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The evolutionary history of 2,658 cancers., , , , , , , , , and 60 other author(s). Nat., 578 (7793): 122-128 (2020)A generalized sparse regression model with adjustment of pedigree structure for variant detection from next generation sequencing data., , , and . BCB, page 191. ACM, (2013)Unified tests for fine scale mapping and identifying sparse high-dimensional sequence associations., , , , and . BCB, page 241-249. ACM, (2015)Scaled sparse high-dimensional tests for localizing sequence variants., , , , and . BCB, page 79-87. ACM, (2014)Identification of significant genetic variants via SLOPE, and its extension to group SLOPE., , and . BCB, page 232-240. ACM, (2015)The effective diagnosis of schizophrenia by using multi-layer RBMs deep networks., , , and . BIBM, page 603-606. IEEE Computer Society, (2015)Inferring structural variant cancer cell fraction, , , , , , , , , and 68 other author(s). Nature Communications, 11 (1): 730-- (2020)A Sparse Regression Method for Group-Wise Feature Selection with False Discovery Rate Control., , , , , and . IEEE ACM Trans. Comput. Biol. Bioinform., 15 (4): 1066-1078 (2018)