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Chemistry & Biodiversity
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November 3, 2022
Termviewer - A Web Application for Streamlined Human Phenotype Ontology (HPO) Tagging and Document Annotation
Anna Nixon, Li Fang, James M Havrilla, et al.
Genome Medicine
|
May 26, 2021
PhenCards: a data resource linking human phenotype information to biomedical knowledge
James M Havrilla, Cong Liu, Xiangchen Dong, et al.
Nature Genetics
|
December 12, 2018
A map of constrained coding regions in the human genome
James M Havrilla, Brent S Pedersen, Ryan M Layer, et al.
Genome Research
|
March 13, 2019
Coexpression patterns define epigenetic regulators associated with neurological dysfunction
Leandros Boukas, James M Havrilla, Peter F Hickey, et al.
BMC Medical Informatics and Decision Making
|
July 28, 2022
PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care
James M Havrilla, Anbumalar Singaravelu, Dennis M Driscoll, et al.
NAR Genomics and Bioinformatics
|
June 6, 2020
Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases
Mengge Zhao, James M Havrilla, Li Fang, et al.
Gigascience
|
June 4, 2018
SV-plaudit: A cloud-based framework for manually curating thousands of structural variants
Jonathan R Belyeu, Thomas J Nicholas, Brent S Pedersen, et al.
F1000Research
|
October 11, 2021
An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates
Ann M Mc Cartney, Medhat Mahmoud, Michael Jochum, et al.
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Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Chemistry & Biodiversity
|
November 3, 2022
Termviewer - A Web Application for Streamlined Human Phenotype Ontology (HPO) Tagging and Document Annotation
Anna Nixon, Li Fang, James M Havrilla, et al.
Genome Medicine
|
May 26, 2021
PhenCards: a data resource linking human phenotype information to biomedical knowledge
James M Havrilla, Cong Liu, Xiangchen Dong, et al.
Nature Genetics
|
December 12, 2018
A map of constrained coding regions in the human genome
James M Havrilla, Brent S Pedersen, Ryan M Layer, et al.
Genome Research
|
March 13, 2019
Coexpression patterns define epigenetic regulators associated with neurological dysfunction
Leandros Boukas, James M Havrilla, Peter F Hickey, et al.
BMC Medical Informatics and Decision Making
|
July 28, 2022
PheNominal: an EHR-integrated web application for structured deep phenotyping at the point of care
James M Havrilla, Anbumalar Singaravelu, Dennis M Driscoll, et al.
NAR Genomics and Bioinformatics
|
June 6, 2020
Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases
Mengge Zhao, James M Havrilla, Li Fang, et al.
Gigascience
|
June 4, 2018
SV-plaudit: A cloud-based framework for manually curating thousands of structural variants
Jonathan R Belyeu, Thomas J Nicholas, Brent S Pedersen, et al.
F1000Research
|
October 11, 2021
An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates
Ann M Mc Cartney, Medhat Mahmoud, Michael Jochum, et al.
Page
of 1