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Mathieu Lemire

Showing results (1-10 of 85) with videos related to

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Nature Genetics|April 28, 2011
Defining rare variants by their frequencies in controls may increase type I errorMathieu Lemire
BMC Genetics|June 29, 2006
SUP: an extension to SLINK to allow a larger number of marker loci to be simulated in pedigrees conditional on trait valuesMathieu Lemire
BMC Proceedings|December 19, 2009
On the association between rheumatoid arthritis and classical HLA class I and class II alleles predicted from single-nucleotide polymorphism dataMathieu Lemire
BMC Genetics|February 3, 2006
A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkageMathieu Lemire
BMC Proceedings|March 1, 2012
Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studiesFrance Gagnon, Nicole M Roslin, Mathieu Lemire
BMC Genomics|May 17, 2017
In silico pathway analysis and tissue specific cis-eQTL for colorectal cancer GWAS risk variantsLenora W M Loo, Mathieu Lemire, Loïc Le Marchand
BMC Proceedings|December 19, 2009
Using a higher criticism statistic to detect modest effects in a genome-wide study of rheumatoid arthritisElena Parkhomenko, David Tritchler, Mathieu Lemire, et al.
American Journal of Human Genetics|August 24, 2004
Transmission-ratio distortion and allele sharing in affected sib pairs: a new linkage statistic with reduced bias, with application to chromosome 6q25.3Mathieu Lemire, Nicole M Roslin, Catherine Laprise, et al.
Human Heredity|July 8, 2011
Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigreesAlejandro A Schäffer, Mathieu Lemire, Jürg Ott, et al.
Clinical Epigenetics|March 16, 2017
The dynamic DNA methylation landscape of the <i>mutL homolog 1</i> shore is altered by <i>MLH1</i>-93G>A polymorphism in normal tissues and colorectal cancerAndrea J Savio, Miralem Mrkonjic, Mathieu Lemire, et al.
Pageof 9

Showing results (1-10 of 85) with videos related to

Sort By:
Pageof 9
Nature Genetics|April 28, 2011
Defining rare variants by their frequencies in controls may increase type I errorMathieu Lemire
BMC Genetics|June 29, 2006
SUP: an extension to SLINK to allow a larger number of marker loci to be simulated in pedigrees conditional on trait valuesMathieu Lemire
BMC Proceedings|December 19, 2009
On the association between rheumatoid arthritis and classical HLA class I and class II alleles predicted from single-nucleotide polymorphism dataMathieu Lemire
BMC Genetics|February 3, 2006
A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkageMathieu Lemire
BMC Proceedings|March 1, 2012
Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studiesFrance Gagnon, Nicole M Roslin, Mathieu Lemire
BMC Genomics|May 17, 2017
In silico pathway analysis and tissue specific cis-eQTL for colorectal cancer GWAS risk variantsLenora W M Loo, Mathieu Lemire, Loïc Le Marchand
BMC Proceedings|December 19, 2009
Using a higher criticism statistic to detect modest effects in a genome-wide study of rheumatoid arthritisElena Parkhomenko, David Tritchler, Mathieu Lemire, et al.
American Journal of Human Genetics|August 24, 2004
Transmission-ratio distortion and allele sharing in affected sib pairs: a new linkage statistic with reduced bias, with application to chromosome 6q25.3Mathieu Lemire, Nicole M Roslin, Catherine Laprise, et al.
Human Heredity|July 8, 2011
Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigreesAlejandro A Schäffer, Mathieu Lemire, Jürg Ott, et al.
Clinical Epigenetics|March 16, 2017
The dynamic DNA methylation landscape of the <i>mutL homolog 1</i> shore is altered by <i>MLH1</i>-93G>A polymorphism in normal tissues and colorectal cancerAndrea J Savio, Miralem Mrkonjic, Mathieu Lemire, et al.
Pageof 9