A Bayesian model integration for mutation calling through data partitioning

MOTIVATION: Detection of somatic mutations from tumor and matched normal sequencing data has become among the most important analysis methods in cancer research. Some existing mutation callers have focused on additional information, e.g. heterozygous single-nucleotide polymorphisms (SNPs) nearby mut...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Bioinformatics
Main Authors: Moriyama, Takuya, Imoto, Seiya, Hayashi, Shuto, Shiraishi, Yuichi, Miyano, Satoru, Yamaguchi, Rui
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2019
Teme:
Original Papers
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6821361/
https://ncbi.nlm.nih.gov/pubmed/30924874
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btz233
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