SNP calling using genotype model selection on high-throughput sequencing data

Motivation: 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-calli...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: You, Na, Murillo, Gabriel, Su, Xiaoquan, Zeng, Xiaowei, Xu, Jian, Ning, Kang, Zhang, Shoudong, Zhu, Jiankang, Cui, Xinping
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2012
Assuntos:
Original Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3338331/
https://ncbi.nlm.nih.gov/pubmed/22253293
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bts001
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados