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Scaling PCR Workflows from
Benchtop to Automation
Broadcast Date: Tuesday, June 29, 2010
Time: 1:00 PM EDT
Sponsored by
Scaling PCR Workflows from
Benchtop to Automation
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Sponsored By
Scaling PCR Workflows from
Benchtop to Automation
Your Moderator
John SterlingEditor-in-Chief
Genetic Engineering & Biotechnology News
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Sponsored By
Scaling PCR Workflows from
Benchtop to Automation
Lawrence J. Wangh, Ph.D.,Professor of Biology
Laboratory of Molecular Medicine and Global Health
Brandeis University
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“Sample Prep for Single Cell Single-Tube LATE-PCR”
Laboratory of Molecular Medicine and Global Health
Department of Biology, Brandeis University, Waltham, MA,
June 29, 2010
Genetic Engineering and Biotechnology News
Webinar
Lawrence J. Wangh, Ph.D.
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Pre-Implantation
Genetic
Diagnosis
Early Cancer
Diagnosis
1997 - Small Sample Size
A Challenge to Conventional PCR
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Limitations of Real-Time PCR
• Low Sensitivity for Small
Number of Initial DNA Targets
• No Quantitative End-Point
Analysis!
Freeman et al., (1999) Biotechniques 26: 122-125
CT Value
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Sample Preparation
in a single tubeImproved SpecificityPrimeSafe
PurAmp&
QuantiLyse
A Whole System ApproachEfficient Amplification
of single-stranded DNA
Dilute’N Go
SequencingVirtual Sequencing
Quantitative End-Point
AnalysisRT –LATE-PCR Multiplexing
Uncoupling ofAnnealing and
Detection
These New Chemistries Result in New Assay Strategies
Lights On/Lights Off Probes
LATE-PCR
see LATE-PCR.org
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Therefore measurements are taken
In real-time, as soon as there are
enough molecules
to detect.
Exponential Amplification: 1,2,4,8.16…..
Amplification is Fast, but unreliable
as it slows down.
detection background
real-time
end-point
Linear After the Exponential (LATE)
Amplification is fast and is reliably
It switches from exponential to linear at
shortly after the detectable level is
reached. Reduced scatter at end-point
detection background
real-time
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Sample Preparation
in a single tubeImproved SpecificityPrimeSafe QuantiLyse
A Whole System ApproachEfficient Amplification
of single-stranded DNA
Dilute’N Go
SequencingVirtual Sequencing
Quantitative End-Point
AnalysisRT –LATE-PCR Multiplexing
Uncoupling ofAnnealing and
Detection
These New Chemistries Result in New Assay Strategies
Lights On/Lights Off Probes
LATE-PCR
Pierce, K., Rice, J., Sanchez, J.A., and Wangh, L.J. (2002) “QuantiLyse: Reliable
DNA Amplification from Single Cells”, BioTechniques 32: 1106-1111.
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The Problem of Scatter at the
CT Among Single Cells
Pierce et al., (2000). Mol Hum Reprod 6:1155-1164
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Optimizing Single-Tube Preparation of Genomic DNA
Chromosome
Packing Density
1:10,000
3 billion base-pairs/CellXY =
In Humans
46
Chromosomes
Per
Somatic Cell
XX =
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QuantiLyse: A Simple Reagent and Method for Reliable Preparation of
Genomic DNA in a Single-Tube Reaction
32
34
36
38
40
42
44
0 10 20 30 40 50 60 70 80
CT V
alu
e
Heat Denature
in Water
Freeze/Thaw
in WaterQuantiLyse
34.4
0.34
35.0
0.66
39.4
2.58
Variations in CT Values Among Replicate Reactions
Reflect Variations in Template Accessibility
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Single Cell, Single Gene, Single Allele
Analysis via Symmetric PCR
Normal Signals 1278 Signals Aberrant Signals- -
-100
400
900
1400
1900
Flu
oresc
en
ce
Normal/NormalA Normal/1278C
-100
400
900
1400
1900
11 15 19 23 27 31 35 39 43 47 51 55 59
Cycle Number
Flu
oresc
en
ce
1278/1278B
11 15 19 23 27 31 35 39 43 47 51 55 59
Cycle Number
D Normal/1278
Rice et al. (2002), Prenat Diagn 22: 1130-1134
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Quality of Genomic DNA Matters!DNA Shearing Increases Scatter
FROZEN/THAWED GENOMIC DNA
Triplex Reaction 2
INTACT GENOMIC DNA: prepared and amplified in the same tube
Triplex Reaction 1
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Sample Preparation
in a single tubeImproved SpecificityPrimeSafe QuantiLyse
A Whole System ApproachEfficient Amplification
of single-stranded DNA
Dilute’N Go
SequencingVirtual Sequencing
Quantitative End-Point
AnalysisRT –LATE-PCR Multiplexing
Uncoupling ofAnnealing and
Detection
These New Chemistries Result in New Assay Strategies
Lights On/Lights Off Probes
LATE-PCR
John Rice, J. Aquiles Sanchez, Kenneth E. Pierce, Arthur H. Reis, Adam Osborne, and
Lawrence J. Wangh (2007) Monoplex/Multiplex Linear-After-The-Exponential (LATE)-PCR
Assays Combined with PrimeSafe® and Dilute-„N‟-Go Sequencing, Nature Protocols 2 #10,
2429-2438.
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Yes PrimeSafe™
No PrimeSafe™
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Quantitative End-Point LATE-PCR
• Low Scatter Among
Replicates
• High Sensitivity Even for
Low Numbers of Targets
-50
0
50
100
150
200
250
300
350
5 10 15 20 25 30 35 40
Cycle Number
TE
T-F
luorescen
ce (
Rn)
10 g
100 g
1000 g
1/25/05
-50
0
50
100
150
200
250
300
350
5 10 15 20 25 30 35 40
Cycle Number
TE
T-F
luorescen
ce (
Rn)
10 g
100 g
1000 g
1/25/05
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Fluo
resc
ence
0
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Fluo
resc
ence
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
0
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Fluo
resc
ence
0
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
20 30 40 50 60 70 80
Cycle Number
Fluo
resc
ence
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
00
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Fluo
resc
ence
0
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Fluo
resc
ence
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
00
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Fluo
resc
ence
0
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
20 30 40 50 60 70 80
Cycle Number
Fluo
resc
ence
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
0000
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Flu
ore
scen
ce
0
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Flu
ore
scen
ce
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
0
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Flu
ore
scen
ce
0
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
20 30 40 50 60 70 80
Cycle Number
Flu
ore
scen
ce
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
00
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Flu
ore
scen
ce
0
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Flu
ore
scen
ce
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
00
500
1000
1500
2000
2500
3000
20 30 40 50 60 70 80
Cycle Number
Flu
ore
scen
ce
0
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
20 30 40 50 60 70 80
Cycle Number
Flu
ore
scen
ce
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
10,000 Genomes
1,000 Genomes
100 Genomes
10 Genomes
0000
• Quantitative End-PointAnalysis
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Sample Preparation
in a single tubeImproved SpecificityPrimeSafe PurAmp&
A Whole System ApproachEfficient Amplification
of single-stranded DNA
Dilute’N Go
SequencingVirtual Sequencing
Quantitative End-Point
AnalysisRT –LATE-PCR Multiplexing
Uncoupling ofAnnealing and
Detection
These New Chemistries Result in New Assay Strategies
Lights On/Lights Off Probes
LATE-PCR
Hartshorn C, Anshelevich A, Wangh LJ. (2005) Rapid, single-tube method for
quantitative preparation and analysis of RNA and DNA in samples as small as one
cell. BMC Biotechnol, 5:2.
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10,000 kilometers
Separation of the Parts, Rather Than Purification
100,000X100,000X
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The Single-tube PurAmp Method
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8 – Cell XX 16 – Cell XX 16 – Cell XY Blastocyst XX
Sheardown et al. Cell 91, 99-107 (1997)
Xist Gene Expression and Nuclear Localization
in Developing Mouse Embryos
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PurAmp is Accurate and Sensitive
Hartshorn et al. (2005) BMC Biotechnology 5:2
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Detection of Xist and Sry in Blastocyst Stage Embryos
Hartshorn et al. (2005) BMC Biotechnology 5:2
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Laser Zona Drilling for Single Cell Isolation
Does it cause heat shock?
Hartshorn et al. (2003) Mol Reprod Dev 64:41-51
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Quantitative Analysis of Hsp 70 Levels
in Single Blastomeres and Whole
Embryos using the PurAmp Method
Hartshorn et al. (2005) Fertility and Sterility 84, no. 5 1547-1550
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Summary of Advantages of Single Tube Sample Preparation
• Separation of Components, Rather than Complete Purification
• Experimentally Convenient and Less Expensive
• Quantitatively More Reliable
optimized for minimum scatter among replicates
• Lower Risk of Laboratory Contamination
• Lower Risk of Sample Contamination
• Gentler on substrates, less shear, less degradation
• Fast and Automatable
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Summary of Our Synergistic Core Technologies
• LATE-PCR: abundant, reliable, single-strand production
• Dilute’N’Go Sequencing, more convenient, less costly
• Quantitative End-Point Analysis, cheaper, fewer errors
• PrimeSafe, cleaner results and easier multiplexing
• Low Temperature Sequence-Specific Probes
• Low Temperature Mis-match Tolerant Probes
• Lights-On/Lights-Off Probes – high resolution
analysis and “virtual sequencing” in a closed tube
All of the above chemistries are automatable!
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Sponsored By
Scaling PCR Workflows from
Benchtop to Automation
Gregory L. Shipley, Ph.D.,Assistant Professor
Director, Quantitative Genomics Laboratory
The University of Texas Health Science Center, Houston
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Scaling Workflows from Bench Top to Automation
Utilizing Automation for Real-Time qPCR
Gregory L. Shipley, Ph.D.
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What do we mean by ‘Automation’?
• Automation refers to using liquid handling robots for
component assembly instead of processing a work flow
manually
• Can be as simple as aspirating and dispensing liquid
from plate A into plate B (or C, D, ... N)
• Can be as complex as automating every step of a
complex workflow utilizing multiple instruments
• Many different kinds of instruments can be integrated
with robot software
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A Robotic Workstation - Components
Instruments (l-r)
1-Cytomat 1
2- DTX-880
3- FX- dual arm
96-tip head &
Span-8
4- Cytomat 2
5- ELx405 plate
washer
(not shown)
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A Robotic Workstation - Complete
Work Station
inside a
Biosero hepa
filtered hood -
aseptic
environment
siRNA &
compound
screening with
live cells or
biochemical
assays
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Why use automation?
• Automation brings a level of accuracy and precision
to an experiment that can not be achieved manually
for large numbers of repetitions
• For small tasks, 1 or 2 96-well plates, it is faster and
can be just as accurate to do the process manually
• However, using automation means that every plate
will be processed the same, every time regardless of
the number of repetitions, complexity or time
required for the task
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What is Involved in using Automation?
• Aside from acquiring the instrumentation, learning to
use the software in a sophisticated way is a critical step
(loops, nested loops, IF statements, variables, etc)
• Requires a dedicated person
• Make sure your assay can be scaled down to 96- or
384-well plates (1536)
• Real-Time qPCR lends itself to this format quite nicely
but not true of all assays
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What Liquid Handling Robot to Buy??
• Don’t consider just what you need today, think about the
future
• Make sure the features give you all the flexibility you require
1- How many tips (1, 4, 8, 96, 384) or tools (1 tip or 8 tips)
2- The more tips, the faster the job will be done
3- Span-8 capability = maximum flexibility & speed
4- Using 96 or 384 tip heads are fast but not as flexible -
work best with another robot
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Pipetting with a Liquid Handling Robot
• By default, robot software set to maximize speed but this
minimizes accuracy
• Slow down aspiration & dispense, volume dependent
• Put in delays, 500 - 1500 ms for aspiration - dispense
• Aspirate (2X), dispense- source (1/2X), dispense- target(s)
(1X), dispense remaining- source
• Pre-wet tips if necessary, depends on solution
• Use appropriate size tips/volume
• Use food color dyes for initial program check
• Use tartrazine (10 mM) to check accuracy/absorbance A427
read - A650 background = 5% - 10% CVs
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Working with 96-Well Plates
• Originally started setting up 96-well qPCR plates with a
Biomek 2000 in 1996
• Used a single channel tool, one well at a time, due to
asymmetric layout of the RT reactions
• 45 minutes+ to set up one 96-well plate - over an hour to
run the RT reaction on a thermocycler
• Added PCR master mix with the 8-channel tool
• Almost 2 H for real-time qPCR on the ABI 7700
• State of the art at the time
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Biomek2000 with Single Channel Tool
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Original 96-Well Plate Layout
Std 1 Std 2 Std 3 Std 4
Std 5 NTC
S #1
S #7
S #1S #1 S #1
S #7 S #7 S #7 S #14 S #14 S #14S #14
S #20 S #20 S #20 S #20
NAC
Sample
Standard
NTC
ASPrimer
4 μl+6 μl
50 μl PCR
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Second Generation 96-Well Plate
Std 1 Std 2 Std 3 Std 4 Std 5 NTC
S #1 S #8S #1S #1 S #1 S #8 S #8 S #8 S #15 S #15 S #15S #15
S #21 S #21 S #21 S #21
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Data from the 96-Well Plate
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Data from the 96-Well Plate
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A Second Assay: 96-Well Plate
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Working with 96- & 384-Well Plates
• 1999 shifted to a Tecan Genesis 100, with Span-8
• Span-8 means the tips can expand/contract in the y-axis
and move independently in the z-axis
• Span-8 allows use of up to 8 tips at once vs 1 previously
• Uses fixed tips, no disposable tip costs
• Use 5% Clorox bleach & H2O washes to clean tips
between samples
• Cut the RT setup time to 17 minutes/plate (384)
• Worth every cent
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Tecan Genesis 100 with Span-8
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Tecan Genesis 100 with Span-8
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384-Well Plate- Multiple Sample Layouts
NTC + Standard Curve, 1 Assay/Plate NAC for each Sample
15 Samples 30 Samples 45 Samples 61 Samples 71 Samples 93 Samples
5 5 4 4 3 3 2 2 1 1
1 1 1 1
93 93 93 93
NTC NTC
NAC
Sample
Standard
NTC
ASPrimer
2 μl+3 μl
20 μl PCR
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Two Assays/Plate- 15, 30 or 45 Samples/Half Plate 1 or 2 Sample Sets
NTC + Standard Curve - 2 Assays, 1 plate NAC for each Sample
15, 30 or 45 Samples, Assay 1, Sample Set 1 15, 30 or 45 Samples, Assay 2, Sample Set 1 or 2
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384-Well Plate Data
ABI 7900HT - Human Probe-based CyclinD1 Assay
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384-Well Plate Data
ABI 7900HT - Human Probe-based CyclinD1 Assay
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Whole-Cell Lysates vs Purified RNADMSO vs Staurosporine
• Comparison of making cDNA from whole cell lysates
vs purified RNA
• Treated cells with Staurosporine or DMSO as carrier
• Made cDNA and added to qPCR SYBR master mix
• One 384-well Tox array (Lonza/Bar Harbor Biotech)
per cell culture
• Used 4 cultures for each group
• Total plates is 16
• Loaded plates utilizing a Biomek2000, single
aspirations with quad dispenses, 8-channel tool
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Whole-Cell Lysates vs Purified RNADMSO vs Staurosporine
Purified RNA
Cell Lysate
18SrRNA
18SrRNA
19 significant
transcript changes
shared between cell
lysates and purified
RNA that validated
with individual
qPCR assays
Automation
essential for this
experiment
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Summary
• Choose the robot platform that fits your workflow,
keeping the future in mind
• Become expert at using the software, dedicated user
• Robots are excellent for repetitive, large scale tasks
• Robots are not good if the work flow changes often
• Using the same robot for plasmid or nucleic acid
preps and setting up qPCR is not a good idea
• Always perform QC on new assays before running
real samples
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Sponsored By
Scaling PCR Workflows from
Benchtop to Automation
David Knorr, Ph.D.,Applications Manager
Automation Solutions Instruments
Agilent Technologies, Inc.
![Page 55: Scaling PCR Workflows from Benchtop to Automationhpst.cz/.../files/attachments/scaling...automation.pdfScaling PCR Workflows from Benchtop to Automation Broadcast Date: Tuesday, June](https://reader034.vdocuments.net/reader034/viewer/2022050315/5f773af0cea7605bbb6067f7/html5/thumbnails/55.jpg)
29 June 2010
Agilent - GEN
Scaling PCR
Automation
• Automation rationale, planning and considerations
• PCR workflow
• Different scales of automation
– single liquid handler
– workstation
– integrated system
29 June 2010
Agilent - GEN
55
David Knorr, Ph.D.
Applications Manager
Agilent Technologies
![Page 56: Scaling PCR Workflows from Benchtop to Automationhpst.cz/.../files/attachments/scaling...automation.pdfScaling PCR Workflows from Benchtop to Automation Broadcast Date: Tuesday, June](https://reader034.vdocuments.net/reader034/viewer/2022050315/5f773af0cea7605bbb6067f7/html5/thumbnails/56.jpg)
29 June 2010
Agilent - GEN
Agilent Technologies
PCR Workflow Solutions
• Instruments for workflow automation
– plate sealer, centrifuge, labeler, stackers, and more
– liquid handlers
› Bravo
› Vertical Pipetting Station (VPrep)
• BenchCel Workstations
• BioCel fully automated systems
• VWorks software
• Reagents
– PCR polymerases (5 choices)
– PCR / qPCR amplification kits
– purification kits for RNA / DNA / PCR product cleanup
29 June 2010
Agilent - GEN
56
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29 June 2010
Agilent - GEN
Automation Rationale
• Capacity or throughput improvements
– shrink research and development timelines
• Quality (product and data) improvements
– process standardization / uniformity
– improve consistency
› reduce error
› reduce subjective data analysis
› enable high-density well formats (e.g. 1536 well plates
• Reduce Operating Costs
• Redistribute brain power - scientists are expensive liquid handlers
29 June 2010
Agilent - GEN
57
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29 June 2010
Agilent - GEN
Plan to Automate
(let the process drive)
• Understand your process;
focus on where you’re going and why
• Scope, Timeline and Cost
– hold onto one and the others will fall into place!
• Review:
– current methods
– up / down stream compatibility and bottlenecks
– flexibility
• A bad process = a bad automated process
29 June 2010
Agilent - GEN
58
Scope
TimeCost
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29 June 2010
Agilent - GEN
Collaborate with a Good Vendor
• Good components
– ease-of-use, loading, teaching, monitoring, cleaning
– reliable, accessible
– safe
• Good track record
• Good people
– project management
– engineering
– software
– technical support
– service
• Be clear with requirements, communicate often
• Identify a super-user
• Use the system immediately
29 June 2010
Agilent - GEN
59
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29 June 2010
Agilent - GEN
PCR Workflow
Real-time PCR
Traditional PCR
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29 June 2010
Agilent - GEN
Nucleic Acid Purification / Isolation
29 June 2010
Agilent - GEN
61
NAPI
• Source material from anything: cells, tissues, fruits, bone fragments, etc.
Each has particular challenges
• Once converted into a liquid (or semi-liquid) nucleic acids can be isolated
usually by some form of affinity chemistry
– magnetic beads
› oligo(dT) or other nucleic acid-binding surface
› requires magnet station & plate-handling robot
– silica-based columns (total nucleic acid DNase or RNase)
› usually require spinning, or vacuum (robotics)
– ChargeSwitch® technology
• Dedicated automation available
– rarely perform all steps
– formats may not fit remainder of workflow
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29 June 2010
Agilent - GEN
Reaction Setup
Determine process strategy
• One sample - many reactions
• Many samples - ~1 reactions
• Layout considerations (tips, reagents, cooling, primers, master mix, etc.)
• Applications using similar workflows:
– conventional sequencing
– RNAi library transfection
– magnetic bead purifications
• Capping / sealing
– downstream processing
29 June 2010
Agilent - GEN
62
Setup
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29 June 2010
Agilent - GEN
PCR Setup: can your head do this?
• Single tip mode - templates in column 1
• Row mode - primers + master mix in row 8
• Aliquot master mix - single row of tips
• Aliquot templates - single column
29 June 2010
Agilent - GEN
63
Setup
1
2
3
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29 June 2010
Agilent - GEN
Agilent PCR Workflow Components
Real-Time PCR
Traditional PCR
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29 June 2010
Agilent - GEN
Bravo Handles PCR Workflow
29 June 2010
Agilent - GEN
65
• Small, versatile, lab-friendly footprint
– hood compatible, easy cleaning
• VWorks software
• Gripper robot
• Quick-change pipetting heads
– 96 & 384 disposable & fixed tip
– pin tool (V&P Scientific)
– high accuracy / precision
– 300 nl – 250 µl range
– SBS plates to 1536 wells
– columns / rows
– tube – plate
– tip tracking
• Many accessories
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29 June 2010
Agilent - GEN
Robots Enable Integrated Platforms:
Workstations & Systems
29 June 2010
Agilent - GEN
66
BenchCel Direct Drive Robot
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29 June 2010
Agilent - GEN
BenchCel Workstations
• 1 – ~4 instruments
• Low complexity assays or protocols
• Complex arrangements possible
29 June 2010
Agilent - GEN
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29 June 2010
Agilent - GEN
WorkStation for PCR setup
• Bravo
• BenchCel 6R
• BenchCel 4R
• PlateLoc
• Plate Centrifuge
• Multidrop Combi
29 June 2010
Agilent - GEN
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29 June 2010
Agilent - GEN
BioCel Systems: Maximum Throughput,
Hands-Off Automation
29 June 2010
Agilent - GEN
69
• Direct Drive Robot
• VWorks scheduler
– event-driven
– error-handling
– 3rd party drivers
• Environmental control
• Customized protocols
• Limitations:
› space
› budget
› imagination
BioCel 1200
BioCel 1800
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29 June 2010
Agilent - GEN
High-Throughput Genotyping BioCel
• Hardware
– dual enclosures
› 3 liquid handlers (magnetic stations and tip washers)
› seal, X-peel, & spin
› 4°C plate storage
(reagents and primers, 189 plates)
› multiple plate stackers
– 10 thermocyclers
– environmental control
• Protocols
– PCR sample preparation
– RT-PCR clean-up
– sequencing-ready amplicons
29 June 2010
Agilent - GEN
70
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29 June 2010
Agilent - GEN
384,000 PCRs from raw samples? Today?
No problem!
› 5 V11 robots, 1 Staubli robot, 2 translators
› 6 VPreps, 1 Tecan Evo
› 5 Thermo Multidrops, 2 Deerac Equators
› 4°C Liconic tube storage
› BioMicroLab XL9 tube reformatting
› 5 VSpins
› 2 PlateLocs
› 2 VCodes
› 1 computer (VWorks)
29 June 2010
Agilent - GEN
71
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Sponsored By
Scaling PCR Workflows from
Benchtop to Automation
Scaling PCR Workflows from
Benchtop to Automation
Q&A
![Page 73: Scaling PCR Workflows from Benchtop to Automationhpst.cz/.../files/attachments/scaling...automation.pdfScaling PCR Workflows from Benchtop to Automation Broadcast Date: Tuesday, June](https://reader034.vdocuments.net/reader034/viewer/2022050315/5f773af0cea7605bbb6067f7/html5/thumbnails/73.jpg)
Scaling PCR Workflows from
Benchtop to Automation
Thank You For Attending
Scaling PCR Workflows from
Benchtop to Automation
Broadcast Date: Tuesday, June 29, 2010
Time: 1:00 PM EDT
Sponsored by