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Gavin Ha

Showing results (1-10 of 94) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|February 16, 2013
Distinguishing somatic and germline copy number events in cancer patient DNA hybridized to whole-genome SNP genotyping arraysGavin Ha, Sohrab Shah
European Journal of Case Reports in Internal Medicine|July 17, 2023
Are Patients with HHV-8 Associated Castleman Disease Successfully Treated with Rituximab at Risk of Subsequently Developing HHV-8 Negative (Idiopathic) Castleman Disease?Gavin Ha, Kelsey Kwong, Bryce Tanaka, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
RCC1 depletion drives protein transport defects and rupture in micronucleiMolly G Zych, Maya Contreras, Manasvita Vashisth, et al.
American Heart Journal Plus : Cardiology Research and Practice|February 7, 2022
Characteristics of Takotsubo cardiomyopathy in patients with COVID-19: Systematic scoping reviewWitina Techasatian, Yoshito Nishimura, Todd Nagamine, et al.
Nature Communications|July 5, 2016
The landscape of chromosomal aberrations in breast cancer mouse models reveals driver-specific routes to tumorigenesisUri Ben-David, Gavin Ha, Prasidda Khadka, et al.
NPJ Precision Oncology|July 13, 2022
Publisher Correction: DNA-based copy number analysis confirms genomic evolution of PDX modelsAnna C H Hoge, Michal Getz, Anat Zimmer, et al.
NPJ Precision Oncology|April 28, 2022
DNA-based copy number analysis confirms genomic evolution of PDX modelsAnna C H Hoge, Michal Getz, Anat Zimmer, et al.
Nature Methods|March 18, 2014
PyClone: statistical inference of clonal population structure in cancerAndrew Roth, Jaswinder Khattra, Damian Yap, et al.
Genome Biology|February 7, 2013
DriverNet: uncovering the impact of somatic driver mutations on transcriptional networks in cancerAli Bashashati, Gholamreza Haffari, Jiarui Ding, et al.
Bioinformatics (Oxford, England)|January 31, 2012
JointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing dataAndrew Roth, Jiarui Ding, Ryan Morin, et al.
Pageof 10

Showing results (1-10 of 94) with videos related to

Sort By:
Pageof 10
Methods in Molecular Biology (Clifton, N.J.)|February 16, 2013
Distinguishing somatic and germline copy number events in cancer patient DNA hybridized to whole-genome SNP genotyping arraysGavin Ha, Sohrab Shah
European Journal of Case Reports in Internal Medicine|July 17, 2023
Are Patients with HHV-8 Associated Castleman Disease Successfully Treated with Rituximab at Risk of Subsequently Developing HHV-8 Negative (Idiopathic) Castleman Disease?Gavin Ha, Kelsey Kwong, Bryce Tanaka, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
RCC1 depletion drives protein transport defects and rupture in micronucleiMolly G Zych, Maya Contreras, Manasvita Vashisth, et al.
American Heart Journal Plus : Cardiology Research and Practice|February 7, 2022
Characteristics of Takotsubo cardiomyopathy in patients with COVID-19: Systematic scoping reviewWitina Techasatian, Yoshito Nishimura, Todd Nagamine, et al.
Nature Communications|July 5, 2016
The landscape of chromosomal aberrations in breast cancer mouse models reveals driver-specific routes to tumorigenesisUri Ben-David, Gavin Ha, Prasidda Khadka, et al.
NPJ Precision Oncology|July 13, 2022
Publisher Correction: DNA-based copy number analysis confirms genomic evolution of PDX modelsAnna C H Hoge, Michal Getz, Anat Zimmer, et al.
NPJ Precision Oncology|April 28, 2022
DNA-based copy number analysis confirms genomic evolution of PDX modelsAnna C H Hoge, Michal Getz, Anat Zimmer, et al.
Nature Methods|March 18, 2014
PyClone: statistical inference of clonal population structure in cancerAndrew Roth, Jaswinder Khattra, Damian Yap, et al.
Genome Biology|February 7, 2013
DriverNet: uncovering the impact of somatic driver mutations on transcriptional networks in cancerAli Bashashati, Gholamreza Haffari, Jiarui Ding, et al.
Bioinformatics (Oxford, England)|January 31, 2012
JointSNVMix: a probabilistic model for accurate detection of somatic mutations in normal/tumour paired next-generation sequencing dataAndrew Roth, Jiarui Ding, Ryan Morin, et al.
Pageof 10