Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Eilbeck

Showing results (71-80 of 86) with videos related to

Pageof 9
Sort By:
Molecular Psychiatry|October 4, 2023
Whole-genome sequencing analysis of suicide deaths integrating brain-regulatory eQTLs data to identify risk loci and genesSeonggyun Han, Emily DiBlasi, Eric T Monson, et al.
Journal of Biomedical Semantics|May 7, 2016
The Non-Coding RNA Ontology (NCRO): a comprehensive resource for the unification of non-coding RNA biologyJingshan Huang, Karen Eilbeck, Barry Smith, et al.
Genome Biology|May 27, 2016
Taxonomer: an interactive metagenomics analysis portal for universal pathogen detection and host mRNA expression profilingSteven Flygare, Keith Simmon, Chase Miller, et al.
Translational Psychiatry|February 16, 2026
Genetic risk of chronic pain conditions associated with risk of suicide death through an integrative analysis of EHR and genomics dataSeonggyun Han, Emily DiBlasi, Eric T Monson, et al.
Bioinformatics (Oxford, England)|September 11, 2019
Unification of miRNA and isomiR research: the mirGFF3 format and the mirtop APIThomas Desvignes, Phillipe Loher, Karen Eilbeck, et al.
International Journal of Data Mining and Bioinformatics|December 20, 2016
The development of non-coding RNA ontologyJingshan Huang, Karen Eilbeck, Barry Smith, et al.
Human Mutation|October 13, 2018
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase GeneDiane B Zastrow, Heather Baudet, Wei Shen, et al.
Journal of the American Medical Informatics Association : JAMIA|January 12, 2026
GARDE-Chat: a scalable, open-source platform for building and deploying health chatbotsGuilherme Del Fiol, Emerson Borsato, Richard L Bradshaw, et al.
Human Molecular Genetics|November 26, 2009
Novel sequence feature variant type analysis of the HLA genetic association in systemic sclerosisDavid R Karp, Nishanth Marthandan, Steven G E Marsh, et al.
The Journal of Molecular Diagnostics : JMD|March 20, 2017
Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical SettingsIra M Lubin, Nazneen Aziz, Lawrence J Babb, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Molecular Psychiatry|October 4, 2023
Whole-genome sequencing analysis of suicide deaths integrating brain-regulatory eQTLs data to identify risk loci and genesSeonggyun Han, Emily DiBlasi, Eric T Monson, et al.
Journal of Biomedical Semantics|May 7, 2016
The Non-Coding RNA Ontology (NCRO): a comprehensive resource for the unification of non-coding RNA biologyJingshan Huang, Karen Eilbeck, Barry Smith, et al.
Genome Biology|May 27, 2016
Taxonomer: an interactive metagenomics analysis portal for universal pathogen detection and host mRNA expression profilingSteven Flygare, Keith Simmon, Chase Miller, et al.
Translational Psychiatry|February 16, 2026
Genetic risk of chronic pain conditions associated with risk of suicide death through an integrative analysis of EHR and genomics dataSeonggyun Han, Emily DiBlasi, Eric T Monson, et al.
Bioinformatics (Oxford, England)|September 11, 2019
Unification of miRNA and isomiR research: the mirGFF3 format and the mirtop APIThomas Desvignes, Phillipe Loher, Karen Eilbeck, et al.
International Journal of Data Mining and Bioinformatics|December 20, 2016
The development of non-coding RNA ontologyJingshan Huang, Karen Eilbeck, Barry Smith, et al.
Human Mutation|October 13, 2018
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase GeneDiane B Zastrow, Heather Baudet, Wei Shen, et al.
Journal of the American Medical Informatics Association : JAMIA|January 12, 2026
GARDE-Chat: a scalable, open-source platform for building and deploying health chatbotsGuilherme Del Fiol, Emerson Borsato, Richard L Bradshaw, et al.
Human Molecular Genetics|November 26, 2009
Novel sequence feature variant type analysis of the HLA genetic association in systemic sclerosisDavid R Karp, Nishanth Marthandan, Steven G E Marsh, et al.
The Journal of Molecular Diagnostics : JMD|March 20, 2017
Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical SettingsIra M Lubin, Nazneen Aziz, Lawrence J Babb, et al.
Pageof 9