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Journal of Hypertension|January 26, 2018
A system view and analysis of essential hypertensionAlon Botzer, Ehud Grossman, John Moult, et al.Plos One|February 23, 2026
Using machine learning to predict and analyze complex trait diseases: Lessons from a simple abstract modelEden Maimon, Ori Bondi, John Moult, et al.Human 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.Proteins|September 24, 2009
Critical assessment of methods of protein structure prediction - Round VIIIJohn Moult, Krzysztof Fidelis, Andriy Kryshtafovych, et al.The Pharmacogenomics Journal|November 6, 2018
Iatrogenic hypertension: a bioinformatic analysisAlon Botzer, Yoram Finkelstein, Ehud Grossman, et al.Pageof 11