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Mark T W Ebbert

Showing results (11-20 of 62) with videos related to

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International Journal of Bioinformatics Research and Applications|December 1, 2007
Pharmacogenomics: analysing SNPs in the CYP2D6 gene using amino acid propertiesMark T W Ebbert, Wesley A Beckstead, Timothy D O'Connor, et al.
BMC Genomics|December 4, 2025
Genome annotations matter: characterizing Ensembl hg38 annotations from 2014 to 2023Madeline L Page, Mark E Wadsworth, Bernardo Aguzzoli Heberle, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|March 22, 2017
Evaluation of the Abbott RealTime HCV genotype II plus RUO (PLUS) assay with reference to core and NS5B sequencingMelanie A Mallory, Danijela Lucic, Mark T W Ebbert, et al.
Genes|August 26, 2022
Web-Based Protein Interactions Calculator Identifies Likely Proteome Coevolution with Alzheimer's Disease-Associated ProteinsKatrisa M Ward, Brandon D Pickett, Mark T W Ebbert, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Sequencing the gaps: dark genomic regions persist in CHM13 despite long-read advancesMark E Wadsworth, Madeline L Page, Bernardo Aguzzoli Heberle, et al.
Scientific Reports|January 12, 2026
Dark and camouflaged genomic regions remain challenging in CHM13Mark E Wadsworth, Madeline L Page, Bernardo Aguzzoli Heberle, et al.
BMC Bioinformatics|July 26, 2016
A novel approach for multi-SNP GWAS and its application in Alzheimer's diseasePaul M Bodily, M Stanley Fujimoto, Justin T Page, et al.
BMC Genomics|July 1, 2016
Variants in ACPP are associated with cerebrospinal fluid Prostatic Acid Phosphatase levelsLyndsay A Staley, Mark T W Ebbert, Daniel Bunker, et al.
BMC Genomics|July 1, 2016
Genome-wide association study of prolactin levels in blood plasma and cerebrospinal fluidLyndsay A Staley, Mark T W Ebbert, Sheradyn Parker, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Decoding the human PBMC isonome: Isoform-level resolution with single-cell long-read transcriptomicsPatricia Hayes Doyle, Madeline L Page, J Anthony Brandon, et al.
Pageof 7

Showing results (11-20 of 62) with videos related to

Sort By:
Pageof 7
International Journal of Bioinformatics Research and Applications|December 1, 2007
Pharmacogenomics: analysing SNPs in the CYP2D6 gene using amino acid propertiesMark T W Ebbert, Wesley A Beckstead, Timothy D O'Connor, et al.
BMC Genomics|December 4, 2025
Genome annotations matter: characterizing Ensembl hg38 annotations from 2014 to 2023Madeline L Page, Mark E Wadsworth, Bernardo Aguzzoli Heberle, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|March 22, 2017
Evaluation of the Abbott RealTime HCV genotype II plus RUO (PLUS) assay with reference to core and NS5B sequencingMelanie A Mallory, Danijela Lucic, Mark T W Ebbert, et al.
Genes|August 26, 2022
Web-Based Protein Interactions Calculator Identifies Likely Proteome Coevolution with Alzheimer's Disease-Associated ProteinsKatrisa M Ward, Brandon D Pickett, Mark T W Ebbert, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Sequencing the gaps: dark genomic regions persist in CHM13 despite long-read advancesMark E Wadsworth, Madeline L Page, Bernardo Aguzzoli Heberle, et al.
Scientific Reports|January 12, 2026
Dark and camouflaged genomic regions remain challenging in CHM13Mark E Wadsworth, Madeline L Page, Bernardo Aguzzoli Heberle, et al.
BMC Bioinformatics|July 26, 2016
A novel approach for multi-SNP GWAS and its application in Alzheimer's diseasePaul M Bodily, M Stanley Fujimoto, Justin T Page, et al.
BMC Genomics|July 1, 2016
Variants in ACPP are associated with cerebrospinal fluid Prostatic Acid Phosphatase levelsLyndsay A Staley, Mark T W Ebbert, Daniel Bunker, et al.
BMC Genomics|July 1, 2016
Genome-wide association study of prolactin levels in blood plasma and cerebrospinal fluidLyndsay A Staley, Mark T W Ebbert, Sheradyn Parker, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Decoding the human PBMC isonome: Isoform-level resolution with single-cell long-read transcriptomicsPatricia Hayes Doyle, Madeline L Page, J Anthony Brandon, et al.
Pageof 7