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Transcriptome and genome sequencing uncovers functional variation in humans, , , , , , , , , and 48 other author(s). Nature, (September 2013)PASSIM - an open source software system for managing information in biomedical studies., , , , , , , , , and 2 other author(s). BMC Bioinform., (2007)What makes a good genetic association study?, and . Lancet, 366 (9493): 1315-23 (October 2005)3971<m:linebreak></m:linebreak>Epidemiologia genètica.SAIL - a software system for sample and phenotype availability across biobanks and cohorts., , , , , , , , and . Bioinform., 27 (4): 589-591 (2011)A System for Information Management in BioMedical Studies - SIMBioMS., , , , , , , , , and 6 other author(s). Bioinform., 25 (20): 2768-2769 (2009)A structural variation reference for medical and population genetics., , , , , , , , , and 174 other author(s). Nat., 581 (7809): 444-451 (2020)Assessing allele-specific expression across multiple tissues from RNA-seq read data., , , , , , and . Bioinform., 31 (15): 2497-2504 (2015)Toppar: an interactive browser for viewing association study results., , , , and . Bioinform., 34 (11): 1922-1924 (2018)Assessing association between protein truncating variants and quantitative traits., , , , , , , , and . Bioinform., 29 (19): 2419-2426 (2013)The Architecture of Gene Regulatory Variation across Multiple Human Tissues: The MuTHER Study, , , , , , , , , and 26 other author(s). PLoS Genet, 7 (2): e1002003 (February 2011)