Loading...
SMASH, a fragmentation and sequencing method for genomic copy number analysis
Copy number variants (CNVs) underlie a significant amount of genetic diversity and disease. CNVs can be detected by a number of means, including chromosomal microarray analysis (CMA) and whole-genome sequencing (WGS), but these approaches suffer from either limited resolution (CMA) or are highly exp...
Na minha lista:
| Udgivet i: | Genome Res |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Cold Spring Harbor Laboratory Press
2016
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4889966/ https://ncbi.nlm.nih.gov/pubmed/27197213 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.201491.115 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|