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SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing data

PloS one, 2012-07, Vol.7 (7), p.e37558-e37558

2012

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Pan-cancer classification of single cells in the tumour microenvironment

Nature communications, 2023-03, Vol.14 (1), p.1615-1615, Article 1615

2023

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The Canadian Partnership for Tomorrow Project: a pan-Canadian platform for research on chronic disease prevention

Canadian Medical Association journal (CMAJ), 2018-06, Vol.190 (23), p.E710-E717

2018

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Gene-by-environment interactions in urban populations modulate risk phenotypes

Nature communications, 2018-03, Vol.9 (1), p.827-12, Article 827

2018

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A Coalescent-Based Method for Detecting and Estimating Recombination From Gene Sequences

Genetics (Austin), 2002-03, Vol.160 (3), p.1231-1241

2002

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Inferring ongoing cancer evolution from single tumour biopsies using synthetic supervised learning

PLoS computational biology, 2022-04, Vol.18 (4), p.e1010007

2022

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De novo transcriptome sequencing in Anopheles funestus using Illumina RNA-seq technology

PloS one, 2010-12, Vol.5 (12), p.e14202-e14202

2010

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Genomic counter-stress changes induced by the relaxation response

PloS one, 2008-07, Vol.3 (7), p.e2576-e2576

2008

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The cell-free DNA methylome captures distinctions between localized and metastatic prostate tumors

Nature communications, 2022-10, Vol.13 (1), p.6467-14, Article 6467

2022

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Interacting evolutionary pressures drive mutation dynamics and health outcomes in aging blood

Nature communications, 2021-08, Vol.12 (1), p.4921-4921, Article 4921

2021

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Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians

PloS one, 2013-04, Vol.8 (4), p.e59494

2013

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Cohort profile: the CARTaGENE Cohort Nutrition Study (Quebec, Canada)

BMJ open, 2024-08, Vol.14 (8), p.e083425

2024

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High-Resolution Genomic Analysis of Human Mitochondrial RNA Sequence Variation

Science (American Association for the Advancement of Science), 2014-04, Vol.344 (6182), p.413-415

2014

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Very few RNA and DNA sequence differences in the human transcriptome

PloS one, 2011-10, Vol.6 (10), p.e25842-e25842

2011

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Normal sex and age-specific parameters in a multi-ethnic population: a cardiovascular magnetic resonance study of the Canadian Alliance for Healthy Hearts and Minds cohort

Journal of cardiovascular magnetic resonance, 2022-01, Vol.24 (1), p.2-2, Article 2

2022

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Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease

PLoS genetics, 2016-10, Vol.12 (10), p.e1006335

2016

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Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis

Neurobiology of aging, 2016, Vol.37, p.209.e17-209.e21

2016

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Genetic evidence of geographical groups among Neanderthals

PloS one, 2009-04, Vol.4 (4), p.e5151-e5151

2009

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Analysis of East Asia genetic substructure using genome-wide SNP arrays

PloS one, 2008-12, Vol.3 (12), p.e3862-e3862

2008

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Evidence for additive and interaction effects of host genotype and infection in malaria

Proceedings of the National Academy of Sciences - PNAS, 2012-10, Vol.109 (42), p.16786-16793

2012

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Antimalarial drug quality in the most severely malarious parts of Africa - a six country study

PloS one, 2008-05, Vol.3 (5), p.e2132-e2132

2008

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GeneDistiller--distilling candidate genes from linkage intervals

PloS one, 2008-12, Vol.3 (12), p.e3874-e3874

2008

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Gain-of-function missense variant in SLC12A2 , encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia

Journal of psychiatric research, 2016-06, Vol.77, p.22-26

2016

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Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4

American journal of human genetics, 2010-07, Vol.87 (1), p.40-51

2010

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SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing data

Pan-cancer classification of single cells in the tumour microenvironment

The Canadian Partnership for Tomorrow Project: a pan-Canadian platform for research on chronic disease prevention

Gene-by-environment interactions in urban populations modulate risk phenotypes

A Coalescent-Based Method for Detecting and Estimating Recombination From Gene Sequences

Inferring ongoing cancer evolution from single tumour biopsies using synthetic supervised learning

De novo transcriptome sequencing in Anopheles funestus using Illumina RNA-seq technology

Genomic counter-stress changes induced by the relaxation response

Genome-wide population-based association study of extremely overweight young adults--the GOYA study

The cell-free DNA methylome captures distinctions between localized and metastatic prostate tumors

Interacting evolutionary pressures drive mutation dynamics and health outcomes in aging blood

Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians

Cohort profile: the CARTaGENE Cohort Nutrition Study (Quebec, Canada)

High-Resolution Genomic Analysis of Human Mitochondrial RNA Sequence Variation

Very few RNA and DNA sequence differences in the human transcriptome

Normal sex and age-specific parameters in a multi-ethnic population: a cardiovascular magnetic resonance study of the Canadian Alliance for Healthy Hearts and Minds cohort

Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis

Genetic evidence of geographical groups among Neanderthals

Analysis of East Asia genetic substructure using genome-wide SNP arrays

Evidence for additive and interaction effects of host genotype and infection in malaria

Antimalarial drug quality in the most severely malarious parts of Africa - a six country study

GeneDistiller--distilling candidate genes from linkage intervals

Gain-of-function missense variant in SLC12A2 , encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia

Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4

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