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lordFAST: sensitive and Fast Alignment Search Tool for LOng noisy Read sequencing Data

MOTIVATION: Recent advances in genomics and precision medicine have been made possible through the application of high throughput sequencing (HTS) to large collections of human genomes. Although HTS technologies have proven their use in cataloging human genome variation, computational analysis of th...

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Detalles Bibliográficos
Publicado en:Bioinformatics
Main Authors: Haghshenas, Ehsan, Sahinalp, S Cenk, Hach, Faraz
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2019
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6298053/
https://ncbi.nlm.nih.gov/pubmed/30561550
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty544
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