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Gabor T Marth

Showing results (41-50 of 61) with videos related to

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Genome Research|January 9, 2024
A Bayesian framework to study tumor subclone-specific expression by combining bulk DNA and single-cell RNA sequencing dataYi Qiao, Xiaomeng Huang, Philip J Moos, et al.
Journal of Clinical and Translational Science|May 1, 2018
Rapid clinical diagnostic variant investigation of genomic patient sequencing data with <i>iobio</i> web toolsAlistair Ward, Mary A Karren, Tonya Di Sera, et al.
Science (New York, N.Y.)|January 17, 2012
A DOC2 protein identified by mutational profiling is essential for apicomplexan parasite exocytosisAndrew Farrell, Sivasakthivel Thirugnanam, Alexander Lorestani, et al.
Bioinformatics (Oxford, England)|June 10, 2011
The variant call format and VCFtoolsPetr Danecek, Adam Auton, Goncalo Abecasis, et al.
Plos One|February 22, 2020
The stochastic nature of errors in next-generation sequencing of circulating cell-free DNADavid A Nix, Sabine Hellwig, Christopher Conley, et al.
Genome Medicine|October 29, 2021
Novel temporal and spatial patterns of metastatic colonization from breast cancer rapid-autopsy tumor biopsiesXiaomeng Huang, Yi Qiao, Samuel W Brady, et al.
Genome Biology|February 5, 2015
Extending reference assembly modelsDeanna M Church, Valerie A Schneider, Karyn Meltz Steinberg, et al.
NPJ Genomic Medicine|August 16, 2018
Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathyBetsy E P Ostrander, Russell J Butterfield, Brent S Pedersen, et al.
Genome Biology|July 2, 2014
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequencesVincenza Colonna, Qasim Ayub, Yuan Chen, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
A precision oncology-focused deep learning framework for personalized selection of cancer therapyCasey Sederman, Chieh-Hsiang Yang, Emilio Cortes-Sanchez, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Genome Research|January 9, 2024
A Bayesian framework to study tumor subclone-specific expression by combining bulk DNA and single-cell RNA sequencing dataYi Qiao, Xiaomeng Huang, Philip J Moos, et al.
Journal of Clinical and Translational Science|May 1, 2018
Rapid clinical diagnostic variant investigation of genomic patient sequencing data with <i>iobio</i> web toolsAlistair Ward, Mary A Karren, Tonya Di Sera, et al.
Science (New York, N.Y.)|January 17, 2012
A DOC2 protein identified by mutational profiling is essential for apicomplexan parasite exocytosisAndrew Farrell, Sivasakthivel Thirugnanam, Alexander Lorestani, et al.
Bioinformatics (Oxford, England)|June 10, 2011
The variant call format and VCFtoolsPetr Danecek, Adam Auton, Goncalo Abecasis, et al.
Plos One|February 22, 2020
The stochastic nature of errors in next-generation sequencing of circulating cell-free DNADavid A Nix, Sabine Hellwig, Christopher Conley, et al.
Genome Medicine|October 29, 2021
Novel temporal and spatial patterns of metastatic colonization from breast cancer rapid-autopsy tumor biopsiesXiaomeng Huang, Yi Qiao, Samuel W Brady, et al.
Genome Biology|February 5, 2015
Extending reference assembly modelsDeanna M Church, Valerie A Schneider, Karyn Meltz Steinberg, et al.
NPJ Genomic Medicine|August 16, 2018
Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathyBetsy E P Ostrander, Russell J Butterfield, Brent S Pedersen, et al.
Genome Biology|July 2, 2014
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequencesVincenza Colonna, Qasim Ayub, Yuan Chen, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2025
A precision oncology-focused deep learning framework for personalized selection of cancer therapyCasey Sederman, Chieh-Hsiang Yang, Emilio Cortes-Sanchez, et al.
Pageof 7