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Ivan Adzhubey

Showing results (1-10 of 4) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Joint estimation and imputation of variant functional effects using high throughput assay dataTian Yu, James D Fife, Ivan Adzhubey, et al.
Cell Genomics|October 10, 2024
FUSE: Improving the estimation and imputation of variant impacts in functional screeningTian Yu, James D Fife, Vineel Bhat, et al.
American Journal of Human Genetics|December 25, 2012
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritisDorothée Diogo, Fina Kurreeman, Eli A Stahl, et al.
Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Joint estimation and imputation of variant functional effects using high throughput assay dataTian Yu, James D Fife, Ivan Adzhubey, et al.
Cell Genomics|October 10, 2024
FUSE: Improving the estimation and imputation of variant impacts in functional screeningTian Yu, James D Fife, Vineel Bhat, et al.
American Journal of Human Genetics|December 25, 2012
Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritisDorothée Diogo, Fina Kurreeman, Eli A Stahl, et al.
Genome Biology|March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY ChallengeCatherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Pageof 1