CoNVEX: copy number variation estimation in exome sequencing data using HMM
<p>Abstract</p> <p>Background</p> <p>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, find...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2013-01-01
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| Series: | BMC Bioinformatics |
| Subjects: |