Evidence map›Paper›PMID 19630541›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2009

A combined expression-interaction model for inferring the temporal activity of transcription factors.

Yanxin Shi, Michael Klutstein, Itamar Simon, Tom Mitchell, Ziv Bar-Joseph

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Computational methods for analyzing dynamic regulatory networks.Methods in molecular biology (Clifton, N.J.) · 2010
    Review
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

5 authors.

Yanxin ShiMachine Learning Department, School of Computer Science, Carnegie Mellon University , Pittsburgh, PA 15213, USA.
Michael Klutstein
Itamar Simon
Tom Mitchell
Ziv Bar-Joseph

Funding

Reconstructing dynamic regulatory networksR01GM085022 · NIGMS · CARNEGIE-MELLON UNIVERSITY · PI BAR-JOSEPH, ZIV · 2008 to 2011
$1.1M
NIGMS NIH HHS 1R01 GM085022
6 · The paper itself

Abstract

Methods suggested for reconstructing regulatory networks can be divided into two sets based on how the activity level of transcription factors (TFs) is inferred. The first group of methods relies on the expression levels of TFs, assuming that the activity of a TF is highly correlated with its mRNA abundance. The second treats the activity level as unobserved and infers it from the expression of the genes that the TF regulates. While both types of methods were successfully applied, each suffers from drawbacks that limit their accuracy. For the first set, the assumption that mRNA levels are correlated with activity is violated for many TFs due to post-transcriptional modifications. For the second, the expression level of a TF which might be informative is completely ignored. Here we present the post-transcriptional modification model (PTMM) that, unlike previous methods, utilizes both sources of data concurrently. Our method uses a switching model to determine whether a TF is transcriptionally or post-transcriptionally regulated. This model is combined with a factorial HMM to reconstruct the interactions in a dynamic regulatory network. Using simulated and real data, we show that PTMM outperforms the other two approaches discussed above. Using real data, we also show that PTMM can recover meaningful TF activity levels and identify post-transcriptionally modified TFs, many of which are supported by other sources. Supporting website: www.sb.cs.cmu.edu/PTMM/PTMM.html.

Indexed as

AlgorithmsGene Regulatory NetworksProtein Processing, Post-TranslationalArtificial IntelligenceModels, GeneticSaccharomyces cerevisiaeTranscription FactorsTranscription Factors

Identifiers

PMID19630541
PMCPMC3154398

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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.