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Nature Genetics
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May 5, 2025
Near-complete Middle Eastern genomes refine autozygosity and enhance disease-causing and population-specific variant discovery
Mohammadmersad Ghorbani, Shabir Moosa, Zenab Siddig, et al.
Nature Communications
|
January 23, 2026
Using the linear references from the pangenome to discover missing autism variants
Yang Sui, Jiadong Lin, Michelle D Noyes, et al.
Cell Reports
|
June 24, 2021
Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7
Bo Meng, Steven A Kemp, Guido Papa, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 8, 2025
Pangenome discovery of missing autism variants
Yang Sui, Jiadong Lin, Michelle D Noyes, et al.
Biorxiv : the Preprint Server for Biology
|
March 22, 2023
Structurally divergent and recurrently mutated regions of primate genomes
Yafei Mao, William T Harvey, David Porubsky, et al.
Biorxiv : the Preprint Server for Biology
|
June 12, 2025
A haplotype-resolved view of human gene regulation
Mitchell R Vollger, Elliott G Swanson, Shane J Neph, et al.
Cell Reports
|
January 30, 2022
Mutations that adapt SARS-CoV-2 to mink or ferret do not increase fitness in the human airway
Jie Zhou, Thomas P Peacock, Jonathan C Brown, et al.
American Journal of Human Genetics
|
June 17, 2026
Complete chromosome 21 centromere sequencing of families with Down syndrome
F Kumara Mastrorosa, Alessia Daponte, Luciana de Gennaro, et al.
Nature Genetics
|
August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Xueya Zhou, Pamela Feliciano, Chang Shu, et al.
Nature
|
August 23, 2023
Assembly of 43 human Y chromosomes reveals extensive complexity and variation
Pille Hallast, Peter Ebert, Mark Loftus, et al.
Page
of 36
Search research articles
Search
Showing results (331-340 of 358) with videos related to
Sort By:
Page
of 36
Nature Genetics
|
May 5, 2025
Near-complete Middle Eastern genomes refine autozygosity and enhance disease-causing and population-specific variant discovery
Mohammadmersad Ghorbani, Shabir Moosa, Zenab Siddig, et al.
Nature Communications
|
January 23, 2026
Using the linear references from the pangenome to discover missing autism variants
Yang Sui, Jiadong Lin, Michelle D Noyes, et al.
Cell Reports
|
June 24, 2021
Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7
Bo Meng, Steven A Kemp, Guido Papa, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 8, 2025
Pangenome discovery of missing autism variants
Yang Sui, Jiadong Lin, Michelle D Noyes, et al.
Biorxiv : the Preprint Server for Biology
|
March 22, 2023
Structurally divergent and recurrently mutated regions of primate genomes
Yafei Mao, William T Harvey, David Porubsky, et al.
Biorxiv : the Preprint Server for Biology
|
June 12, 2025
A haplotype-resolved view of human gene regulation
Mitchell R Vollger, Elliott G Swanson, Shane J Neph, et al.
Cell Reports
|
January 30, 2022
Mutations that adapt SARS-CoV-2 to mink or ferret do not increase fitness in the human airway
Jie Zhou, Thomas P Peacock, Jonathan C Brown, et al.
American Journal of Human Genetics
|
June 17, 2026
Complete chromosome 21 centromere sequencing of families with Down syndrome
F Kumara Mastrorosa, Alessia Daponte, Luciana de Gennaro, et al.
Nature Genetics
|
August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes
Xueya Zhou, Pamela Feliciano, Chang Shu, et al.
Nature
|
August 23, 2023
Assembly of 43 human Y chromosomes reveals extensive complexity and variation
Pille Hallast, Peter Ebert, Mark Loftus, et al.
Page
of 36