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Genome-wide genetic data on $\sim$500,000 UK Biobank participants, , , , , , , , , and 6 other author(s). bioRxiv, (2017)Accurate, scalable and integrative haplotype estimation, , , , and . Nature Communications, 10 (1): 5436-- (2019)ISHAPE: new rapid and accurate software for haplotyping., , , , , and . BMC Bioinform., (2007)Phasing for medical sequencing using rare variants and large haplotype reference panels., , , and . Bioinform., 32 (13): 1974-1980 (2016)MBV: a method to solve sample mislabeling and detect technical bias in large combined genotype and sequencing assay datasets., , , , , , and . Bioinform., 33 (12): 1895-1897 (2017)A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness, , , , , , , , , and 17 other author(s). PLoS Genet, 10 (4): e1004234 (April 2014)Fast and efficient QTL mapper for thousands of molecular phenotypes., , , , and . Bioinform., 32 (10): 1479-1485 (2016)Shape-IT: new rapid and accurate algorithm for haplotype inference., , and . BMC Bioinform., (2008)The impact of rare variation on gene expression across tissues., , , , , , , , , and 65 other author(s). Nat., 550 (7675): 239-243 (2017)XSI - a genotype compression tool for compressive genomics in large biobanks., , , , and . Bioinform., 38 (15): 3778-3784 (2022)