A carregar...
Integrative DNA copy number detection and genotyping from sequencing and array-based platforms
MOTIVATION: Copy number variations (CNVs) are gains and losses of DNA segments and have been associated with disease. Many large-scale genetic association studies are performing CNV analysis using whole exome sequencing (WES) and whole genome sequencing (WGS). In many of these studies, previous sing...
Na minha lista:
| Publicado no: | Bioinformatics |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6041760/ https://ncbi.nlm.nih.gov/pubmed/29992253 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty104 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|