Allele-specific transcription factor binding to common and rare variants associated with disease and gene expression

Genome-wide association studies (GWAS) have identified a large number of disease-associated SNPs, but in few cases the functional variant and the gene it controls have been identified. To systematically identify candidate regulatory variants, we sequenced ENCODE cell lines and used public ChIP-seq d...

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Detalhes bibliográficos
Publicado no:Hum Genet
Main Authors: Cavalli, Marco, Pan, Gang, Nord, Helena, Wallerman, Ola, Wallén Arzt, Emelie, Berggren, Olof, Elvers, Ingegerd, Eloranta, Maija-Leena, Rönnblom, Lars, Lindblad Toh, Kerstin, Wadelius, Claes
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2016
Assuntos:
Original Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4835527/
https://ncbi.nlm.nih.gov/pubmed/26993500
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-016-1654-x
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