Targeted Sequencing Using Droplet-Based Microfluidics. Keith Brown Director, Sales

Similar documents
Novel methods for RNA and DNA- Seq analysis using SMART Technology. Andrew Farmer, D. Phil. Vice President, R&D Clontech Laboratories, Inc.

HHS Public Access Author manuscript Nat Biotechnol. Author manuscript; available in PMC 2010 May 01.

SureSelect Target Enrichment for the Ion Proton TM Next Generation Sequencing System

RIPTIDE HIGH THROUGHPUT RAPID LIBRARY PREP (HT-RLP)

Matthew Tinning Australian Genome Research Facility. July 2012

Services Presentation Genomics Experts

Get to Know Your DNA. Every Single Fragment.

Next-generation sequencing technologies

Improved Library Quantification with

Surely Better Target Enrichment from Sample to Sequencer

QIAseq SPE technology for Illumina : Redefining amplicon sequencing

Factors affecting PCR

SEQUENCING FROM SAMPLE TO SEQUENCE READY

Target Enrichment Strategies for Next Generation Sequencing

Genome Resequencing. Rearrangements. SNPs, Indels CNVs. De novo genome Sequencing. Metagenomics. Exome Sequencing. RNA-seq Gene Expression

March 20-23, 2010 Sacramento, CA

The Agilent Technologies

Deep Sequencing technologies

PrimePCR Assay Validation Report

Supplementary Information for:

Incorporating Molecular ID Technology. Accel-NGS 2S MID Indexing Kits

PrimePCR Assay Validation Report

DNA concentration and purity were initially measured by NanoDrop 2000 and verified on Qubit 2.0 Fluorometer.

High Throughput Sequencing the Multi-Tool of Life Sciences. Lutz Froenicke DNA Technologies and Expression Analysis Cores UCD Genome Center

Next Generation Sequencing Lecture Saarbrücken, 19. March Sequencing Platforms

HaloPlex HS. Get to Know Your DNA. Every Single Fragment. Kevin Poon, Ph.D.

How is genome sequencing done?

PrimePCR Assay Validation Report

The Agilent Technologies SureSelect Platform for Target Enrichment

Introduction to RNA-Seq in GeneSpring NGS Software

Overview of Next Generation Sequencing technologies. Céline Keime

HyperCap, an automatable workflow on the Agilent Bravo B

Integrated NGS Sample Preparation Solutions for Limiting Amounts of RNA and DNA. March 2, Steven R. Kain, Ph.D. ABRF 2013

PrimePCR Assay Validation Report

Increase Sequencing Efficiency with the SeqCap EZ Prime Exome

PrimePCR Assay Validation Report

SMARTer Ultra Low RNA Kit for Illumina Sequencing Two powerful technologies combine to enable sequencing with ultra-low levels of RNA

Contact us for more information and a quotation

Bioinformatics Advice on Experimental Design

Wet-lab Considerations for Illumina data analysis

Surely Better Target Enrichment from Sample to Sequencer and Analysis

SUPPLEMENTARY DATA. Table S1 Clinical features of new SS/MF patients enrolled in SNP6.0 and 10K analysis. % of TCRVß+ within CD3+CD4+

PrimePCR Assay Validation Report

DNA METHYLATION RESEARCH TOOLS

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

Next Generation Sequencing. Target Enrichment

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

Genomic systems 67. Pathologus Kongresszus Keszthely, október 9-11.

Amplicon Sequencing Template Preparation

Sequence Annotation & Designing Gene-specific qpcr Primers (computational)

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

DNBseq TM SERVICE OVERVIEW Plant and Animal Whole Genome Re-Sequencing

Human Genome Sequencing Over the Decades The capacity to sequence all 3.2 billion bases of the human genome (at 30X coverage) has increased

PrimePCR Assay Validation Report

Reading Lecture 8: Lecture 9: Lecture 8. DNA Libraries. Definition Types Construction

Supplementary Information

G E N OM I C S S E RV I C ES

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

The New Genome Analyzer IIx Delivering more data, faster, and easier than ever before. Jeremy Preston, PhD Marketing Manager, Sequencing

TECHNICAL BULLETIN. SeqPlex DNA Amplification Kit for use with high throughput sequencing technologies. Catalog Number SEQX Storage Temperature 20 C

PrimePCR Assay Validation Report

Requirements for Illumina Sequencing: Constructed Library Submission

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

Next-Generation Sequencing. Technologies

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

Cancer Genetics Solutions

PrimePCR Assay Validation Report

High Throughput Sequencing Technologies. J Fass UCD Genome Center Bioinformatics Core Monday June 16, 2014

Welcome to the NGS webinar series

Implementation of Ion AmpliSeq in molecular diagnostics

New Frontiers of Genetic Profiling Achieve Higher Sensitivity and Greater Insights with Molecular Barcodes, Long Read Capture and Optimized Exomes

Sample to Insight. Dr. Bhagyashree S. Birla NGS Field Application Scientist

Aaron Liston, Oregon State University Botany 2012 Intro to Next Generation Sequencing Workshop

UHT Sequencing Course Large-scale genotyping. Christian Iseli January 2009

Access Array BRCA1 / BRCA2 / TP53 Target-Specific Panel Build the highest quality amplicon libraries with qualified assays

Introduction Bioo Scientific

Targeted RNA sequencing reveals the deep complexity of the human transcriptome.

MHC Region. MHC expression: Class I: All nucleated cells and platelets Class II: Antigen presenting cells

Introductory Next Gen Workshop

PrimePCR Assay Validation Report

PrimePCR Assay Validation Report

High Throughput Sequencing the Multi-Tool of Life Sciences. Lutz Froenicke DNA Technologies and Expression Analysis Cores UCD Genome Center

The Diploid Genome Sequence of an Individual Human

Molecular Biology and Functional Genomic Core Facility

Successful gene expression studies using validated qpcr assays. Jan Hellemans, CEO Biogazelle webinar October 28 th, 2015

C3BI. VARIANTS CALLING November Pierre Lechat Stéphane Descorps-Declère

KAPA hgdna QUANTIFICATION AND QC KIT:

Transcription:

Targeted Sequencing Using Droplet-Based Microfluidics Keith Brown Director, Sales brownk@raindancetech.com

Who we are: is a Provider of Microdroplet-based Solutions The Company s RainStorm TM Technology Produces Picoliter-sized Droplets at a Rate of 10 million Per Hour 30 micron (16 pl) droplets: 3,000 / second Each droplet is the functional equivalent of an individual test tube and can contain a single molecule, cell or reaction Accelerating Human Health and Disease Research 2

Custom Order Primer Libraries upload gene list customer RefSeq ID CCDS Genomic coordinates Sequence Primer Library aliquots primer design oligo synthesis primer library production 3

Primer Design Criteria Parameter Spec Notes SNP Filter Amplicon Length (bp) 454 FLX 454 Titanium Illumina / SOLiD Avoid known SNPs in primers 150-250 200-600 200-600 Amplicon GC Content (%) 30-70% 50% optimal Using latest info in dbsnp Padding Region 50 bp Max. position for 3 end of primer outside of target region. Overlap (for tiled amplicons) 20-100 bp Upstream of primer sequence of overlapping amplicons Primer Tm ( C) 56-60 ispcr 1 product 2 products 3-5 products Max product size (bp) 100% 4000 Percent of amplicons with products predicted by ispcr BLASTN word size of 7; >80% overall identity and perfect match of 4 bp at 3 end OR perfect match of 11 bp at 3 end Max allowable product size for nonspecific ispcr amplicon to be considered.

RainDance Primer Library Production 1. Primer Design Customer s regions of interest Primer Pair #1 Primer Pair #2 Primer Pair #3 Primer Pair #4 Primer Pair #5 2. Primer Synthesis Forward and reverse primer pair 3. Primer Droplet Aliquot Manufacture Controlled droplet volume Controlled droplet count 4. Primer Library 5

Primer Library Quality Control Image Analysis: Droplet size Uniformity 6

Primer Library Quality Control Real-time QC of droplet representation, ~ 6,266,496 droplets Average Number of Droplets = 16,319* Std Dev = 184 *representative of ~5% of all droplets 7

RDT Polymerase Chain Reaction Inputs Output Genomic DNA Template Droplet 33 microns - 18 pl Merge 5 3 fwd rev 3 5 Primer Pair Droplet 25 microns - 8 pl PCR Droplet 37 microns - 26 pl 8

RDT 1000 Droplet-Based PCR Primer Library Genomic DNA Template Mix 9

RDT 1000 Droplet-Based PCR Primer Library Genomic DNA Template Mix 1 million droplets 45 minutes per run PCR Library Droplet Merge Area 10

Targeted Sequencing Workflow Off-Chip Process 50 ul of droplets per sample 10 minute process Break Emulsion Purified Amplicon DNA PCR Library PCR Amplification Sequencing 11

RDT 4000 Member Library Genes associated with core signaling pathways in pancreatic cancer Calculated Amplicon Peaks Total Amplicon Bases = 1.63 Mb Total Targeted Region = 1.34 Mb Primer Library Specifications: Primer Length 17-30 bp Primer Tm 55.4-61.2 C Amplicon Length 299-659 bp Amplicon GC 25.1-81.5% Agilent Bioanalyzer Analysis HapMap Sample NA18858 Sequenced using 454 and Illumina ½ 454 FLX run 2 lanes on Illumina GAII Jones S, Core signaling pathways in human pancreatic cancers revealed by global genomic analyses. Science 2008; 1801-6 12

RDT 4000 Member Library Exon Sequencing Results (1.34 Mb / 3976 exons) Targeted Sequencing Results 454 FLX Illumina GAII Percent of Target Amplicons Covered (Completeness) Target Representation Bias (<5-fold) (Sequencing Efficiency) Target Representation Bias (<10-fold) (Sequencing Efficiency) 96.9% 99.7% 89% 81% 93% 93% Targeted Bases Greater Than 10x Coverage 87% 86% Sequenced using 454 and Illumina ½ 454 FLX run 2 lanes on Illumina GAII 13

RDT 4000 Member Library: SNP Analysis 454 FLX Illumina GAII SNP s Detected (Coverage > 20x) 1675 1852 Concordant SNP s 1648 1824 Percent Concordant 98.4% 98.5% Allelic ratios for SNPs Mean - 49.5% STD 9.8% Discordant calls with HapMap 18858 reference 27 28 14

Discordant SNP Analysis 454 FLX Illumina GAII Likely Cause of Error Primary discordant calls with HapMap 18858 reference 27 28 1. SNPs not in database confirmed by both 454 and Illumina 2. SNP in database not found by either Illumina or 454 13 13 Novel 8 8 Database Error 3. SNP in database found in either 454 or Illumina but not both 4 4 Sequencing Platform Error 4. SNPs not in database confirmed by either 454 or Illumina but not both 5. SNPs in database not found by Illumina with insufficient reads by 454 2 Unknown 3 Unknown Concordance after removing Database Errors and Sequencing Platform Errors 2/1675 (99.8%) 3/1852 (99.8%) 15

Points to Consider for Targeted Sequencing What percent of target bases are represented at a minimum coverage? How much sequencing capacity is required? 16

Cumulative Coverage Profile Comparison Percent of Target Bases with Mapped Reads 100% 95% 90% 85% 80% 75% 70% 65% 60% 55% Represents 88% of Target 50% 0.0 20X 0.2 0.4 0.6 0.8 100X 1.0 Sequence Coverage normalized to Mean RDT 454 RDT Illumina Hyb Illumina Process % of Bases with 0.2X of Mean RDT (454) 96% RDT (Illumina) 94% Hyb (Illumina) 80% 64% 17 Hybridization (Hyb) data from Gnirke et al. 2009

RDT 1000 18