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Runjun D Kumar

Showing results (1-10 of 25) with videos related to

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Scientific Reports|July 27, 2017
Analysis of somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer typesRunjun D Kumar, Ron Bose
Nature Genetics|September 13, 2016
Unsupervised detection of cancer driver mutations with parsimony-guided learningRunjun D Kumar, S Joshua Swamidass, Ron Bose
Plos One|July 5, 2013
Prioritizing Potentially Druggable Mutations with dGene: An Annotation Tool for Cancer Genome Sequencing DataRunjun D Kumar, Li-Wei Chang, Matthew J Ellis, et al.
Clinical and Translational Medicine|December 30, 2020
A TMPRSS2-ERG gene signature predicts prognosis of patients with prostate adenocarcinomaEmily Zhou, Baoyi Zhang, Kenneth Zhu, et al.
American Journal of Medical Genetics. Part A|April 1, 2022
The germline p53 activation syndrome: A new patient further refines the clinical phenotypeRunjun D Kumar, Mustafa Tosur, Seema R Lalani, et al.
Clinical Pediatrics|January 18, 2020
Facial Nerve Palsy in a Child With Fever of Unknown OriginCharmaine P Mutucumarana, Runjun D Kumar, Dana M Foradori, et al.
Bioinformatics (Oxford, England)|July 26, 2015
Statistically identifying tumor suppressors and oncogenes from pan-cancer genome-sequencing dataRunjun D Kumar, Adam C Searleman, S Joshua Swamidass, et al.
Cancer Genetics|September 30, 2021
Selection for or against escape from nonsense mediated decay is a novel signature for the detection of cancer genesRunjun D Kumar, Briana A Burns, Paul J Vandeventer, et al.
Molecular Genetics and Metabolism Reports|January 25, 2021
A deep intronic variant is a common cause of OTC deficiency in individuals with previously negative genetic testingRunjun D Kumar, Lindsay C Burrage, Jan Bartos, et al.
American Journal of Medical Genetics. Part A|September 6, 2022
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysisRunjun D Kumar, Linyan Meng, Pengfei Liu, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Scientific Reports|July 27, 2017
Analysis of somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer typesRunjun D Kumar, Ron Bose
Nature Genetics|September 13, 2016
Unsupervised detection of cancer driver mutations with parsimony-guided learningRunjun D Kumar, S Joshua Swamidass, Ron Bose
Plos One|July 5, 2013
Prioritizing Potentially Druggable Mutations with dGene: An Annotation Tool for Cancer Genome Sequencing DataRunjun D Kumar, Li-Wei Chang, Matthew J Ellis, et al.
Clinical and Translational Medicine|December 30, 2020
A TMPRSS2-ERG gene signature predicts prognosis of patients with prostate adenocarcinomaEmily Zhou, Baoyi Zhang, Kenneth Zhu, et al.
American Journal of Medical Genetics. Part A|April 1, 2022
The germline p53 activation syndrome: A new patient further refines the clinical phenotypeRunjun D Kumar, Mustafa Tosur, Seema R Lalani, et al.
Clinical Pediatrics|January 18, 2020
Facial Nerve Palsy in a Child With Fever of Unknown OriginCharmaine P Mutucumarana, Runjun D Kumar, Dana M Foradori, et al.
Bioinformatics (Oxford, England)|July 26, 2015
Statistically identifying tumor suppressors and oncogenes from pan-cancer genome-sequencing dataRunjun D Kumar, Adam C Searleman, S Joshua Swamidass, et al.
Cancer Genetics|September 30, 2021
Selection for or against escape from nonsense mediated decay is a novel signature for the detection of cancer genesRunjun D Kumar, Briana A Burns, Paul J Vandeventer, et al.
Molecular Genetics and Metabolism Reports|January 25, 2021
A deep intronic variant is a common cause of OTC deficiency in individuals with previously negative genetic testingRunjun D Kumar, Lindsay C Burrage, Jan Bartos, et al.
American Journal of Medical Genetics. Part A|September 6, 2022
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysisRunjun D Kumar, Linyan Meng, Pengfei Liu, et al.
Pageof 3