Evidence map›Paper›PMID 23173746›Full record

ArticleBMC proceedings2012

An efficient heuristic method for active feature acquisition and its application to protein-protein interaction prediction.

Mohamed Thahir, Tarun Sharma, Madhavi K Ganapathiraju

Open access · goldAbstract read
In one paragraph

Article in BMC proceedings, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 94% of its field
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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Active feature elicitation: An unified framework.Frontiers in artificial intelligence · 2023
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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

3 authors at 2 institutions in 1 country.

Mohamed ThahirDepartment of Biomedical Informatics, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA. madhavi@pitt.edu.
Tarun Sharma
Madhavi K Ganapathiraju
University of Pittsburgh · USCarnegie Mellon University · US

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

backgroundMachine learning approaches for classification learn the pattern of the feature space of different classes, or learn a boundary that separates the feature space into different classes. The features of the data instances are usually available, and it is only the class-labels of the instances that are unavailable. For example, to classify text documents into different topic categories, the words in the documents are features and they are readily available, whereas the topic is what is predicted. However, in some domains obtaining features may be resource-intensive because of which not all features may be available. An example is that of protein-protein interaction prediction, where not only are the labels ('interacting' or 'non-interacting') unavailable, but so are some of the features. It may be possible to obtain at least some of the missing features by carrying out a few experiments as permitted by the available resources. If only a few experiments can be carried out to acquire missing features, which proteins should be studied and which features of those proteins should be determined? From the perspective of machine learning for PPI prediction, it would be desirable that those features be acquired which when used in training the classifier, the accuracy of the classifier is improved the most. That is, the utility of the feature-acquisition is measured in terms of how much acquired features contribute to improving the accuracy of the classifier. Active feature acquisition (AFA) is a strategy to preselect such instance-feature combinations (i.e. protein and experiment combinations) for maximum utility. The goal of AFA is the creation of optimal training set that would result in the best classifier, and not in determining the best classification model itself.

resultsWe present a heuristic method for active feature acquisition to calculate the utility of acquiring a missing feature. This heuristic takes into account the change in belief of the classification model induced by the acquisition of the feature under consideration. As compared to random selection of proteins on which the experiments are performed and the type of experiment that is performed, the heuristic method reduces the number of experiments to as few as 40%. Most notable characteristic of this method is that it does not require re-training of the classification model on every possible combination of instance, feature and feature-value tuples. For this reason, our method is far less computationally expensive as compared with previous AFA strategies.

conclusionsThe results show that our heuristic method for AFA creates an optimal training set with far less features acquired as compared to random acquisition. This shows the value of active feature acquisition to aid in protein-protein interaction prediction where feature acquisition is costly. Compared to previous methods, the proposed method reduces computational cost while also achieving a better F-score. The proposed method is valuable as it presents a direction to AFA with a far lesser computational expense by removing the need for the first time, of training a classifier for every combination of instance, feature and feature-value tuples which would be impractical for several domains.

Identifiers

PMID23173746
PMCPMC3504800
OpenAlexW1978328358

What OpenQuestion holds

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LicenceCC BY
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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.