HashSeq: a Simple, Scalable, and Conservative <i>De Novo</i> Variant Caller for 16S rRNA Gene Data Sets.

Fouladi, Farnaz; Young, Jacqueline B; Fodor, Anthony A

HashSeq: a Simple, Scalable, and Conservative De Novo Variant Caller for 16S rRNA Gene Data Sets.

Fouladi, Farnaz; Young, Jacqueline B; Fodor, Anthony A.

Afiliación

Fouladi F; Department of Bioinformatics and Genomics, University of North Carolina at Charlottegrid.266859.6, Charlotte, North Carolina, USA.
Young JB; Department of Bioinformatics and Genomics, University of North Carolina at Charlottegrid.266859.6, Charlotte, North Carolina, USA.
Fodor AA; Department of Bioinformatics and Genomics, University of North Carolina at Charlottegrid.266859.6, Charlotte, North Carolina, USA.

mSystems ; 6(6): e0069721, 2021 Dec 21.

Article en En | MEDLINE | ID: mdl-34751586

Palabras clave

16S rRNA gene sequence variant; microbiome; sequence variant; sequencing error

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: MSystems Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos