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Whole-genome sequencing analysis of copy number variation... | ResearchHub
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Whole-genome sequencing analysis of copy number variation (CNV) using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis
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Authors
Bo Zhou
6 more
Bo Zhou
•
Steve Ho
4 more
•
Alexander Urban
Published
April 28, 2018
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Preprint Server
Topics
Biology
Genetics And Genomics
Computer Science
Genetics
Copy-Number Variation
Show all topics
DOI
10.1101/192310
License
CC-BY-NC-ND
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Genetics And Genomics
Computer Science
Genetics
Copy-Number Variation
Show all topics
DOI
10.1101/192310
License
CC-BY-NC-ND
Other Formats
PDF
