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IUBMB Life
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June 17, 2008
Microarray-based DNA profiling to study genomic aberrations
Nic Waddell
Idrugs : the Investigational Drugs Journal
|
November 4, 2010
The clinical potential and challenges of sequencing cancer genomes for personalized medical genomics
Nicole Cloonan, Nic Waddell, Sean M Grimmond
Integrative Biology : Quantitative Biosciences From Nano to Macro
|
February 8, 2011
Sequencing transcriptomes in toto
Karin S Kassahn, Nic Waddell, Sean M Grimmond
BMC Cancer
|
June 19, 2012
The application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genes
Julie K Johnson, Nic Waddell, , et al.
Breast Cancer Research and Treatment
|
March 22, 2012
Germline copy number variants are not associated with globally acquired copy number changes in familial breast tumours
Logan C Walker, Lutz Krause, , et al.
Breast Cancer Research and Treatment
|
December 21, 2007
Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers
Logan C Walker, Nic Waddell, Anette Ten Haaf, et al.
Plos Genetics
|
February 23, 2010
Use of DNA-damaging agents and RNA pooling to assess expression profiles associated with BRCA1 and BRCA2 mutation status in familial breast cancer patients
Logan C Walker, Bryony A Thompson, Nic Waddell, et al.
Studies in Health Technology and Informatics
|
August 10, 2019
Running Genomic Analyses in the Cloud
Conrad Leonard, Scott Wood, Oliver Holmes, et al.
BMC Cancer
|
July 9, 2015
Comparative microRNA profiling of sporadic and BRCA1 associated basal-like breast cancers
Max Yan, Kristy Shield-Artin, David Byrne, et al.
Breast Cancer Research : BCR
|
April 28, 2012
Enhanced RAD21 cohesin expression confers poor prognosis in BRCA2 and BRCAX, but not BRCA1 familial breast cancers
Max Yan, Huiling Xu, Nic Waddell, et al.
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of 4
Search research articles
Search
Showing results (1-10 of 39) with videos related to
Sort By:
Page
of 4
IUBMB Life
|
June 17, 2008
Microarray-based DNA profiling to study genomic aberrations
Nic Waddell
Idrugs : the Investigational Drugs Journal
|
November 4, 2010
The clinical potential and challenges of sequencing cancer genomes for personalized medical genomics
Nicole Cloonan, Nic Waddell, Sean M Grimmond
Integrative Biology : Quantitative Biosciences From Nano to Macro
|
February 8, 2011
Sequencing transcriptomes in toto
Karin S Kassahn, Nic Waddell, Sean M Grimmond
BMC Cancer
|
June 19, 2012
The application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genes
Julie K Johnson, Nic Waddell, , et al.
Breast Cancer Research and Treatment
|
March 22, 2012
Germline copy number variants are not associated with globally acquired copy number changes in familial breast tumours
Logan C Walker, Lutz Krause, , et al.
Breast Cancer Research and Treatment
|
December 21, 2007
Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers
Logan C Walker, Nic Waddell, Anette Ten Haaf, et al.
Plos Genetics
|
February 23, 2010
Use of DNA-damaging agents and RNA pooling to assess expression profiles associated with BRCA1 and BRCA2 mutation status in familial breast cancer patients
Logan C Walker, Bryony A Thompson, Nic Waddell, et al.
Studies in Health Technology and Informatics
|
August 10, 2019
Running Genomic Analyses in the Cloud
Conrad Leonard, Scott Wood, Oliver Holmes, et al.
BMC Cancer
|
July 9, 2015
Comparative microRNA profiling of sporadic and BRCA1 associated basal-like breast cancers
Max Yan, Kristy Shield-Artin, David Byrne, et al.
Breast Cancer Research : BCR
|
April 28, 2012
Enhanced RAD21 cohesin expression confers poor prognosis in BRCA2 and BRCAX, but not BRCA1 familial breast cancers
Max Yan, Huiling Xu, Nic Waddell, et al.
Page
of 4