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A sparse model based detection of copy number variations from exome sequencing data
GOAL: Whole-exome sequencing provides a more cost-effective way than whole-genome sequencing for detecting genetic variants such as copy number variations (CNVs). Although a number of approaches have been proposed to detect CNVs from whole-genome sequencing, a direct adoption of these approaches to...
Gardado en:
| Publicado en: | IEEE Trans Biomed Eng |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2016
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4808620/ https://ncbi.nlm.nih.gov/pubmed/26258935 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1109/TBME.2015.2464674 |
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