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Medrxiv : the Preprint Server for Health Sciences
|
December 3, 2025
MaveMD: A functional data resource for genomic medicine
Abbye E McEwen, Jeremy Stone, Malvika Tejura, et al.
Biorxiv : the Preprint Server for Biology
|
July 9, 2024
Mapping MAVE data for use in human genomics applications
Jeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Genome Biology
|
June 25, 2025
Mapping MAVE data for use in human genomics applications
Jeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Genome Biology
|
January 22, 2025
MaveDB 2024: a curated community database with over seven million variant effects from multiplexed functional assays
Alan F Rubin, Jeremy Stone, Aisha Haley Bianchi, et al.
Biorxiv : the Preprint Server for Biology
|
February 23, 2026
A scalable approach to resolving variants of uncertain significance
Malvika Tejura, Yile Chen, Abbye E McEwen, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Medrxiv : the Preprint Server for Health Sciences
|
December 3, 2025
MaveMD: A functional data resource for genomic medicine
Abbye E McEwen, Jeremy Stone, Malvika Tejura, et al.
Biorxiv : the Preprint Server for Biology
|
July 9, 2024
Mapping MAVE data for use in human genomics applications
Jeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Genome Biology
|
June 25, 2025
Mapping MAVE data for use in human genomics applications
Jeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Genome Biology
|
January 22, 2025
MaveDB 2024: a curated community database with over seven million variant effects from multiplexed functional assays
Alan F Rubin, Jeremy Stone, Aisha Haley Bianchi, et al.
Biorxiv : the Preprint Server for Biology
|
February 23, 2026
A scalable approach to resolving variants of uncertain significance
Malvika Tejura, Yile Chen, Abbye E McEwen, et al.
Page
of 1