Evidence map›Paper›PMID 24564884›Full record

ArticleBMC proceedings2013

Conceptualization of molecular findings by mining gene annotations.

Vicky Chen, Xinghua Lu

Abstract read
In one paragraph

Article in BMC proceedings, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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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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

4 citing papers in PubMed.

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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.

Vicky Chen
Xinghua Lu

Funding

The internship in Biomedical Research, Informatics, and Computer Science (iBRIC): Biomedical Informatics and Data Science research experiences for students from Minority Serving InstitutionsT15LM007059 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARRY S HOCHHEISER · 1987 to 2026
$23.9M
Ontology-Driven Methods for Knowledge Acquisition and Knowledge DiscoveryR01LM011155 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LU, XINGHUA · 2011 to 2014
$1.2M
NLM NIH HHS R01 LM011155NLM NIH HHS T15 LM007059
6 · The paper itself

Abstract

backgroundThe Gene Ontology (GO) is an ontology representing molecular biology concepts related to genes and their products. Current annotations from the GO Consortium tend to be highly specific, and contemporary genome-scale studies often return a long list of genes of potential interest, such as genes in a cancer tumor that are differentially expressed than those found in normal tissue. It is therefore a challenging task to reveal, at a conceptual level, the major functional themes in which genes are involved. Presently, there is a need for tools capable of revealing such themes through mining and representing semantic information in an objective and quantitative manner.

methodsIn this study, we utilized the hierarchical organization of the GO to derive a more abstract representation of the major biological processes of a list of genes based on their annotations. We cast the task as follows: given a list of genes, identify non-disjoint, functionally coherent subsets, such that the functions of the genes in a subset are summarized by an informative GO term that accurately captures the semantic information of the original annotations.

resultsWe evaluated different metrics for assessing information loss when merging GO terms, and different statistical schemes to assess the functional coherence of a set of genes. We found that the best discriminative power was achieved by using a combination of the information-content-based measure as the information-loss metric, and the graph-based statistics derived from a Steiner tree connecting genes in an augmented GO graph.

conclusionsOur methods provide an objective and quantitative approach to capturing the major directions of gene functions in a context-specific fashion.

Identifiers

PMID24564884
PMCPMC4042834

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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.