An investigation of causes of false positive single nucleotide polymorphisms using simulated reads from a small eukaryote genome

BACKGROUND: Single Nucleotide Polymorphisms (SNPs) are widely used molecular markers, and their use has increased massively since the inception of Next Generation Sequencing (NGS) technologies, which allow detection of large numbers of SNPs at low cost. However, both NGS data and their analysis are...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:BMC Bioinformatics
Main Authors: Ribeiro, Antonio, Golicz, Agnieszka, Hackett, Christine Anne, Milne, Iain, Stephen, Gordon, Marshall, David, Flavell, Andrew J., Bayer, Micha
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2015
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4642669/
https://ncbi.nlm.nih.gov/pubmed/26558718
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0801-z
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares