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Family reunion via error correction: an efficient analysis of duplex sequencing data
BACKGROUND: Duplex sequencing is the most accurate approach for identification of sequence variants present at very low frequencies. Its power comes from pooling together multiple descendants of both strands of original DNA molecules, which allows distinguishing true nucleotide substitutions from PC...
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| Publicat a: | BMC Bioinformatics |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7057607/ https://ncbi.nlm.nih.gov/pubmed/32131723 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-020-3419-8 |
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