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SiNPle: Fast and Sensitive Variant Calling for Deep Sequencing Data

Current high-throughput sequencing technologies can generate sequence data and provide information on the genetic composition of samples at very high coverage. Deep sequencing approaches enable the detection of rare variants in heterogeneous samples, such as viral quasi-species, but also have the un...

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Detalles Bibliográficos
Publicado en:Genes (Basel)
Main Authors: Ferretti, Luca, Tennakoon, Chandana, Silesian, Adrian, Freimanis, Graham, Ribeca, Paolo
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2019
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6722845/
https://ncbi.nlm.nih.gov/pubmed/31349684
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10080561
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