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

Similar documents
Abstract. Optimization strategy of Copy Number Variant calling using Multiplicom solutions APPLICATION NOTE. Introduction

NGS in tissue and liquid biopsy

Nature Genetics: doi: /ng Supplementary Figure 1. Details of sequencing analysis.

Supplementary Figure 1. Estimation of tumour content

Nature Biotechnology: doi: /nbt Supplementary Figure 1. PL gene expression in tomato fruit.

Vertical Magnetic Separation of Circulating Tumor Cells and Somatic Genomic-Alteration Analysis in Lung Cancer Patients

SUPPLEMENTARY INFORMATION

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

Performance Characteristics BRCA MASTR Plus Dx

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

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

Disclosure. Summary. Circulating DNA and NGS technology 3/27/2017. Disclosure of Relevant Financial Relationships. JS Reis-Filho, MD, PhD, FRCPath

Advance Your Genomic Research Using Targeted Resequencing with SeqCap EZ Library

Detection of low-frequent mitochondrial DNA variants using SMRT sequencing

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

Supplemental Data: Detailed Characteristics of Patients with MKRN3. Patient 1 was born after an uneventful pregnancy. She presented in our

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

Host Double Strand Break Repair Generates HIV-1 Strains Resistant to CRISPR/Cas9

Supplementary Material

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

Nature Biotechnology: doi: /nbt.1904

Supplementary Figure 1. Generation of knockin mice expressing L-selectinN138G. (a) Schematics of the Sellg allele (top), the targeting vector, the

Supplementary Figure 1

Supplementary Figure 1: Features of IGLL5 Mutations in CLL: a) Representative IGV screenshot of first

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

Supplementary Figure 1

Genome-editing via Oviductal Nucleic Acids Delivery (GONAD) system: a novel microinjection-independent genome engineering method in mice

Nature Genetics: doi: /ng.2995

Accel-Amplicon Panels

p.r623c p.p976l p.d2847fs p.t2671 p.d2847fs p.r2922w p.r2370h p.c1201y p.a868v p.s952* RING_C BP PHD Cbp HAT_KAT11

Whole Genome and Transcriptome Analysis of Anaplastic Meningioma. Patrick Tarpey Cancer Genome Project Wellcome Trust Sanger Institute

Hands-On Ten The BRCA1 Gene and Protein

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

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

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

Prevalence of HPV-16 genomic variant carrying a 63-bp duplicated sequence within the E1 gene in Slovenian women

Supplemental Information For: The genetics of splicing in neuroblastoma

NEXT GENERATION SEQUENCING. R. Piazza (MD, PhD) Dept. of Medicine and Surgery, University of Milano-Bicocca

SUPPLEMENTARY INFORMATION

DNA-seq Bioinformatics Analysis: Copy Number Variation

SUPPLEMENTARY FIGURES

Supplementary information to:

PG-Seq NGS Kit for Preimplantation Genetic Screening

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

Nature Immunology: doi: /ni Supplementary Figure 1. Characteristics of SEs in T reg and T conv cells.

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

Nature Structural & Molecular Biology: doi: /nsmb.2419

AD (Leave blank) TITLE: Genomic Characterization of Brain Metastasis in Non-Small Cell Lung Cancer Patients

Nature Genetics: doi: /ng Supplementary Figure 1. SEER data for male and female cancer incidence from

Characterisation of structural variation in breast. cancer genomes using paired-end sequencing on. the Illumina Genome Analyser

Nature Getetics: doi: /ng.3471

Supplementary Figure 1: High-throughput profiling of survival after exposure to - radiation. (a) Cells were plated in at least 7 wells in a 384-well

Supplementary Appendix

MEDICAL GENOMICS LABORATORY. Next-Gen Sequencing and Deletion/Duplication Analysis of NF1 Only (NF1-NG)

Introduction. Introduction

Nature Genetics: doi: /ng Supplementary Figure 1. Mutational signatures in BCC compared to melanoma.

Nature Genetics: doi: /ng Supplementary Figure 1. Somatic coding mutations identified by WES/WGS for 83 ATL cases.

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

Please Silence Your Cell Phones. Thank You

Supplementary Information

Integration of Cancer Genome into GECCO- Genetics and Epidemiology of Colorectal Cancer Consortium

AP VP DLP H&E. p-akt DLP

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

To test the possible source of the HBV infection outside the study family, we searched the Genbank

Studying The Role Of DNA Mismatch Repair In Brain Cancer Malignancy

Illumina Trusight Myeloid Panel validation A R FHAN R A FIQ

Supplementary Tables. Supplementary Figures

Supplementary Materials and Methods

Nature Genetics: doi: /ng Supplementary Figure 1. Clinical timeline for the discovery WES cases.

Diagnostic with alternative sample types (liquid biopsy)

Transform genomic data into real-life results

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

a) SSR with core motif > 2 and repeats number >3. b) MNR with repeats number>5.

Introduction of an NGS gene panel into the Haemato-Oncology MPN service

Nature Immunology: doi: /ni Supplementary Figure 1. DNA-methylation machinery is essential for silencing of Cd4 in cytotoxic T cells.

Liquid biopsy in lung cancer: The EGFR paradigm

Monitoring for Drug Resistance by Genotyping. Urvi M Parikh, PhD MTN Virology Core Lab

7SK ChIRP-seq is specifically RNA dependent and conserved between mice and humans.

Table S1. Total and mapped reads produced for each ChIP-seq sample

Table S1. Relative abundance of AGO1/4 proteins in different organs. Table S2. Summary of smrna datasets from various samples.

Dr Rick Tearle Senior Applications Specialist, EMEA Complete Genomics Complete Genomics, Inc.

EXAMPLE. - Potentially responsive to PI3K/mTOR and MEK combination therapy or mtor/mek and PKC combination therapy. ratio (%)

CITATION FILE CONTENT/FORMAT

BIOL2005 WORKSHEET 2008

Exosome DNA Extraction Kits

Research Strategy: 1. Background and Significance

SUPPLEMENTARY INFORMATION

Section D: The Molecular Biology of Cancer

EGFR shrna A: CCGGCGCAAGTGTAAGAAGTGCGAACTCGAGTTCGCACTTCTTACACTTGCG TTTTTG. EGFR shrna B: CCGGAGAATGTGGAATACCTAAGGCTCGAGCCTTAGGTATTCCACATTCTCTT TTTG

underlying metastasis and recurrence in HNSCC, we analyzed two groups of patients. The

Shape-based retrieval of CNV regions in read coverage data. Sangkyun Hong and Jeehee Yoon*

Supplementary Materials for

CDH1 truncating alterations were detected in all six plasmacytoid-variant bladder tumors analyzed by whole-exome sequencing.

Introduction to Systems Biology of Cancer Lecture 2

EPIGENETIC RE-EXPRESSION OF HIF-2α SUPPRESSES SOFT TISSUE SARCOMA GROWTH

Supplementary Materials for

Inhibition of Cdk5 Promotes β-cell Differentiation from Ductal Progenitors

Exploring the Presence of microdnas in Prostate Cancer Cell Lines,

The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep

Transcription:

Supplementary Figure 1. Schematic diagram of o2n-seq. Double-stranded DNA was sheared, end-repaired, and underwent A-tailing by standard protocols. A-tailed DNA was ligated to T-tailed dutp adapters, circularized using single-strand DNA ligase, and used for second strand synthesis followed by strand displacement amplification. The amplified DNA is shown as step 6, and was subsequently used to prepare the standard NGS libraries.

a b c Supplementary Figure 2. Read depth distribution of Cir-seq, Duplex-seq, o2n-seq, and Droplet-CirSeq libraries. (a) Read depth CV (coefficient of variance) for Cir-seq for poliovirus, Cir-seq for phix174, Droplet- CirSeq, o2n-seq, and STD-NGS libraries (means ±s.d.). The o2n-seq libraries exhibited a depth CV 3.6 times lower than that of Cir-seq for poliovirus libraries, 4.22 times lower than that of Cir-seq for phix174 libraries and 2.5 times lower than that of Droplet-CirSeq libraries. The o2n-seq library depth CV was closer to that of the standard NGS library. Two-tailed Student s t-test was used for statistical analysis. (b) Boxplot of read depth distribution. Y-axis represents the log(e) ratio of depth over mean of the genome. Three replicates of Cir-seqpoliovirus, three replicates of Cir-seq-phix174, one replicate of Duplex-seq, three replicates of o2n-seq, and one standard NGS (insert size: 90 bp) were plotted. (c) Read depth distribution of Cir-seq-poliovirus, Cir-seqphix174, Droplet-CirSeq and o2n-seq. This figure showed the o2n-seq had a more highly concentrated read depth distribution than Cir-seq and Droplet-seq, and each site depth for o2n-seq was closer to the mean value of depth.

Supplementary Figure 3. Mutation types obtained by o2n-seq for 3X, 4X or 5X CSs (three experimental replicates, means ±s.d.). Supplementary Figure 4. Number of mutations detected by o2n-seq and Cir-seq. (a) Number of true positive (TP) mutations detected using o2n-seq (three experimental replicates, means ±s.d.) and Cir-seq (three experimental replicates, means ±s.d.) under different CSs criteria. Two-tailed Student s t-test was used for statistical analysis. (b, c) Total mutations, including both TP and FP mutations, detected by o2n-seq (three experimental replicates, means ±s.d.) and Cir-seq (three experimental replicates, means ±s.d.). Twotailed Student s t-test was used for statistical analysis.

Supplementary Figure 5. Mutation frequency distribution of FP and TP variants detected by o2n-seq under different CSs (3X-5X) for the 1:100 mixture of E.coli. Supplementary Figure 6. Sensitivity and FPR of mutation detection of o2n-seq by different CSs criteria (3X-9X) under different total CSs coverage (5,000-25,000 ) for the 1: 1,000 mix of phix174 (the other experimental replicate). Dash lines were used to display the overlapped results.

Supplementary Figure 7. Samples collection. Tumor tissues were embedded in O.C.T. and sliced into 1-mmthick pieces. One normal sample (N1) two tumor samples (T1, T2) were collected from one 1-mm-thick slice.

Supplementary Figure 8. Distribution of mutation type for high frequency somatic mutations in tumor samples (T1 and T2). Supplementary Figure 9. The MAF (detected by VarScan) of high frequency somatic mutation distribution for tumor samples (T1 and T2). Different MAF patterns for different samples suggest different heterogeneity levels.

Supplementary Figure 10. Validation of low-frequency mutations by ultra-deep amplicon sequencing for N1, T1, T2, and T3. The x-axis represents ± 2 bp homozygous neighbors (blue) and the candidate locus (red). The y-axis represents the MAF of mutations.

Supplementary Figure 11. Validated ultralow-frequency mutations in normal sample by digital droplet PCR. T1 was chosen as the positive control (frequency of mutant allele: 40%). N1 is the sample and NC is the negative control (normal individual). Signal from a single droplet is one dot on the graph. Comp-PTM1 represents the signal for the mutant allele (MU), and Comp-PTM2 represents the signal for the wild-type (WT) allele. NA represents the droplets that do not contain any probe targets. Numbers below the WT/MU/NA labels are the droplet number with corresponding signal.