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Carlo Sidore

Showing results (1-10 of 63) with videos related to

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BMC Genomics|September 23, 2017
XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experimentsAlberto Magi, Tommaso Pippucci, Carlo Sidore
Genome Research|April 5, 2011
Low-coverage sequencing: implications for design of complex trait association studiesYun Li, Carlo Sidore, Hyun Min Kang, et al.
Genetic Epidemiology|December 20, 2018
Relative impact of indels versus SNPs on complex diseaseSarah 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 familiesBingshan 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 JapanMinhui Chen, Carlo Sidore, Masato Akiyama, et al.
Genome Research|October 16, 2012
Genotype calling and haplotyping in parent-offspring triosWei Chen, Bingshan Li, Zhen Zeng, et al.
Communications Biology|January 25, 2019
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigreeSahar 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 samplePaolo Francalacci, Daria Sanna, Antonella Useli, et al.
Diabetologia|April 8, 2021
Analysis of overlapping genetic association in type 1 and type 2 diabetesJamie 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 sequencesYong Qian, Thomas J Butler, Krista Opsahl-Ong, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
BMC Genomics|September 23, 2017
XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experimentsAlberto Magi, Tommaso Pippucci, Carlo Sidore
Genome Research|April 5, 2011
Low-coverage sequencing: implications for design of complex trait association studiesYun Li, Carlo Sidore, Hyun Min Kang, et al.
Genetic Epidemiology|December 20, 2018
Relative impact of indels versus SNPs on complex diseaseSarah 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 familiesBingshan 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 JapanMinhui Chen, Carlo Sidore, Masato Akiyama, et al.
Genome Research|October 16, 2012
Genotype calling and haplotyping in parent-offspring triosWei Chen, Bingshan Li, Zhen Zeng, et al.
Communications Biology|January 25, 2019
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigreeSahar 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 samplePaolo Francalacci, Daria Sanna, Antonella Useli, et al.
Diabetologia|April 8, 2021
Analysis of overlapping genetic association in type 1 and type 2 diabetesJamie 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 sequencesYong Qian, Thomas J Butler, Krista Opsahl-Ong, et al.
Pageof 7