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Biorxiv : the Preprint Server for Biology|April 8, 2025
Evaluating genetic-ancestry inference from single-cell RNA-seq dataJianing Yao, Steven Gazal
HGG Advances|January 9, 2026
Evaluating genetic-ancestry inference from single-cell transcriptomic datasetsJianing Yao, Steven Gazal
Medrxiv : the Preprint Server for Health Sciences|October 31, 2023
Ancestry-specific regulatory and disease architectures are likely due to cell-type-specific gene-by-environment interactionsJuehan Wang, Steven Gazal
Theoretical Population Biology|October 4, 2015
Relationship inference from the genetic data on parents or offspring: A comparative studySteven Gazal, Emmanuelle Génin, Anne-Louise Leutenegger
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
A machine-learning framework to characterize functional disease architectures and prioritize disease variantsSiliangyu Cheng, Artem Kim, Dhrithi Deshpande, et al.
American Journal of Human Genetics|February 10, 2022
Partitioning gene-mediated disease heritability without eQTLsDaniel J Weiner, Steven Gazal, Elise B Robinson, et al.
European Journal of Human Genetics : EJHG|March 3, 2011
Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?Anne-Louise Leutenegger, Mourad Sahbatou, Steven Gazal, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Efficient count-based models improve power and robustness for large-scale single-cell eQTL mappingZixuan Eleanor Zhang, Artem Kim, Noah Suboc, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
A scalable variational approach to characterize pleiotropic components across thousands of human diseases and complex traits using GWAS summary statisticsZixuan Zhang, Junghyun Jung, Artem Kim, et al.
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