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Constructing a meaningful evolutionary average at the phylogenetic center of mass., and . BMC Bioinform., (2007)Genome-wide analysis of transcription factor binding sites based on ChIP-Seq data., , , , , , , and . Nat. Methods, 5 (9): 829-34 (2008)Chaining Algorithms for Alignment of Draft Sequence., , , , and . WABI, volume 3240 of Lecture Notes in Computer Science, page 326-337. Springer, (2004)De novo mutational signature discovery in tumor genomes using SparseSignatures., , , , and . PLoS Comput. Biol., (2021)SHRiMP: Accurate Mapping of Short Color-space Reads., , , , , and . PLoS Comput. Biol., (2009)ABC: software for interactive browsing of genomic multiple sequence alignment data., , and . BMC Bioinform., (2004)Extensive sequencing of seven human genomes to characterize benchmark reference materials, , , , , , , , , and 43 other author(s). Scientific Data, (June 2016)Extensive sequencing of seven human genomes to characterize benchmark reference materials, , , , , , , , , and 40 other author(s). bioRxiv, (2015)svviz: a read viewer for validating structural variants., , , and . Bioinform., 31 (24): 3994-3996 (2015)