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Omics : a Journal of Integrative Biology|July 19, 2016
Consensus Genome-Wide Expression Quantitative Trait Loci and Their Relationship with Human Complex Trait DiseaseChen-Hsin Yu, Lipika R Pal, John MoultBMC Genomics|June 26, 2015
Insights from GWAS: emerging landscape of mechanisms underlying complex trait diseaseLipika R Pal, Chen-Hsin Yu, Stephen M Mount, et al.Journal of Molecular Biology|May 5, 2015
Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association StudiesLipika R Pal, John MoultHuman Mutation|November 5, 2019
Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype-weighted knowledge in the CAGI SickKids5 clinical genomes challengeLipika R Pal, Kunal Kundu, Yizhou Yin, et al.Human Mutation|May 13, 2017
Determination of disease phenotypes and pathogenic variants from exome sequence data in the CAGI 4 gene panel challengeKunal Kundu, Lipika R Pal, Yizhou Yin, et al.Human Mutation|May 18, 2017
CAGI4 SickKids clinical genomes challenge: A pipeline for identifying pathogenic variantsLipika R Pal, Kunal Kundu, Yizhou Yin, et al.Human Mutation|May 18, 2017
CAGI4 Crohn's exome challenge: Marker SNP versus exome variant models for assigning risk of Crohn diseaseLipika R Pal, Kunal Kundu, Yizhou Yin, et al.Plos Computational Biology|December 27, 2018
Harnessing formal concepts of biological mechanism to analyze human diseaseLindley Darden, Kunal Kundu, Lipika R Pal, et al.Human Mutation|May 26, 2017
Ensemble variant interpretation methods to predict enzyme activity and assign pathogenicity in the CAGI4 NAGLU (Human N-acetyl-glucosaminidase) and UBE2I (Human SUMO-ligase) challengesYizhou Yin, Kunal Kundu, Lipika R Pal, et al.Human Mutation|July 24, 2019
Reports from the fifth edition of CAGI: The Critical Assessment of Genome InterpretationGaia Andreoletti, Lipika R Pal, John Moult, et al.Pageof 14