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Inferring copy number and genotype in tumour exome data
BACKGROUND: Using whole exome sequencing to predict aberrations in tumours is a cost effective alternative to whole genome sequencing, however is predominantly used for variant detection and infrequently utilised for detection of somatic copy number variation. RESULTS: We propose a new method to inf...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4162913/ https://ncbi.nlm.nih.gov/pubmed/25167919 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-732 |
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