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Journal of Crohn'S & Colitis|August 13, 2025
Phenome-wide association study of monogenic inflammatory bowel disease genes in diverse biobanks identifies population-specific and shared Goldilocks alleles: implications for Precision MedicineMichelle M Bao, Meltem Ece Kars, David Zhang, et al.Human Genetics|November 9, 2022
Identifying shared genetic factors underlying epilepsy and congenital heart disease in EuropeansYiming Wu, Cigdem Sevim Bayrak, Bosi Dong, et al.Molecular Biology and Evolution|August 13, 2011
Herders of Indian and European cattle share their predominant allele for lactase persistenceIrene Gallego Romero, Chandana Basu Mallick, Anke Liebert, et al.Genome Medicine|December 1, 2023
Genome-wide prediction of pathogenic gain- and loss-of-function variants from ensemble learning of a diverse feature setDavid Stein, Meltem Ece Kars, Yiming Wu, et al.Plos One|July 17, 2008
A meta-analysis of microarray gene expression in mouse stem cells: redefining stemnessYvonne J K Edwards, Kevin Bryson, David T JonesBioinformatics (Oxford, England)|January 20, 2021
Adversarial generation of gene expression dataRamon Viñas, Helena Andrés-Terré, Pietro Liò, et al.The New Zealand Medical Journal|March 21, 2024
Improving community antibiotic prescribing to keep antibiotics working in Aotearoa New ZealandMark G ThomasPharmacogenetics and Genomics|May 4, 2016
Contrasting exome constancy and regulatory region variation in the gene encoding CYP3A4: an examination of the extent and potential implicationsOlivia J Creemer, Naser Ansari-Pour, Rosemary Ekong, et al.Bioinformatics (Oxford, England)|December 15, 2012
SwiftLink: parallel MCMC linkage analysis using multicore CPU and GPUAlan Medlar, Dorota Głowacka, Horia Stanescu, et al.Proceedings of the National Academy of Sciences of the United States of America|April 2, 2015
Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variantsAziz Belkadi, Alexandre Bolze, Yuval Itan, et al.Pageof 30