Evidence map›Paper›PMID 23812993›Full record

ArticleBioinformatics (Oxford, England)2013

Automated annotation of gene expression image sequences via non-parametric factor analysis and conditional random fields.

Iulian Pruteanu-Malinici, William H Majoros, Uwe Ohler

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

2 citing papers in PubMed.

  1. Article
  2. Stability-driven nonnegative matrix factorization to interpret spatial gene expression and build local gene networks.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
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

3 authors.

Iulian Pruteanu-MaliniciInstitute for Genome Sciences & Policy, Duke University, Durham, NC 27708, USA.
William H Majoros
Uwe Ohler

Funding

Computational Biology and Bioinformatics Training ProgramT32GM071340 · NIGMS · DUKE UNIVERSITY · PI MAGWENE, PAUL MITAARI · 2005 to 2020
$3.3M
NIGMS NIH HHS T32 GM071340
6 · The paper itself

Abstract

motivationComputational approaches for the annotation of phenotypes from image data have shown promising results across many applications, and provide rich and valuable information for studying gene function and interactions. While data are often available both at high spatial resolution and across multiple time points, phenotypes are frequently annotated independently, for individual time points only. In particular, for the analysis of developmental gene expression patterns, it is biologically sensible when images across multiple time points are jointly accounted for, such that spatial and temporal dependencies are captured simultaneously.

methodsWe describe a discriminative undirected graphical model to label gene-expression time-series image data, with an efficient training and decoding method based on the junction tree algorithm. The approach is based on an effective feature selection technique, consisting of a non-parametric sparse Bayesian factor analysis model. The result is a flexible framework, which can handle large-scale data with noisy incomplete samples, i.e. it can tolerate data missing from individual time points.

resultsUsing the annotation of gene expression patterns across stages of Drosophila embryonic development as an example, we demonstrate that our method achieves superior accuracy, gained by jointly annotating phenotype sequences, when compared with previous models that annotate each stage in isolation. The experimental results on missing data indicate that our joint learning method successfully annotates genes for which no expression data are available for one or more stages.

Indexed as

Models, StatisticalAlgorithmsAnimalsBayes TheoremDrosophilaEmbryonic DevelopmentFactor Analysis, StatisticalGene Expression ProfilingImage Processing, Computer-AssistedIn Situ HybridizationRNA, MessengerStatistics, NonparametricVocabulary, ControlledRNA, Messenger

Identifiers

PMID23812993
PMCPMC3694682

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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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.