SNP calling using genotype model selection on high-throughput sequencing data
Author(s) -
Na You,
Gabriel Murillo,
Xiaoquan Su,
Xiaowei Zeng,
Jian Xu,
Kang Ning,
Shoudong Zhang,
JianKang Zhu,
Xinping Cui
Publication year - 2012
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/bts001
Subject(s) - snp , selection (genetic algorithm) , throughput , genotype , computer science , dna sequencing , computational biology , genetics , biology , single nucleotide polymorphism , data mining , artificial intelligence , gene , telecommunications , wireless
A review of the available single nucleotide polymorphism (SNP) calling procedures for Illumina high-throughput sequencing (HTS) platform data reveals that most rely mainly on base-calling and mapping qualities as sources of error when calling SNPs. Thus, errors not involved in base-calling or alignment, such as those in genomic sample preparation, are not accounted for.
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