Literature DB >> 34504351

Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study.

Jonathan Foox1,2, Scott W Tighe3, Charles M Nicolet4, Justin M Zook5, Marta Byrska-Bishop6, Wayne E Clarke6, Michael M Khayat7,8, Medhat Mahmoud7,8, Phoebe K Laaguiby3, Zachary T Herbert9, Derek Warner10, George S Grills11, Jin Jen12, Shawn Levy13, Jenny Xiang1, Alicia Alonso1, Xia Zhao14,15, Wenwei Zhang14, Fei Teng14, Yonggang Zhao14,16, Haorong Lu14,17, Gary P Schroth18, Giuseppe Narzisi6, William Farmerie19, Fritz J Sedlazeck20,21, Don A Baldwin22, Christopher E Mason23,24,25,26.   

Abstract

Assessing the reproducibility, accuracy and utility of massively parallel DNA sequencing platforms remains an ongoing challenge. Here the Association of Biomolecular Resource Facilities (ABRF) Next-Generation Sequencing Study benchmarks the performance of a set of sequencing instruments (HiSeq/NovaSeq/paired-end 2 × 250-bp chemistry, Ion S5/Proton, PacBio circular consensus sequencing (CCS), Oxford Nanopore Technologies PromethION/MinION, BGISEQ-500/MGISEQ-2000 and GS111) on human and bacterial reference DNA samples. Among short-read instruments, HiSeq 4000 and X10 provided the most consistent, highest genome coverage, while BGI/MGISEQ provided the lowest sequencing error rates. The long-read instrument PacBio CCS had the highest reference-based mapping rate and lowest non-mapping rate. The two long-read platforms PacBio CCS and PromethION/MinION showed the best sequence mapping in repeat-rich areas and across homopolymers. NovaSeq 6000 using 2 × 250-bp read chemistry was the most robust instrument for capturing known insertion/deletion events. This study serves as a benchmark for current genomics technologies, as well as a resource to inform experimental design and next-generation sequencing variant calling.
© 2021. The Author(s), under exclusive licence to Springer Nature America, Inc.

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Year:  2021        PMID: 34504351      PMCID: PMC8985210          DOI: 10.1038/s41587-021-01049-5

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


  43 in total

1.  Tandem repeats finder: a program to analyze DNA sequences.

Authors:  G Benson
Journal:  Nucleic Acids Res       Date:  1999-01-15       Impact factor: 16.971

2.  Reproducibility and quantitation of amplicon sequencing-based detection.

Authors:  Jizhong Zhou; Liyou Wu; Ye Deng; Xiaoyang Zhi; Yi-Huei Jiang; Qichao Tu; Jianping Xie; Joy D Van Nostrand; Zhili He; Yunfeng Yang
Journal:  ISME J       Date:  2011-02-24       Impact factor: 10.302

3.  ClinVar at five years: Delivering on the promise.

Authors:  Melissa J Landrum; Brandi L Kattman
Journal:  Hum Mutat       Date:  2018-11       Impact factor: 4.878

4.  College of American Pathologists' laboratory standards for next-generation sequencing clinical tests.

Authors:  Nazneen Aziz; Qin Zhao; Lynn Bry; Denise K Driscoll; Birgit Funke; Jane S Gibson; Wayne W Grody; Madhuri R Hegde; Gerald A Hoeltge; Debra G B Leonard; Jason D Merker; Rakesh Nagarajan; Linda A Palicki; Ryan S Robetorye; Iris Schrijver; Karen E Weck; Karl V Voelkerding
Journal:  Arch Pathol Lab Med       Date:  2014-08-25       Impact factor: 5.534

5.  Proficiency Testing of Standardized Samples Shows Very High Interlaboratory Agreement for Clinical Next-Generation Sequencing-Based Oncology Assays.

Authors:  Jason D Merker; Kelly Devereaux; A John Iafrate; Suzanne Kamel-Reid; Annette S Kim; Joel T Moncur; Stephen B Montgomery; Rakesh Nagarajan; Bryce P Portier; Mark J Routbort; Craig Smail; Lea F Surrey; Patricia Vasalos; Alexander J Lazar; Neal I Lindeman
Journal:  Arch Pathol Lab Med       Date:  2018-10-30       Impact factor: 5.534

6.  A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium.

Authors: 
Journal:  Nat Biotechnol       Date:  2014-08-24       Impact factor: 54.908

7.  OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders.

Authors:  Joanna S Amberger; Carol A Bocchini; François Schiettecatte; Alan F Scott; Ada Hamosh
Journal:  Nucleic Acids Res       Date:  2014-11-26       Impact factor: 19.160

8.  UpSetR: an R package for the visualization of intersecting sets and their properties.

Authors:  Jake R Conway; Alexander Lex; Nils Gehlenborg
Journal:  Bioinformatics       Date:  2017-09-15       Impact factor: 6.937

9.  An open resource for accurately benchmarking small variant and reference calls.

Authors:  Justin M Zook; Jennifer McDaniel; Nathan D Olson; Justin Wagner; Hemang Parikh; Haynes Heaton; Sean A Irvine; Len Trigg; Rebecca Truty; Cory Y McLean; Francisco M De La Vega; Chunlin Xiao; Stephen Sherry; Marc Salit
Journal:  Nat Biotechnol       Date:  2019-04-01       Impact factor: 54.908

10.  DELLY: structural variant discovery by integrated paired-end and split-read analysis.

Authors:  Tobias Rausch; Thomas Zichner; Andreas Schlattl; Adrian M Stütz; Vladimir Benes; Jan O Korbel
Journal:  Bioinformatics       Date:  2012-09-15       Impact factor: 6.937

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  15 in total

1.  Diagnostic accuracy of the metagenomic next-generation sequencing (mNGS) for detection of bacterial meningoencephalitis: a systematic review and meta-analysis.

Authors:  Rimjhim Kanaujia; Manisha Biswal; Archana Angrup; Pallab Ray
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2022-04-26       Impact factor: 3.267

2.  Comprehensive pan-cancer analysis identifies cellular senescence as a new therapeutic target for cancer: multi-omics analysis and single-cell sequencing validation.

Authors:  Qiuhuan Zhang; Yi Tang; Guimei Hu; Zhuoer Yuan; Shengyue Zhang; Yucao Sun; Chencheng Dong; Jiehua Zhao; Guo Wu; Xiaoliang Huang; Jianrong Yang; Yuntian Tang
Journal:  Am J Cancer Res       Date:  2022-09-15       Impact factor: 5.942

3.  Development of a versatile high-throughput mutagenesis assay with multiplexed short-read NGS using DNA-barcoded supF shuttle vector library amplified in E. coli.

Authors:  Hidehiko Kawai; Ren Iwata; Shungo Ebi; Ryusei Sugihara; Shogo Masuda; Chiho Fujiwara; Shingo Kimura; Hiroyuki Kamiya
Journal:  Elife       Date:  2022-10-10       Impact factor: 8.713

4.  Detecting cell-of-origin and cancer-specific methylation features of cell-free DNA from Nanopore sequencing.

Authors:  Efrat Katsman; Shari Orlanski; Filippo Martignano; Silvestro G Conticello; Benjamin P Berman; Ilana Fox-Fisher; Ruth Shemer; Yuval Dor; Aviad Zick; Amir Eden; Iacopo Petrini
Journal:  Genome Biol       Date:  2022-07-15       Impact factor: 17.906

Review 5.  Loop-Mediated Isothermal Amplification Detection of SARS-CoV-2 and Myriad Other Applications.

Authors:  Keith J M Moore; Jeremy Cahill; Guy Aidelberg; Rachel Aronoff; Ali Bektaş; Daniela Bezdan; Daniel J Butler; Sridar V Chittur; Martin Codyre; Fernan Federici; Nathan A Tanner; Scott W Tighe; Randy True; Sarah B Ware; Anne L Wyllie; Evan E Afshin; Andres Bendesky; Connie B Chang; Richard Dela Rosa; Eran Elhaik; David Erickson; Andrew S Goldsborough; George Grills; Kathrin Hadasch; Andrew Hayden; Seong-Young Her; Julie A Karl; Chang Hee Kim; Alison J Kriegel; Thomas Kunstman; Zeph Landau; Kevin Land; Bradley W Langhorst; Ariel B Lindner; Benjamin E Mayer; Lee A McLaughlin; Matthew T McLaughlin; Jenny Molloy; Christopher Mozsary; Jerry L Nadler; Melinee D'Silva; David Ng; David H O'Connor; Jerry E Ongerth; Olayinka Osuolale; Ana Pinharanda; Dennis Plenker; Ravi Ranjan; Michael Rosbash; Assaf Rotem; Jacob Segarra; Stephan Schürer; Scott Sherrill-Mix; Helena Solo-Gabriele; Shaina To; Merly C Vogt; Albert D Yu; Christopher E Mason
Journal:  J Biomol Tech       Date:  2021-09

6.  RNA-combine: a toolkit for comprehensive analyses on transcriptome data from different sequencing platforms.

Authors:  Xuemin Dong; Shanshan Dong; Shengkai Pan; Xiangjiang Zhan
Journal:  BMC Bioinformatics       Date:  2022-01-06       Impact factor: 3.169

7.  Hidden biases in germline structural variant detection.

Authors:  Michael M Khayat; Sayed Mohammad Ebrahim Sahraeian; Samantha Zarate; Andrew Carroll; Huixiao Hong; Bohu Pan; Leming Shi; Richard A Gibbs; Marghoob Mohiyuddin; Yuanting Zheng; Fritz J Sedlazeck
Journal:  Genome Biol       Date:  2021-12-20       Impact factor: 13.583

8.  Studying mutation rate evolution in primates-a need for systematic comparison of computational pipelines.

Authors:  Lucie A Bergeron; Søren Besenbacher; Mikkel H Schierup; Guojie Zhang
Journal:  Gigascience       Date:  2021-10-21       Impact factor: 6.524

9.  The Sequencing Quality Control 2 study: establishing community standards for sequencing in precision medicine.

Authors:  Tim R Mercer; Joshua Xu; Christopher E Mason; Weida Tong
Journal:  Genome Biol       Date:  2021-11-08       Impact factor: 13.583

Review 10.  Towards accurate and reliable resolution of structural variants for clinical diagnosis.

Authors:  Zhichao Liu; Ruth Roberts; Timothy R Mercer; Joshua Xu; Fritz J Sedlazeck; Weida Tong
Journal:  Genome Biol       Date:  2022-03-03       Impact factor: 17.906

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