Iso-Seq Method Updates and Target Enrichment Without Amplification for SMRT Sequencing

Similar documents
CRISPR/Cas9 Enrichment and Long-read WGS for Structural Variant Discovery

Binding Calculator Parameters

FRAGILE X MOLECULAR DIAGNOSTICS ORDERING INFORMATION. FragilEaseTM FRAGILEASETM ASSAY CHARACTERISTICS WORKFLOW. PCR Purification.

Analysis of Massively Parallel Sequencing Data Application of Illumina Sequencing to the Genetics of Human Cancers

Selective depletion of abundant RNAs to enable transcriptome analysis of lowinput and highly-degraded RNA from FFPE breast cancer samples

Simple, rapid, and reliable RNA sequencing

Eukaryotic Gene Regulation

Advance Your Genomic Research Using Targeted Resequencing with SeqCap EZ Library

A complete next-generation sequencing workfl ow for circulating cell-free DNA isolation and analysis

RNA SEQUENCING AND DATA ANALYSIS

Accessing and Using ENCODE Data Dr. Peggy J. Farnham

Computational Analysis of UHT Sequences Histone modifications, CAGE, RNA-Seq

Detection of low-frequent mitochondrial DNA variants using SMRT sequencing

High Throughput TruSeq Stranded mrna Library Construction on the Biomek FX P

Supplemental Figure S1. Expression of Cirbp mrna in mouse tissues and NIH3T3 cells.

genomics for systems biology / ISB2020 RNA sequencing (RNA-seq)

AbSeq on the BD Rhapsody system: Exploration of single-cell gene regulation by simultaneous digital mrna and protein quantification

AVENIO family of NGS oncology assays ctdna and Tumor Tissue Analysis Kits

RNA-seq Introduction

Regulation of Gene Expression in Eukaryotes

RNA SEQUENCING AND DATA ANALYSIS

AVENIO ctdna Analysis Kits The complete NGS liquid biopsy solution EMPOWER YOUR LAB

MODULE 3: TRANSCRIPTION PART II

Fragile X Syndrome. Genetics, Epigenetics & the Role of Unprogrammed Events in the expression of a Phenotype

Phosphate buffered saline (PBS) for washing the cells TE buffer (nuclease-free) ph 7.5 for use with the PrimePCR Reverse Transcription Control Assay

Nature Structural & Molecular Biology: doi: /nsmb Supplementary Figure 1

CONTRACTING ORGANIZATION: Johns Hopkins University, Baltimore, MD

EPIGENOMICS PROFILING SERVICES

Transcriptional control in Eukaryotes: (chapter 13 pp276) Chromatin structure affects gene expression. Chromatin Array of nuc

Introduction to Systems Biology of Cancer Lecture 2

P. Tang ( 鄧致剛 ); PJ Huang ( 黄栢榕 ) g( ); g ( ) Bioinformatics Center, Chang Gung University.

Supplementary Figure 1. Schematic diagram of o2n-seq. Double-stranded DNA was sheared, end-repaired, and underwent A-tailing by standard protocols.

Breast and ovarian cancer in Serbia: the importance of mutation detection in hereditary predisposition genes using NGS

Ch. 18 Regulation of Gene Expression

Multiplex target enrichment using DNA indexing for ultra-high throughput variant detection

KAPA Stranded RNA-Seq Library Preparation Kit

Cellecta Overview. Started Operations in 2007 Headquarters: Mountain View, CA

Circulating Cell-Free DNA Pre-analytics: Importance of ccfdna Stabilization and Extraction for Liquid Biopsy Applications

The functional investigation of the interaction between TATA-associated factor 3 (TAF3) and p53 protein

Deploying the full transcriptome using RNA sequencing. Jo Vandesompele, CSO and co-founder The Non-Coding Genome May 12, 2016, Leuven

Breast cancer. Risk factors you cannot change include: Treatment Plan Selection. Inferring Transcriptional Module from Breast Cancer Profile Data

Ambient temperature regulated flowering time

MODULE 4: SPLICING. Removal of introns from messenger RNA by splicing

ncounter TM Analysis System

Supplementary Figures

Prokaryotes and eukaryotes alter gene expression in response to their changing environment

RNA-Seq Preparation Comparision Summary: Lexogen, Standard, NEB

Where Splicing Joins Chromatin And Transcription. 9/11/2012 Dario Balestra

Effects of UBL5 knockdown on cell cycle distribution and sister chromatid cohesion

ACE ImmunoID Biomarker Discovery Solutions ACE ImmunoID Platform for Tumor Immunogenomics

Variant Classification. Author: Mike Thiesen, Golden Helix, Inc.

WHITE PAPER. Increasing Ligation Efficiency and Discovery of mirnas for Small RNA NGS Sequencing Library Prep with Plant Samples

Morphogens: What are they and why should we care?

Nature Genetics: doi: /ng.3731

The value of Omics to chemical risk assessment

LEIDEN, THE NETHERLANDS

Profiles of gene expression & diagnosis/prognosis of cancer. MCs in Advanced Genetics Ainoa Planas Riverola

From reference genes to global mean normalization

Evaluation of MIA FORA NGS HLA test and software. Lisa Creary, PhD Department of Pathology Stanford Blood Center Research & Development Group

2/10/2016. Evaluation of MIA FORA NGS HLA test and software. Disclosure. NGS-HLA typing requirements for the Stanford Blood Center

Detection of aneuploidy in a single cell using the Ion ReproSeq PGS View Kit

mirna Dr. S Hosseini-Asl

ncounter Data Analysis Guidelines for Copy Number Variation (CNV) Molecules That Count NanoString Technologies, Inc.

Mutation Detection and CNV Analysis for Illumina Sequencing data from HaloPlex Target Enrichment Panels using NextGENe Software for Clinical Research

NGS in Cancer Pathology After the Microscope: From Nucleic Acid to Interpretation

Genetics. Instructor: Dr. Jihad Abdallah Transcription of DNA

Fluxion Biosciences and Swift Biosciences Somatic variant detection from liquid biopsy samples using targeted NGS

Overview: Conducting the Genetic Orchestra Prokaryotes and eukaryotes alter gene expression in response to their changing environment

Nature Structural & Molecular Biology: doi: /nsmb Supplementary Figure 1

COMPARISON OF HIV DRUG-RESISTANT MUTANT DETECTION BY NGS WITH AND WITHOUT UNIQUE MOLECULAR IDENTIFIERS (UMI)

Deep-Sequencing of HIV-1

CHAPTER 4 RESULTS. showed that all three replicates had similar growth trends (Figure 4.1) (p<0.05; p=0.0000)

Mechanisms of alternative splicing regulation

The Avatar System TM Yields Biologically Relevant Results

Epigenetics: The Future of Psychology & Neuroscience. Richard E. Brown Psychology Department Dalhousie University Halifax, NS, B3H 4J1

Circular RNAs (circrnas) act a stable mirna sponges

Bio 111 Study Guide Chapter 17 From Gene to Protein

Population Screening for Fragile X Syndrome

Best practice DNA prep for SMRT. Olga Vinnere Pettersson, PhD Project coordinator NGI-Sweden / SciLifeLab (UU)

Detection of copy number variations in PCR-enriched targeted sequencing data

RNA- seq Introduc1on. Promises and pi7alls

Gene Regulation Part 2

Transcriptome and isoform reconstruc1on with short reads. Tangled up in reads

Supplemental Methods RNA sequencing experiment

Phylogenomics. Antonis Rokas Department of Biological Sciences Vanderbilt University.

Development of subcutaneously administered RNAi therapeutic ARO-HBV for chronic hepatitis B virus infection

AquaPreserve DNA/RNA/Protein Order # Preservation and Extraction Kit 8001MT, 8060MT

An epigenetic approach to understanding (and predicting?) environmental effects on gene expression

Single-strand DNA library preparation improves sequencing of formalin-fixed and paraffin-embedded (FFPE) cancer DNA

Comparison of open chromatin regions between dentate granule cells and other tissues and neural cell types.

Lecture 8 Understanding Transcription RNA-seq analysis. Foundations of Computational Systems Biology David K. Gifford

Genetics and Genomics in Medicine Chapter 6 Questions

Cytogenetics 101: Clinical Research and Molecular Genetic Technologies

Functional validation of cancer susceptibility genes using gene editing

Introduction. Introduction

Proteogenomic analysis of alternative splicing: the search for novel biomarkers for colorectal cancer Gosia Komor

Fragile X One gene, three very different disorders for which Genetic Technology is essential. Significance of Fragile X. Significance of Fragile X

PG-Seq NGS Kit for Preimplantation Genetic Screening

Norgen s HIV proviral DNA PCR Kit was developed and validated to be used with the following PCR instruments: Qiagen Rotor-Gene Q BioRad icycler

Norgen s HIV Proviral DNA PCR Kit was developed and validated to be used with the following PCR instruments: Qiagen Rotor-Gene Q BioRad T1000 Cycler

Transcription:

Iso-Seq Method Updates and Target Enrichment Without Amplification for SMRT Sequencing PacBio Americas User Group Meeting Sample Prep Workshop June.27.2017 Tyson Clark, Ph.D. For Research Use Only. Not for use in diagnostics procedures. Copyright 2017 by Pacific Biosciences of California, Inc. All rights reserved.

AGENDA - Iso-Seq Method Updates -Overview of New Iso-Seq Method Workflow for Sequel Systems -Example Sequel System Iso-Seq Method Datasets -Size Selection Option for Iso-Seq Method on the Sequel System -Sequencing and Experimental Design Recommendations -Summary - Target Enrichment R&D Updates -Targeted Sequencing Using a CRISPR/Cas9-based Non-Amplification Method -Conclusion

Iso-Seq Method Updates

DETERMINATION OF TRANSCRIPT ISOFORMS Gene mrna isoforms Short-read technologies: PacBio s Iso-Seq Analysis solution: Insufficient Connectivity Splice Isoform Uncertainty Full-length cdna Sequence Reads Splice Isoform Certainty No Assembly Required Reads spanning splice junctions

Sequel System Iso-Seq Procedure Overview

EXISTING ISO-SEQ SAMPLE PREP WORKFLOW ON THE PACBIO RS II INVOLVES EXTENSIVE SIZE SELECTION Total RNA 1-2 2-3 3-6 5-10 Optional Poly-A Selection Re-Amplification PCR Optimization polya+ RNA Full Length 1 st Strand cdna Amplified cdna Reverse Transcription Large Scale Amplification 1-2 1-2 2-3 2-3 3-6 3-6 3-6 5-10 5-10 5-10 SMRTbell Template Preparation Optional Size Selection (BluePippin or SageELF) Size Selection (BluePippin, SageELF, or gel) SMRT Sequencing 1-2 2-3 3-6 5-10 Optional 5-10 size fraction

DECREASED LOADING BIAS IN SEQUEL SYSTEM REDUCES NEED FOR SIZE SELECTION Sequel SYSTEM output correlates with input SMRTbell library size distribution Full-length Transcript Sizes - Histogram plot of number of full-length sequences by transcript length for a Magbead-loaded, non-size selected Iso-Seq library sequenced on both the PacBio RS II and the Sequel System. BioAnalyzer trace of a non-size selected Iso-Seq Library - The full-length cdna sequences run on the Sequel System closely resemble the size distribution of the input SMRTbell library

NEW STREAMLINED ISO-SEQ WORKFLOW FOR SEQUEL

Example Sequel System Iso-Seq Method Datasets

EXAMPLE SEQUEL SYSTEM ISO-SEQ METHOD DATASET: PRIMARY SEQUENCING METRICS Sample [On- Plate] Total Gb Movie Pol RL (bp) Longest Subread 1x + 0.4x 50 pm 4.89 360 11766 2816 339905 (32.8%) 1x + 0.4x 40 pm 7.57 600 13845 2855 172510 (17%) 1x + 0.4x 50 pm 7.17 600 12015 2928 102676 (10%) P0 (%) P1 (%) P2 (%) 415685 (40.1%) 546423 (53%) 596453 (58%) 281207 (27.1%) 317867 (31%) 337671 (33%) - Target P1 ~50%, P0 10% - MagBead loading - Pre-extension = 120 mins - Polymerase Read Length increases with increasing movie time - Obtained 4.5 Gb for a 6-h movie and 7 Gb for a 10-h movie

EXAMPLE SEQUEL SYSTEM ISO-SEQ METHOD DATASET: SECONDARY ANALYSIS METRICS ( ISO-SEQ PROTOCOL) Sample [On-Plate] Movie #CCS CCS RL #FLNC (%) FLNC RL # Polished HQ Isoforms # Polished LQ Isoforms 1x + 0.4x 50 pm 360 415,539 2602 202,328 (48.7%) 1x + 0.4x 40 pm 600 545,724 2535 264,779 (48.5%) 1x + 0.4x 50 pm 600 595,533 2597 244,521 (41.1%) 2892 14,722 96,755 2867 20,386 132,119 3019 17,765 125,467-1 Sequel SMRT Cell typically yields 200 K Full-length non-chimeric (FLNC) reads - Number of FLNC and HQ isoforms drops with increased loading concentration (40 pm to 50 pm on-plate) even though the # CCS increases

Size Selection Option for Iso-Seq Method on the Sequel System

NEW STREAMLINED ISO-SEQ WORKFLOW FOR SEQUEL

EFFECT OF USING SIZE SELECTION OPTION WITH ISO-SEQ METHOD ON THE SEQUEL SYSTEM Non-size selected Non-size selected plus >4 size selected library (co-loaded) - BluePippin (or SageELF) size-selected library (4.5 10 ) can be pooled with non-size selected library and co-loaded together onto a single Sequel SMRT Cell Full-length Transcript Sizes

Transcript Count RECOMMENDATIONS FOR EXISTING SIZE-SELECTED FRACTIONS 0.5-2 1.5-3 2.5-6 4.5-10 Full-Length Transcript Size - Anneal and Bind size-selected fractions separately - Pool fractions by equimolar pooling (Make adjustments where necessary) - Data shown for 4 size bins pooled together and sequenced on a single Sequel SMRT Cell

AVAILABLE TECHNICAL RESOURCES FOR ISO-SEQ ANALYSIS Iso-Seq Best Practices NimbleGen Targeted Iso-Seq Barcoding Iso-Seq Iso-Seq on Sequel IDT Targeted Iso-Seq

SUMMARY - Prepare full-length transcripts using the Clontech SMARTer PCR cdna Synthesis Kit with as little as 1 ng of poly A+ RNA or 2 ng of total RNA - Sequel System loading protocols reduce need for size selection for transcripts <4 - Optional size-selection protocols to enrich for transcripts >4 - Survey transcriptomes in 1 2 SMRT Cells on the Sequel System - Increase sequencing depth for more comprehensive transcriptome characterization - Compatible with standard target enrichment methods, such as NimbleGen SeqCap EZ or IDT xgen Lockdown Probes - Multiplex transcripts or full transcriptomes with sample barcoding - Profile transcripts from multiplexed samples in a single Sequel SMRT Cell 1M - Data analysis protocols and tools available through SMRT Analysis and PacBio DevNet to generate high-quality, full-length transcript sequences with no assembly required - Run Iso-Seq analysis in either de novo (no genome reference required) or reference-based mode - Run Iso-Seq with Mapping analysis (map isoforms to GMAP) to enable studying gene families, gene fusion, accurate identification of unique isoforms.

Target Enrichment R&D Updates

Targeted SMRT Sequencing of Repeat- Expansion Disease Causative Genomic Regions Using a CRISPR/Cas9, Non-Amplification Based Method For Research Use Only. Not for use in diagnostics procedures. Copyright 2015 by Pacific Biosciences of California, Inc. All rights reserved.

REPEAT EXPANSION DISEASES 23

CRISPR/CAS9 SYSTEM Bacterial Adaptive Immunity RNA-guided DNA Endonuclease Some in vivo applications: - Gene silencing - Homology-directed repair - Transient gene silencing or transcriptional repression - Transient activation of endogenous genes - Transgenic animals and embryonic stem cells

PCR-FREE TARGET ENRICHMENT VIA CAS9 DIGESTION: METHOD OVERVIEW (CURRENTLY IN DEVELOPMENT)

USING CRISPR/CAS9 TO ENRICH FOR REPEAT EXPANSION DISORDERS * * *Restriction Enzyme Number of individual molecules sequenced - Improved on-target rate with complexity reduction: - Restriction enzymes are used to degrade unwanted SMRTbell templates - Additional starting DNA is required to maintain input into Cas9 digestion step - Multiplexing: - Multiple regions can be targeted in the same reaction - Patient samples could be barcoded during initial SMRTbell library preparation

COVERAGE ACROSS THE GENOME

RICARDO MOURO PINTO WILL BE DISCUSSING HUNTINGTON S DISEASE TOMORROW

FRAGILE X SYNDROME - Most common heritable form of cognitive impairment - Caused by expansion of a CGG trinucleotide repeat in the 5 UTR of the FMR1 gene fraxa.org

>700 CGG REPEATS SEQUENCED FROM THE FMR1 GENE

AGG INTERRUPTIONS REDUCE THE CHANCES OF PRE- TO FULL- MUTATION TRANSMISSION CGG CGG CGG CGG AGG CGG Difference in risk is greatest near 75-80 CGG repeats Having full sequence information is medically relevant Yrigollen et al. (2012) Genet Med 80% 60% 15% Maternal CGG repeat number 2 CGG CGG CGG CGG AGG CGG CGG CGG CGG CGG CGG CGG CGG CGG AGG CGG 1 CGG CGG CGG CGG AGG CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG 0 CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG CGG Yrigollen et al. (2012) Genet Med 14:729 736

DIRECT DETECTION OF METHYLATION

METHYLATION DETECTION OF FMR1 SAMPLE

METHYLATION DETECTION OF FMR1 SAMPLE CGG repeat region appears to be heavily methylated (5mC)

CONCLUSION Amplification-free enrichment with CRISPR/Cas9 and SMRT Sequencing achieves the base-level resolution required to understand the underlying biology of repeat expansion disorders - Target any hard-to-amplify genomic region regardless of sequence context - Avoid PCR bias and PCR errors - Accurately sequence through long repetitive and low-complexity regions - Count repeats and identify sequence interruptions - Detect and characterize epigenetic modification signals - Detect sample mosaicism

For Research Use Only. Not for use in diagnostics procedures. Copyright 2017 by Pacific Biosciences of California, Inc. All rights reserved. Pacific Biosciences, the Pacific Biosciences logo, PacBio, SMRT, SMRTbell, Iso-Seq, and Sequel are trademarks of Pacific Biosciences. BluePippin and SageELF are trademarks of Sage Science. NGS-go and NGSengine are trademarks of GenDx. All other trademarks are the sole property of their respective owners.