Join a team of forensic DNA analysts from the Sacramento County District Attorney’s Crime Lab as they experience the new Applied Biosystems SeqStudio Flex Genetic Analyzer for the first time. You’ll see first-hand all the technological advances for increased flexibility, easier operation, enhanced connectivity, and remote serviceability. Designed using capillary electrophoresis (CE) technology trusted by HID labs for over 25 years, SeqStudio Flex Series Genetic Analyzers for Human Identification deliver the flexibility and accuracy your work demands. The Select Science 2023 Scientists’ Choice Awards winning SeqStudio Flex Genetic Analyzers are validated for human identification applications according to DNA Advisory Board (DAB) Quality Assurance Standards (July 1, 2020) and the Scientific Working Group for DNA Analysis Methods (SWGDAM, December 2016) guidelines across a variety of Applied Biosystems PCR amplification kits. A summary of the developmental validation studies using Applied Biosystems GeneMapper ID-X Software v1.7 will be presented. In this webinar, you will learn how the SeqStudio Flex systems can deliver reliable STR data faster and easier. Flexibility—available in 8- or 24 capillary configurations with four-plate capacity, continuous plate loading, and urgent sample reprioritization Usability—intuitive user interface, one button start-up, auto-spectral calibration, redesigned capillary array, and on-instrument training videos to get you up and running quickly Lab-friendly connectivity—integrate the instrument into your lab via local area network (LAN), Wi-Fi, USB ports, or LIMS compatibility; set up plates and monitor progress from anywhere using the Thermo Fisher Connect Platform Serviceability—remote troubleshooting with Smart Help and Remote Support capabilities may resolve up to 70% of issues using real time audio/video collaboration tools to minimize your downtime.
0:00
Hello, and welcome to Flex Your Power with the Seek Studio Flex Genetic Analy
0:05
zer for
0:05
Human Identification, brought to you by Forensic and sponsored by Thermo Fisher
0:09
Scientific.
0:11
My name is Michelle Taylor, Editor-in-Chief of Forensic, and I will be your
0:14
moderator
0:14
throughout.
0:15
For today's webinar, you can earn one hour of continuing education credit.
0:19
Following the conclusion of the webinar, you will receive an email with
0:22
information on
0:23
how to obtain CE Credit Documentation.
0:25
We have a great lineup scheduled to present to you today, but before we begin,
0:29
I'd like
0:29
to take just a moment to cover a few logistics.
0:33
At the end of the presentations, we will hold a question and answer session.
0:37
To ask a question, click on the "Ask a Question" tab in the upper right corner
0:40
of your screen.
0:42
Please also take note that the right side of the screen features an overview of
0:44
today's
0:45
webinar, as well as more information about our speakers.
0:48
If you have a technical question during today's event, click on the "Test your
0:51
Connection"
0:52
button at the bottom of your screen.
0:54
From there, you can access additional webinar support.
0:57
Please note that we will also have a few polling questions for you in between
1:01
the presentation.
1:02
We also invite you to use the social media widgets beneath the webinar to share
1:05
with
1:06
your friends and colleagues.
1:08
Today, you will join three forensic experts from the Sacramento County District
1:13
Attorney's
1:14
Crime Lab as they experience a new applied biosystems, SEEC Studio, FlexGenetic
1:19
Analyzer
1:20
for the first time.
1:21
Nick Andrews, Product Manager at Thermofisher Scientific will lead the big
1:25
reveal.
1:26
Nick was a practicing forensic scientist in the UK before moving to the US in
1:30
2015 to
1:31
advance his career in human identification at Thermofisher Scientific.
1:35
Nick went from supporting customers as a field application scientist to
1:39
applying his customer-centric
1:40
focus to product management, making sure the challenging work of a forensic
1:44
scientist
1:44
is easy, informative, and innovative.
1:47
When Nick is not working on the future of HIV, he can be found making fun,
1:50
informative
1:51
and YouTube videos to make forensic scientists life just that much more fun.
1:56
Aquabecriminalists successfully complete the first run on the HIV version of
2:01
the SEEC Studio
2:01
Flex, Jill Muelling, Senior Technical Application Specialist at Thermofisher
2:06
Scientific will
2:07
join us for a short technical presentation, reviewing the product's features
2:11
and some
2:11
validation data.
2:13
Jill started her forensic career at a US government laboratory, first as a
2:17
technician,
2:17
and then as a criminalist in the DNA database unit for a total of eight years.
2:22
She then spent five with a research organization working on the Cancer Genome
2:26
Atlas Project.
2:27
Jill joined Thermofisher Scientific in 2016 as a North America field
2:31
application scientist,
2:33
covering the Western states for two years before moving over to HIV technical
2:37
support
2:37
in 2018.
2:38
Jill has spent the last three years in the Forensic Science Applications Group,
2:43
providing
2:43
subject matter expertise during new product development and escalation support
2:47
for global
2:48
HIV field teams.
2:51
Thank you for joining us for today's webinar, and please keep your eyes open
2:53
for an invitation
2:54
to our next one in November.
2:56
Now, without further ado, I'll hand it over to Nick to get us started.
2:59
I'm Nick Andrews, Product Manager at Thermofisher Scientific, part of the Human
3:19
Identification
3:20
team, or HID as it's known.
3:22
Today, we're here in sunny Pleasanton, California, the home of the HID Research
3:27
and Development
3:28
team.
3:29
We have something super exciting to share with you today.
3:32
We are ready to unveil the latest and greatest genetic analyzer, the Seek
3:37
Studio Flex.
3:38
Now you may know that the Seek Studio Flex has been available for the research
3:42
community,
3:42
but we're ready for forensic prime time.
3:45
So today, we have three forensic experts from the Sacramento County Crime Lab
3:50
who are
3:50
here to put it through its paces.
3:52
They'll get to see all the greatest features, like the foreplay deck with
3:55
continuous plate
3:56
loading, sample re-prioritization, the integrated data collection software, and
4:01
the remote monitoring
4:02
and remote troubleshooting features.
4:04
I know this instrument is going to blow them away, and it's going to blow you
4:08
away too.
4:08
So let's go meet the team.
4:09
I cannot wait to see what they think.
4:17
My name is Ryan Nickel, and I work for the Sacramento County Crime Lab.
4:20
I'm a criminalist there, and I'm also a crime scene lead at the laboratory.
4:24
I'm Natalie Jones.
4:25
I also work at the Sacramento County Crime Lab as a criminalist, and I'm also
4:29
the local
4:29
codist administrator.
4:30
I'm Danielle Frost.
4:32
I'm also a criminalist at the Sacramento County Crime Lab, and I'm in training.
4:36
Thank you so much for introducing yourselves, and thank you very much for
4:39
coming in.
4:40
This is great.
4:41
You all seem to have a lot of different experiences, so this is going to be a
4:43
really exciting time.
4:45
Just to confirm, you're all forensic scientists, none of you are paid actors.
4:48
No, I'm an actor.
4:50
So what do you actually know about the Seek Studio Flex?
4:53
It's been out for the research community for a while, so have you heard
4:55
anything about
4:56
it?
4:57
Nothing.
4:58
Only the name, which I saw in the email that we got.
5:00
CE Instrument.
5:01
Yep, that's right.
5:02
It's our brand new latest and greatest genetic analyzer that we have.
5:05
It got released for our research community a while ago, and now we're ready to
5:10
unveil
5:11
it for the HID market.
5:12
So we want you guys to be the first look at this instrument.
5:15
So we're the first forensic scientist to this.
5:18
You're going to be the first forensic scientist in the world to touch this
5:21
instrument.
5:21
Wow.
5:22
That's exciting.
5:23
This is going to be exciting.
5:24
It's cool.
5:25
It's going to be great.
5:27
So if you had a new CE Instrument for your lab, what would you want it to do?
5:31
Would there be anything you'd be looking for?
5:33
I would probably something along the lines of if one plate is running, if you
5:38
could actually
5:39
load a plate on while the other plate is running would be great.
5:44
That would be a big help in our laboratory, for sure.
5:46
Yeah, glad you say that.
5:47
I think it would be nice to be able to load more than two plates.
5:51
Or maybe six.
5:53
That way we can get everyone at the lab working on at the same time and just
5:57
turn the instrument
5:58
on and let it go.
5:59
I would love for the software to be really user friendly and to be able to
6:05
easily load
6:06
on your plate and press buttons.
6:09
That's smart.
6:10
Say go.
6:11
And you mentioned that you were currently in training.
6:14
So how has it been learning how to use CE in the application of forensic DNA?
6:21
It's been challenging just learning memorizing the steps.
6:27
There's so many steps that come with the CE in managing the software.
6:34
So it's a question of where do I look for this button.
6:39
It's kind of hidden away in this corner.
6:41
That's been difficult.
6:43
Right.
6:44
Yes.
6:45
I know for my time in the lab.
6:46
You all have 3,500s in your lab, correct?
6:48
Yes.
6:49
Yeah.
6:50
What's using about the 3,500 or how has it helped you?
6:52
I like the anode and cathode buffer that it's just you don't have to load it or
6:58
make any
6:58
mixture.
6:59
It comes in a pre-made box.
7:01
You can throw that right on.
7:02
I also like the, you know, it scans the polymer for us and tells us how many
7:08
injections.
7:09
So that's nice.
7:10
I like that we have our lab uses 24 capillaries.
7:15
So we can get through a lot of samples pretty quick.
7:17
Yeah.
7:18
We use USBs.
7:19
We have to go into the run room, load it onto the USB, take it back to our desk
7:23
, load it
7:24
into the software.
7:25
So I hadn't thought about that, but that would be nice if we could like remote
7:28
into
7:28
that computer from our desk, pull our data, put it right into the software.
7:33
I would love that.
7:34
Yeah.
7:35
I'm sure actually other analysts that are, you know, we're allowed to work from
7:38
home
7:39
a couple days a week, would actually like to remote in, get their data and
7:42
actually
7:42
analyze data from home.
7:43
So if you need some re-injections, you don't have to worry about re-plating
7:47
when you come
7:47
in the next day.
7:48
Yes.
7:49
Yes.
7:50
Can this instrument tell us at our desk that something's wrong?
7:54
We can pop in there and fix it.
7:56
Well, I don't want to give too much away, but it might have some of these
8:00
speeches that
8:01
you've been looking for.
8:02
I like it.
8:03
I'm pretty happy that you brought these up, but I think maybe we should
8:06
probably get
8:06
in there and actually see this instrument.
8:08
All right.
8:09
Let's see it.
8:10
Cool.
8:11
Let's do it.
8:12
Okay.
8:19
Oh, Ryan, Natalie, Danielle, Eager Beaver.
8:37
I would very much like to introduce to you the new six new blocks.
8:42
Wow.
8:43
Very sleek.
8:44
Yes.
8:45
Ooh.
8:46
That is cool.
8:47
No, can I have that?
8:49
Yeah.
8:50
How can we touch it?
8:52
Go ahead.
8:53
I had my phone.
8:54
Now you can get in there.
8:55
It looks very similar back there.
8:58
Yeah.
8:59
Can we take a closer look?
9:00
Please.
9:01
I'm assuming touch screen.
9:03
I want to know how many plates.
9:04
Can I touch the screen?
9:06
Can we open it?
9:07
Yeah.
9:08
Boo.
9:09
Four plates, guys.
9:10
Four.
9:11
Let's see.
9:12
The door is unlocked.
9:13
Go ahead.
9:14
To, oh, they're not there.
9:17
They're there.
9:18
Yep.
9:19
That's fun.
9:20
Oh.
9:21
So you can load while it's running.
9:23
Yes.
9:24
Wow.
9:25
Continuous plate loading.
9:27
Sample re-prioritization.
9:29
So you can load a plate.
9:30
It could be injecting.
9:31
You could then load another plate.
9:32
You could say my injection is more important.
9:34
You could put that to the top of the list and it will take that plate.
9:37
You could have four plates in there.
9:39
When one plate is finished, you could open that drawer, take it off.
9:41
And there's a new spot open again.
9:43
You could maybe wait until the end of the day, load four plates at once and it
9:46
can just
9:47
run all night and then you can come back into data in the morning.
9:50
I know one of your concerns might have been about, well, what happens if there
9:54
's an injection
9:55
failure or something like that?
9:56
But this also has a remote monitoring.
9:57
So you can get alerts at your computer.
10:00
You can get them on your phone.
10:02
You can even do re-injections from your phone with this instrument.
10:05
So if you are working remotely, you can do that.
10:07
Yes.
10:08
And for those of you who may be using 3130 back in the day, or you had the
10:11
bottom, you can get the barn doors.
10:12
This instrument has the same type from there.
10:15
Very cool.
10:16
Easy to get in there.
10:17
Obviously your oven door.
10:20
You may not be able to newly designed array as well.
10:23
So it's actually easier to install than even the 3500.
10:26
I love that.
10:28
It looks easier too.
10:29
You can kind of see just where the little buttons are there.
10:32
Pop in out.
10:33
Exactly.
10:34
So can I open the drawer right now to the instrument?
10:36
Yeah.
10:37
As long as that screen says the drawer is unlocked, you can open that drawer at
10:39
any
10:40
point.
10:41
Go ahead.
10:44
My question was, is there like an arm that kind of grabs those plates and takes
10:48
it up
10:48
to be analyzed?
10:49
That's exactly right.
10:50
So the arm will pick up the plate and move it up to where the capillaries are
10:55
so you
10:55
can actually do the injection itself.
10:58
So that drawer is unlocked at any point during the run so you can load plates.
11:01
The only time it would be locked is when an injection is in place.
11:05
Just for safety reasons, you've got high voltage running through there.
11:08
But otherwise you can load plates on there.
11:10
That screen will also tell you when you have plates that are present on there
11:13
so you can
11:14
see what is linked and you know if there's available space on it.
11:18
And do this plates set in or do they clip in?
11:21
They just sit on top of there.
11:23
So as long as you put them in that plate cradle, then they just sit in there
11:25
and they wait
11:26
for the arm to come and pick them up.
11:27
Very cool.
11:28
What about the runtime?
11:30
It's actually about the same as the 3500.
11:32
So it's kind of around the same time that you had before.
11:34
A couple of other features while we have the drawer open, there's also an
11:37
integrated barcode
11:38
scanner in there.
11:39
So if you use barcoded plates, it can read that so that you actually know what
11:43
you're
11:43
linking and you can verify it.
11:45
As before, you just have to make sure that you put the plate in the right place
11:49
This time you don't.
11:50
I see two USB ports right there.
11:53
Is that to like bring in our data and it automatically kind of populates into
11:57
the screen
11:58
there?
11:59
So we knew that there's obviously a lot of different options that you can have
12:01
when you
12:01
want to transfer data.
12:03
This instrument does have cloud connectivity and local area network as well.
12:07
So you can network the instrument on your local area network in the lab.
12:12
You can set up your plates from your office and you can have those plates
12:15
loaded directly
12:16
onto the instrument through a piece of software called plate manager, which we
12:19
'll show you
12:19
in a bit.
12:20
And then you could also do a USB so you can put it into like your standard CSV
12:24
or text
12:24
file, load it onto the instrument or you could do it through the cloud.
12:29
So you could use plate manager on the cloud, set up your plate and it will
12:32
remotely send
12:33
that plate to the instrument itself.
12:36
That's cool.
12:37
A bunch of different options.
12:39
One thing I did want to do is introduce you to two of our R&D scientists who've
12:43
been working
12:44
really hard on the validation of this instrument.
12:46
They are going to help us set up a run and get the instrument going and teach
12:49
you how
12:49
to use the instrument thoroughly.
12:51
So what do you say we go meet them?
12:53
Yeah.
12:54
All right.
12:55
Hi everybody.
12:56
My name is Dan Sunil.
12:57
I'm a staff scientist and summer fisher.
12:59
I've been working on this project for over one year.
13:03
So today I'm going to show you how to use the plate manager.
13:08
That's software used for creating your files for running the samples on six UDF
13:15
lex.
13:16
So we have two different versions.
13:19
So one version is on the cloud.
13:22
Another version is on the desktop.
13:25
So this is the version on cloud.
13:28
So you can create your file from the scratch by clicking on the sky here or you
13:35
can open
13:36
a file which has been saved on cloud or from your computer.
13:42
Or if you want to use a recently used file, you can click on this one.
13:49
You can check to see whether it's correct or not.
13:52
Everything is correct so you can send this to the machine directly.
13:58
You can choose multiple instruments at the same time and click on OK.
14:03
So then this file would be sent to your instruments.
14:07
Or you can just choose one of them.
14:09
So like today, I'm going to just send this one to this instrument.
14:14
So after you see it, you just click on OK.
14:18
So now the file is on your instrument.
14:21
You're ready to run your sample on the instrument.
14:26
And also, I'm going to show you how to create a file using the plate manager.
14:35
I will be using the desktop version today.
14:39
So I'm going to show you how to create a plate file from the scratch.
14:43
So to do that, just click on this one here.
14:47
Then you get all of these things by default.
14:51
You can change your name here.
14:54
You can change the name of the file.
14:56
Or you can just use the default file name.
15:00
If you say OK, all the parameters here are correct.
15:05
So you click on Next.
15:08
Then you can click on the carbon.
15:12
You want to put your samples in.
15:14
Then you can come here.
15:17
From here, you choose the injection protocol.
15:22
So today, I'm going to show you how to choose this one.
15:26
That's for the J6 die.
15:30
So after you click on that, see all the other parameters, you know, show up
15:36
here.
15:37
After that, you click on here.
15:39
So then you can put the name of the files in there.
15:44
So what I do, I just, you know, I have prepared everything.
15:49
So I just copy the thing here and then paste it to the software.
15:59
Sample name, I click on this one and contove it.
16:02
So then the file names are pasty here.
16:05
And also, you can put the panel names here.
16:12
So these are the panel names.
16:14
All of them here, I use a global file, IQC panel.
16:20
So click on the software here.
16:25
So then you get to this panel.
16:30
OK, so you click on the first one, you click on Contove here.
16:36
So the file, these are the panel names.
16:40
And then I put the catalynx here.
16:43
Highlight everything here and then Contove C.
16:52
And put it into the first custom fields.
17:00
Then Contove.
17:01
OK, after that, you go here.
17:06
You save it and then it's saved.
17:12
After you saved, you can put send it to the instrument.
17:16
Or you can export it into your USB drive.
17:22
So I can export it to either my computer or USB drive.
17:26
So save.
17:29
Now, it's saved in this USB drive.
17:33
And then I'm ready to use it.
17:37
Is the computer attached or connected to the instrument at all?
17:42
Yeah, so these computer is connected to the instrument
17:47
through Wi-Fi.
17:48
Gotcha.
17:49
Nice.
17:50
And at our lab, we use an Excel program.
17:53
Our sample names and information.
17:57
So we would be able to export that in a CSV file
18:01
and then load it into the software rather than manually
18:04
setting up our plate.
18:06
Yeah, so you can do that.
18:07
So basically, after you set up the plate,
18:10
use the plane manager.
18:11
Or you have a CSV file installed in the--
18:16
on your computer or USB drive.
18:19
So instead of a computer, can you use your phone to do this?
18:24
Yeah, you can use your smartphone.
18:27
Do the same thing.
18:29
You can monitor your rung.
18:31
And also, you can unlink or link your plate.
18:34
If you found that after you go home,
18:36
or if you are somewhere else far, far away,
18:40
if you just thought, oh, I made a mistake.
18:44
So you can make the revision of your protocol using your cell
18:50
phone or your computer remotely.
18:52
Nice.
18:53
That's really cool.
18:54
A good feature.
18:55
Yeah.
18:55
Oh, now the plate is in the same location.
18:59
Right.
18:59
You don't even need to come here to unlink the plate.
19:03
You can just use that with your--
19:05
Or set my injection before his.
19:07
[LAUGHTER]
19:08
Right.
19:09
OK.
19:10
I also really loved that each injection was a different color.
19:13
That was very pleasing to the eye.
19:15
Yeah, exactly.
19:15
And I knew too.
19:18
So if there's somebody at your lab that always thinks their case
19:22
is the most important and wants to jump in front of everybody
19:26
all the time, is there a way to prevent plates
19:30
from getting bumped to the front?
19:32
I think that would be a very good feature.
19:34
But all these things should be tracked in the SAE feature.
19:40
So we could know who jumped in front of my run.
19:43
Got it.
19:43
Exactly.
19:44
[MUSIC PLAYING]
19:47
Hi, my name is Jimmy Lee.
19:52
I am a staff engineer at Thermo Fisher.
19:54
I will be showing you the 6-3 of Flex.
19:56
So this is their new instrument.
19:58
So I'll have Ryan come and play with the instrument,
20:00
if you want to.
20:01
Sure.
20:02
All right.
20:03
So if you want to load, I know Leonton helps you set up a plate.
20:07
So here, I'm going to hand you that plate.
20:09
You can open the drawer.
20:10
So there's positions A, B, C, and D.
20:16
Already two have been filled.
20:17
So you can put it in C or D.
20:18
OK.
20:19
I'm going to go with D.
20:21
Oh, I already--
20:22
Oh, Zuzi.
20:22
--flight it in.
20:24
There you go.
20:25
It will lock once you close it.
20:26
But now you can link your plate, which has already
20:28
been loaded on by Leonton.
20:29
So click Link Plate.
20:31
Yep.
20:32
Go to My Instrument.
20:35
And it's right there at a demo 8 cap.
20:37
OK.
20:40
And then you can check all of the properties.
20:42
So you click on Application.
20:46
Click on Application.
20:47
Oh, there it is.
20:47
OK.
20:48
So you're already on HID 96 will plate.
20:51
36 centimeter pop 4.
20:52
Click Done.
20:54
Go to Plate Screen.
20:57
And here we're going to do an injection from column 2.
21:00
OK.
21:00
Yeah.
21:00
If you want to see what it is, you can go and highlight it.
21:04
And those are your parameters.
21:06
And you can click on the pencil button.
21:09
And then you can scroll and see all the configurations.
21:13
Nice.
21:13
Side-standard.
21:14
OK.
21:15
For the most part, you have your J6 sample in there.
21:18
Yep.
21:18
You click Done.
21:20
And when you're ready to run, click Start.
21:22
Start Run.
21:23
Yeah.
21:23
Is there a way to check the names of the samples that are in there?
21:27
Go back to that pencil.
21:29
You can go to a sample name.
21:30
Click on multiple.
21:32
And here is where you can enter all of your names in.
21:34
Oh, gotcha.
21:34
And it's already pre-named in here.
21:36
Right.
21:37
There's the A.
21:37
And you go to Sample Type.
21:39
And change the--
21:40
You can go there.
21:41
And then he's the first one to a little glatter.
21:44
The rest are sample.
21:44
Gotcha.
21:45
OK.
21:46
Cool.
21:46
Yeah.
21:47
And then--
21:47
And then--
21:48
Start.
21:48
Start Run.
21:49
There you go.
21:49
Right on.
21:50
Go do some free checks to make sure
21:52
the consumables are not expired.
21:53
And it'll give you an estimated end time.
21:57
And there it goes.
21:58
Nice.
21:59
That starts up really fast.
22:00
Yeah, it did.
22:01
Did it have to preheat?
22:03
So if you did impreheat your oven,
22:05
then it will have to preheat.
22:05
You can actually do that before you run.
22:07
If you hit that speedometer symbol on the top.
22:09
Yep.
22:10
If you scroll to the left, there's a pre-oven option.
22:16
But it's already heating up right now.
22:17
So it's disabled.
22:19
OK.
22:19
So you don't have to worry about that.
22:20
But you see the oven temperature is already at 31 degrees.
22:23
So--
22:23
Do you guys recommend preheating?
22:25
Or is it not necessary?
22:26
If it's already warmed up, it'll run faster.
22:29
How long to preheat?
22:30
Maybe like 10 minutes before you start your run.
22:32
Yeah.
22:32
I like that the things you can't select are grayed out
22:36
and things you can are blue.
22:38
So you can also turn on the LED to highlight
22:40
some of the instrument stuff.
22:41
So--
22:43
There.
22:43
Turn on some of the consumables.
22:45
Yeah.
22:46
Since it's running, you can't really open a door.
22:47
But there's that CBC buffer right there.
22:50
It's going with the polymer pouch and then the ABC buffer.
22:54
Same array.
22:54
It's slightly different from the 3500,
22:56
but similar format here.
22:58
So this is the 24 cap array.
23:01
OK.
23:01
So you open the oven.
23:02
You just easily install it and you want it to.
23:05
OK.
23:05
Did you change anything on the consumables as far as like--
23:09
they can only be on the instrument for two weeks?
23:11
Yeah.
23:11
So if you go back to the right on the screen,
23:14
it shows you all of your status of the consumables.
23:16
So the capillary, how many injections
23:19
has left, the polymer, and the installation date
23:22
and the expiration date, as well as your buffer.
23:25
And here's your spatial calibration, your remaining
23:28
injections, and then all the calibrations that
23:30
were done for your die sets that you can run.
23:32
And then on this side, you should see
23:34
some of the maintenance stuff that needs to be done.
23:37
Some of them you might need a software update from time
23:39
or time, but it'll tell you when you need to do all your maintenance.
23:42
OK.
23:43
And like the wizards for that stuff.
23:46
Yeah.
23:47
Good.
23:47
Yeah.
23:47
You want to go to that, to X out of that?
23:49
Sure.
23:51
Click on action.
23:53
Click on maintenance.
23:56
Yep.
23:56
And then maintenance wizards.
23:59
So here you have a list of anything
24:00
you want to do for maintenance.
24:01
You can change your array, change your polymer type,
24:04
change your buffer, change your polymer.
24:06
And each of them have a video embedded,
24:08
so you can actually watch some of them for a little bit.
24:11
So now, like I showed you before,
24:14
you can actually run multiple plates at a time.
24:16
So click home.
24:19
So now it's unlocked, so you can open it up.
24:21
OK.
24:22
You put that in position C. All right.
24:28
Oh, lock again, but now you can link a plate.
24:31
So create a new plate file.
24:34
And here, you can name your plate.
24:37
So just click click name.
24:38
Yep.
24:40
Type whatever you-- today's date.
24:42
OK.
24:44
Play 2.
24:45
All right, enter.
24:47
Go to application type.
24:49
Like that.
24:51
Change it from sequencing to HID.
24:54
Yeah?
24:54
Done.
24:55
Yeah, done.
24:56
Go to your plate.
24:58
And then you can click on the pencil button.
25:01
Click on injection protocol one time.
25:05
Yeah.
25:05
And then you can pick which die set you want to run.
25:08
OK.
25:10
And then you can change any of the--
25:12
so this injection protocol pre-populates these fields
25:14
for you.
25:15
If you want to do any of the custom ones,
25:16
you can change them here.
25:19
So done.
25:20
Done.
25:21
And start.
25:21
Start.
25:23
So will it run in the order that you set it?
25:27
So this will run after the first one is done.
25:30
If you wanted to change it--
25:31
since it's already started, you can't do that.
25:33
But you go to run queue, you'll see the order of things
25:36
that will be done.
25:37
So I can take plate 2 and go--
25:40
Right.
25:40
Right.
25:41
--top of the list.
25:42
Right.
25:42
So these ones are completed.
25:44
So plate D is running.
25:46
So your plate C is going to run afterwards.
25:48
So it's in queue.
25:51
And it'll show you the estimated start at end time.
25:53
OK.
25:54
So you have to remember where you loaded it.
25:57
Exactly.
25:57
OK.
25:58
Nope.
25:59
So you can click close.
26:02
And since these are already done,
26:03
you can actually look at some of the data on there.
26:05
So you click on the screen.
26:07
Click real sample list.
26:10
So that's what we ran.
26:11
This is just the installation run.
26:12
So you click done.
26:14
Click on action.
26:15
So you can either unlink.
26:19
But if you want to look at the data,
26:21
click on the green icon.
26:23
And that's what was run on that plate.
26:25
So you can use the screen to scroll through,
26:28
expand that blue bar if you want to.
26:31
That's cool.
26:34
No.
26:35
Click on any of those--
26:37
the bullet point buttons.
26:39
And then you can select dies that you want to see.
26:41
Oh.
26:42
I have been.
26:44
Yep.
26:44
So you just turned off blue.
26:46
Oh, I'm turning off.
26:47
Yep.
26:47
Good.
26:48
Yep. So now you're just looking at the size standard orange.
26:53
There you go.
26:54
And then when you want to bring the samples back in,
26:56
just click on the color again.
27:00
And on the right side, there's another option
27:04
where you can zoom in and--
27:08
Oh, there you go.
27:09
Mm.
27:12
And then the middle button is the EPT.
27:15
So it shows you the record of all of your run.
27:19
It's the oven temperature, your current, your voltage
27:23
throughout your entire run.
27:24
So same thing, same touch face, touch me in the face.
27:28
And then when you're done with that, stick done.
27:31
Good done.
27:33
I like that black background.
27:34
It's so much easier to see the colors than the white.
27:37
Yeah.
27:38
So let's say you want to run another plate.
27:40
These all are filled.
27:41
You can unlink a plate by just pressing B.
27:43
Do you want to try it?
27:44
OK.
27:45
Sure.
27:46
Unlink the plate.
27:47
It's going to confirm that you want to do that.
27:50
So now you can open the drawer.
27:51
Right.
27:52
Remove the plate.
27:54
And if you have another one ready to go, you can pop it.
27:56
Oh, and it shows that it's removed.
27:58
It will sense the plate right over there.
28:00
Yep.
28:00
So I'll take that.
28:01
OK.
28:02
So now you can leave it there, load another plate, or--
28:06
Awesome.
28:07
I have it on standby.
28:08
Yep.
28:08
Very cool.
28:10
I noticed this is your computer now.
28:12
You're not hooked up to a computer.
28:13
So currently, we--
28:17
to do like a reboot of the system every two weeks,
28:19
we'll shut down, shut down, restart, restart.
28:21
So you don't need to do that for these?
28:23
Yeah.
28:23
If you want to restart for any reason,
28:25
you can just power off when no place are on there,
28:27
not running, and power back on.
28:29
Is that something recommended, or can we just leave it on?
28:31
You can leave it on.
28:32
Yeah.
28:33
No reason I would need to turn it off, though.
28:36
Nice.
28:36
Nice.
28:37
Yeah, yeah.
28:38
We talked a little bit earlier about having the computer
28:41
and the instrument hooked up to Wi-Fi,
28:43
and being able to control it from your phone and everything.
28:46
Forensic labs are always concerned about security.
28:49
So I wanted to ask about that.
28:50
Right.
28:50
So these instruments can be controlled with SAE.
28:53
So it's the security audit and the e-signature functions.
28:56
So if you have it on the network,
28:58
if anyone logs in, they have to have their own account login.
29:01
If they want to start a run, they
29:03
have to have permission to sign off.
29:05
If you don't want to have it on a network,
29:06
you can have a local computer attached to the instrument.
29:09
And it's also controlled by SAE.
29:11
Wi-Fi free, just local area, just within house.
29:15
So no internet needed.
29:16
Yeah.
29:17
And then as soon as this run is done,
29:19
we can access it on the computer, any computer,
29:23
with a Wi-Fi on our phone.
29:26
Yeah, you can do remote access.
29:28
I do have it on my phone.
29:29
It can monitor run, and I can show it at as well.
29:32
[MUSIC PLAYING]
29:34
So for my remote monitoring app, you can do remote monitoring
29:41
your run.
29:42
So here it has a run that's already completed.
29:44
Click on your raw plot.
29:46
And now, Ryan, you can scroll the data on the phone,
29:49
just like you would on the flex.
29:53
You can see all the peaks.
29:55
And you can click on different capillaries on top.
29:59
And then you can feel it's bright color.
30:02
And then just--
30:03
On the back.
30:04
Still.
30:05
Yeah.
30:06
Apply.
30:07
There you go.
30:07
That's always your size standard.
30:09
Yeah.
30:11
Scroll and go to all the capillaries.
30:15
And it will save your preference on color.
30:16
All right.
30:20
Nice.
30:21
There you go.
30:22
So what's coming off the instrument is being directly
30:26
screened to your phone.
30:27
Exactly.
30:28
Yep.
30:29
Like it.
30:29
Thank you.
30:30
[MUSIC PLAYING]
30:33
[CHEERING]
30:35
[MUSIC PLAYING]
30:37
[CHEERING]
30:38
[MUSIC PLAYING]
30:41
So we'll have a look at the seats to be a flex a bit.
30:43
I know we talked about how the consumables are the same,
30:47
except from the array.
30:48
So I just wanted to show you really quickly
30:49
how you can change the array in that sort of process.
30:52
But you could open it up these big barn doors.
30:56
And then if you want to open up the array,
30:58
that means we'll get you to do it.
30:59
Just show you how easy it is.
31:01
Open the array door.
31:02
Unscrew the detection cell.
31:07
Loosen the cap bundle.
31:12
Here you go.
31:13
And then loosen the bottom door.
31:17
It's down here.
31:20
There you go.
31:20
And you can slide that out slightly.
31:23
And then you can just use this little handle here
31:29
and just pull that out of there.
31:32
And it will hold it in place.
31:35
Let's remove it.
31:38
Great.
31:39
Where am I?
31:39
So the very nice thing about these new arrays
31:41
are they have--
31:44
to make it easier to do it one-handed, they lock in place.
31:47
So you can hold it to it and you can install the array one-handed.
31:50
So it'll stay like this when you want to load it back
31:52
into the instrument.
31:53
Just slide it in place like that.
31:58
And then you can release it.
32:01
Feed it into the bottom.
32:02
The detection window is automatically there.
32:04
It's in the right place.
32:05
The instrument knows where it is.
32:07
So you can just tighten everything back up again.
32:09
Close the doors.
32:10
Tighten your football.
32:17
The feral at the end.
32:18
And that's it.
32:19
That's changing the array.
32:20
Easy, easy.
32:20
Wow.
32:21
Very easy.
32:23
The nice thing about this instrument, the very cool thing
32:26
is, when you change your array, what do you normally
32:28
have to do after that?
32:30
You run a spectral and a spatial.
32:32
Right.
32:32
So you run the spatial because that's
32:34
how the instrument knows where each of the capillaries are.
32:37
You run the spectral because that's
32:38
teaching the instrument the die set
32:39
that you're going to be using for that.
32:41
And to make sure it's applied to this new array.
32:45
The nice thing about this instrument,
32:46
you only need to run that spectral once.
32:49
That's crazy.
32:51
Throughout the entire life of the instrument.
32:53
Correct.
32:53
The instrument will remember the spectral you have run.
32:56
As long as you're running the same die set for that chemistry,
32:59
it will continue to apply that every time you change the array.
33:03
That's really cool.
33:04
It's incredible.
33:05
Yeah. That's amazing.
33:06
I'll get them remembers it.
33:07
It makes sure your data is still there.
33:09
The only time you will ever need to run the spectral
33:11
is if you change die sets.
33:12
So a different type of chemistry.
33:14
Or you are troubleshooting.
33:16
Wow.
33:17
So it can save you a lot of time running this instrument.
33:22
Especially it's one of those things.
33:23
It's like, I feel like we do it, but not enough to really learn it well.
33:28
Every time you do it.
33:29
So we never have to learn it again.
33:32
Exactly.
33:32
Break out the manual every time.
33:35
Every single time.
33:36
And the other thing.
33:37
So obviously, a lot of these things on the instrument,
33:39
you don't have to do that often.
33:40
So what we do have on this instrument as well
33:42
is to help you is called the learning center.
33:45
So if you go to Actions and then Learning Center,
33:50
from here, you have helpful videos that you can run
33:54
that will walk you through when you need to do
33:57
different steps on the instrument.
33:59
So if you want us to learn about how to set up a run on the instrument.
34:02
And it will take you through all the steps you need to
34:14
on how to run and set up a run.
34:16
Wow.
34:17
That's cool.
34:19
For me, I learned a lot better with videos, too.
34:21
Like, hey, here's how you do this.
34:22
Instead of reading something that makes it a lot,
34:26
a lot more difficult to be like, oh, take the plate and put it here,
34:29
do this.
34:29
It's like, oh, video shows you exactly how to do it.
34:32
So now we have everything for a visual, kinesthetic,
34:35
learners, no matter what you do.
34:37
Yep.
34:37
This is really great for new analysts also.
34:41
New analysts, maybe analysts who haven't run the CE in a while,
34:44
you're just coming back into the lab.
34:47
It's just making it so that it's easy.
34:48
It's approachable, and you just know what you're doing.
34:50
Yeah.
34:51
Yeah.
34:51
So you can always feel confident when you run the CE in Studio Flex.
34:56
So back to the old school almost.
34:59
Barn doors feels nice.
35:01
But I also like the familiarity with it, too.
35:04
It has this-- you haven't changed everything inside.
35:08
We don't have to learn an entirely new instrument.
35:10
It's just almost like an upgrade to the instruments
35:14
with a whole bunch of cool features.
35:16
[MUSIC PLAYING]
35:20
All right, guys.
35:24
We've had a really exciting day and an action-packed day
35:27
learning all about the CE in Studio Flex.
35:29
I really just want to know what you guys think about it.
35:30
It's awesome.
35:32
I think that design is really sleek.
35:34
It's user-friendly.
35:36
You can take your data on the go.
35:39
Yes, I love the onboard computer,
35:42
so you don't have to restart and link these two separate things.
35:46
And that you can remote in and from home or from your desk,
35:50
monitor your run, set re-injections,
35:53
put your plate before your coworkers.
35:56
Exactly.
35:57
Yeah.
35:57
And I even heard you ask some really important questions
35:59
about data security and stuff while you were there.
36:01
I mean, that is something that we know
36:03
is a huge challenge for forensic labs.
36:06
The world is moving connectivity and cloud-based things.
36:08
And that's why at Thermofisher, we
36:09
have a group that is dedicated to testing vulnerabilities
36:14
on our software and our cloud-based systems.
36:16
And we have teams that are actually there helping you
36:18
so you can bring online and work with your IT groups
36:21
within your lab to figure out what is possible to do
36:24
within your lab.
36:25
Because what we're finding is there's a lot of stuff
36:27
that we can actually do and still be very secure.
36:29
The old-school methods of actually using USBs
36:32
is not the secure method anymore.
36:33
It's actually having connectivity with encryptions
36:36
and secure passwords.
36:38
So it's going to be really exciting for the future.
36:40
And this instrument is definitely going to take us there.
36:43
I also like the footprint of this instrument.
36:46
For something that can hold four plates
36:48
and kind of run all of these things,
36:49
it's about almost the same size as the 3500.
36:53
So it's taken up a nice small amount of space.
36:57
As long as it's deep enough at your lab,
36:59
you can get a couple of these, I think.
37:02
And you don't need that control computer, either,
37:05
if you don't need to.
37:05
So there's a special bench real estate here.
37:08
A lot less.
37:09
Yeah.
37:10
And being able to put another plate in the queue,
37:12
while one is running, that feature I absolutely love.
37:15
I've spent a lot of time waiting for my co-workers
37:18
to finish up their run before I can even
37:20
start propping my plate.
37:22
And how do you think that this would benefit you
37:24
in your lab?
37:24
New instruments or kind of new technology
37:27
comes out once every five years or so, I feel like.
37:29
And this is just kind of taking us to that next step
37:32
of the fact that it has the Wi-Fi capability
37:36
or the cloud-based capability.
37:37
It just kind of has that feel of, hey,
37:40
we are getting into that next generation of instrumentation.
37:45
So I like it.
37:47
It's staying current with everybody else's phones
37:52
and computers and what we're used to instead
37:55
of running on some old instruments.
37:57
Exactly.
37:58
And if your lab is not ready for that,
38:00
you can also do it the standard way as well.
38:01
So it's very versatile in that sense.
38:04
But it's going to be ready for the future when we're there.
38:07
Yeah, the fact that you still have the USB, people
38:09
like to get in their steps still.
38:11
So it's like, hey, you don't have to use your phone.
38:13
Go and get those steps and walk to the instrument again.
38:17
Take it off and take it back to your desk.
38:20
And what do you think about the onboard learning center?
38:23
Yeah, do you think that will help you in the lab?
38:24
I do.
38:26
Because I know sometimes when you have to put new polymer on
38:30
and you haven't had to do that in eight months,
38:32
I have to pull out that manual and figure out
38:35
how to reload my polymer or something.
38:37
So now I can just play, see how to do it, pop it on,
38:40
and I don't have to worry about it.
38:41
Yeah, the fact that you can actually pause the video too
38:44
and do that while you're doing it.
38:48
The doors are separate from the computer screen.
38:50
So you can just pause it, do that, OK, click play
38:54
and continue on.
38:55
It's nice.
38:56
And watching the video of it happening in real time
38:59
is a lot easier than having to read through the wizard
39:02
like we do now.
39:03
So that's really nice.
39:04
And what about the startup sequence?
39:06
Do you guys think about that?
39:08
I think it's great because currently, like I said,
39:11
earlier with the computer next to your instrument,
39:15
you have to turn this off, turn this off, turn this on,
39:18
turn this on, wait for a green light, open your software.
39:21
So now it's just one button, turn the instrument on,
39:24
and you're ready to go.
39:25
And what do you think about the array?
39:27
This was absolutely amazing.
39:28
So can I--
39:29
Yeah, please.
39:30
So you literally just squeeze that and it releases.
39:36
That's really cool.
39:37
Exactly.
39:38
That was something I didn't know that I needed.
39:39
Yeah.
39:40
Exactly.
39:41
No more fumbling around with the detection cell window,
39:43
trying to get that in place with the magnets
39:45
and then making sure it's just right.
39:47
Not breaking it?
39:49
Not breaking the array.
39:50
That's key as well.
39:52
But yeah.
39:53
Yeah, I was always worried.
39:54
I'm like, ah, capillary needs to be changed.
39:57
I'm like, maybe I'll just pretend I didn't see it
39:59
on the instrument.
40:00
Someone else will change it because it's like this thing.
40:02
It was like, you know, kind of all over the place.
40:04
So it's nice that it's everything's kind of in place.
40:07
You know, a couple clicks, a couple knobs to turn
40:10
and it's in and ready to go.
40:12
Yeah, you can do it one-handed.
40:15
No more three hands and tape kneaded.
40:18
I know we've had an action-packed day.
40:20
It has been super exciting from our side.
40:21
Then we're Fisher Scientific has loved having you here.
40:24
So thank you so much for taking the time.
40:26
It has been great.
40:26
I really hope you got a lot out of it.
40:28
And I can't wait until the next video.
40:30
Thanks so much for having us.
40:31
This is wonderful.
40:32
I had a blast.
40:33
You were the first accredited forensic scientist
40:36
to do a run on the HID version of the Seac Studio Flex.
40:41
This is great.
40:41
Thank you guys so much.
40:42
Thank you.
40:43
Thank you.
40:43
[MUSIC PLAYING]
40:46
Hi.
40:56
Good morning.
40:57
Good afternoon.
40:58
Good evening.
40:59
I'm Jill Muelling, senior technical application specialist
41:02
with Thermo Fisher Scientific.
41:05
Today we're going to review some of the features you saw
41:08
in the unveiling video and go through some validation data.
41:12
So let's get started.
41:14
The first thing we're going to talk about is usability.
41:17
Let's take a minute and recap some of the new features
41:20
the Flex offers that increase usability.
41:23
One of those is the user interface,
41:26
which has the same design as our other newer applied biosystem
41:30
instruments, making it intuitive and easy to use.
41:34
Advancements with the Flex include a run queue screen
41:37
that allows users to reorder injections
41:40
and prioritize newly loaded samples.
41:43
On this screen, I'm showing a plate in position A.
41:46
So plates could be loaded in positions B, C, and D
41:49
in the plate drawer, as long as the instrument is not
41:52
actively injecting.
41:54
Any injections on those plates can then
41:56
be reordered by moving injections up and down in the queue.
42:00
Similar to the 3,500, you can also
42:02
decide to re-inject samples with either the same injection
42:05
parameters or different parameters,
42:08
say if you wanted to change the injection time.
42:12
On the next screen here, you'll see
42:14
one of the new support screens that we have enabled
42:16
on the seek studio Flex.
42:19
SmartHelp allows users to connect with our technical support
42:22
and instrument services team by email or voice message
42:25
and easily select the option to include any instrument log
42:29
files.
42:30
These features do require a thorough Fisher Connect
42:32
account to be enabled.
42:34
The instrument also has a remote support function
42:38
that only requires an internet connection
42:41
if you need to troubleshoot quickly,
42:42
within an engineer, or tech support
42:45
so the representative can remote into the instrument computer
42:48
and see what the user is seeing.
42:50
Another powerful improvement is that on instrument data
42:53
can now be analyzed from anywhere
42:55
using the remote monitoring software
42:58
through Thermo Fisher Connect.
43:00
Here I'm showing an allelic ladder from Global Filer Express,
43:03
along with its associated sample quality flags
43:06
and sizing quality for the entire injection.
43:09
When sizing quality flags are present,
43:12
a reinjection can be set up remotely,
43:14
or the run can be paused until you
43:16
are able to get in front of the instrument to troubleshoot.
43:18
When we look at the features of the Flex
43:21
and then combine it with the new features available in GMAP
43:24
or IDX version 1.7, the analysis time
43:27
can be reduced even further.
43:29
Some of the GMAP or IDX features include the option
43:33
to add a text block directly to the Electrophirogram
43:36
for second review without printing
43:39
and easier ways to view Stutter and Marker specific thresholds.
43:43
On this Electrophirogram, the Stutter peaks
43:45
that are filtered are shown here in gray.
43:48
Marker specific thresholds are seen on the right side
43:51
of any of the marker headers.
43:53
In this example, a Marker specific threshold of 500 RFUs
43:57
was applied to DYS 391.
44:00
Pullup detection is a new algorithm
44:02
that can either delete or label
44:04
a identified pullup as an artifact
44:07
that isn't removed by the auto spectral calibration.
44:10
All right, so here's what that means in GMAP or IDX.
44:13
You can see the analytical threshold
44:15
and Stutter visualization are both plot settings
44:19
that can be turned on and off simply
44:21
by going to those checkboxes.
44:24
The pullup ratio is in the analysis method
44:27
and is applied to the data.
44:29
Our validation specifically used the default values shown here
44:34
and looked at labeling or deleting pullup
44:36
that was less than 5% and that was offset
44:39
from the parent peak by no more than two data points.
44:42
Manual pullup can be a bit more subjective
44:45
and could expand out past half a base pair.
44:48
So a lab would really want to optimize
44:50
and validate these settings as part of their workflow.
44:53
All right, let's now get into resolution.
44:56
With any new CE system,
44:58
you want to be confident that you're getting the same
45:01
one base pair resolution, precision,
45:04
inaccuracy that you're used to.
45:06
So let's take a look at the data quality that you expect.
45:10
First, I want to go through how we develop
45:13
our minimum thresholds for developmental validation.
45:17
We look at data on a per instrument basis
45:20
and then holistically get a sense of how the instruments
45:23
will perform in the field.
45:25
Negative template controls from each of our chemistries are amped
45:28
and run under standard recommendations.
45:31
For this validation, we analyzed with GMAP or IDX
45:34
version 1.7 at one RFU.
45:37
We manually review the data for any spikes
45:40
or other known artifacts and then determine the average RFU
45:44
and standard deviation for each Dye channel.
45:47
The average RFU plus three standard deviations
45:51
is the LOD or limit of detection.
45:53
The average RFU plus 10 standard deviations
45:56
is our LOQ or limit of quantification.
46:00
We expect nearly any background noise to fall below
46:03
this value.
46:05
For certain studies such as pull up and mixture analysis,
46:08
we will utilize the minimum threshold values,
46:10
which are rounded up to the closest factor of five
46:14
from the limit of quantification value.
46:18
For other studies such as sensitivity,
46:20
we will use the eight times limit of detection number
46:23
as the peak analytical threshold.
46:25
So what that looks like is here,
46:29
if we compare the 3500 data collection for minimum values
46:33
that we use in our developmental validation,
46:36
this is one eight flex and one 24 flex.
46:39
And you can see the values are all very similar
46:42
across the two platforms, which is what we would expect.
46:46
For each of the chemistries we looked at during validation,
46:49
we used five total seek studio flex instruments,
46:53
two eight cap and three 24 cap instruments.
46:56
Minimum thresholds were calculated for each instrument
46:59
and then averaged across for analysis
47:02
with GMAP or IDX 1.7.
47:05
Looking at all the chemistries across the flex validation,
47:08
our newer chemistries have minimum thresholds
47:10
all around 50 RFUs or lower,
47:13
while our legacy kits with older dies
47:15
have slightly higher noise and minimum thresholds.
47:18
If we take a closer look at the negative controls
47:21
that were run with global fliler IQC,
47:23
this is for one seek studio eight flex
47:26
and one seek studio 24 flex.
47:29
And don't forget in this particular kit with global
47:31
fliler IQC we have the internal quality markers
47:34
that help with analysis of amplification data.
47:37
So we have a small and a large to determine degradation
47:40
in inhibition and we look at those,
47:43
the data, the noise is all really well below 25 RFUs.
47:47
So low signal to noise ratio.
47:49
All right, so we also want to make sure
47:50
that we are getting similar peak heights.
47:53
In this particular instance,
47:55
we independently amplified and ran 10 single source samples
47:58
with global fliler IQC.
48:01
These are actually 10 different samples.
48:04
So they're not exactly the same
48:06
that were run on a 3500 and the flex,
48:09
but overall these normalized heterozygous peak heights
48:12
show that the data is consistent across the two platforms.
48:17
Another thing to keep in mind with peak heights,
48:19
we introduced off-scale recovery with 3500 data collection four
48:24
and we include it with the flex as a default
48:26
for all sample types on the seek studio flex.
48:30
Single source samples are directly amplified
48:33
and do not become saturated with the homozygous allele call.
48:36
I added text box here for the homozygous locide
48:39
that were near legacy saturation of 32,000.
48:43
Three of the loci here are above the threshold
48:46
but are not saturated with off-scale recovery enabled,
48:49
which allows for minimal off-scale calls
48:51
and increased first-past success rate of these samples.
48:55
All right, another thing we want to make sure
48:57
is that we're getting the same one base pair resolution
49:00
that you expect with our CE systems.
49:03
Here's the global filer IQC ladder
49:05
and I've highlighted here any of the one base pair
49:09
resolved peaks that are in that ladder.
49:11
So those are all shown here.
49:13
We also use the NIST standard 2391D
49:18
for one base pair resolution looking in mixtures.
49:21
For the three chemistries that are shown here,
49:24
we injected this standard 14 times
49:26
on both an 8-cap and 24-cap.
49:29
All injections were able to resolve the minor peak.
49:33
We did use GMEP or IDX 1.7 for this
49:35
and analyzed with all filters turned off.
49:38
All right, just a closer look at some additional mixtures.
49:41
We have here our positive control 007 and 9947A
49:46
as a one to seven mixture,
49:48
and all the genotypes were concordant across the two samples.
49:53
For this particular sample,
49:54
default marker-specific stutter thresholds were used
49:57
and pull-up detection was enabled in GMEP or IDX.
50:01
Okay, with this one, we are also using 9947A and 007,
50:05
but in this case, we're trying to mimic a sexual assault sample
50:09
and can clearly see that the Y profile has come through
50:12
strongly with Y-filer plus.
50:15
And then just to make sure, we ran a similar mixture
50:19
of two males on the 3,500 and the flex.
50:23
So here first is the 3,500 data and then the flex data.
50:27
So you can really see that data quality peak heights
50:30
and balance of the peaks are all very similar
50:33
on the two platforms.
50:35
And then finally, when it comes to resolution,
50:37
we have a three-person 111 mixture with global phyler IQC.
50:43
And again, you can see here that each of the three samples
50:47
is shown here and easy to distinguish.
50:51
All right, so now let's talk about some of the features
50:54
that make the flex faster for your laboratory.
50:57
So the seek studio flex enhances the pull-up reduction feature
51:01
that was introduced with data collection,
51:03
3,500 data collection for.
51:05
An initial manual spectral calibration has to be done
51:09
with the first use of any die set and polymer combination.
51:13
Subsequent injections will determine if the sample quality
51:16
within a capillary meets specific quality criteria.
51:20
If it does, the spectral calibration for that capillary
51:23
will be updated for the current sample.
51:26
This is an iterative process so that with each injection,
51:30
the spectral calibration is updating from the previous.
51:33
Even when a new capillary array is installed,
51:36
a spectral calibration is no longer required
51:39
because the last good spectral calibration
51:41
will be stored and applied.
51:44
In the sample highlighted, the quality has a green flag.
51:48
And if we want to take a closer look,
51:50
we can click on the eye icon
51:52
and see the spectral status of that particular sample.
51:56
Here you can see that the auto spectral calibration
51:59
for this sample was successful and applied.
52:02
If the auto spectral calibration is not successful,
52:05
the status will report the previous passing calibration data
52:09
that was applied to the sample.
52:11
We took a look at both auto spectral enabled on
52:15
and auto spectral off.
52:17
And we amped 007 24 times and then injected it
52:22
each, well, twice for a total of 48 injections on a 24 flex.
52:28
We also took 23 single source samples
52:31
and injected them twice.
52:35
And when you look at the parent peak heights
52:37
for both data sets, they're, you know,
52:40
pretty equivalent with both auto spectral on and off.
52:45
When we used the minimum thresholds that we discussed
52:48
earlier, with auto spectral on,
52:50
we had around 1,800 pull up peak calls for these data sets
52:55
when evaluating with an internal development tool.
52:59
On the same hand, auto spectral off,
53:01
we had nearly double this pull up calls
53:04
with over 5,000 calls.
53:06
And average pull up peak height was nearly the same
53:10
for when the auto spectral calibration is disabled.
53:13
So again, a great way to reduce your pull up data.
53:18
And here's what that looks like when we look
53:20
on an individual sample and die basis.
53:23
This is the blue channel of a one
53:25
anagram extracted single source sample
53:27
that was analyzed at 50 RFU at all markers
53:31
and defaults that are filters were applied.
53:33
On the top, we ran with the flex with auto spectral on
53:36
and pull up detection enabled in GMAP or IDX 1.7.
53:41
There are actually zero calls that are made by the software
53:44
because the spectral calibration for this sample
53:46
effectively removed any pull up signal.
53:50
On the bottom, we ran the flex with auto spectral off
53:53
and did not enable pull up detection in GMAP or IDX.
53:58
Nine calls were manually annotated for this channel alone.
54:02
Peaks that were already labeled as an artifact
54:04
in this particular sample, such as the OMR here,
54:07
were not further defined.
54:09
When we take a look at the green channel,
54:13
similarly at the top panel, we have the flex instrument
54:16
with auto spectral on as default and pull up detection
54:19
enabled in GMAP or IDX.
54:23
GMAP or IDX labeled five peaks as pull up
54:26
based on the data point range and max pull up percent
54:29
sets in GMAP or IDX analysis method.
54:32
These pull up calls are labeled as artifacts
54:35
and therefore don't appear as a wheel calls
54:37
in the sizing table.
54:39
The three manual calls were made due to the way
54:41
the filters are set up for pull up analysis.
54:43
So again, that's something the lab would want
54:45
to optimize and validate.
54:47
The bottom panel shows the same sample injected
54:51
on the flex with auto spectral off
54:53
and pull up detection disabled.
54:55
And you can see that sample actually had 12 manual
54:59
pull up calls that were noted.
55:01
All right, so let's recap what we've discussed so far.
55:05
The seek pseudo flex has improved usability
55:08
with a newly designed array for even easier installation
55:11
in the ability to load four plates at any one time.
55:15
For resolution, the data is equivalent to the data
55:20
you already expect on our applied biosystems
55:23
to E systems like the 3500.
55:25
You have one base per resolution, low background noise
55:29
and peak heights are equivalent to the 3500.
55:31
In addition, you get faster results
55:35
with auto spectral calibration enabled combined
55:39
with GMAP or IDX 1.7 to allow for less time spent
55:42
analyzing data for pull up.
55:44
When we put all this together, it has the potential
55:49
to make your lab stronger and more efficient.
55:52
So flex your power.
55:56
Thank you for attending.
55:58
Please put your questions in the chat
56:00
and we will get to as many as we can today.
56:02
If you want in more in depth validation studies,
56:06
please refer to the seek studio flex for HIV user bulletin
56:09
and go to the link here.
56:11
- Thank you, Nick and Jill
56:15
for those interesting and informative presentations.
56:18
Now it's about time for the Q&A.
56:20
If you have questions, please submit it
56:22
through the Q&A panel on your screen.
56:25
While we wait for everyone to submit their questions,
56:27
I have a few polling questions for you.
56:29
First up, which of the following
56:32
will most increase your lab's productivity?
56:35
For play deck with continuous loading,
56:38
sample re-prioriturization,
56:40
spectral auto calibration and pull up reduction,
56:44
on instrument learning center with videos and wizards,
56:47
smart help/remote support.
56:49
Please take a moment, if you will,
56:52
to answer our polling questions,
56:54
so we keep in tune.
56:55
Right, well, it looks like the majority of you said,
56:59
four-plate deck with continuous loading
57:01
would help the most to increase your lab's productivity.
57:04
Our second question is,
57:07
the last time we went with agency IT
57:10
on instrumentation connectivity,
57:12
the answer was A, we've never asked
57:15
because we know we can.
57:17
B, not.
57:18
C, local area network.
57:21
LAN, only.
57:22
D, LAN and approved outside port.
57:25
Again, please take a minute to give us your answer
57:30
so we can understand more about your connectivity problems.
57:33
All right, thank you so much.
57:36
And our very last polling question for you
57:38
is coming right now.
57:40
This would you like to receive more information
57:42
on today's webinar topics?
57:44
Please select all that apply.
57:46
If you can go ahead and give us your answer,
57:49
then we will move on to our Q&A portion of the webinar.
57:54
Again, if you have a question,
57:56
please go ahead and make sure you get that in
57:58
and we'll try to address it.
58:00
Here is our first question.
58:05
And it is going to Nick.
58:08
Nick, are you ready for us?
58:10
- I am indeed.
58:11
Hello, everyone.
58:13
- I'm perfect.
58:14
All right, Nick.
58:15
- So, does the smartphone and instrument
58:18
need to be on the same Wi-Fi connection
58:21
for remote access function to work?
58:23
- Oh, that's a great question.
58:26
No, it does not need to be on the same network.
58:29
So the remote connection that we saw in the video,
58:33
that's going through a platform
58:35
called the ThermoConnect platform.
58:37
So how that works is the instrument is connected
58:40
to that platform and then your phone is connected
58:43
to that platform.
58:44
And that's how you gain access to the instrument.
58:46
You don't have to be on the same network.
58:48
This gives you the ability to be at home anywhere in the world
58:53
that you can safely and securely log on
58:55
to the ThermoConnect platform.
58:56
You can see the status of the instruments
58:58
and what is currently happening.
59:00
Really cool feature.
59:03
- Perfect.
59:04
- Thank you.
59:04
- All right, next question.
59:07
And Jill, this one's actually for you.
59:09
You ready for us?
59:11
- I'm ready.
59:13
- Perfect.
59:14
So Jill, does Seek Studio Flex have the OSR feature
59:18
as found in the 3500?
59:20
- It does.
59:22
So OSR or off-scale recovery is a default
59:27
that is enabled on the runs.
59:30
You have the ability to turn it off,
59:34
but we thought for efficiency reasons
59:37
that we would make it standard as default
59:39
on the HRD application runs.
59:43
- Okay, so yeah, that makes sense.
59:46
All right, here's another one for you.
59:49
So you explain more on the three different ways
59:52
to set up a plate?
59:54
- Yeah, absolutely.
59:56
So there's a number of nice ways to set up a plate.
01:00:00
So of course, there is the instrument GUI
01:00:05
that you can set up a plate on.
01:00:08
You can also use our plate manager software,
01:00:12
which is included.
01:00:14
So there is both a desktop version
01:00:17
and a version that is available with the thermophisher
01:00:21
connect similar to the remote monitoring.
01:00:24
So you can set up the plate on there.
01:00:26
And you can also create a .csv file.
01:00:30
And then those can be uploaded to the instrument via USB
01:00:35
or an internet or network connection.
01:00:39
So there's a number of ways to get a plate record
01:00:42
onto the instrument.
01:00:46
- That's okay.
01:00:48
And Nick, we have another question here that has come in for you.
01:00:54
What is the difference in the learning center
01:00:57
compared with the wizard?
01:01:00
- Another great question.
01:01:02
So there are two places you can go on the CStudio Flex
01:01:06
to get information.
01:01:08
So the learning center is what is new in the CStudio Flex.
01:01:13
If you go in there, you'll find a bunch of videos
01:01:16
that are narrated.
01:01:18
You can pause them and they help you set up plates.
01:01:22
They look at different aspects of the instrument.
01:01:25
They show you how to do things.
01:01:27
So this makes it really useful for people who haven't used
01:01:31
the instrument in a while.
01:01:33
It means that they can come up to the instrument
01:01:35
and just set up a plate and run very easily.
01:01:38
If they've forgotten anything,
01:01:39
they can use these videos to help them.
01:01:41
The wizards, anyone who has used the .3, 1/30 or the .3, 500
01:01:46
will know about the wizards.
01:01:48
We made them look much nicer in the .3, 500.
01:01:51
They're even better in the CStudio Flex now.
01:01:53
And they will take you step by step through guide
01:01:56
through the maintenance that you have to perform on the instrument.
01:01:59
So making sure the bubbles are gone from the polymer,
01:02:03
making sure that everything is accurate and done correctly
01:02:07
so you can be confident that the instrument is going to keep
01:02:09
giving you that data that you expect.
01:02:12
Perfect. Thank you.
01:02:15
So we are back to you, actually.
01:02:18
We have a researcher who says,
01:02:22
"Will I see less pull-up peaks with the systems?"
01:02:27
Absolutely. And I think I shared some of that in the slides
01:02:31
that I presented.
01:02:33
So we also enabled the auto-spectral calibration as default
01:02:39
in HID to enable less pull-up.
01:02:46
And when you use that in coordination with GeneMapper IDX 1.7,
01:02:50
you can really reduce the number of pull-up calls.
01:02:54
So we actually initiated or first launched a pull-up reduction feature
01:03:00
with the 3,500 data collection for the only thing that we've --
01:03:06
I'm sorry -- we enhanced it on the Flex to allow it to carry the information
01:03:12
through, and so it continuously updates per sample.
01:03:18
And so that's why if you put a new capillary on,
01:03:22
you don't actually have to run a new spectral calibration
01:03:27
because it saved that data.
01:03:30
On the 3,500, you weren't able to save that data.
01:03:33
It looked at the data, compared it to a manual calibration,
01:03:37
and then updated it if it could.
01:03:40
Now it's released since you can use the samples on the Flex.
01:03:44
It continues to improve upon itself,
01:03:47
so it's much better than the manual.
01:03:51
And so we did show that also with the auto-spectral calibration
01:03:57
on versus the auto-spectral calibration off.
01:04:01
You've got more than twice, maybe even three times the number of pull-up peaks
01:04:06
when you actually disabled auto-spectral calibration off.
01:04:10
So we did validate the instrument with it only enabled.
01:04:15
So we would definitely recommend using that feature.
01:04:20
Perfect, thank you Joe, that's really informative.
01:04:25
Okay, next, back to you now.
01:04:28
Can you tell us why the decision was made to redesign the array?
01:04:36
Well, we have to do something to make it better.
01:04:42
Well, looking back, when we were designing the Peak Studio Flex,
01:04:46
we did a lot of voice of customer.
01:04:48
We spoke to a lot of customers around the world and tried to understand
01:04:52
what the pain points they were feeling.
01:04:54
If you speak to any customer or anyone who has ever run a 3130
01:04:58
who then went on to a 3500, they would probably tell you that
01:05:02
it was just light years ahead in terms of usability and the ease of use of it.
01:05:08
There wasn't really much that people thought that we could do to improve it
01:05:12
until you look at just the simple change that we made with the array.
01:05:16
And putting in this retractor tab, it means that you can one insert the array
01:05:22
single-handed, which is lovely.
01:05:25
You don't have to worry about breaking any of those capillaries on there.
01:05:28
The other thing is that you can confidently just slide in the cap bundle
01:05:34
and the detection window is going to be seated perfectly where it needs to be
01:05:38
so that the instrument can run that spectral calibration,
01:05:41
you can run that spectral calibration and get on with your
01:05:45
the work that you need to do.
01:05:47
So it really is just making life that much easier for anyone who's using the
01:05:52
instrument.
01:05:53
Well, and that's what forensic experts want. So that sounds like good plan.
01:05:58
Yes, ease of use all the way.
01:06:01
Our next last question for you then.
01:06:07
What can we do with remote monitoring?
01:06:14
So remote monitoring is a pretty awesome feature that we brought in with the
01:06:20
Seek Studio Flex.
01:06:22
This is going to give you the ability to check in on the instrument,
01:06:26
see how the instrument is running, see if there are any positions free to load
01:06:31
samples, to load plates.
01:06:33
You're going to be able to see if there are any issues with the instruments.
01:06:37
So that is really helpful.
01:06:39
A lot of times people will find that the post amplification lab
01:06:43
is not really frequented that much or it's not populated that often with
01:06:48
scientists.
01:06:49
People actually have to go down there when they think that their run is ready.
01:06:53
With the remote monitoring it makes it really easy just to quickly check to see
01:06:56
if everything is ready so that you can go down there if you need to or if there
01:07:00
are any errors.
01:07:01
The other things that is kind of adjacent to the remote monitoring that you can
01:07:06
do is the remote support.
01:07:08
So through this, if you are at the instrument, something goes wrong,
01:07:12
you recognize an issue, you can open up tech support cases directly from the
01:07:17
instrument.
01:07:18
So that means that you can open up the case, someone up there in my Fisher
01:07:22
and in support can get hold of that and then they can call you back.
01:07:25
And then even on to the next level of things is the ability that our engineers
01:07:31
can remote into that instrument and help you fix a bunch of issues remotely
01:07:37
without even having to come in.
01:07:39
So the instrument in your lab does not have to go down.
01:07:42
If there's an issue we can remote in and we can fix it much quicker
01:07:45
than if you had to wait for an engineer to come to you.
01:07:48
So a lot of different features that are all about connectivity.
01:07:51
We're living in a connected world and now the forensic lab is starting to get
01:07:56
there too.
01:07:57
Of course that makes sense.
01:08:01
All right audience, well that wraps up the time we have for Q&A today.
01:08:06
I'd like to thank our fantastic presenters, Nick and Jill,
01:08:09
as well as the real Fisher scientific sponsor for a trade webinar.
01:08:12
In 24 hours or less, this webinar will be available on demand
01:08:16
if you would like to share it with friends and colleagues or maybe even watch
01:08:20
it again.
01:08:21
Additionally, please keep your eyes open for an invitation to our next one in
01:08:25
November.
01:08:26
Until then, thank you so much for attending today and we hope to see you next
01:08:29
time.
01:08:30
[BLANK_AUDIO]