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Single-molecule sequencing detection of N6-methyladenine in microbial reference materials.
McIntyre, Alexa B R; Alexander, Noah; Grigorev, Kirill; Bezdan, Daniela; Sichtig, Heike; Chiu, Charles Y; Mason, Christopher E.
Afiliación
  • McIntyre ABR; Department of Physiology and Biophysics, Weill Cornell Medicine, New York, 10065, NY, USA.
  • Alexander N; Tri-Institutional Training Program in Computational Biology and Medicine, New York, 10065, NY, USA.
  • Grigorev K; Department of Physiology and Biophysics, Weill Cornell Medicine, New York, 10065, NY, USA.
  • Bezdan D; Department of Physiology and Biophysics, Weill Cornell Medicine, New York, 10065, NY, USA.
  • Sichtig H; Department of Physiology and Biophysics, Weill Cornell Medicine, New York, 10065, NY, USA.
  • Chiu CY; US Food and Drug Administration, Silver Spring, 20993, MD, USA.
  • Mason CE; Department of Laboratory Medicine, University of California San Francisco, San Francisco, 94107, CA, USA.
Nat Commun ; 10(1): 579, 2019 02 04.
Article en En | MEDLINE | ID: mdl-30718479
The DNA base modification N6-methyladenine (m6A) is involved in many pathways related to the survival of bacteria and their interactions with hosts. Nanopore sequencing offers a new, portable method to detect base modifications. Here, we show that a neural network can improve m6A detection at trained sequence contexts compared to previously published methods using deviations between measured and expected current values as each adenine travels through a pore. The model, implemented as the mCaller software package, can be extended to detect known or confirm suspected methyltransferase target motifs based on predictions of methylation at untrained contexts. We use PacBio, Oxford Nanopore, methylated DNA immunoprecipitation sequencing (MeDIP-seq), and whole-genome bisulfite sequencing data to generate and orthogonally validate methylomes for eight microbial reference species. These well-characterized microbial references can serve as controls in the development and evaluation of future methods for the identification of base modifications from single-molecule sequencing data.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Adenosina / Análisis de Secuencia de ADN / Metilación de ADN Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Adenosina / Análisis de Secuencia de ADN / Metilación de ADN Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos