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Systematic and Comprehensive Survey of Genomic Loci Associated with Complex Diseases and Traits.

, , , , and . BIBM, page 1447-1452. IEEE, (2020)

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Systematic Exploration in Tissue-Pathway Associations of Complex Traits Using Comprehensive eQTLs Catalog., , , , and . Frontiers Big Data, (2021)Systematic and Comprehensive Survey of Genomic Loci Associated with Complex Diseases and Traits., , , , and . BIBM, page 1447-1452. IEEE, (2020)Prioritizing Intellectual Disability Candidate Genes and Understanding Family Diseases Using Machine Learning., and . BIBM, page 2886-2892. IEEE, (2022)Identification of genome-wide non-canonical spliced regions and analysis of biological functions for spliced sequences using Read-Split-Fly., , , , , and . BMC Bioinform., 18 (S-11): 37-48 (2017)MMiRNA-Viewer2, a bioinformatics tool for visualizing functional annotation for MiRNA and MRNA pairs in a network., , , , , , , , and . BMC Bioinform., 21-S (4): 247 (2020)End-to-end Deep Learning Methods for Automated Damage Detection in Extreme Events at Various Scales., , and . ICPR, page 6640-6647. IEEE, (2020)Computational identification of key pathways and differentially-expressed gene signatures in ovarian cancer stem cells., , and . BIBM, page 1843-1848. IEEE, (2020)Identification of Key Biomarkers Associated with Ductal Breast Cancer in Spatial Transcriptomics Data., , , , , and . BIBM, page 3840-3847. IEEE, (2023)Orthogonal analysis of variants in APOE gene using in-silico approaches reveals novel disrupting variants., , , , , and . Frontiers Bioinform., (May 2023)A Bioinformatics Pipeline for the identification of disease-causing variants in humans that can change protein structure., , , , , and . BIBM, page 3849-3851. IEEE, (2022)