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Paper Details

Familial long-read sequencing increases yield of de novo mutations.
Am J Hum Genet
27
2022
CHM13, DNM, DNMs, GRCh38, SNVs, T2T, autism, children, germline, heterochromatic satellites, human, nucleotide, reference genome, short, tandem repeats
Author NameAffiliation
Tina GravesMcDonnell Genome Institute, Washington University
Tina GravesMcDonnell Genome Institute, Washington University
Younes MokrabQatar College of Health and Life Sciences, Hamad Bin Khalifa University
Michael C Zody
Michael C Zody
Jan O Korbel
Jan O Korbel
Evan E EichlerUniversity of Washington School of Medicine, USA Howard Hughes Medical Institute, University of Washington
Evan E EichlerUniversity of Washington School of Medicine, USA Howard Hughes Medical Institute, University of Washington
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