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      Accelerated Profile HMM Searches

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      PLoS Computational Biology
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          Abstract

          Profile hidden Markov models (profile HMMs) and probabilistic inference methods have made important contributions to the theory of sequence database homology search. However, practical use of profile HMM methods has been hindered by the computational expense of existing software implementations. Here I describe an acceleration heuristic for profile HMMs, the “multiple segment Viterbi” (MSV) algorithm. The MSV algorithm computes an optimal sum of multiple ungapped local alignment segments using a striped vector-parallel approach previously described for fast Smith/Waterman alignment. MSV scores follow the same statistical distribution as gapped optimal local alignment scores, allowing rapid evaluation of significance of an MSV score and thus facilitating its use as a heuristic filter. I also describe a 20-fold acceleration of the standard profile HMM Forward/Backward algorithms using a method I call “sparse rescaling”. These methods are assembled in a pipeline in which high-scoring MSV hits are passed on for reanalysis with the full HMM Forward/Backward algorithm. This accelerated pipeline is implemented in the freely available HMMER3 software package. Performance benchmarks show that the use of the heuristic MSV filter sacrifices negligible sensitivity compared to unaccelerated profile HMM searches. HMMER3 is substantially more sensitive and 100- to 1000-fold faster than HMMER2. HMMER3 is now about as fast as BLAST for protein searches.

          Author Summary

          Searching sequence databases is one of the most important applications in computational molecular biology. The main workhorse in the field is the BLAST suite of programs. Since the introduction of BLAST in the 1990's, important theoretical advances in homology search methodology have been made using probabilistic inference methods and hidden Markov models (HMMs). However, previous software implementations of these newer probabilistic methods were slower than BLAST by about 100-fold. This hindered their utility, because computation speed is so critical with the rapidly increasing size of modern sequence databases. Here I describe the acceleration methods I implemented in a new, freely available profile HMM software package, HMMER3. HMMER3 makes profile HMM searches about as fast as BLAST, while retaining the power of using probabilistic inference technology.

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          Most cited references44

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          Identification of common molecular subsequences.

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            Hidden Markov model speed heuristic and iterative HMM search procedure

            Background Profile hidden Markov models (profile-HMMs) are sensitive tools for remote protein homology detection, but the main scoring algorithms, Viterbi or Forward, require considerable time to search large sequence databases. Results We have designed a series of database filtering steps, HMMERHEAD, that are applied prior to the scoring algorithms, as implemented in the HMMER package, in an effort to reduce search time. Using this heuristic, we obtain a 20-fold decrease in Forward and a 6-fold decrease in Viterbi search time with a minimal loss in sensitivity relative to the unfiltered approaches. We then implemented an iterative profile-HMM search method, JackHMMER, which employs the HMMERHEAD heuristic. Due to our search heuristic, we eliminated the subdatabase creation that is common in current iterative profile-HMM approaches. On our benchmark, JackHMMER detects 14% more remote protein homologs than SAM's iterative method T2K. Conclusions Our search heuristic, HMMERHEAD, significantly reduces the time needed to score a profile-HMM against large sequence databases. This search heuristic allowed us to implement an iterative profile-HMM search method, JackHMMER, which detects significantly more remote protein homologs than SAM's T2K and NCBI's PSI-BLAST.
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              Hidden Markov models in computational biology. Applications to protein modeling.

              Hidden Markov Models (HMMs) are applied to the problems of statistical modeling, database searching and multiple sequence alignment of protein families and protein domains. These methods are demonstrated on the globin family, the protein kinase catalytic domain, and the EF-hand calcium binding motif. In each case the parameters of an HMM are estimated from a training set of unaligned sequences. After the HMM is built, it is used to obtain a multiple alignment of all the training sequences. It is also used to search the SWISS-PROT 22 database for other sequences that are members of the given protein family, or contain the given domain. The HMM produces multiple alignments of good quality that agree closely with the alignments produced by programs that incorporate three-dimensional structural information. When employed in discrimination tests (by examining how closely the sequences in a database fit the globin, kinase and EF-hand HMMs), the HMM is able to distinguish members of these families from non-members with a high degree of accuracy. Both the HMM and PROFILESEARCH (a technique used to search for relationships between a protein sequence and multiply aligned sequences) perform better in these tests than PROSITE (a dictionary of sites and patterns in proteins). The HMM appears to have a slight advantage over PROFILESEARCH in terms of lower rates of false negatives and false positives, even though the HMM is trained using only unaligned sequences, whereas PROFILESEARCH requires aligned training sequences. Our results suggest the presence of an EF-hand calcium binding motif in a highly conserved and evolutionary preserved putative intracellular region of 155 residues in the alpha-1 subunit of L-type calcium channels which play an important role in excitation-contraction coupling. This region has been suggested to contain the functional domains that are typical or essential for all L-type calcium channels regardless of whether they couple to ryanodine receptors, conduct ions or both.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Comput Biol
                plos
                ploscomp
                PLoS Computational Biology
                Public Library of Science (San Francisco, USA )
                1553-734X
                1553-7358
                October 2011
                October 2011
                20 October 2011
                25 October 2011
                : 7
                : 10
                : e1002195
                Affiliations
                [1]HHMI Janelia Farm Research Campus, Ashburn, Virginia, United States of America
                University of Virginia, United States of America
                Author notes

                Conceived and designed the experiments: SRE. Performed the experiments: SRE. Analyzed the data: SRE. Contributed reagents/materials/analysis tools: SRE. Wrote the paper: SRE.

                Article
                PCOMPBIOL-D-11-00572
                10.1371/journal.pcbi.1002195
                3197634
                22039361
                647dfa9d-460a-453f-a4ea-11fed9b902c3
                Sean R. Eddy. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 27 April 2011
                : 29 July 2011
                Page count
                Pages: 16
                Categories
                Research Article
                Biology
                Computational Biology
                Sequence Analysis

                Quantitative & Systems biology
                Quantitative & Systems biology

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