SEMPLR: an R package for transcription factor binding prediction.
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- Record sourced from PubMed, PMID 42286344.
- Also identified by DOI 10.1093/bioinformatics/btag383.
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Abstract
SEMPLR is an R package that predicts transcription factor binding and variant effects using SNP Effect Matrices (SEMs), providing efficient, genome-wide scoring, enrichment testing, and visualization tools for comprehensive analysis of regulatory sequences. Available on GitHub at https://github.com/grkenney/SEMPLR and on Bioconductor at https://bioconductor.org/packages/release/bioc/html/SEMPLR.html. Supplementary data are available at Bioinformatics online.