Evidence map›Paper›PMID 21551143›Full record

ArticleBioinformatics (Oxford, England)2011

A multiple network learning approach to capture system-wide condition-specific responses.

Sushmita Roy, Margaret Werner-Washburne, Terran Lane

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
  4. Review
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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

3 authors.

Sushmita RoyDepartment of Computer Science, University of New Mexico, Albuquerque, NM 87131, USA. sroy@broadinstitute.org
Margaret Werner-Washburne
Terran Lane

Funding

UNM Initiative to Maximize Student Diversity (IMSD)R25GM060201 · NIGMS · UNIVERSITY OF NEW MEXICO · PI WERNER-WASHBURNE, MARGRET C. · 2000 to 2017
$9.9M
A compendium of gene expression in stationary phaseR01GM067593 · NIGMS · UNIVERSITY OF NEW MEXICO · PI WERNER-WASHBURNE, MARGARET C. · 2002 to 2005
$1.6M
CRCNS: Bayesian Analysis of Neural-Behavioral Interactions in Mental IllnessR01MH076282 · NIMH · UNIVERSITY OF NEW MEXICO · PI LANE, TERRAN D. R. · 2005 to 2007
$964k
NIGMS NIH HHS GM-060201NIGMS NIH HHS GM-67593NIGMS NIH HHS R01 GM067593NIGMS NIH HHS R25 GM060201NIMH NIH HHS 1R01MH076282-03NIMH NIH HHS R01 MH076282
6 · The paper itself

Abstract

motivationCondition-specific networks capture system-wide behavior under varying conditions such as environmental stresses, cell types or tissues. These networks frequently comprise parts that are unique to each condition, and parts that are shared among related conditions. Existing approaches for learning condition-specific networks typically identify either only differences or only similarities across conditions. Most of these approaches first learn networks per condition independently, and then identify similarities and differences in a post-learning step. Such approaches do not exploit the shared information across conditions during network learning.

resultsWe describe an approach for learning condition-specific networks that identifies the shared and unique subgraphs during network learning simultaneously, rather than as a post-processing step. Our approach learns networks across condition sets, shares data from different conditions and produces high-quality networks that capture biologically meaningful information. On simulated data, our approach outperformed an existing approach that learns networks independently for each condition, especially for small training datasets. On microarray data of hundreds of deletion mutants in two, yeast stationary-phase cell populations, the inferred network structure identified several common and population-specific effects of these deletion mutants and several high-confidence cases of double-deletion pairs, which can be experimentally tested. Our results are consistent with and extend the existing knowledge base of differentiated cell populations in yeast stationary phase. AVAILABILITY AND IMPLEMENTATION: C++ code can be accessed from http://www.broadinstitute.org/~sroy/condspec/ .

Indexed as

Artificial IntelligenceComputational BiologyComputer SimulationSaccharomyces cerevisiae

Identifiers

PMID21551143
PMCPMC3117363

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.