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This article is part of the supplement: Probabilistic Modeling and Machine Learning in Structural and Systems Biology .

Open AccessResearch

Methods for estimating human endogenous retrovirus activities from EST databases

Merja Oja1,2 email, Jaakko Peltonen2 email, Jonas Blomberg3 email and Samuel Kaski2 email

Department of Computer Science, University of Helsinki, P.O. Box 68, FI-00014 University of Helsinki, Finland

Helsinki Institute for Information Technology, Laboratory of Computer and Information Science, Helsinki University of Technology, P.O. Box 5400, FI-02015 TKK, Finland

Section of Virology, Department of Medical Sciences, Uppsala University, Academic Hospital, 751 85 Uppsala, Sweden

author email corresponding author email

BMC Bioinformatics 2007, 8(Suppl 2):S11doi:10.1186/1471-2105-8-S2-S11

Published: 3 May 2007

Abstract

Background

Human endogenous retroviruses (HERVs) are surviving traces of ancient retrovirus infections and now reside within the human DNA. Recently HERV expression has been detected in both normal tissues and diseased patients. However, the activities (expression levels) of individual HERV sequences are mostly unknown.

Results

We introduce a generative mixture model, based on Hidden Markov Models, for estimating the activities of the individual HERV sequences from EST (expressed sequence tag) databases. We use the model to estimate the relative activities of 181 HERVs. We also empirically justify a faster heuristic method for HERV activity estimation and use it to estimate the activities of 2450 HERVs. The majority of the HERV activities were previously unknown.

Conclusion

(i) Our methods estimate activity accurately based on experiments on simulated data. (ii) Our estimate on real data shows that 7% of the HERVs are active. The active ones are spread unevenly into HERV groups and relatively uniformly in terms of estimated age. HERVs with the retroviral env gene are more often active than HERVs without env. Few of the active HERVs have open reading frames for retroviral proteins.


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