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NGS based haplotype assembly using matrix completion
We apply matrix completion methods for haplotype assembly from NGS reads to develop the new HapSVT, HapNuc, and HapOPT algorithms. This is performed by applying a mathematical model to convert the reads to an incomplete matrix and estimating unknown components. This process is followed by quantizing...
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| I publikationen: | PLoS One |
|---|---|
| Huvudupphovsmän: | , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Public Library of Science
2019
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6435133/ https://ncbi.nlm.nih.gov/pubmed/30913270 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0214455 |
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