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Journal of Medical Genetics
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November 13, 2024
Long-read sequencing for detection and subtyping of Prader-Willi and Angelman syndromes
Vahid Akbari, Sarah Dada, Yaoqing Shen, et al.
Genome Research
|
September 11, 2012
Spark: a navigational paradigm for genomic data exploration
Cydney B Nielsen, Hamid Younesy, Henriette O'Geen, et al.
Molecular Genetics & Genomic Medicine
|
November 25, 2020
Matching methods in precision oncology: An introduction and illustrative example
Deirdre Weymann, Janessa Laskin, Steven J M Jones, et al.
BMC Cancer
|
December 19, 2015
The genomic and transcriptomic landscape of anaplastic thyroid cancer: implications for therapy
Katayoon Kasaian, Sam M Wiseman, Blair A Walker, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2022
Long-read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmia
Pierre K Boerkoel, Katherine Dixon, Carrie Fitzsimons, et al.
BMC Medical Genomics
|
September 7, 2022
TMBur: a distributable tumor mutation burden approach for whole genome sequencing
Emma Titmuss, Richard D Corbett, Scott Davidson, et al.
The Journal of Biological Chemistry
|
October 23, 2012
Bromodomain-containing protein 4 (BRD4) regulates RNA polymerase II serine 2 phosphorylation in human CD4+ T cells
Weishi Zhang, Celine Prakash, Calvin Sum, et al.
Genome Research
|
May 5, 2004
Sockeye: a 3D environment for comparative genomics
Stephen B Montgomery, Tamara Astakhova, Mikhail Bilenky, et al.
Genome Research
|
August 23, 2007
Identification and analysis of internal promoters in Caenorhabditis elegans operons
Peiming Huang, Erin D Pleasance, Jason S Maydan, et al.
The Canadian Journal of Cardiology
|
January 28, 2014
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect
Steven C Greenway, Ross McLeod, Stacey Hume, et al.
Page
of 78
Search research articles
Search
Showing results (501-510 of 771) with videos related to
Sort By:
Page
of 78
Journal of Medical Genetics
|
November 13, 2024
Long-read sequencing for detection and subtyping of Prader-Willi and Angelman syndromes
Vahid Akbari, Sarah Dada, Yaoqing Shen, et al.
Genome Research
|
September 11, 2012
Spark: a navigational paradigm for genomic data exploration
Cydney B Nielsen, Hamid Younesy, Henriette O'Geen, et al.
Molecular Genetics & Genomic Medicine
|
November 25, 2020
Matching methods in precision oncology: An introduction and illustrative example
Deirdre Weymann, Janessa Laskin, Steven J M Jones, et al.
BMC Cancer
|
December 19, 2015
The genomic and transcriptomic landscape of anaplastic thyroid cancer: implications for therapy
Katayoon Kasaian, Sam M Wiseman, Blair A Walker, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2022
Long-read genome sequencing resolves a complex 13q structural variant associated with syndromic anophthalmia
Pierre K Boerkoel, Katherine Dixon, Carrie Fitzsimons, et al.
BMC Medical Genomics
|
September 7, 2022
TMBur: a distributable tumor mutation burden approach for whole genome sequencing
Emma Titmuss, Richard D Corbett, Scott Davidson, et al.
The Journal of Biological Chemistry
|
October 23, 2012
Bromodomain-containing protein 4 (BRD4) regulates RNA polymerase II serine 2 phosphorylation in human CD4+ T cells
Weishi Zhang, Celine Prakash, Calvin Sum, et al.
Genome Research
|
May 5, 2004
Sockeye: a 3D environment for comparative genomics
Stephen B Montgomery, Tamara Astakhova, Mikhail Bilenky, et al.
Genome Research
|
August 23, 2007
Identification and analysis of internal promoters in Caenorhabditis elegans operons
Peiming Huang, Erin D Pleasance, Jason S Maydan, et al.
The Canadian Journal of Cardiology
|
January 28, 2014
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect
Steven C Greenway, Ross McLeod, Stacey Hume, et al.
Page
of 78