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American Journal of Human Genetics
|
May 26, 2023
Estimating clinical risk in gene regions from population sequencing cohort data
James D Fife, Christopher A Cassa
Medrxiv : the Preprint Server for Health Sciences
|
January 30, 2023
Estimating clinical risk in gene regions from population sequencing cohort data
James D Fife, Christopher A Cassa
Medrxiv : the Preprint Server for Health Sciences
|
January 30, 2023
Joint estimation and imputation of variant functional effects using high throughput assay data
Tian Yu, James D Fife, Ivan Adzhubey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 28, 2022
Informing variant assessment using structured evidence from prior classifications (PS1, PM5, and PVS1 sequence variant interpretation criteria)
Vineel Bhat, Ivan A Adzhubei, James D Fife, et al.
Cell Genomics
|
October 10, 2024
FUSE: Improving the estimation and imputation of variant impacts in functional screening
Tian Yu, James D Fife, Vineel Bhat, et al.
Nature Communications
|
June 18, 2022
Peptide fusion improves prime editing efficiency
Minja Velimirovic, Larissa C Zanetti, Max W Shen, et al.
Cell Genomics
|
May 25, 2023
Systematic elucidation of genetic mechanisms underlying cholesterol uptake
Marisa C Hamilton, James D Fife, Ersin Akinci, et al.
Biorxiv : the Preprint Server for Biology
|
January 30, 2023
Systematic elucidation of genetic mechanisms underlying cholesterol uptake
Marisa C Hamilton, James D Fife, Ersin Akinci, et al.
Biorxiv : the Preprint Server for Biology
|
September 2, 2020
Elucidation of remdesivir cytotoxicity pathways through genome-wide CRISPR-Cas9 screening and transcriptomics
Ersin Akinci, Minsun Cha, Lin Lin, et al.
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Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
American Journal of Human Genetics
|
May 26, 2023
Estimating clinical risk in gene regions from population sequencing cohort data
James D Fife, Christopher A Cassa
Medrxiv : the Preprint Server for Health Sciences
|
January 30, 2023
Estimating clinical risk in gene regions from population sequencing cohort data
James D Fife, Christopher A Cassa
Medrxiv : the Preprint Server for Health Sciences
|
January 30, 2023
Joint estimation and imputation of variant functional effects using high throughput assay data
Tian Yu, James D Fife, Ivan Adzhubey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 28, 2022
Informing variant assessment using structured evidence from prior classifications (PS1, PM5, and PVS1 sequence variant interpretation criteria)
Vineel Bhat, Ivan A Adzhubei, James D Fife, et al.
Cell Genomics
|
October 10, 2024
FUSE: Improving the estimation and imputation of variant impacts in functional screening
Tian Yu, James D Fife, Vineel Bhat, et al.
Nature Communications
|
June 18, 2022
Peptide fusion improves prime editing efficiency
Minja Velimirovic, Larissa C Zanetti, Max W Shen, et al.
Cell Genomics
|
May 25, 2023
Systematic elucidation of genetic mechanisms underlying cholesterol uptake
Marisa C Hamilton, James D Fife, Ersin Akinci, et al.
Biorxiv : the Preprint Server for Biology
|
January 30, 2023
Systematic elucidation of genetic mechanisms underlying cholesterol uptake
Marisa C Hamilton, James D Fife, Ersin Akinci, et al.
Biorxiv : the Preprint Server for Biology
|
September 2, 2020
Elucidation of remdesivir cytotoxicity pathways through genome-wide CRISPR-Cas9 screening and transcriptomics
Ersin Akinci, Minsun Cha, Lin Lin, et al.
Page
of 1