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BMC Genomics
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September 23, 2017
XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments
Alberto Magi, Tommaso Pippucci, Carlo Sidore
Genome Research
|
April 5, 2011
Low-coverage sequencing: implications for design of complex trait association studies
Yun Li, Carlo Sidore, Hyun Min Kang, et al.
Genetic Epidemiology
|
December 20, 2018
Relative impact of indels versus SNPs on complex disease
Sarah A Gagliano, Sebanti Sengupta, Carlo Sidore, et al.
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.
American Journal of Human Genetics
|
June 14, 2020
Evidence of Polygenic Adaptation in Sardinia at Height-Associated Loci Ascertained from the Biobank Japan
Minhui Chen, Carlo Sidore, Masato Akiyama, et al.
Genome Research
|
October 16, 2012
Genotype calling and haplotyping in parent-offspring trios
Wei Chen, Bingshan Li, Zhen Zeng, et al.
Communications Biology
|
January 25, 2019
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree
Sahar V Mozaffari, Jeanne M DeCara, Sanjiv J Shah, et al.
BMC Research Notes
|
May 1, 2015
Detection of phylogenetically informative polymorphisms in the entire euchromatic portion of human Y chromosome from a Sardinian sample
Paolo Francalacci, Daria Sanna, Antonella Useli, et al.
Diabetologia
|
April 8, 2021
Analysis of overlapping genetic association in type 1 and type 2 diabetes
Jamie R J Inshaw, Carlo Sidore, Francesco Cucca, et al.
Bioinformatics (Oxford, England)
|
April 29, 2017
fastMitoCalc: an ultra-fast program to estimate mitochondrial DNA copy number from whole-genome sequences
Yong Qian, Thomas J Butler, Krista Opsahl-Ong, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 63) with videos related to
Sort By:
Page
of 7
BMC Genomics
|
September 23, 2017
XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments
Alberto Magi, Tommaso Pippucci, Carlo Sidore
Genome Research
|
April 5, 2011
Low-coverage sequencing: implications for design of complex trait association studies
Yun Li, Carlo Sidore, Hyun Min Kang, et al.
Genetic Epidemiology
|
December 20, 2018
Relative impact of indels versus SNPs on complex disease
Sarah A Gagliano, Sebanti Sengupta, Carlo Sidore, et al.
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.
American Journal of Human Genetics
|
June 14, 2020
Evidence of Polygenic Adaptation in Sardinia at Height-Associated Loci Ascertained from the Biobank Japan
Minhui Chen, Carlo Sidore, Masato Akiyama, et al.
Genome Research
|
October 16, 2012
Genotype calling and haplotyping in parent-offspring trios
Wei Chen, Bingshan Li, Zhen Zeng, et al.
Communications Biology
|
January 25, 2019
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree
Sahar V Mozaffari, Jeanne M DeCara, Sanjiv J Shah, et al.
BMC Research Notes
|
May 1, 2015
Detection of phylogenetically informative polymorphisms in the entire euchromatic portion of human Y chromosome from a Sardinian sample
Paolo Francalacci, Daria Sanna, Antonella Useli, et al.
Diabetologia
|
April 8, 2021
Analysis of overlapping genetic association in type 1 and type 2 diabetes
Jamie R J Inshaw, Carlo Sidore, Francesco Cucca, et al.
Bioinformatics (Oxford, England)
|
April 29, 2017
fastMitoCalc: an ultra-fast program to estimate mitochondrial DNA copy number from whole-genome sequences
Yong Qian, Thomas J Butler, Krista Opsahl-Ong, et al.
Page
of 7