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BMC Proceedings
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December 17, 2016
Independent test assessment using the extreme value distribution theory
Marcio Almeida, Lucy Blondell, Juan M Peralta, et al.
Nature Protocols
|
November 1, 2024
Seq-Scope: repurposing Illumina sequencing flow cells for high-resolution spatial transcriptomics
Yongsung Kim, Weiqiu Cheng, Chun-Seok Cho, et al.
Psychophysiology
|
November 13, 2014
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes
Scott I Vrieze, Stephen M Malone, Uma Vaidyanathan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 24, 2025
Human genomic regions of systemic interindividual epigenetic variation are implicated in neurodevelopmental and metabolic disorders
Wen-Jou Chang, Uditha Maduranga, Chathura J Gunasekara, et al.
Circulation
|
June 20, 2018
Proteomic Architecture of Human Coronary and Aortic Atherosclerosis
David M Herrington, Chunhong Mao, Sarah J Parker, et al.
Science (New York, N.Y.)
|
May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
Jacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.
Circulation. Genomic and Precision Medicine
|
November 4, 2021
Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation
Yunju Yang, Traci M Bartz, Michael R Brown, et al.
American Journal of Human Genetics
|
May 3, 2022
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data
Le Huang, Jonathan D Rosen, Quan Sun, et al.
Human Molecular Genetics
|
November 8, 2014
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes
Andrew R Wood, Marcus A Tuke, Mike Nalls, et al.
BMC Proceedings
|
December 17, 2016
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19
John Blangero, Tanya M Teslovich, Xueling Sim, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 70) with videos related to
Sort By:
Page
of 7
BMC Proceedings
|
December 17, 2016
Independent test assessment using the extreme value distribution theory
Marcio Almeida, Lucy Blondell, Juan M Peralta, et al.
Nature Protocols
|
November 1, 2024
Seq-Scope: repurposing Illumina sequencing flow cells for high-resolution spatial transcriptomics
Yongsung Kim, Weiqiu Cheng, Chun-Seok Cho, et al.
Psychophysiology
|
November 13, 2014
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes
Scott I Vrieze, Stephen M Malone, Uma Vaidyanathan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 24, 2025
Human genomic regions of systemic interindividual epigenetic variation are implicated in neurodevelopmental and metabolic disorders
Wen-Jou Chang, Uditha Maduranga, Chathura J Gunasekara, et al.
Circulation
|
June 20, 2018
Proteomic Architecture of Human Coronary and Aortic Atherosclerosis
David M Herrington, Chunhong Mao, Sarah J Parker, et al.
Science (New York, N.Y.)
|
May 19, 2012
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
Jacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, et al.
Circulation. Genomic and Precision Medicine
|
November 4, 2021
Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation
Yunju Yang, Traci M Bartz, Michael R Brown, et al.
American Journal of Human Genetics
|
May 3, 2022
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data
Le Huang, Jonathan D Rosen, Quan Sun, et al.
Human Molecular Genetics
|
November 8, 2014
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes
Andrew R Wood, Marcus A Tuke, Mike Nalls, et al.
BMC Proceedings
|
December 17, 2016
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19
John Blangero, Tanya M Teslovich, Xueling Sim, et al.
Page
of 7