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Paper Details

Measuring coverage and accuracy of whole-exome sequencing in clinical context.
Genet Med
39
2018
Blood samples, exome, genes, heterozygous indels, homozygous indels, pharmacogenes, single-nucleotide variants, variants
Exome, Exome Sequencing, Female, Genome, Human, Genomics, Heterozygote, Homozygote, Humans, INDEL Mutation, Male, Molecular Sequence Annotation
Author NameAffiliation
Sek Won KongBoston Children's Hospital
Sek Won KongHarvard Medical School
In-Hee LeeBoston Children's Hospital
In-Hee LeeHarvard Medical School
In-Hee LeeBoston Children's Hospital
In-Hee LeeHarvard Medical School
Xuanshi LiuBoston Children's Hospital
Xuanshi LiuHarvard Medical School
Joel N HirschhornHarvard Medical School
Joel N HirschhornBroad Institute
Joel N HirschhornHarvard Medical School
Joel N HirschhornBroad Institute
Kenneth D MandlBoston Children's Hospital
Kenneth D MandlHarvard Medical School
Kenneth D MandlHarvard Medical School
Kenneth D MandlBoston Children's Hospital
Kenneth D MandlHarvard Medical School
Kenneth D MandlHarvard Medical School
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