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Tackling the widespread and critical impact of batch effects in high-throughput data., , , , , , , , and . Nat Rev Genet, 11 (10): 733--739 (October 2010)Detection of de novo copy number deletions from targeted sequencing of trios., , , , , , , and . Bioinform., 35 (4): 571-578 (2019)Fast detection of de novo copy number variants from SNP arrays for case-parent trios., , , , , and . BMC Bioinform., (2012)Detecting and quantifying antibody reactivity in PhIP-Seq data with BEER., , , , and . Bioinform., 38 (19): 4647-4649 (2022)Performance assessment of copy number microarray platforms using a spike-in experiment., , , , , , , , , and 6 other author(s). Bioinform., 27 (8): 1052-1060 (2011)Estimation of cancer cell fractions and clone trees from multi-region sequencing of tumors., , , , and . Bioinform., 38 (15): 3677-3683 (2022)SNPchip: R classes and methods for SNP array data., , , and . Bioinform., 23 (5): 627-628 (2007)Detection of rare disease variants in extended pedigrees using RVS., , , , and . Bioinform., 35 (14): 2509-2511 (2019)3D genomic mapping reveals multifocality of human pancreatic precancers., , , , , , , , , and 35 other author(s). Nat., 629 (8012): 679-687 (2024)