SNP2TFBS – a database of regulatory SNPs affecting predicted transcription factor binding site affinity
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/45/D1/D139/8846719/gkw1064.pdf
Reference20 articles.
1. Genetic variation in the non-coding genome: involvement of micro-RNAs and long non-coding RNAs in disease;Hrdlickova;Biochim. et Biophys. Acta,2014
2. Genetic and epigenetic fine mapping of causal autoimmune disease variants
3. The Genetic and Mechanistic Basis for Variation in Gene Regulation
4. atSNP: transcription factor binding affinity testing for regulatory SNP detection
5. Transcription factor binding predictions using TRAP for the analysis of ChIP-seq data and regulatory SNPs
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