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

Kenneth D Doig

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 14, 2023
Homologous Recombination Repair Deficiency: An Overview for PathologistsKenneth D Doig, Andrew P Fellowes, Stephen B Fox
Pathology|February 14, 2022
Tumour mutational burden: an overview for pathologistsKenneth D Doig, Andrew Fellowes, Prudence Scott, et al.
BMC Medical Genomics|March 29, 2022
Findings from precision oncology in the clinic: rare, novel variants are a significant contributor to scaling molecular diagnosticsKenneth D Doig, Christopher G Love, Thomas Conway, et al.
Journal of Bacteriology|December 4, 2012
Complete genome sequence of the frog pathogen Mycobacterium ulcerans ecovar LiflandiiNicholas J Tobias, Kenneth D Doig, Marnix H Medema, et al.
BMC Bioinformatics|December 17, 2017
Canary: an atomic pipeline for clinical amplicon assaysKenneth D Doig, Jason Ellul, Andrew Fellowes, et al.
Biodata Mining|October 30, 2025
Using artificial intelligence (AI) to model clinical variant reporting for next generation sequencing (NGS) oncology assaysKenneth D Doig, Rashindrie Perera, Yamuna Kankanige, et al.
BMC Genomics|June 21, 2012
On the origin of Mycobacterium ulcerans, the causative agent of Buruli ulcerKenneth D Doig, Kathryn E Holt, Janet A M Fyfe, et al.
Genome Medicine|April 26, 2017
PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratoriesKenneth D Doig, Andrew Fellowes, Anthony H Bell, et al.
American Journal of Human Genetics|November 4, 2022
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretationEmma Tudini, James Andrews, David M Lawrence, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 14, 2023
Homologous Recombination Repair Deficiency: An Overview for PathologistsKenneth D Doig, Andrew P Fellowes, Stephen B Fox
Pathology|February 14, 2022
Tumour mutational burden: an overview for pathologistsKenneth D Doig, Andrew Fellowes, Prudence Scott, et al.
BMC Medical Genomics|March 29, 2022
Findings from precision oncology in the clinic: rare, novel variants are a significant contributor to scaling molecular diagnosticsKenneth D Doig, Christopher G Love, Thomas Conway, et al.
Journal of Bacteriology|December 4, 2012
Complete genome sequence of the frog pathogen Mycobacterium ulcerans ecovar LiflandiiNicholas J Tobias, Kenneth D Doig, Marnix H Medema, et al.
BMC Bioinformatics|December 17, 2017
Canary: an atomic pipeline for clinical amplicon assaysKenneth D Doig, Jason Ellul, Andrew Fellowes, et al.
Biodata Mining|October 30, 2025
Using artificial intelligence (AI) to model clinical variant reporting for next generation sequencing (NGS) oncology assaysKenneth D Doig, Rashindrie Perera, Yamuna Kankanige, et al.
BMC Genomics|June 21, 2012
On the origin of Mycobacterium ulcerans, the causative agent of Buruli ulcerKenneth D Doig, Kathryn E Holt, Janet A M Fyfe, et al.
Genome Medicine|April 26, 2017
PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratoriesKenneth D Doig, Andrew Fellowes, Anthony H Bell, et al.
American Journal of Human Genetics|November 4, 2022
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretationEmma Tudini, James Andrews, David M Lawrence, et al.
Pageof 1