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A Pipeline NanoTRF as a New Tool for De Novo Satellite DNA Identification in the Raw Nanopore Sequencing Reads of Plant Genomes.
Kirov, Ilya; Kolganova, Elizaveta; Dudnikov, Maxim; Yurkevich, Olga Yu; Amosova, Alexandra V; Muravenko, Olga V.
Afiliação
  • Kirov I; All-Russia Research Institute of Agricultural Biotechnology, Timiryazevskaya Str. 42, Moscow 127550, Russia.
  • Kolganova E; Moscow Institute of Physics and Technology, Dolgoprudny 141701, Russia.
  • Dudnikov M; All-Russia Research Institute of Agricultural Biotechnology, Timiryazevskaya Str. 42, Moscow 127550, Russia.
  • Yurkevich OY; All-Russia Research Institute of Agricultural Biotechnology, Timiryazevskaya Str. 42, Moscow 127550, Russia.
  • Amosova AV; Moscow Institute of Physics and Technology, Dolgoprudny 141701, Russia.
  • Muravenko OV; Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.
Plants (Basel) ; 11(16)2022 Aug 12.
Article em En | MEDLINE | ID: mdl-36015406
ABSTRACT
High-copy tandemly organized repeats (TRs), or satellite DNA, is an important but still enigmatic component of eukaryotic genomes. TRs comprise arrays of multi-copy and highly similar tandem repeats, which makes the elucidation of TRs a very challenging task. Oxford Nanopore sequencing data provide a valuable source of information on TR organization at the single molecule level. However, bioinformatics tools for de novo identification of TRs in raw Nanopore data have not been reported so far. We developed NanoTRF, a new python pipeline for TR repeat identification, characterization and consensus monomer sequence assembly. This new pipeline requires only a raw Nanopore read file from low-depth (<1×) genome sequencing. The program generates an informative html report and figures on TR genome abundance, monomer sequence and monomer length. In addition, NanoTRF performs annotation of transposable elements (TEs) sequences within or near satDNA arrays, and the information can be used to elucidate how TR−TE co-evolve in the genome. Moreover, we validated by FISH that the NanoTRF report is useful for the evaluation of TR chromosome organization­clustered or dispersed. Our findings showed that NanoTRF is a robust method for the de novo identification of satellite repeats in raw Nanopore data without prior read assembly. The obtained sequences can be used in many downstream analyses including genome assembly assistance and gap estimation, chromosome mapping and cytogenetic marker development.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article