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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
Danny Miller
38 more
Danny Miller
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Arvis Sulovari
36 more
•
Evan Eichler
Published November 4, 2020
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Topics
#biology
#genetics-and-genomics
#genetics
#single-nucleotide-polymorphism
#copy-number-variation
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
#single-nucleotide-polymorphism
#copy-number-variation
Show all topics
DOI
10.1101/2020.11.03.365395
License
CC-BY-ND
Other Formats
PDF