Search research articles
Contact Us
Filters
Showing results (1-10 of 35) with videos related to
Page
of 4
Sort By:
Plos Genetics
|
October 12, 2012
A likelihood-based framework for variant calling and de novo mutation detection in families
Bingshan Li, Wei Chen, Xiaowei Zhan, et al.
BMC Bioinformatics
|
April 18, 2015
Comparing variant calling algorithms for target-exon sequencing in a large sample
Yancy Lo, Hyun M Kang, Matthew R Nelson, et al.
Plos Genetics
|
January 10, 2013
Systems genetic analysis of osteoblast-lineage cells
Gina Calabrese, Brian J Bennett, Luz Orozco, et al.
International Journal of Molecular Sciences
|
February 11, 2023
Correlations between H<sub>2</sub> Permeation and Physical/Mechanical Properties in Ethylene Propylene Diene Monomer Polymers Blended with Carbon Black and Silica Fillers
Jae K Jung, Ji H Lee, Sang K Jeon, et al.
The Journal of Investigative Dermatology
|
January 21, 2014
Transcriptome analysis of psoriasis in a large case-control sample: RNA-seq provides insights into disease mechanisms
Bingshan Li, Lam C Tsoi, William R Swindell, et al.
Genome Biology
|
February 28, 2015
Analysis of long non-coding RNAs highlights tissue-specific expression patterns and epigenetic profiles in normal and psoriatic skin
Lam C Tsoi, Matthew K Iyer, Philip E Stuart, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 28, 2020
Whole-Genome Sequencing Identifies Novel Functional Loci Associated with Lung Function in Puerto Rican Youth
Eunice Y Lee, Angel C Y Mak, Donglei Hu, et al.
Plos Genetics
|
August 11, 2011
Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability
Serena Sanna, Bingshan Li, Antonella Mulas, et al.
Plos Genetics
|
June 23, 2011
Comparative analysis of proteome and transcriptome variation in mouse
Anatole Ghazalpour, Brian Bennett, Vladislav A Petyuk, et al.
European Journal of Human Genetics : EJHG
|
October 9, 2014
Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs
Giorgio Pistis, Eleonora Porcu, Scott I Vrieze, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
Plos Genetics
|
October 12, 2012
A likelihood-based framework for variant calling and de novo mutation detection in families
Bingshan Li, Wei Chen, Xiaowei Zhan, et al.
BMC Bioinformatics
|
April 18, 2015
Comparing variant calling algorithms for target-exon sequencing in a large sample
Yancy Lo, Hyun M Kang, Matthew R Nelson, et al.
Plos Genetics
|
January 10, 2013
Systems genetic analysis of osteoblast-lineage cells
Gina Calabrese, Brian J Bennett, Luz Orozco, et al.
International Journal of Molecular Sciences
|
February 11, 2023
Correlations between H<sub>2</sub> Permeation and Physical/Mechanical Properties in Ethylene Propylene Diene Monomer Polymers Blended with Carbon Black and Silica Fillers
Jae K Jung, Ji H Lee, Sang K Jeon, et al.
The Journal of Investigative Dermatology
|
January 21, 2014
Transcriptome analysis of psoriasis in a large case-control sample: RNA-seq provides insights into disease mechanisms
Bingshan Li, Lam C Tsoi, William R Swindell, et al.
Genome Biology
|
February 28, 2015
Analysis of long non-coding RNAs highlights tissue-specific expression patterns and epigenetic profiles in normal and psoriatic skin
Lam C Tsoi, Matthew K Iyer, Philip E Stuart, et al.
American Journal of Respiratory and Critical Care Medicine
|
May 28, 2020
Whole-Genome Sequencing Identifies Novel Functional Loci Associated with Lung Function in Puerto Rican Youth
Eunice Y Lee, Angel C Y Mak, Donglei Hu, et al.
Plos Genetics
|
August 11, 2011
Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability
Serena Sanna, Bingshan Li, Antonella Mulas, et al.
Plos Genetics
|
June 23, 2011
Comparative analysis of proteome and transcriptome variation in mouse
Anatole Ghazalpour, Brian Bennett, Vladislav A Petyuk, et al.
European Journal of Human Genetics : EJHG
|
October 9, 2014
Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs
Giorgio Pistis, Eleonora Porcu, Scott I Vrieze, et al.
Page
of 4