Evidence map›Paper›PMID 21047389›Full record

ArticleBMC genomics2010

Identifying functional relationships within sets of co-expressed genes by combining upstream regulatory motif analysis and gene expression information.

Viktor Martyanov, Robert H Gross

Abstract read
In one paragraph

Article in BMC genomics, 2010. 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

2 authors.

Viktor MartyanovDepartment of Biological Sciences, Dartmouth College, Hanover, NH 03755, USA. viktor.martyanov@dartmouth.edu
Robert H Gross

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExisting clustering approaches for microarray data do not adequately differentiate between subsets of co-expressed genes. We devised a novel approach that integrates expression and sequence data in order to generate functionally coherent and biologically meaningful subclusters of genes. Specifically, the approach clusters co-expressed genes on the basis of similar content and distributions of predicted statistically significant sequence motifs in their upstream regions.

resultsWe applied our method to several sets of co-expressed genes and were able to define subsets with enrichment in particular biological processes and specific upstream regulatory motifs.

conclusionsThese results show the potential of our technique for functional prediction and regulatory motif identification from microarray data.

Indexed as

Cluster AnalysisAlgorithmsGene Expression ProfilingGene Expression RegulationOligonucleotide Array Sequence AnalysisSaccharomyces cerevisiaeSequence Analysis, DNA

Identifiers

PMID21047389
PMCPMC2975146

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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.