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Finding differentially expressed regions of arbitrary length in quantitative genomic data based on marked point process model

Motivation: High-throughput nucleotide sequencing technologies provide large amounts of quantitative genomic data at nucleotide resolution, which are important for the present and future biomedical researches; for example differential analysis of base-level RNA expression data will improve our under...

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Detalles Bibliográficos
Autor principal: Hatsuda, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436798/
https://www.ncbi.nlm.nih.gov/pubmed/22962492
http://dx.doi.org/10.1093/bioinformatics/bts371
Descripción
Sumario:Motivation: High-throughput nucleotide sequencing technologies provide large amounts of quantitative genomic data at nucleotide resolution, which are important for the present and future biomedical researches; for example differential analysis of base-level RNA expression data will improve our understanding of transcriptome, including both coding and non-coding genes. However, most studies of these data have relied on existing genome annotations and thus are limited to the analysis of known transcripts. Results: In this article, we propose a novel method based on a marked point process model to find differentially expressed genomic regions of arbitrary length without using genome annotations. The presented method conducts a statistical test for differential analysis in regions of various lengths at each nucleotide and searches the optimal configuration of the regions by using a Monte Carlo simulation. We applied the proposed method to both synthetic and real genomic data, and their results demonstrate the effectiveness of our method. Availability: The program used in this study is available at https://sites.google.com/site/hiroshihatsuda/. Contact: H.Hatsuda@warwick.ac.uk