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Showing results (251-260 of 279) with videos related to

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Biorxiv : the Preprint Server for Biology|September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologiesJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Cell Reports. Medicine|May 24, 2023
Tumor biology and immune infiltration define primary liver cancer subsets linked to overall survival after immunotherapyAnuradha Budhu, Erica C Pehrsson, Aiwu He, et al.
Biorxiv : the Preprint Server for Biology|April 27, 2026
Single-cell full-length transcriptome of human lung reveals genetic effects on isoform regulation beyond gene-level expressionBolun Li, Thong Luong, Elelta Sisay, et al.
Scientific Data|November 10, 2021
Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark studyYongmei Zhao, Li Tai Fang, Tsai-Wei Shen, et al.
Circulation Research|December 28, 2023
Blood Monocyte Phenotype Is A Marker of Cardiovascular Risk in Type 2 DiabetesJean-Baptiste Julla, Diane Girard, Marc Diedisheim, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2024
Toward a CRISPR-based mouse model of <i>Vhl</i>-deficient clear cell kidney cancer: Initial experience and lessons learnedLaura A Stransky, Wenhua Gao, Laura S Schmidt, et al.
Nature Biotechnology|October 16, 2025
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomaticJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Severus: accurate detection and characterization of somatic structural variation in tumor genomes using long readsAyse Keskus, Asher Bryant, Tanveer Ahmad, et al.
Genome Biology|December 13, 2022
Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologiesKeyur Talsania, Tsai-Wei Shen, Xiongfong Chen, et al.
Cancer Discovery|January 30, 2023
Extrachromosomal DNA Amplification Contributes to Small Cell Lung Cancer Heterogeneity and Is Associated with Worse OutcomesLőrinc Sándor Pongor, Christopher W Schultz, Lorenzo Rinaldi, et al.
Pageof 28

Showing results (251-260 of 279) with videos related to

Sort By:
Pageof 28
Biorxiv : the Preprint Server for Biology|September 4, 2024
DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologiesJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Cell Reports. Medicine|May 24, 2023
Tumor biology and immune infiltration define primary liver cancer subsets linked to overall survival after immunotherapyAnuradha Budhu, Erica C Pehrsson, Aiwu He, et al.
Biorxiv : the Preprint Server for Biology|April 27, 2026
Single-cell full-length transcriptome of human lung reveals genetic effects on isoform regulation beyond gene-level expressionBolun Li, Thong Luong, Elelta Sisay, et al.
Scientific Data|November 10, 2021
Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark studyYongmei Zhao, Li Tai Fang, Tsai-Wei Shen, et al.
Circulation Research|December 28, 2023
Blood Monocyte Phenotype Is A Marker of Cardiovascular Risk in Type 2 DiabetesJean-Baptiste Julla, Diane Girard, Marc Diedisheim, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 4, 2024
Toward a CRISPR-based mouse model of <i>Vhl</i>-deficient clear cell kidney cancer: Initial experience and lessons learnedLaura A Stransky, Wenhua Gao, Laura S Schmidt, et al.
Nature Biotechnology|October 16, 2025
Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomaticJimin Park, Daniel E Cook, Pi-Chuan Chang, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Severus: accurate detection and characterization of somatic structural variation in tumor genomes using long readsAyse Keskus, Asher Bryant, Tanveer Ahmad, et al.
Genome Biology|December 13, 2022
Structural variant analysis of a cancer reference cell line sample using multiple sequencing technologiesKeyur Talsania, Tsai-Wei Shen, Xiongfong Chen, et al.
Cancer Discovery|January 30, 2023
Extrachromosomal DNA Amplification Contributes to Small Cell Lung Cancer Heterogeneity and Is Associated with Worse OutcomesLőrinc Sándor Pongor, Christopher W Schultz, Lorenzo Rinaldi, et al.
Pageof 28