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Preferred analysis methods for single genomic regions in RNA sequencing revealed by p

This is a discussion on Preferred analysis methods for single genomic regions in RNA sequencing revealed by p within the Analytic News Feeds forums, part of the Analytics category; Preferred analysis methods for single genomic regions in RNA sequencing revealed by processing the shape of coverage. Nucleic Acids Res. 2011 Dec 30; Authors: Okoniewski MJ, Lesniewska A, Szabelska A, ...


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Old 3rd January 2012, 09:26 PM   #1
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Default Preferred analysis methods for single genomic regions in RNA sequencing revealed by p

Preferred analysis methods for single genomic regions in RNA sequencing revealed by processing the shape of coverage.

Nucleic Acids Res. 2011 Dec 30;

Authors: Okoniewski MJ, Lesniewska A, Szabelska A, Zyprych-Walczak J, Ryan M, Wachtel M, Morzy T, Schäffer B, Schlapbach R

Abstract
The informational content of RNA sequencing is currently far from being completely explored. Most of the analyses focus on processing tables of counts or finding isoform deconvolution via exon junctions. This article presents a comparison of several techniques that can be used to estimate differential expression of exons or small genomic regions of expression, based on their coverage function shapes. The problem is defined as finding the differentially expressed exons between two samples using local expression profile normalization and statistical measures to spot the differences between two profile shapes. Initial experiments have been done using synthetic data, and real data modified with synthetically created differential patterns. Then, 160 pipelines (5 types of generator × 4 normalizations × 8 difference measures) are compared. As a result, the best analysis pipelines are selected based on linearity of the differential expression estimation and the area under the ROC curve. These platform-independent techniques have been implemented in the Bioconductor package rnaSeqMap. They point out the exons with differential expression or internal splicing, even if the counts of reads may not show this. The areas of application include significant difference searches, splicing identification algorithms and finding suitable regions for QPCR primers.


PMID: 22210855 [PubMed - as supplied by publisher]



PubMed comprises more than 19 million citations for biomedical articles from MEDLINE and life science journals. This RSS feed searches for mentions of Bioconductor - the open source and open development software project for the analysis and comprehension of genomic data.
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