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Paper Details

Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomes.
Genome Res
11
2017
31, BWT, FM, GRCh37, GRCh38, base position, full, genomes, human, human T-lymphotropic virus 1, human genomes, human reference assembly versions, sequencing reads, variant alleles, viral genomes
Author NameAffiliation
Jared T SimpsonOntario Institute for Cancer Research
Jared T SimpsonUniversity of Toronto
Richard DurbinWellcome Trust Sanger Institute
Richard DurbinWellcome Trust Sanger Institute
Shane McCarthyWellcome Trust Sanger Institute
Shane McCarthyWellcome Trust Sanger Institute
Thomas M KeaneWellcome Trust Sanger Institute
Thomas M KeaneEuropean Bioinformatics Institute
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