De novo species identification using 16S rRNA gene nanopore sequencing
Author(s) -
Inga Leena Angell,
Morten Nilsen,
Karin C. Lødrup Carlsen,
KaiHåkon Carlsen,
Gunilla Hedlin,
Christine Monceyron Jonassen,
Benjamin J. Marsland,
Björn Nordlund,
Eva Maria Rehbinder,
Carina Madelen Saunders,
Håvard Ove Skjerven,
Anne Cathrine Staff,
Cilla Söderhäll,
Riyas Vettukattil,
Knut Rudi
Publication year - 2020
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.10029
Subject(s) - nanopore sequencing , random hexamer , biology , nanopore , computational biology , identification (biology) , species identification , dna sequencing , metagenomics , ribosomal rna , sequence assembly , evolutionary biology , gene , genetics , ecology , nanotechnology , microbiology and biotechnology , transcriptome , materials science , gene expression
Nanopore sequencing is rapidly becoming more popular for use in various microbiota-based applications. Major limitations of current approaches are that they do not enable de novo species identification and that they cannot be used to verify species assignments. This severely limits applicability of the nanopore sequencing technology in taxonomic applications. Here, we demonstrate the possibility of de novo species identification and verification using hexamer frequencies in combination with k-means clustering for nanopore sequencing data. The approach was tested on the human infant gut microbiota of 3-month-old infants. Using the hexamer k-means approach we identified two new low abundant species associated with vaginal delivery. In addition, we confirmed both the vaginal delivery association for two previously identified species and the overall high levels of bifidobacteria. Taxonomic assignments were further verified by mock community analyses. Therefore, we believe our de novo species identification approach will have widespread application in analyzing microbial communities in the future.
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