Detection of copy number variation from array intensity and sequencing read depth using a stepwise Bayesian model
<p>Abstract</p> <p>Background</p> <p>Copy number variants (CNVs) have been demonstrated to occur at a high frequency and are now widely believed to make a significant contribution to the phenotypic variation in human populations. Array-based comparative genomic hybridization (array-CGH) and newly de...
Wedi'i Gadw mewn:
| Prif Awduron: | , |
|---|---|
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BMC
2010-10-01
|
| Cyfres: | BMC Bioinformatics |
| Mynediad Ar-lein: | http://www.biomedcentral.com/1471-2105/11/539 |
| Tagiau: |
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!
|