Evidence map›Paper›PMID 23812987›Full record

ArticleBioinformatics (Oxford, England)2013

Multitask learning for host-pathogen protein interactions.

Meghana Kshirsagar, Jaime Carbonell, Judith Klein-Seetharaman

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

  1. Article
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  9. Article
  10. Prediction of host-pathogen protein interactions by extended network model.Turkish journal of biology = Turk biyoloji dergisi · 2021
    Article
  11. Article
  12. Article
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  14. Review
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  18. A review on host-pathogen interactions: classification and prediction.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2016
    Review
  19. Article
  20. 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.

Meghana KshirsagarLanguage Technologies Institute, School of Computer Science, Carnegie Mellon University, 5000 Forbes Ave, PA 15213, USA.
Jaime Carbonell
Judith Klein-Seetharaman

Funding

X-Ray Core P50GM082251 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CALERO, GUILLERMO ALBERTO · 2007 to 2018
$48.1M
Bridging Sequence Patterns and Structural DynamicsR01LM007994 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BAHAR, IVET · 2004 to 2011
$3.0M
NIGMS NIH HHS P50 GM082251NIGMS NIH HHS P50GM082251NLM NIH HHS 2R01LM007994-05NLM NIH HHS R01 LM007994
6 · The paper itself

Abstract

motivationAn important aspect of infectious disease research involves understanding the differences and commonalities in the infection mechanisms underlying various diseases. Systems biology-based approaches study infectious diseases by analyzing the interactions between the host species and the pathogen organisms. This work aims to combine the knowledge from experimental studies of host-pathogen interactions in several diseases to build stronger predictive models. Our approach is based on a formalism from machine learning called 'multitask learning', which considers the problem of building models across tasks that are related to each other. A 'task' in our scenario is the set of host-pathogen protein interactions involved in one disease. To integrate interactions from several tasks (i.e. diseases), our method exploits the similarity in the infection process across the diseases. In particular, we use the biological hypothesis that similar pathogens target the same critical biological processes in the host, in defining a common structure across the tasks.

resultsOur current work on host-pathogen protein interaction prediction focuses on human as the host, and four bacterial species as pathogens. The multitask learning technique we develop uses a task-based regularization approach. We find that the resulting optimization problem is a difference of convex (DC) functions. To optimize, we implement a Convex-Concave procedure-based algorithm. We compare our integrative approach to baseline methods that build models on a single host-pathogen protein interaction dataset. Our results show that our approach outperforms the baselines on the training data. We further analyze the protein interaction predictions generated by the models, and find some interesting insights. AVAILABILITY: The predictions and code are available at: http://www.cs.cmu.edu/∼mkshirsa/ismb2013_paper320.html . SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Artificial IntelligenceHost-Pathogen InteractionsAlgorithmsBacterial ProteinsHumansProtein Interaction MappingBacterial Proteins

Identifiers

PMID23812987
PMCPMC3694681

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.