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iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data., , , , , , , and . BMC Syst. Biol., 7 (S-6): S8 (2013)VarySysDB: a human genetic polymorphism database based on all H-InvDB transcripts., , , , , , , , and . Nucleic Acids Res., 37 (Database-Issue): 810-815 (2009)Estimating copy numbers of alleles from population-scale high-throughput sequencing data., , , , , , and . BMC Bioinform., 16 (S-1): S4 (2015)A statistical variant calling approach from pedigree information and local haplotyping with phase informative reads., , , , , , and . Bioinform., 29 (22): 2835-2843 (2013)HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data., , , , , , , , and . BMC Genom., 16 (S-2): S7 (2015)SVEM: A Structural Variant Estimation Method Using Multi-mapped Reads on Breakpoints., , , , , , , , and . AlCoB, volume 8542 of Lecture Notes in Computer Science, page 208-219. Springer, (2014)HapMonster: A Statistically Unified Approach for Variant Calling and Haplotyping Based on Phase-Informative Reads., , , , , , and . AlCoB, volume 8542 of Lecture Notes in Computer Science, page 107-118. Springer, (2014)