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Custom Enrichment Panels for Targeted Next
Generation Sequencing
Rami Zahr, NGS Field Application Specialist
Integrated DNA Technologies
What is Target Enrichment?
Whole Genome
Sequencing

Target
Enrichment

Genomic DNA

Perform Fragmentation

Attach Adapters

Perform
Hybrid Capture

Generate
Amplicons

Sequence

Samples in Experiment
Target Analysis Size

Primary Applications

1–10 Samples

100s–1000s

3 Gb

Variable: 5 kb–60 Mb

Discovery
Building a reference (de novo)

Rare variant discovery
Variant detection

2
IDT xGen® Target Enrichment Products
xGen® Lockdown® Probes
 Individually synthesized and quality control (QC) tested
 Lengths of 60–120 nt
 7–10 business day TAT

xGen® Acute Myeloid Leukemia Cancer Panel v1.0
 260 genes, 11.7K probes, 1.2 Mb
 Based on findings published by The Cancer Genome Atlas Research Network (2013)
[N Engl J Med, 368:2059–2074]

xGen® Universal Blocking Oligos
 Single oligo sequence blocks many barcoded adapters simultaneously
 Consistent on-target performance even with high multiplex captures

xGen® 4-Hour Capture Protocol
 4-hour hybridization, 2–4 hours hands-on time
 High uniformity of enrichment

3
Probe Performance and Validation—Design of Tm Experiment
1, 3, or 7 bp (All T)

7 bp (All T or All C)

Top strand = 121, 123, or 127 bp respectively

120 bp

7 bp (All T or All C)

Top strand = 134 bp

120 bp

1 bp mismatch (G-T or T-T)

120 bp

120 bp

Ultramer® Oligonucleotides with 1, 3, or 7 G-T or T-T mismatches

120 bp

120 bp

4
Probe Performance and Validation—Conclusion
 1–7 base mismatches had <5°C ΔTm
 One or two 1–7 base insertions had <4°C ΔTm
 These small changes in Tm will not affect capture
 Thus use of a 120mer capture probe is sufficient

5
AML Panel Performance—Fold Enrichment
300

Average Coverage
Depth

Fold Enrichment

750

700

250
650

600

550
150
500

100

Fold Enrichment

Average Coverage Depth

200

450

400
50
350

0

300
#10

#11

#17

#23

#10

#11

#17

#23

6
AML Panel Performance—Alignment Breakdown
Off-target

Duplicate On-Target

500 bp Flank

On-Target

100%
90%
80%
70%

% of Reads

60%
50%
40%
30%
20%
10%
0%
#10

#11

#17

#23

#10

#11

#17

#23

7
AML Panel Performance—Uniformity
>0.2 x Mean Coverage

>0.5 x Mean Coverage

>1.0 x Mean Coverage

1
0.9
0.8

% of Targets

0.7
0.6
0.5
0.4
0.3
0.2
0.1
0
1

2

Replicate Number

3

4

8
xGen® Universal Blocking Oligos
60.00

On-Target Reads (%)

50.00

40.00

30.00

20.00

10.00

xGen® Universal Blocking
Oligos

xGen® Standard Blocking
Oligos
w/ no inosines

Standard Blocking Oligos
w/ inosine barcodes

9
Summary
 xGen® Lockdown® Probes are high quality, individually quality
controlled oligos

 The xGen® AML Panel v1.0 provides a large list of genes that
researchers can use as a starting point to create a customized panel
at low cost, for high performance

 xGen® Standard Blocking Oligos used with xGen® Lockdown® Probes
increase on-target capture, and xGen® Universal Blocking Oligos can
block many indices
10

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Custom Enrichment Panels for Targeted Next Generation Sequencing

  • 1. Custom Enrichment Panels for Targeted Next Generation Sequencing Rami Zahr, NGS Field Application Specialist Integrated DNA Technologies
  • 2. What is Target Enrichment? Whole Genome Sequencing Target Enrichment Genomic DNA Perform Fragmentation Attach Adapters Perform Hybrid Capture Generate Amplicons Sequence Samples in Experiment Target Analysis Size Primary Applications 1–10 Samples 100s–1000s 3 Gb Variable: 5 kb–60 Mb Discovery Building a reference (de novo) Rare variant discovery Variant detection 2
  • 3. IDT xGen® Target Enrichment Products xGen® Lockdown® Probes  Individually synthesized and quality control (QC) tested  Lengths of 60–120 nt  7–10 business day TAT xGen® Acute Myeloid Leukemia Cancer Panel v1.0  260 genes, 11.7K probes, 1.2 Mb  Based on findings published by The Cancer Genome Atlas Research Network (2013) [N Engl J Med, 368:2059–2074] xGen® Universal Blocking Oligos  Single oligo sequence blocks many barcoded adapters simultaneously  Consistent on-target performance even with high multiplex captures xGen® 4-Hour Capture Protocol  4-hour hybridization, 2–4 hours hands-on time  High uniformity of enrichment 3
  • 4. Probe Performance and Validation—Design of Tm Experiment 1, 3, or 7 bp (All T) 7 bp (All T or All C) Top strand = 121, 123, or 127 bp respectively 120 bp 7 bp (All T or All C) Top strand = 134 bp 120 bp 1 bp mismatch (G-T or T-T) 120 bp 120 bp Ultramer® Oligonucleotides with 1, 3, or 7 G-T or T-T mismatches 120 bp 120 bp 4
  • 5. Probe Performance and Validation—Conclusion  1–7 base mismatches had <5°C ΔTm  One or two 1–7 base insertions had <4°C ΔTm  These small changes in Tm will not affect capture  Thus use of a 120mer capture probe is sufficient 5
  • 6. AML Panel Performance—Fold Enrichment 300 Average Coverage Depth Fold Enrichment 750 700 250 650 600 550 150 500 100 Fold Enrichment Average Coverage Depth 200 450 400 50 350 0 300 #10 #11 #17 #23 #10 #11 #17 #23 6
  • 7. AML Panel Performance—Alignment Breakdown Off-target Duplicate On-Target 500 bp Flank On-Target 100% 90% 80% 70% % of Reads 60% 50% 40% 30% 20% 10% 0% #10 #11 #17 #23 #10 #11 #17 #23 7
  • 8. AML Panel Performance—Uniformity >0.2 x Mean Coverage >0.5 x Mean Coverage >1.0 x Mean Coverage 1 0.9 0.8 % of Targets 0.7 0.6 0.5 0.4 0.3 0.2 0.1 0 1 2 Replicate Number 3 4 8
  • 9. xGen® Universal Blocking Oligos 60.00 On-Target Reads (%) 50.00 40.00 30.00 20.00 10.00 xGen® Universal Blocking Oligos xGen® Standard Blocking Oligos w/ no inosines Standard Blocking Oligos w/ inosine barcodes 9
  • 10. Summary  xGen® Lockdown® Probes are high quality, individually quality controlled oligos  The xGen® AML Panel v1.0 provides a large list of genes that researchers can use as a starting point to create a customized panel at low cost, for high performance  xGen® Standard Blocking Oligos used with xGen® Lockdown® Probes increase on-target capture, and xGen® Universal Blocking Oligos can block many indices 10