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Long-read genome sequencing identifies causal structural ... | ResearchHub
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Long-read genome sequencing identifies causal structural variation in a Mendelian disease
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Authors
Jason Merker
18 more
Jason Merker
•
Aaron Wenger
16 more
•
Euan Ashley
Published
June 22, 2017
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Journal
Genetics in Medicine
Topics
Biology
Genomics
Cardiology And Cardiovascular Medicine
Molecular Biology
Genetics
Show all topics
DOI
10.1038/gim.2017.86
License
publisher-specific-oa
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Genetics in Medicine
Topics
Biology
Genomics
Cardiology And Cardiovascular Medicine
Molecular Biology
Genetics
Show all topics
DOI
10.1038/gim.2017.86
License
publisher-specific-oa
