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Noise-cancelling repeat finder: uncovering tandem repeats in error-prone long-read sequencing data

SUMMARY: Tandem DNA repeats can be sequenced with long-read technologies, but cannot be accurately deciphered due to the lack of computational tools taking high error rates of these technologies into account. Here we introduce Noise-Cancelling Repeat Finder (NCRF) to uncover putative tandem repeats...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Bioinformatics
Päätekijät: Harris, Robert S, Cechova, Monika, Makova, Kateryna D
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2019
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6853708/
https://ncbi.nlm.nih.gov/pubmed/31290946
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btz484
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