Evidence map›Paper›PMID 16503966›Full record

ArticleBMC bioinformatics2006

Gene annotation and network inference by phylogenetic profiling.

Jie Wu, Zhenjun Hu, Charles DeLisi

Abstract read
In one paragraph

Article in BMC bioinformatics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
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  14. The Schistosoma mansoni transcriptome: an update.Experimental parasitology · 2007
    Review
  15. Article
  16. 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

3 authors.

Jie WuDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, USA. jiewu@bu.edu
Zhenjun Hu
Charles DeLisi

Funding

PERTURBATION ANALYSIS OF PI3 KINASE /ERK SIGNALINGP20GM066401 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DELISI, CHARLES · 2002 to 2004
$1.2M
NIGMS NIH HHS GM66401NIGMS NIH HHS P20 GM066401
6 · The paper itself

Abstract

backgroundPhylogenetic analysis is emerging as one of the most informative computational methods for the annotation of genes and identification of evolutionary modules of functionally related genes. The effectiveness with which phylogenetic profiles can be utilized to assign genes to pathways depends on an appropriate measure of correlation between gene profiles, and an effective decision rule to use the correlate. Current methods, though useful, perform at a level well below what is possible, largely because performance of the latter deteriorates rapidly as coverage increases.

resultsWe introduce, test and apply a new decision rule, correlation enrichment (CE), for assigning genes to functional categories at various levels of resolution. Among the results are: (1) CE performs better than standard guilt by association (SGA, assignment to a functional category when a simple correlate exceeds a pre-specified threshold) irrespective of the number of genes assigned (i.e. coverage); improvement is greatest at high coverage where precision (positive predictive value) of CE is approximately 6-fold higher than that of SGA. (2) CE is estimated to allocate each of the 2918 unannotated orthologs to KEGG pathways with an average precision of 49% (approximately 7-fold higher than SGA) (3) An estimated 94% of the 1846 unannotated orthologs in the COG ontology can be assigned a function with an average precision of 0.4 or greater. (4) Dozens of functional and evolutionarily conserved cliques or quasi-cliques can be identified, many having previously unannotated genes.

conclusionThe method serves as a general computational tool for annotating large numbers of unknown genes, uncovering evolutionary and functional modules. It appears to perform substantially better than extant stand alone high throughout methods.

Indexed as

AlgorithmsPhylogenyGene Expression ProfilingGene Expression RegulationOligonucleotide Array Sequence AnalysisSequence Analysis, DNASignal Transduction

Identifiers

PMID16503966
PMCPMC1388238

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Registered trials

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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.