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Paper Details

Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome.
Genome Res
3
2021
NRF1, PRDM9, PRDM9 binding sites, PRDM9-bound sites, SV breakpoints, TFBS motif, TFBSs, chromatin, germline, germline TFBSs, human, human genome, human spermatogonia, motif sites, neural enhancers, proliferative cell type, rare, regulatory regions, regulatory sites, spermatogonia, variant breakpoints
Author NameAffiliation
David R FitzPatrickMRC Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital
Martin S TaylorMRC Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital
Martin S TaylorMRC Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital
Colin A SempleMRC Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital
Colin A SempleMRC Institute of Genetics and Cancer, The University of Edinburgh, Western General Hospital
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