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Detection of copy number variants and loss of heterozygosity from impure tumor samples using whole exome sequencing data
Using whole-exome sequencing (WES) for the detection of chromosomal aberrations from tumor samples has become increasingly popular, as it is cost-effective and time efficient. However, factors which present in WES tumor samples, including diversity in exon size, batch effect and tumor impurity, can...
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| Gepubliceerd in: | Oncol Lett |
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| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
D.A. Spandidos
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6126229/ https://ncbi.nlm.nih.gov/pubmed/30214605 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2018.9150 |
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