Evidence map›Paper›PMID 28073302›Full record

ArticleJournal of bioinformatics and computational biology2016

Is the average shortest path length of gene set a reflection of their biological relatedness?

Varsha Embar, Adam Handen, Madhavi K Ganapathiraju

Abstract read
In one paragraph

Article in Journal of bioinformatics and computational biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
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  6. FOBI: an ontology to represent food intake data and associate it with metabolomic data.Database : the journal of biological databases and curation · 2020
    Article
  7. 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.

Varsha Embar* Language Technologies Institute, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Adam Handen† Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Madhavi K Ganapathiraju† Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA 15213, USA.

Funding

Discovery of Mental Health and Inflammation (MHAIN) InteractomeR01MH094564 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GANAPATHIRAJU, MADHAVI K · 2011 to 2015
$1.9M
NIMH NIH HHS R01 MH094564
6 · The paper itself

Abstract

When a set of genes are identified to be related to a disease, say through gene expression analysis, it is common to examine the average distance among their protein products in the human interactome as a measure of biological relatedness of these genes. The reasoning for this is that, genes associated with a disease would tend to be functionally related, and that functionally related genes would be closely connected to each other in the interactome. Typically, average shortest path length (ASPL) of disease genes (although referred to as genes in the context of disease-associations, the interactions are among protein-products of these genes) is compared to ASPL of randomly selected genes or to ASPL in a randomly permuted network. We examined whether the ASPL of a set of genes is indeed a good measure of biological relatedness or whether it is simply a characteristic of the degree distribution of those genes. We examined the ASPL of genes sets of some disease and pathway associations and compared them to ASPL of three types of randomly selected control sets: uniform selection, from entire proteome, degree-matched selection, and random permutation of the network. We found that disease associated genes and their degree-matched random genes have comparable ASPL. In other words, ASPL is a characteristic of the degree of the genes and the network topology, and not that of functional coherence.

Indexed as

Gene Regulatory NetworksModels, BiologicalHumansProtein Interaction MapsRandom Allocationdisease genesInteractome networkprotein-protein interactionsshortest path distance

Identifiers

PMID28073302
PMCPMC5726383

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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.