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SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes., , , , , , , , , and 4 other author(s). Nucleic Acids Res., 34 (Database-Issue): 617-621 (2006)GLOSSI: a method to assess the association of genetic loci-sets with complex diseases., , , , , and . BMC Bioinform., (2009)SNPPicker: High quality tag SNP selection across multiple populations., , , , and . BMC Bioinform., (2011)PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data., , , , , , , , , and 6 other author(s). Bioinform., 30 (18): 2678-2680 (2014)Robust and efficient identification of biomarkers by classifying features on graphs., , , , , , , and . Bioinform., 24 (18): 2023-2029 (2008)Measure transcript integrity using RNA-seq data., , , , , , , , , and 4 other author(s). BMC Bioinform., (2016)NCBI's LocusLink and RefSeq., , , and . Nucleic Acids Res., 28 (1): 126-128 (2000)MAP-RSeq: Mayo Analysis Pipeline for RNA sequencing., , , , , , , , , and 5 other author(s). BMC Bioinform., (2014)