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Nature Genetics
|
April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M Werling, Harrison Brand, Joon-Yong An, et al.
Nature
|
February 5, 2011
Mapping copy number variation by population-scale genome sequencing
Ryan E Mills, Klaudia Walter, Chip Stewart, et al.
NPJ Genomic Medicine
|
March 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit
Sabrina Malone Jenkins, Rachel N Palmquist, Barry Moore, et al.
Nature Communications
|
April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Mark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
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of 11
Search research articles
Search
Showing results (101-110 of 104) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 104 results.
Nature Genetics
|
April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Donna M Werling, Harrison Brand, Joon-Yong An, et al.
Nature
|
February 5, 2011
Mapping copy number variation by population-scale genome sequencing
Ryan E Mills, Klaudia Walter, Chip Stewart, et al.
NPJ Genomic Medicine
|
March 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unit
Sabrina Malone Jenkins, Rachel N Palmquist, Barry Moore, et al.
Nature Communications
|
April 18, 2019
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Mark J P Chaisson, Ashley D Sanders, Xuefang Zhao, et al.
Page
of 11