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ExomeAI: detection of recurrent allelic imbalance in tumors using whole-exome sequencing data
Summary: Whole-exome sequencing (WES) has extensively been used in cancer genome studies; however, the use of WES data in the study of loss of heterozygosity or more generally allelic imbalance (AI) has so far been very limited, which highlights the need for user-friendly and flexible software that...
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| Vydáno v: | Bioinformatics |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4308664/ https://ncbi.nlm.nih.gov/pubmed/25297069 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu665 |
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