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Exploiting genetic variation to uncover rules of transcription factor binding and chromatin accessibility

Single-nucleotide variants that underlie phenotypic variation can affect chromatin occupancy of transcription factors (TFs). To delineate determinants of in vivo TF binding and chromatin accessibility, we introduce an approach that compares ChIP-seq and DNase-seq data sets from genetically divergent...

詳細記述

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書誌詳細
出版年:Nat Commun
主要な著者: Behera, Vivek, Evans, Perry, Face, Carolyne J., Hamagami, Nicole, Sankaranarayanan, Laavanya, Keller, Cheryl A., Giardine, Belinda, Tan, Kai, Hardison, Ross C., Shi, Junwei, Blobel, Gerd A.
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group UK 2018
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5823854/
https://ncbi.nlm.nih.gov/pubmed/29472540
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-018-03082-6
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