Loading...
CoNVEX: copy number variation estimation in exome sequencing data using HMM
BACKGROUND: One of the main types of genetic variations in cancer is Copy Number Variations (CNV). Whole exome sequenicng (WES) is a popular alternative to whole genome sequencing (WGS) to study disease specific genomic variations. However, finding CNV in Cancer samples using WES data has not been f...
Na minha lista:
| Main Authors: | , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2013
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3549847/ https://ncbi.nlm.nih.gov/pubmed/23368785 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-S2-S2 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|