Skip to Main Content

Paper Details

Basset: learning the regulatory code of the accessible genome with deep convolutional neural networks.
Genome Research
451
2016
164 cell types, DNA sequences, DNase, Genome-wide association study (GWAS) SNPs, SNPs, accessible genome, accessible genomic sites, cell type, chromatin accessibility code, eukaryotic gene, human, noncoding genome, noncoding variants, regulatory code, variant alleles
Author NameAffiliation
David R KelleyHarvard University
John L RinnHarvard University
  • 1 - 2

Datasets

Release 1.2