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Human Mutation
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August 22, 2018
hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update
Meng Wang, Keith M Callenberg, Raymond Dalgleish, et al.
Human Mutation
|
November 30, 2020
Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals
Jan Higgins, Raymond Dalgleish, Johan T den Dunnen, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 10, 2024
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery
Daniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
HGG Advances
|
October 12, 2024
A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discovery
Daniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 14) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 14 results.
Human Mutation
|
August 22, 2018
hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update
Meng Wang, Keith M Callenberg, Raymond Dalgleish, et al.
Human Mutation
|
November 30, 2020
Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals
Jan Higgins, Raymond Dalgleish, Johan T den Dunnen, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 10, 2024
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery
Daniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
HGG Advances
|
October 12, 2024
A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discovery
Daniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
Page
of 2