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Nature Communications
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January 22, 2024
Pangenome graphs improve the analysis of structural variants in rare genetic diseases
Cristian Groza, Carl Schwendinger-Schreck, Warren A Cheung, et al.
Clinical Immunology (Orlando, Fla.)
|
March 19, 2025
Total plasma cfDNA methylation in pediatric kidney transplant recipients provides insight into acute allograft rejection pathophysiology
Benjamin L Spector, Boryana S Koseva, Drinnan Sante, et al.
Nature Communications
|
February 25, 2026
Evolving epigenomics of immune cells at single-nucleus resolution in children en route to type 1 diabetes
Tomi Pastinen, Elin Grundberg, Todd Bradley, et al.
Nature Communications
|
September 18, 2024
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation
Craig Smail, Bing Ge, Marissa R Keever-Keigher, et al.
Genome Biology
|
July 18, 2015
Epigenome data release: a participant-centered approach to privacy protection
Stephanie O M Dyke, Warren A Cheung, Yann Joly, et al.
Genome Biology
|
December 25, 2015
Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation
Stephan Busche, Xiaojian Shao, Maxime Caron, et al.
Nature Communications
|
August 10, 2023
Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape
Kaela M Varberg, Esteban M Dominguez, Boryana Koseva, et al.
Nature Communications
|
March 16, 2019
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements
Fiona Allum, Åsa K Hedman, Xiaojian Shao, et al.
Nature Metabolism
|
February 19, 2020
Single-cell analysis of human adipose tissue identifies depot and disease specific cell types
Jinchu Vijay, Marie-Frédérique Gauthier, Rebecca L Biswell, et al.
Nature Biotechnology
|
January 3, 2024
Characterization and visualization of tandem repeats at genome scale
Egor Dolzhenko, Adam English, Harriet Dashnow, et al.
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Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Nature Communications
|
January 22, 2024
Pangenome graphs improve the analysis of structural variants in rare genetic diseases
Cristian Groza, Carl Schwendinger-Schreck, Warren A Cheung, et al.
Clinical Immunology (Orlando, Fla.)
|
March 19, 2025
Total plasma cfDNA methylation in pediatric kidney transplant recipients provides insight into acute allograft rejection pathophysiology
Benjamin L Spector, Boryana S Koseva, Drinnan Sante, et al.
Nature Communications
|
February 25, 2026
Evolving epigenomics of immune cells at single-nucleus resolution in children en route to type 1 diabetes
Tomi Pastinen, Elin Grundberg, Todd Bradley, et al.
Nature Communications
|
September 18, 2024
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation
Craig Smail, Bing Ge, Marissa R Keever-Keigher, et al.
Genome Biology
|
July 18, 2015
Epigenome data release: a participant-centered approach to privacy protection
Stephanie O M Dyke, Warren A Cheung, Yann Joly, et al.
Genome Biology
|
December 25, 2015
Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation
Stephan Busche, Xiaojian Shao, Maxime Caron, et al.
Nature Communications
|
August 10, 2023
Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape
Kaela M Varberg, Esteban M Dominguez, Boryana Koseva, et al.
Nature Communications
|
March 16, 2019
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements
Fiona Allum, Åsa K Hedman, Xiaojian Shao, et al.
Nature Metabolism
|
February 19, 2020
Single-cell analysis of human adipose tissue identifies depot and disease specific cell types
Jinchu Vijay, Marie-Frédérique Gauthier, Rebecca L Biswell, et al.
Nature Biotechnology
|
January 3, 2024
Characterization and visualization of tandem repeats at genome scale
Egor Dolzhenko, Adam English, Harriet Dashnow, et al.
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of 4