Evidence map›Paper›PMID 27600224›Full record

ArticleMicroarrays (Basel, Switzerland)2015

Data Integration for Microarrays: Enhanced Inference for Gene Regulatory Networks.

Alina Sîrbu, Martin Crane, Heather J Ruskin

Abstract read
In one paragraph

Article in Microarrays (Basel, Switzerland), 2015. 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

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

2 citing papers in PubMed.

  1. Review
  2. 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.

Alina SîrbuDepartment of Computer Science and Engineering, University of Bologna, Via Mura Anteo Zamboni 7, Bologna 40126, Italy. alina.sirbu@unibo.it.
Martin CraneCenter for Scientific Computing and Complex Systems Modelling, School of Computing, Dublin City University, Glasnevin, Dublin 9, Ireland. mcrane@computing.dcu.ie.
Heather J RuskinCenter for Scientific Computing and Complex Systems Modelling, School of Computing, Dublin City University, Glasnevin, Dublin 9, Ireland. hruskin@computing.dcu.ie.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microarray technologies have been the basis of numerous important findings regarding gene expression in the few last decades. Studies have generated large amounts of data describing various processes, which, due to the existence of public databases, are widely available for further analysis. Given their lower cost and higher maturity compared to newer sequencing technologies, these data continue to be produced, even though data quality has been the subject of some debate. However, given the large volume of data generated, integration can help overcome some issues related, e.g., to noise or reduced time resolution, while providing additional insight on features not directly addressed by sequencing methods. Here, we present an integration test case based on public Drosophila melanogaster datasets (gene expression, binding site affinities, known interactions). Using an evolutionary computation framework, we show how integration can enhance the ability to recover transcriptional gene regulatory networks from these data, as well as indicating which data types are more important for quantitative and qualitative network inference. Our results show a clear improvement in performance when multiple datasets are integrated, indicating that microarray data will remain a valuable and viable resource for some time to come.

Indexed as

data integrationgene regulatory networksmicroarraysreverse engineeringtranscriptional regulation

Identifiers

PMID27600224
PMCPMC4996389

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.