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Anjali D Zimmer

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Proceedings of the National Academy of Sciences of the United States of America|October 30, 2016
Differential roles of the RNases H in preventing chromosome instabilityAnjali D Zimmer, Douglas Koshland
BMC Genomics|April 19, 2018
A machine learning model to determine the accuracy of variant calls in capture-based next generation sequencingJeroen van den Akker, Gilad Mishne, Anjali D Zimmer, et al.
Molecular Biology of the Cell|March 21, 2014
Multiple inputs control sulfur-containing amino acid synthesis in Saccharomyces cerevisiaeMeru J Sadhu, James J Moresco, Anjali D Zimmer, et al.
Genetics in Medicine Open|May 25, 2026
Rates of unbalanced chromosome rearrangements associated with pericentric and paracentric inversions: Analysis of molecular chromosome results in embryo samplesKatrina Merrion, Jessica Adsit, Katherine L Howard, et al.
Database : the Journal of Biological Databases and Curation|February 14, 2019
A scalable, aggregated genotypic-phenotypic database for human disease variationRyan Barrett, Cynthia L Neben, Anjali D Zimmer, et al.
Journal of the National Cancer Institute|September 22, 2018
Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online InitiativeJennifer L Caswell-Jin, Anjali D Zimmer, Will Stedden, et al.
Human Mutation|March 17, 2020
LEAP: Using machine learning to support variant classification in a clinical settingCarmen Lai, Anjali D Zimmer, Robert O'Connor, et al.
Database : the Journal of Biological Databases and Curation|November 12, 2020
Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasetsMark J Berger, Hannah E Williams, Ryan Barrett, et al.
The Journal of Molecular Diagnostics : JMD|February 23, 2021
Intronic Breakpoint Signatures Enhance Detection and Characterization of Clinically Relevant Germline Structural VariantsJeroen van den Akker, Lawrence Hon, Anjana Ondov, et al.
The Journal of Molecular Diagnostics : JMD|June 16, 2019
Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing GuidelinesCynthia L Neben, Anjali D Zimmer, Will Stedden, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Proceedings of the National Academy of Sciences of the United States of America|October 30, 2016
Differential roles of the RNases H in preventing chromosome instabilityAnjali D Zimmer, Douglas Koshland
BMC Genomics|April 19, 2018
A machine learning model to determine the accuracy of variant calls in capture-based next generation sequencingJeroen van den Akker, Gilad Mishne, Anjali D Zimmer, et al.
Molecular Biology of the Cell|March 21, 2014
Multiple inputs control sulfur-containing amino acid synthesis in Saccharomyces cerevisiaeMeru J Sadhu, James J Moresco, Anjali D Zimmer, et al.
Genetics in Medicine Open|May 25, 2026
Rates of unbalanced chromosome rearrangements associated with pericentric and paracentric inversions: Analysis of molecular chromosome results in embryo samplesKatrina Merrion, Jessica Adsit, Katherine L Howard, et al.
Database : the Journal of Biological Databases and Curation|February 14, 2019
A scalable, aggregated genotypic-phenotypic database for human disease variationRyan Barrett, Cynthia L Neben, Anjali D Zimmer, et al.
Journal of the National Cancer Institute|September 22, 2018
Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online InitiativeJennifer L Caswell-Jin, Anjali D Zimmer, Will Stedden, et al.
Human Mutation|March 17, 2020
LEAP: Using machine learning to support variant classification in a clinical settingCarmen Lai, Anjali D Zimmer, Robert O'Connor, et al.
Database : the Journal of Biological Databases and Curation|November 12, 2020
Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasetsMark J Berger, Hannah E Williams, Ryan Barrett, et al.
The Journal of Molecular Diagnostics : JMD|February 23, 2021
Intronic Breakpoint Signatures Enhance Detection and Characterization of Clinically Relevant Germline Structural VariantsJeroen van den Akker, Lawrence Hon, Anjana Ondov, et al.
The Journal of Molecular Diagnostics : JMD|June 16, 2019
Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing GuidelinesCynthia L Neben, Anjali D Zimmer, Will Stedden, et al.
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