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Targeted long-read sequencing resolves complex structural... | ResearchHub
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Targeted long-read sequencing resolves complex structural variants and identifies missing disease-causing variants
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Authors
Danny Miller
38 more
Danny Miller
•
Arvis Sulovari
36 more
•
Evan Eichler
Published
November 4, 2020
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Preprint Server
Topics
Biology
Genetics And Genomics
Genetics
Gene
Computational Biology
Show all topics
DOI
10.1101/2020.11.03.365395
License
CC-BY-ND
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Genetics
Gene
Computational Biology
Show all topics
DOI
10.1101/2020.11.03.365395
License
CC-BY-ND
Other Formats
PDF
