AIRVF: a filtering toolbox for precise variant calling in Ion Torrent sequencing
Author:
Affiliation:
1. Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, South Korea
2. Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, South Korea
Funder
National Research Foundation of Korea
NRF
Korea Health Industry Development Institute
Yonsei University College of Medicine
Publisher
Oxford University Press (OUP)
Subject
Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability
Link
http://academic.oup.com/bioinformatics/article-pdf/34/7/1232/25119652/btx719.pdf
Reference8 articles.
1. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples;Cibulskis;Nat. Biotechnol,2013
2. Systematic comparison of variant calling pipelines using gold standard personal exome variants;Hwang,2015
3. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing;Koboldt;Genome Res,2012
4. Performance comparison of illumina and ion torrent next-generation sequencing platforms for 16S rRNA-based bacterial community profiling;Salipante;Appl. Environ. Microbiol,2014
5. Characterization of sequence-specific errors in various next-generation sequencing systems;Shin;Mol. Biosyst,2016
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1. PipeIT;The Journal of Molecular Diagnostics;2019-09
2. Identification of single nucleotide variants using position-specific error estimation in deep sequencing data;BMC Medical Genomics;2019-08-02
3. Identification of single nucleotide variants using position-specific error estimation in deep sequencing data;2018-11-23
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