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Major copy proportion analysis of tumor samples using SNP arrays., , , , , , and . BMC Bioinformatics, (2008)Analyses of non-coding somatic drivers in 2,658 cancer whole genomes., , , , , , , , , and 179 other author(s). Nat., 578 (7793): 102-111 (2020)A Mathematical Methodology for Determining the Temporal Order of Pathway Alterations Arising during Gliomagenesis., , , , , and . PLoS Computational Biology, (2012)Inferring Loss-of-Heterozygosity from Unpaired Tumors Using High-Density Oligonucleotide SNP Arrays., , , , , , , , , and 6 other author(s). PLoS Computational Biology, (2006)SeqLib: a C ++ API for rapid BAM manipulation, sequence alignment and sequence assembly., and . Bioinform., 33 (5): 751-753 (2017)Allele-Specific Amplification in Cancer Revealed by SNP Array Analysis., , , , , , , and . PLoS Computational Biology, (2005)Correction: Inferring Loss-of-Heterozygosity from Unpaired Tumors Using High-Density Oligonucleotide SNP Arrays., , , , , , , , , and 6 other author(s). PLoS Computational Biology, (2007)VariantBam: filtering and profiling of next-generational sequencing data using region-specific rules., , , and . Bioinform., 32 (13): 2029-2031 (2016)