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Paper Details

Inferring compound heterozygosity from large-scale exome sequencing data.
bioRxiv
1
2023
Mendelian conditions, Recessive diseases, chromosome, co-occurring variants, coding variants, maternal and, patient, patients, rare variant pairs, recessive disease
Author NameAffiliation
Michael H GuoHospital of the University of the Pennsylvania
Michael H GuoBroad Institute of MIT and Harvard
Nicholas A WattsBroad Institute of MIT and Harvard
Nicholas A WattsMassachusetts General Hospital
Moriel Singer-BerkBroad Institute of MIT and Harvard
Samantha BaxterBroad Institute of MIT and Harvard
Samantha BaxterBroad Institute of MIT and Harvard
Grace TiaoBroad Institute of MIT and Harvard
Grace TiaoMassachusetts General Hospital
Benjamin M NealeBroad Institute of MIT and Harvard
Benjamin M NealeStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Benjamin M NealeMassachusetts General Hospital
Benjamin M NealeBroad Institute of MIT and Harvard
Benjamin M NealeMassachusetts General Hospital
Benjamin M NealeStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Joel N HirschhornBroad Institute of MIT and Harvard
Joel N HirschhornCenter for Basic and Translational Obesity Research, Boston Children's Hospital
Joel N HirschhornBoston Children's Hospital
Joel N HirschhornBlavatnik Institute, Harvard Medical School
Joel N HirschhornBroad Institute of MIT and Harvard
Joel N HirschhornBlavatnik Institute, Harvard Medical School
Joel N HirschhornBoston Children's Hospital
Joel N HirschhornCenter for Basic and Translational Obesity Research, Boston Children's Hospital
Heidi L RehmBroad Institute of MIT and Harvard
Heidi L RehmCenter for Genomic Medicine, Massachusetts General Hospital
Heidi L RehmMassachusetts General Hospital
Heidi L RehmBroad Institute of MIT and Harvard
Heidi L RehmMassachusetts General Hospital
Heidi L RehmCenter for Genomic Medicine, Massachusetts General Hospital
Mark J DalyBroad Institute of MIT and Harvard
Mark J DalyInstitute for Molecular Medicine Finland
Mark J DalyMassachusetts General Hospital
Mark J DalyBroad Institute of MIT and Harvard
Mark J DalyMassachusetts General Hospital
Mark J DalyInstitute for Molecular Medicine Finland
Anne O'Donnell-LuriaBroad Institute of MIT and Harvard
Anne O'Donnell-LuriaCenter for Genomic Medicine, Massachusetts General Hospital
Anne O'Donnell-LuriaBoston Children's Hospital
Anne O'Donnell-LuriaMassachusetts General Hospital
Anne O'Donnell-LuriaBroad Institute of MIT and Harvard
Anne O'Donnell-LuriaMassachusetts General Hospital
Anne O'Donnell-LuriaBoston Children's Hospital
Anne O'Donnell-LuriaCenter for Genomic Medicine, Massachusetts General Hospital
Konrad J KarczewskiBroad Institute of MIT and Harvard
Konrad J KarczewskiCenter for Genomic Medicine, Massachusetts General Hospital
Konrad J KarczewskiMassachusetts General Hospital
Konrad J KarczewskiBroad Institute of MIT and Harvard
Konrad J KarczewskiMassachusetts General Hospital
Konrad J KarczewskiCenter for Genomic Medicine, Massachusetts General Hospital
Daniel G MacArthurBroad Institute of MIT and Harvard
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