Detecting differential copy number variation between groups of samples

We present a method to detect copy number variants (CNVs) that are differentially present between two groups of sequenced samples. We use a finite-state transducer where the emitted read depth is conditioned on the mappability and GC-content of all reads that occur at a given base position. In this...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Genome Res
Main Authors: Lowe, Craig B., Sanchez-Luege, Nicelio, Howes, Timothy R., Brady, Shannon D., Daugherty, Rhea R., Jones, Felicity C., Bell, Michael A., Kingsley, David M.
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2018
Assuntos:
Method
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5793789/
https://ncbi.nlm.nih.gov/pubmed/29229672
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.206938.116
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados