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Detection of structural variations in densely-labelled optical DNA barcodes: A hidden Markov model approach.
Dvirnas, Albertas; Stewart, Callum; Müller, Vilhelm; Bikkarolla, Santosh Kumar; Frykholm, Karolin; Sandegren, Linus; Kristiansson, Erik; Westerlund, Fredrik; Ambjörnsson, Tobias.
Afiliação
  • Dvirnas A; Department of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
  • Stewart C; Department of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
  • Müller V; Division of Chemical Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
  • Bikkarolla SK; Division of Chemical Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
  • Frykholm K; Division of Chemical Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
  • Sandegren L; Department of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
  • Kristiansson E; Department of Mathematical Sciences, Chalmers University of Technology and the University of Gothenburg, Gothenburg, Sweden.
  • Westerlund F; Division of Chemical Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
  • Ambjörnsson T; Department of Astronomy and Theoretical Physics, Lund University, Lund, Sweden.
PLoS One ; 16(11): e0259670, 2021.
Article em En | MEDLINE | ID: mdl-34739528
ABSTRACT
Large-scale genomic alterations play an important role in disease, gene expression, and chromosome evolution. Optical DNA mapping (ODM), commonly categorized into sparsely-labelled ODM and densely-labelled ODM, provides sequence-specific continuous intensity profiles (DNA barcodes) along single DNA molecules and is a technique well-suited for detecting such alterations. For sparsely-labelled barcodes, the possibility to detect large genomic alterations has been investigated extensively, while densely-labelled barcodes have not received as much attention. In this work, we introduce HMMSV, a hidden Markov model (HMM) based algorithm for detecting structural variations (SVs) directly in densely-labelled barcodes without access to sequence information. We evaluate our approach using simulated data-sets with 5 different types of SVs, and combinations thereof, and demonstrate that the method reaches a true positive rate greater than 80% for randomly generated barcodes with single variations of size 25 kilobases (kb). Increasing the length of the SV further leads to larger true positive rates. For a real data-set with experimental barcodes on bacterial plasmids, we successfully detect matching barcode pairs and SVs without any particular assumption of the types of SVs present. Instead, our method effectively goes through all possible combinations of SVs. Since ODM works on length scales typically not reachable with other techniques, our methodology is a promising tool for identifying arbitrary combinations of genomic alterations.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Código de Barras de DNA Taxonômico Tipo de estudo: Diagnostic_studies / Health_economic_evaluation Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Código de Barras de DNA Taxonômico Tipo de estudo: Diagnostic_studies / Health_economic_evaluation Idioma: En Ano de publicação: 2021 Tipo de documento: Article