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Warren A Cheung

Showing results (1-10 of 32) with videos related to

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Genome Medicine|October 2, 2012
Inferring novel gene-disease associations using Medical Subject Heading Over-representation ProfilesWarren A Cheung, Bf Francis Ouellette, Wyeth W Wasserman
BMC Medical Genomics|July 4, 2013
Compensating for literature annotation bias when predicting novel drug-disease relationships through Medical Subject Heading Over-representation Profile (MeSHOP) similarityWarren A Cheung, B F Francis Ouellette, Wyeth W Wasserman
BMC Bioinformatics|September 29, 2012
Quantitative biomedical annotation using medical subject heading over-representation profiles (MeSHOPs)Warren A Cheung, B F Francis Ouellette, Wyeth W Wasserman
Genome Research|March 20, 2025
Expanded methylome and quantitative trait loci detection by long-read profiling of personal DNACristian Groza, Bing Ge, Warren A Cheung, et al.
Clinical Epigenetics|April 24, 2015
Risk of re-identification of epigenetic methylation data: a more nuanced response is neededYann Joly, Stephanie Om Dyke, Warren A Cheung, et al.
Chemical Biology & Drug Design|October 15, 2010
Optimization of antibacterial peptides by genetic algorithms and cheminformaticsChristopher D Fjell, Håvard Jenssen, Warren A Cheung, et al.
Nutrients|July 11, 2023
Adverse Maternal Environments Perturb Hepatic DNA Methylome and Transcriptome Prior to the Adult-Onset Non-Alcoholic Fatty Liver Disease in Mouse OffspringQi Fu, Warren A Cheung, Amber V Majnik, et al.
Scientific Reports|August 6, 2021
Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age rangeKonner Winkley, Dithi Banerjee, Todd Bradley, et al.
Journal of Medicinal Chemistry|March 20, 2009
Identification of novel antibacterial peptides by chemoinformatics and machine learningChristopher D Fjell, Håvard Jenssen, Kai Hilpert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scoresCas LeMaster, Carl Schwendinger-Schreck, Bing Ge, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Genome Medicine|October 2, 2012
Inferring novel gene-disease associations using Medical Subject Heading Over-representation ProfilesWarren A Cheung, Bf Francis Ouellette, Wyeth W Wasserman
BMC Medical Genomics|July 4, 2013
Compensating for literature annotation bias when predicting novel drug-disease relationships through Medical Subject Heading Over-representation Profile (MeSHOP) similarityWarren A Cheung, B F Francis Ouellette, Wyeth W Wasserman
BMC Bioinformatics|September 29, 2012
Quantitative biomedical annotation using medical subject heading over-representation profiles (MeSHOPs)Warren A Cheung, B F Francis Ouellette, Wyeth W Wasserman
Genome Research|March 20, 2025
Expanded methylome and quantitative trait loci detection by long-read profiling of personal DNACristian Groza, Bing Ge, Warren A Cheung, et al.
Clinical Epigenetics|April 24, 2015
Risk of re-identification of epigenetic methylation data: a more nuanced response is neededYann Joly, Stephanie Om Dyke, Warren A Cheung, et al.
Chemical Biology & Drug Design|October 15, 2010
Optimization of antibacterial peptides by genetic algorithms and cheminformaticsChristopher D Fjell, Håvard Jenssen, Warren A Cheung, et al.
Nutrients|July 11, 2023
Adverse Maternal Environments Perturb Hepatic DNA Methylome and Transcriptome Prior to the Adult-Onset Non-Alcoholic Fatty Liver Disease in Mouse OffspringQi Fu, Warren A Cheung, Amber V Majnik, et al.
Scientific Reports|August 6, 2021
Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age rangeKonner Winkley, Dithi Banerjee, Todd Bradley, et al.
Journal of Medicinal Chemistry|March 20, 2009
Identification of novel antibacterial peptides by chemoinformatics and machine learningChristopher D Fjell, Håvard Jenssen, Kai Hilpert, et al.
Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scoresCas LeMaster, Carl Schwendinger-Schreck, Bing Ge, et al.
Pageof 4