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  Dealing with Sparse Data in Predicting Outcomes of HIV Combination Therapies

Bogojeska, J., Bickel, S., Altmann, A., & Lengauer, T. (2010). Dealing with Sparse Data in Predicting Outcomes of HIV Combination Therapies. Bioinformatics, 26(17), 2085-2092. doi:10.1093/bioinformatics/btq361.

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Genre: Journal Article
Latex : Dealing with Sparse Data in Predicting Outcomes of {HIV} Combination Therapies

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Copyright © 2010 Oxford University Press
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 Creators:
Bogojeska, Jasmina1, Author           
Bickel, Steffen2, Author           
Altmann, André1, Author           
Lengauer, Thomas1, Author           
Affiliations:
1Computational Biology and Applied Algorithmics, MPI for Informatics, Max Planck Society, ou_40046              
2Machine Learning, MPI for Informatics, Max Planck Society, ou_1116552              

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 Abstract: Motivation: As there exists no cure or vaccine for the infection with human
immunodeficiency virus (HIV), the standard approach to treating HIV patients is
to repeatedly administer different combinations of several antiretroviral
drugs. Because of the large number of possible drug combinations, manually
finding a successful regimen becomes practically impossible. This presents a
major challenge for HIV treatment. The application of machine learning methods
for predicting virological responses to potential therapies is a possible
approach to solving this problem. However, due to evolving trends in treating
HIV patients the available clinical datasets have a highly unbalanced
representation, which might negatively affect the usefulness of derived
statistical models.

Results: This article presents an approach that tackles the problem of
predicting virological response to combination therapies by learning a separate
logistic regression model for each therapy. The models are fitted by using not
only the data from the target therapy but also the information from similar
therapies. For this purpose, we introduce and evaluate two different measures
of therapy similarity. The models are also able to incorporate phenotypic
knowledge on the therapy outcomes through a Gaussian prior. With our approach
we balance the uneven therapy representation in the datasets and produce higher
quality models for therapies with very few training samples. According to the
results from the computational experiments our therapy similarity model
performs significantly better than training separate models for each therapy by
using solely their examples. Furthermore, the model's performance is as good as
an approach that encodes therapy information in the input feature space with
the advantage of delivering better results for therapies with very few training
samples.

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Language(s): eng - English
 Dates: 2010-06-302010
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 536640
DOI: 10.1093/bioinformatics/btq361
URI: http://bioinformatics.oxfordjournals.org/content/26/17/2085.full
Other: Local-ID: C125673F004B2D7B-3E1FBC4FF547FA99C12577F40059916E-Bogojeska2010
BibTex Citekey: Bogojeska-et-al_Bioinformatics10
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Title: Bioinformatics
Source Genre: Journal
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Publ. Info: Oxford : Oxford University Press
Pages: - Volume / Issue: 26 (17) Sequence Number: - Start / End Page: 2085 - 2092 Identifier: ISSN: 1367-4803
CoNE: https://pure.mpg.de/cone/journals/resource/954926969991