MAC: identifying and correcting annotation for multi-nucleotide variations

BACKGROUND: Next-Generation Sequencing (NGS) technologies have rapidly advanced our understanding of human variation in cancer. To accurately translate the raw sequencing data into practical knowledge, annotation tools, algorithms and pipelines must be developed that keep pace with the rapidly evolv...

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Detalhes bibliográficos
Publicado no:BMC Genomics
Main Authors: Wei, Lei, Liu, Lu T., Conroy, Jacob R., Hu, Qiang, Conroy, Jeffrey M., Morrison, Carl D., Johnson, Candace S., Wang, Jianmin, Liu, Song
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4521406/
https://ncbi.nlm.nih.gov/pubmed/26231518
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-015-1779-7
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