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Bioinformatics (Oxford, England)
|
August 8, 2009
R/Bioconductor software for Illumina's Infinium whole-genome genotyping BeadChips
Matthew E Ritchie, Benilton S Carvalho, Kurt N Hetrick, et al.
American Journal of Human Genetics
|
October 30, 2012
Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data
Goo Jun, Matthew Flickinger, Kurt N Hetrick, et al.
Molecular Syndromology
|
January 8, 2015
Novel Deletion of SERPINF1 Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian Families
Renata Moldenhauer Minillo, Nara Sobreira, Maria de Fatima de Faria Soares, et al.
Current Protocols in Human Genetics
|
January 12, 2017
Generating Exome Enriched Sequencing Libraries from Formalin-Fixed, Paraffin-Embedded Tissue DNA for Next-Generation Sequencing
Beth A Marosy, Brian D Craig, Kurt N Hetrick, et al.
Plos One
|
August 11, 2011
Copy number variation in familial Parkinson disease
Nathan Pankratz, Alexandra Dumitriu, Kurt N Hetrick, et al.
Ebiomedicine
|
June 4, 2018
Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma
Zhaoxi Wang, Yongyue Wei, Ruyang Zhang, et al.
Nature Communications
|
March 6, 2014
Mutations in Alström protein impair terminal differentiation of cardiomyocytes
Lincoln T Shenje, Peter Andersen, Marc K Halushka, et al.
Journal of the National Cancer Institute
|
August 28, 2020
Germline Sequencing DNA Repair Genes in 5545 Men With Aggressive and Nonaggressive Prostate Cancer
Burcu F Darst, Tokhir Dadaev, Ed Saunders, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 15, 2023
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients
Yi-Hui Zhou, Paul J Gallins, Rhonda G Pace, et al.
JAMA Oncology
|
September 21, 2023
Germline Sequencing Analysis to Inform Clinical Gene Panel Testing for Aggressive Prostate Cancer
Burcu F Darst, Ed Saunders, Tokhir Dadaev, et al.
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of 2
Search research articles
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Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Bioinformatics (Oxford, England)
|
August 8, 2009
R/Bioconductor software for Illumina's Infinium whole-genome genotyping BeadChips
Matthew E Ritchie, Benilton S Carvalho, Kurt N Hetrick, et al.
American Journal of Human Genetics
|
October 30, 2012
Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data
Goo Jun, Matthew Flickinger, Kurt N Hetrick, et al.
Molecular Syndromology
|
January 8, 2015
Novel Deletion of SERPINF1 Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian Families
Renata Moldenhauer Minillo, Nara Sobreira, Maria de Fatima de Faria Soares, et al.
Current Protocols in Human Genetics
|
January 12, 2017
Generating Exome Enriched Sequencing Libraries from Formalin-Fixed, Paraffin-Embedded Tissue DNA for Next-Generation Sequencing
Beth A Marosy, Brian D Craig, Kurt N Hetrick, et al.
Plos One
|
August 11, 2011
Copy number variation in familial Parkinson disease
Nathan Pankratz, Alexandra Dumitriu, Kurt N Hetrick, et al.
Ebiomedicine
|
June 4, 2018
Multi-Omics Analysis Reveals a HIF Network and Hub Gene EPAS1 Associated with Lung Adenocarcinoma
Zhaoxi Wang, Yongyue Wei, Ruyang Zhang, et al.
Nature Communications
|
March 6, 2014
Mutations in Alström protein impair terminal differentiation of cardiomyocytes
Lincoln T Shenje, Peter Andersen, Marc K Halushka, et al.
Journal of the National Cancer Institute
|
August 28, 2020
Germline Sequencing DNA Repair Genes in 5545 Men With Aggressive and Nonaggressive Prostate Cancer
Burcu F Darst, Tokhir Dadaev, Ed Saunders, et al.
American Journal of Respiratory and Critical Care Medicine
|
March 15, 2023
Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 Patients
Yi-Hui Zhou, Paul J Gallins, Rhonda G Pace, et al.
JAMA Oncology
|
September 21, 2023
Germline Sequencing Analysis to Inform Clinical Gene Panel Testing for Aggressive Prostate Cancer
Burcu F Darst, Ed Saunders, Tokhir Dadaev, et al.
Page
of 2