Evidence map›Paper›PMID 30753300›Full record

ArticleBioinformatics (Oxford, England)2019

PairedFB: a full hierarchical Bayesian model for paired RNA-seq data with heterogeneous treatment effects.

Yuanyuan Bian, Chong He, Jie Hou, Jianlin Cheng, Jing Qiu

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yuanyuan BianDepartment of Statistics, University of Missouri, Columbia, MO, USA.
Chong HeDepartment of Statistics, University of Missouri, Columbia, MO, USA.
Jie HouDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO, USA.
Jianlin ChengDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO, USA.
Jing QiuDepartment of Applied Economics and Statistics, University of Delaware, Newark, DE, USA.

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI Anjana Narayan Bhat · 2012 to 2026
$67.2M
NIGMS NIH HHS P20 GM103446
6 · The paper itself

Abstract

motivationSeveral methods have been proposed for the paired RNA-seq analysis. However, many of them do not consider the heterogeneity in treatment effect among pairs that can naturally arise in real data. In addition, it has been reported in literature that the false discovery rate (FDR) control of some popular methods has been problematic. In this paper, we present a full hierarchical Bayesian model for the paired RNA-seq count data that accounts for variation of treatment effects among pairs and controls the FDR through the posterior expected FDR.

resultsOur simulation studies show that most competing methods can have highly inflated FDR for small to moderate sample sizes while PairedFB is able to control FDR close to the nominal levels. Furthermore, PairedFB has overall better performance in ranking true differentially expressed genes (DEGs) on the top than others, especially when the sample size gets bigger or when the heterogeneity level of treatment effects is high. In addition, PairedFB can be applied to identify the biologically significant DEGs with controlled FDR. The real data analysis also indicates PairedFB tends to find more biologically relevant genes even when the sample size is small. PairedFB is also shown to be robust with respect to the model misspecification in terms of its relative performance compared to others. AVAILABILITY AND IMPLEMENTATION: Software to implement this method (PairedFB) can be downloaded at: https://sites.google.com/a/udel.edu/qiujing/publication. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

RNA-SeqSoftwareBayes TheoremExome SequencingGene Expression ProfilingSequence Analysis, RNA

Identifiers

PMID30753300
PMCPMC7963077

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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.