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Paper Details

A framework for the detection of de novo mutations in family-based sequencing data.
Eur J Hum Genet
17
2017
DNMs, X chromosome, X-chromosome, human, human DNA sequence, indels, single nucleotide
Author NameAffiliation
Kiran GarimellaUniversity of Oxford
Menachem FromerMassachusetts General Hospital
Menachem FromerIcahn School of Medicine at Mount Sinai
Menachem FromerIcahn School of Medicine at Mount Sinai
Menachem FromerThe Broad Institute of Harvard and MIT
Kaitlin E SamochaMassachusetts General Hospital
Kaitlin E SamochaThe Broad Institute of Harvard and MIT
Benjamin M NealeMassachusetts General Hospital
Benjamin M NealeThe Broad Institute of Harvard and MIT
Benjamin M NealeMassachusetts General Hospital
Benjamin M NealeThe Broad Institute of Harvard and MIT
Mark J DalyMassachusetts General Hospital
Mark J DalyThe Broad Institute of Harvard and MIT
Mark J DalyMassachusetts General Hospital
Mark J DalyThe Broad Institute of Harvard and MIT
Eric BanksThe Broad Institute of Harvard and MIT
Eric BanksThe Broad Institute of Harvard and MIT
Mark A DePristoThe Broad Institute of Harvard and MIT
Paul I W de BakkerCenter for Molecular Medicine, University Medical Center Utrecht
Paul I W de BakkerJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht
Paul I W de BakkerCenter for Molecular Medicine, University Medical Center Utrecht
Paul I W de BakkerJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht
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