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L Griffith

Showing results (651-660 of 715) with videos related to

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Veterinary and Comparative Oncology|February 22, 2026
Whole Exome Sequencing of Feline Oral Squamous Cell Carcinoma Reveals Genomic Parallels With Human Head and Neck Squamous Cell CarcinomaShirley Chu, Zachary L Skidmore, Wes Warren, et al.
Experimental Hematology|August 2, 2017
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomesJin Zhang, Malachi Griffith, Christopher A Miller, et al.
Molecular Cancer Research : MCR|August 18, 2019
Targeting the Mevalonate Pathway to Overcome Acquired Anti-HER2 Treatment Resistance in Breast CancerVidyalakshmi Sethunath, Huizhong Hu, Carmine De Angelis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2018
Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samplesErica K Barnell, Peter Ronning, Katie M Campbell, et al.
Nature Communications|March 23, 2023
Integrated analysis of genomic and transcriptomic data for the discovery of splice-associated variants in cancerKelsy C Cotto, Yang-Yang Feng, Avinash Ramu, et al.
Blood Advances|July 26, 2023
Mutations associated with progression in follicular lymphoma predict inferior outcomes at diagnosis: Alliance A151303David A Russler-Germain, Kilannin Krysiak, Cody Ramirez, et al.
Nature Methods|October 15, 2013
DGIdb: mining the druggable genomeMalachi Griffith, Obi L Griffith, Adam C Coffman, et al.
Cell Genomics|April 9, 2026
ClinGen API platform for classification of human genetic variantsNeethu Shah, Tierra Farris, Arturo Alejandro Zuniga, et al.
Arxiv|July 3, 2026
pVACtools v6: A comprehensive suite for neoantigen prediction, visualization, and therapy designMy H Hoang, Susanna Kiwala, Megan Richters, et al.
Genome Medicine|November 30, 2019
Standard operating procedure for curation and clinical interpretation of variants in cancerArpad M Danos, Kilannin Krysiak, Erica K Barnell, et al.
Pageof 72

Showing results (651-660 of 715) with videos related to

Sort By:
Pageof 72
Veterinary and Comparative Oncology|February 22, 2026
Whole Exome Sequencing of Feline Oral Squamous Cell Carcinoma Reveals Genomic Parallels With Human Head and Neck Squamous Cell CarcinomaShirley Chu, Zachary L Skidmore, Wes Warren, et al.
Experimental Hematology|August 2, 2017
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomesJin Zhang, Malachi Griffith, Christopher A Miller, et al.
Molecular Cancer Research : MCR|August 18, 2019
Targeting the Mevalonate Pathway to Overcome Acquired Anti-HER2 Treatment Resistance in Breast CancerVidyalakshmi Sethunath, Huizhong Hu, Carmine De Angelis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2018
Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samplesErica K Barnell, Peter Ronning, Katie M Campbell, et al.
Nature Communications|March 23, 2023
Integrated analysis of genomic and transcriptomic data for the discovery of splice-associated variants in cancerKelsy C Cotto, Yang-Yang Feng, Avinash Ramu, et al.
Blood Advances|July 26, 2023
Mutations associated with progression in follicular lymphoma predict inferior outcomes at diagnosis: Alliance A151303David A Russler-Germain, Kilannin Krysiak, Cody Ramirez, et al.
Nature Methods|October 15, 2013
DGIdb: mining the druggable genomeMalachi Griffith, Obi L Griffith, Adam C Coffman, et al.
Cell Genomics|April 9, 2026
ClinGen API platform for classification of human genetic variantsNeethu Shah, Tierra Farris, Arturo Alejandro Zuniga, et al.
Arxiv|July 3, 2026
pVACtools v6: A comprehensive suite for neoantigen prediction, visualization, and therapy designMy H Hoang, Susanna Kiwala, Megan Richters, et al.
Genome Medicine|November 30, 2019
Standard operating procedure for curation and clinical interpretation of variants in cancerArpad M Danos, Kilannin Krysiak, Erica K Barnell, et al.
Pageof 72