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sCNAphase: using haplotype resolved read depth to genotyp... | ResearchHub
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sCNAphase: using haplotype resolved read depth to genotype somatic copy number alterations from low cellularity aneuploid tumors
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Authors
Wenhan Chen
4 more
Wenhan Chen
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Wenhan Chen
2 more
•
Lachlan Coin
Published
July 19, 2016
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Preprint Server
Topics
Biology
Bioinformatics
Loss Of Heterozygosity
Copy-Number Variation
Copy Number Analysis
Show all topics
DOI
10.1101/038828
License
CC-BY-NC-ND
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Preprint Server
Topics
Biology
Bioinformatics
Loss Of Heterozygosity
Copy-Number Variation
Copy Number Analysis
Show all topics
DOI
10.1101/038828
License
CC-BY-NC-ND
Other Formats
PDF
