Evidence map›Paper›PMID 28595376›Full record

ArticleBioinformatics (Oxford, England)2017

DEIsoM: a hierarchical Bayesian model for identifying differentially expressed isoforms using biological replicates.

Hao Peng, Yifan Yang, Shandian Zhe, Jian Wang, Michael Gribskov, Yuan Qi

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Article in Bioinformatics (Oxford, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Hao PengDepartment of Computer Science.
Yifan YangDepartment of Computer Science.
Shandian ZheDepartment of Computer Science.
Jian WangEli Lilly and Company, Indianapolis, IN 46285, USA.
Michael GribskovDepartment of Computer Science.
Yuan QiDepartment of Computer Science.

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No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationHigh-throughput mRNA sequencing (RNA-Seq) is a powerful tool for quantifying gene expression. Identification of transcript isoforms that are differentially expressed in different conditions, such as in patients and healthy subjects, can provide insights into the molecular basis of diseases. Current transcript quantification approaches, however, do not take advantage of the shared information in the biological replicates, potentially decreasing sensitivity and accuracy.

resultsWe present a novel hierarchical Bayesian model called Differentially Expressed Isoform detection from Multiple biological replicates (DEIsoM) for identifying differentially expressed (DE) isoforms from multiple biological replicates representing two conditions, e.g. multiple samples from healthy and diseased subjects. DEIsoM first estimates isoform expression within each condition by (1) capturing common patterns from sample replicates while allowing individual differences, and (2) modeling the uncertainty introduced by ambiguous read mapping in each replicate. Specifically, we introduce a Dirichlet prior distribution to capture the common expression pattern of replicates from the same condition, and treat the isoform expression of individual replicates as samples from this distribution. Ambiguous read mapping is modeled as a multinomial distribution, and ambiguous reads are assigned to the most probable isoform in each replicate. Additionally, DEIsoM couples an efficient variational inference and a post-analysis method to improve the accuracy and speed of identification of DE isoforms over alternative methods. Application of DEIsoM to an hepatocellular carcinoma (HCC) dataset identifies biologically relevant DE isoforms. The relevance of these genes/isoforms to HCC are supported by principal component analysis (PCA), read coverage visualization, and the biological literature. AVAILABILITY AND IMPLEMENTATION: The software is available at https://github.com/hao-peng/DEIsoM. CONTACT: pengh@alumni.purdue.edu. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Gene Expression ProfilingSequence Analysis, RNABayes TheoremCarcinoma, HepatocellularComputer SimulationHumansLiver NeoplasmsRNA IsoformsSoftwareRNA Isoforms

Identifiers

PMID28595376
PMCPMC5870796

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.