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Bioinformatic pipelines for whole transcriptome sequencing data exploitation in leukemia patients with complex structural variants

BACKGROUND: Extensive genome rearrangements, known as chromothripsis, have been recently identified in several cancer types. Chromothripsis leads to complex structural variants (cSVs) causing aberrant gene expression and the formation of de novo fusion genes, which can trigger cancer development, or...

詳細記述

保存先:
書誌詳細
出版年:PeerJ
主要な著者: Hynst, Jakub, Plevova, Karla, Radova, Lenka, Bystry, Vojtech, Pal, Karol, Pospisilova, Sarka
フォーマット: Artigo
言語:Inglês
出版事項: PeerJ Inc. 2019
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6571010/
https://ncbi.nlm.nih.gov/pubmed/31223530
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.7071
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