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Estimating copy numbers of alleles from population-scale high-throughput sequencing data
BACKGROUND: With the recent development of microarray and high-throughput sequencing (HTS) technologies, a number of studies have revealed catalogs of copy number variants (CNVs) and their association with phenotypes and complex traits. In parallel, a number of approaches to predict CNV regions and...
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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4331703/ https://ncbi.nlm.nih.gov/pubmed/25707811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-16-S1-S4 |
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