Evidence map›Paper›PMID 28557607›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2017

A Poisson Log-Normal Model for Constructing Gene Covariation Network Using RNA-seq Data.

Yoonha Choi, Marc Coram, Jie Peng, Hua Tang

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2017. 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
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yoonha Choi1 Department of Genetics, Stanford University , Stanford, California.
Marc Coram2 Department of Health Research and Policy, Stanford University , Stanford, California.
Jie Peng3 Department of Statistics, University of California , Davis, Davis, California.
Hua Tang1 Department of Genetics, Stanford University , Stanford, California.

Funding

Genetic Architecture of Complex Traits in Admixed PopulationsR01GM073059 · NIGMS · STANFORD UNIVERSITY · PI TANG, HUA · 2005 to 2016
$2.4M
NIGMS NIH HHS R01 GM073059
6 · The paper itself

Abstract

Constructing expression networks using transcriptomic data is an effective approach for studying gene regulation. A popular approach for constructing such a network is based on the Gaussian graphical model (GGM), in which an edge between a pair of genes indicates that the expression levels of these two genes are conditionally dependent, given the expression levels of all other genes. However, GGMs are not appropriate for non-Gaussian data, such as those generated in RNA-seq experiments. We propose a novel statistical framework that maximizes a penalized likelihood, in which the observed count data follow a Poisson log-normal distribution. To overcome the computational challenges, we use Laplace's method to approximate the likelihood and its gradients, and apply the alternating directions method of multipliers to find the penalized maximum likelihood estimates. The proposed method is evaluated and compared with GGMs using both simulated and real RNA-seq data. The proposed method shows improved performance in detecting edges that represent covarying pairs of genes, particularly for edges connecting low-abundant genes and edges around regulatory hubs.

Indexed as

Gene Regulatory NetworksLikelihood FunctionsModels, StatisticalPoisson DistributionAlgorithmsComputer SimulationEthnicityGene Expression RegulationHigh-Throughput Nucleotide SequencingHumansLymphocytesMetagenomicsSequence Analysis, RNAalternating directions method of multipliersGaussian graphical modelpenalized likelihoodPoisson log-normal distributionRNA-seq

Identifiers

PMID28557607
PMCPMC5510689

What OpenQuestion holds

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Registered trials

None linked

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.