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Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Integration of transcriptomics and long-read genomics prioritizes structural variants in rare diseaseTanner D Jensen, Bohan Ni, Chloe M Reuter, et al.
Nature|October 13, 2017
The impact of rare variation on gene expression across tissuesXin Li, Yungil Kim, Emily K Tsang, et al.
Plos Genetics|April 26, 2012
Patterns of cis regulatory variation in diverse human populationsBarbara E Stranger, Stephen B Montgomery, Antigone S Dimas, et al.
Elife|June 12, 2013
Passive and active DNA methylation and the interplay with genetic variation in gene regulationMaria Gutierrez-Arcelus, Tuuli Lappalainen, Stephen B Montgomery, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 23, 2017
Long-read genome sequencing identifies causal structural variation in a Mendelian diseaseJason D Merker, Aaron M Wenger, Tam Sneddon, et al.
Plos Genetics|January 31, 2015
Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicingMaria Gutierrez-Arcelus, Halit Ongen, Tuuli Lappalainen, et al.
Genome Research|May 20, 2016
Impact of the X Chromosome and sex on regulatory variationKimberly R Kukurba, Princy Parsana, Brunilda Balliu, et al.
Biorxiv : the Preprint Server for Biology|October 9, 2023
Integrated single-cell multiome analysis reveals muscle fiber-type gene regulatory circuitry modulated by endurance exerciseAliza B Rubenstein, Gregory R Smith, Zidong Zhang, et al.
Genome Biology|September 11, 2020
Impact of admixture and ancestry on eQTL analysis and GWAS colocalization in GTExNicole R Gay, Michael Gloudemans, Margaret L Antonio, et al.
Nature Communications|July 9, 2016
Integrative functional genomics identifies regulatory mechanisms at coronary artery disease lociClint L Miller, Milos Pjanic, Ting Wang, et al.
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