ArticleBMC bioinformatics2007
An evolutionary method for learning HMM structure: prediction of protein secondary structure.
Article in BMC bioinformatics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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.
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.
Who cites it
15 citing papers in PubMed.
- Efficient Mining and Characterization of Two Novel Keratinases from Metagenomic Database.Biomolecules · 2025Article
- Tokenization and deep learning architectures in genomics: A comprehensive review.Computational and structural biotechnology journal · 2025Review
- Visual Analytics: A Method to Explore Natural Histories of Oral Epithelial Dysplasia.Frontiers in oral health · 2021Article
- A secondary structure-based position-specific scoring matrix applied to the improvement in protein secondary structure prediction.PloS one · 2021Article
- ProbPFP: a multiple sequence alignment algorithm combining hidden Markov model optimized by particle swarm optimization with partition function.BMC bioinformatics · 2019Article
- Protein Secondary Structure Prediction Based on Data Partition and Semi-Random Subspace Method.Scientific reports · 2018Article
- Protein secondary structure prediction using a small training set (compact model) combined with a Complex-valued neural network approach.BMC bioinformatics · 2016Article
- A review of three different studies on hidden markov models for epigenetic problems: a computational perspective.Genomics & informatics · 2014Review
- Evolving stochastic context--free grammars for RNA secondary structure prediction.BMC bioinformatics · 2012Article
- SPINE X: improving protein secondary structure prediction by multistep learning coupled with prediction of solvent accessible surface area and backbone torsion angles.Journal of computational chemistry · 2012Article
- Learning sparse models for a dynamic Bayesian network classifier of protein secondary structure.BMC bioinformatics · 2011Article
- The identification of novel cyclic AMP-dependent protein kinase anchoring proteins using bioinformatic filters and peptide arrays.Protein engineering, design & selection : PEDS · 2011Article
- Improving protein secondary structure prediction using a simple k-mer model.Bioinformatics (Oxford, England) · 2010Article
- Template-based protein modeling: recent methodological advances.Current topics in medicinal chemistry · 2010Review
- Hidden Markov Models and their Applications in Biological Sequence Analysis.Current genomics · 2009Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe prediction of the secondary structure of proteins is one of the most studied problems in bioinformatics. Despite their success in many problems of biological sequence analysis, Hidden Markov Models (HMMs) have not been used much for this problem, as the complexity of the task makes manual design of HMMs difficult. Therefore, we have developed a method for evolving the structure of HMMs automatically, using Genetic Algorithms (GAs).
resultsIn the GA procedure, populations of HMMs are assembled from biologically meaningful building blocks. Mutation and crossover operators were designed to explore the space of such Block-HMMs. After each step of the GA, the standard HMM estimation algorithm (the Baum-Welch algorithm) was used to update model parameters. The final HMM captures several features of protein sequence and structure, with its own HMM grammar. In contrast to neural network based predictors, the evolved HMM also calculates the probabilities associated with the predictions. We carefully examined the performance of the HMM based predictor, both under the multiple- and single-sequence condition.
conclusionWe have shown that the proposed evolutionary method can automatically design the topology of HMMs. The method reads the grammar of protein sequences and converts it into the grammar of an HMM. It improved previously suggested evolutionary methods and increased the prediction quality. Especially, it shows good performance under the single-sequence condition and provides probabilistic information on the prediction result. The protein secondary structure predictor using HMMs (P.S.HMM) is on-line available http://www.binf.ku.dk/~won/pshmm.htm. It runs under the single-sequence condition.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.