Literature DB >> 24067931

Three-stage quality control strategies for DNA re-sequencing data.

Yan Guo, Fei Ye, Quanghu Sheng, Travis Clark, David C Samuels.   

Abstract

Advances in next-generation sequencing (NGS) technologies have greatly improved our ability to detect genomic variants for biomedical research. In particular, NGS technologies have been recently applied with great success to the discovery of mutations associated with the growth of various tumours and in rare Mendelian diseases. The advance in NGS technologies has also created significant challenges in bioinformatics. One of the major challenges is quality control of the sequencing data. In this review, we discuss the proper quality control procedures and parameters for Illumina technology-based human DNA re-sequencing at three different stages of sequencing: raw data, alignment and variant calling. Monitoring quality control metrics at each of the three stages of NGS data provides unique and independent evaluations of data quality from differing perspectives. Properly conducting quality control protocols at all three stages and correctly interpreting the quality control results are crucial to ensure a successful and meaningful study.
© The Author 2013. Published by Oxford University Press. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  FASTQ; alignment; quality control; sequencing; variant calling

Mesh:

Substances:

Year:  2013        PMID: 24067931      PMCID: PMC4492405          DOI: 10.1093/bib/bbt069

Source DB:  PubMed          Journal:  Brief Bioinform        ISSN: 1467-5463            Impact factor:   11.622


  43 in total

1.  HiTEC: accurate error correction in high-throughput sequencing data.

Authors:  Lucian Ilie; Farideh Fazayeli; Silvana Ilie
Journal:  Bioinformatics       Date:  2010-11-26       Impact factor: 6.937

2.  VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing.

Authors:  Daniel C Koboldt; Qunyuan Zhang; David E Larson; Dong Shen; Michael D McLellan; Ling Lin; Christopher A Miller; Elaine R Mardis; Li Ding; Richard K Wilson
Journal:  Genome Res       Date:  2012-02-02       Impact factor: 9.043

3.  Base-calling of automated sequencer traces using phred. I. Accuracy assessment.

Authors:  B Ewing; L Hillier; M C Wendl; P Green
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

4.  The use of next generation sequencing technology to study the effect of radiation therapy on mitochondrial DNA mutation.

Authors:  Yan Guo; Qiuyin Cai; David C Samuels; Fei Ye; Jirong Long; Chung-I Li; Jeanette F Winther; E Janet Tawn; Marilyn Stovall; Päivi Lähteenmäki; Nea Malila; Shawn Levy; Christian Shaffer; Yu Shyr; Xiao-Ou Shu; John D Boice
Journal:  Mutat Res       Date:  2012-02-24       Impact factor: 2.433

5.  Fast gapped-read alignment with Bowtie 2.

Authors:  Ben Langmead; Steven L Salzberg
Journal:  Nat Methods       Date:  2012-03-04       Impact factor: 28.547

6.  SomaticSniper: identification of somatic point mutations in whole genome sequencing data.

Authors:  David E Larson; Christopher C Harris; Ken Chen; Daniel C Koboldt; Travis E Abbott; David J Dooling; Timothy J Ley; Elaine R Mardis; Richard K Wilson; Li Ding
Journal:  Bioinformatics       Date:  2011-12-06       Impact factor: 6.937

7.  Exome sequencing identifies PDE4D mutations in acrodysostosis.

Authors:  Hane Lee; John M Graham; David L Rimoin; Ralph S Lachman; Pavel Krejci; Stuart W Tompson; Stanley F Nelson; Deborah Krakow; Daniel H Cohn
Journal:  Am J Hum Genet       Date:  2012-03-29       Impact factor: 11.025

8.  Exome sequencing identifies PDE4D mutations as another cause of acrodysostosis.

Authors:  Caroline Michot; Carine Le Goff; Alice Goldenberg; Avinash Abhyankar; Céline Klein; Esther Kinning; Anne-Marie Guerrot; Philippe Flahaut; Alice Duncombe; Genevieve Baujat; Stanislas Lyonnet; Caroline Thalassinos; Patrick Nitschke; Jean-Laurent Casanova; Martine Le Merrer; Arnold Munnich; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2012-03-29       Impact factor: 11.025

9.  Transition and transversion rate in the evolution of animal mitochondrial DNA.

Authors:  C Lanave; S Tommasi; G Preparata; C Saccone
Journal:  Biosystems       Date:  1986       Impact factor: 1.973

10.  Quality control and preprocessing of metagenomic datasets.

Authors:  Robert Schmieder; Robert Edwards
Journal:  Bioinformatics       Date:  2011-01-28       Impact factor: 6.937

View more
  65 in total

1.  Mitochondria sequence mapping strategies and practicability of mitochondria variant detection from exome and RNA sequencing data.

Authors:  Pan Zhang; David C Samuels; Brian Lehmann; Thomas Stricker; Jennifer Pietenpol; Yu Shyr; Yan Guo
Journal:  Brief Bioinform       Date:  2015-08-05       Impact factor: 11.622

2.  Optimized Protocol for Simple Extraction of High-Quality Genomic DNA from Clostridium difficile for Whole-Genome Sequencing.

Authors:  James Heng Chiak Sim; Victoria Anikst; Akshar Lohith; Nader Pourmand; Niaz Banaei
Journal:  J Clin Microbiol       Date:  2015-04-15       Impact factor: 5.948

3.  Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.

Authors:  Adam C Naj; Honghuang Lin; Badri N Vardarajan; Simon White; Daniel Lancour; Yiyi Ma; Michael Schmidt; Fangui Sun; Mariusz Butkiewicz; William S Bush; Brian W Kunkle; John Malamon; Najaf Amin; Seung Hoan Choi; Kara L Hamilton-Nelson; Sven J van der Lee; Namrata Gupta; Daniel C Koboldt; Mohamad Saad; Bowen Wang; Alejandro Q Nato; Harkirat K Sohi; Amanda Kuzma; Li-San Wang; L Adrienne Cupples; Cornelia van Duijn; Sudha Seshadri; Gerard D Schellenberg; Eric Boerwinkle; Joshua C Bis; Josée Dupuis; William J Salerno; Ellen M Wijsman; Eden R Martin; Anita L DeStefano
Journal:  Genomics       Date:  2018-05-29       Impact factor: 5.736

Review 4.  High-throughput sequencing in mitochondrial DNA research.

Authors:  Fei Ye; David C Samuels; Travis Clark; Yan Guo
Journal:  Mitochondrion       Date:  2014-05-20       Impact factor: 4.160

5.  A Distributed Network for Social Cognition Enriched for Oxytocin Receptors.

Authors:  Mariela Mitre; Bianca J Marlin; Jennifer K Schiavo; Egzona Morina; Samantha E Norden; Troy A Hackett; Chiye J Aoki; Moses V Chao; Robert C Froemke
Journal:  J Neurosci       Date:  2016-02-24       Impact factor: 6.167

6.  Single nucleotide variant counts computed from RNA sequencing and cellular traffic into human kidney allografts.

Authors:  Gaurav Thareja; Hua Yang; Shahina Hayat; Franco B Mueller; John R Lee; Michelle Lubetzky; Darshana M Dadhania; Aziz Belkadi; Surya V Seshan; Karsten Suhre; Manikkam Suthanthiran; Thangamani Muthukumar
Journal:  Am J Transplant       Date:  2018-05-15       Impact factor: 8.086

7.  Differential maturation of vesicular glutamate and GABA transporter expression in the mouse auditory forebrain during the first weeks of hearing.

Authors:  Troy A Hackett; Amanda R Clause; Toru Takahata; Nicholas J Hackett; Daniel B Polley
Journal:  Brain Struct Funct       Date:  2015-07-10       Impact factor: 3.270

8.  Strategies for processing and quality control of Illumina genotyping arrays.

Authors:  Shilin Zhao; Wang Jing; David C Samuels; Quanghu Sheng; Yu Shyr; Yan Guo
Journal:  Brief Bioinform       Date:  2018-09-28       Impact factor: 11.622

Review 9.  Single-nucleotide variants in human RNA: RNA editing and beyond.

Authors:  Yan Guo; Hui Yu; David C Samuels; Wei Yue; Scott Ness; Ying-Yong Zhao
Journal:  Brief Funct Genomics       Date:  2019-02-14       Impact factor: 4.241

10.  Mitochondria single nucleotide variation across six blood cell types.

Authors:  Pan Zhang; David C Samuels; Jing Wang; Shilin Zhao; Yu Shyr; Yan Guo
Journal:  Mitochondrion       Date:  2016-03-05       Impact factor: 4.160

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.