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Methods in Molecular Biology (Clifton, N.J.)
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February 16, 2013
Distinguishing somatic and germline copy number events in cancer patient DNA hybridized to whole-genome SNP genotyping arrays
Gavin Ha, Sohrab Shah
European Journal of Case Reports in Internal Medicine
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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
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September 16, 2024
RCC1 depletion drives protein transport defects and rupture in micronuclei
Molly 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 review
Witina 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 tumorigenesis
Uri 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 models
Anna 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 models
Anna C H Hoge, Michal Getz, Anat Zimmer, et al.
Nature Methods
|
March 18, 2014
PyClone: statistical inference of clonal population structure in cancer
Andrew Roth, Jaswinder Khattra, Damian Yap, et al.
Genome Biology
|
February 7, 2013
DriverNet: uncovering the impact of somatic driver mutations on transcriptional networks in cancer
Ali 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 data
Andrew Roth, Jiarui Ding, Ryan Morin, et al.
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of 10
Search research articles
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Showing results (1-10 of 94) with videos related to
Sort By:
Page
of 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 arrays
Gavin 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 micronuclei
Molly 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 review
Witina 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 tumorigenesis
Uri 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 models
Anna 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 models
Anna C H Hoge, Michal Getz, Anat Zimmer, et al.
Nature Methods
|
March 18, 2014
PyClone: statistical inference of clonal population structure in cancer
Andrew Roth, Jaswinder Khattra, Damian Yap, et al.
Genome Biology
|
February 7, 2013
DriverNet: uncovering the impact of somatic driver mutations on transcriptional networks in cancer
Ali 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 data
Andrew Roth, Jiarui Ding, Ryan Morin, et al.
Page
of 10