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AeQTL: eQTL analysis using region-based aggregation of rare genomic variants., , , , and . PSB, WorldScientific, (2021)Gap statistics for whole genome shotgun DNA sequencing projects., and . Bioinform., 20 (10): 1527-1534 (2004)Optimizing Cancer Genome Sequencing and Analysis, , , , , , , , , and 17 other author(s). Cell Systems, 1 (3): 210--223 (Sep 9, 2015)MSIsensor-ct: microsatellite instability detection using cfDNA sequencing data., , , , , , , , , and 2 other author(s). Briefings Bioinform., (2021)Random Covering of Multiple One-Dimensional Domains with an Application to DNA Sequencing.. SIAM J. Appl. Math., 68 (3): 890-905 (2008)Systematic discovery of complex insertions and deletions in human cancers, , , , , , , , , and 10 other author(s). Nature Medicine, 22 (1): 97--104 (2016)MuSiC: Identifying mutational significance in cancer genomes, , , , , , , , , and 2 other author(s). Genome Research, 22 (8, /content/22/8.cover.gif): 1589-1598 (2012)A General Coverage Theory for Shotgun DNA Sequencing.. J. Comput. Biol., 13 (6): 1177-1196 (2006)Collision probability between sets of random variables. Statistics & Probability Letters, 64 (3): 249 - 254 (2003)Design and implementation of a generalized laboratory data model., , , , , , , , , and 4 other author(s). BMC Bioinform., (2007)