1k citations · 1k across the 2 of their papers we have counts for
2 papers
q-bio.GN2014★ 1k cited
SAMBLASTER: fast duplicate marking and structural variant read extraction
Gregory G. Faust, Ira M. Hall
Motivation: Illumina DNA sequencing is now the predominant source of raw genomic data, and data volumes are growing rapidly. Bioinformatic analysis pipelines are having trouble kee…
q-bio.GN2012★ 2 cited
LUMPY: A probabilistic framework for structural variant discovery
Ryan M. Layer, Ira M. Hall, Aaron R. Quinlan
Comprehensive discovery of structural variation (SV) in human genomes from DNA sequencing requires the integration of multiple alignment signals including read-pair, split-read and…