Evidence map›Paper›PMID 18793458›Full record

ArticleBMC bioinformatics2008

Clustering ionic flow blockade toggles with a mixture of HMMs.

Alexander Churbanov, Stephen Winters-Hilt

Abstract read
In one paragraph

Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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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.

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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

2 authors.

Alexander ChurbanovThe Research Institute for Children, 200 Henry Clay Ave, New Orleans, LA 70118, USA. atchourb@cs.uno.edu
Stephen Winters-Hilt

Funding

Electronic Sequencing in NanoporesR01HG003703 · NHGRI · HARVARD UNIVERSITY · PI BRANTON, DANIEL NONE, GOLOVCHENKO, JENE A · 2005 to 2014
$16.1M
Nanopore study of single antibody-antigen interactionsK22LM008794 · NLM · CHILDREN'S HOSPITAL (NEW ORLEANS) · PI WINTERS-HILT, STEPHEN · 2005 to 2007
$486k
A Comprehensive Structural and Dynamic Map of DNA Duplex EndsR21GM073617 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI AKESON, MARK A · 2006 to 2008
$417k
NHGRI NIH HHS R01 HG003703NHGRI NIH HHS R01HG003703NIGMS NIH HHS R21 GM073617NIGMS NIH HHS R21GM073617NLM NIH HHS K22 LM008794NLM NIH HHS K22LM008794
6 · The paper itself

Abstract

backgroundIonic current blockade signal processing, for use in nanopore detection, offers a promising new way to analyze single molecule properties with potential implications for DNA sequencing. The alpha-Hemolysin transmembrane channel interacts with a translocating molecule in a nontrivial way, frequently evidenced by a complex ionic flow blockade pattern with readily distinguishable modes of toggling. Effective processing of such signals requires developing machine learning methods capable of learning the various blockade modes for classification and knowledge discovery purposes. Here we propose a method aimed to improve our stochastic analysis capabilities to better understand the discriminatory capabilities of the observed the nanopore channel interactions with analyte.

resultsWe tailored our memory-sparse distributed implementation of a Mixture of Hidden Markov Models (MHMMs) to the problem of channel current blockade clustering and associated analyte classification. By using probabilistic fully connected HMM profiles as mixture components we were able to cluster the various 9 base-pair hairpin channel blockades. We obtained very high Maximum a Posteriori (MAP) classification with a mixture of 12 different channel blockade profiles, each with 4 levels, a configuration that can be computed with sufficient speed for real-time experimental feedback. MAP classification performance depends on several factors such as the number of mixture components, the number of levels in each profile, and the duration of a channel blockade event. We distribute Baum-Welch Expectation Maximization (EM) algorithms running on our model in two ways. A distributed implementation of the MHMM data processing accelerates data clustering efforts. The second, simultanteous, strategy uses an EM checkpointing algorithm to lower the memory use and efficiently distribute the bulk of EM processing in processing large data sequences (such as for the progressive sums used in the HMM parameter estimates).

conclusionThe proposed distributed MHMM method has many appealing properties, such as precise classification of analyte in real-time scenarios, and the ability to incorporate new domain knowledge into a flexible, easily distributable, architecture. The distributed HMM provides a feature extraction that is equivalent to that of the sequential HMM with a speedup factor approximately equal to the number of independent CPUs operating on the data. The MHMM topology learns clusters existing within data samples via distributed HMM EM learning. A Java implementation of the MHMM algorithm is available at http://logos.cs.uno.edu/~achurban.

Indexed as

AlgorithmsArtificial IntelligenceBase SequenceBiological AssayDNAEscherichia coli ProteinsHemolysin ProteinsIon Channel GatingIon ChannelsMarkov ChainsMolecular Sequence DataPattern Recognition, AutomatedSequence Analysis, DNADNAEscherichia coli ProteinsHemolysin ProteinsHlya protein, E coliIon Channels

Identifiers

PMID18793458
PMCPMC2537564

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LicenceCC BY
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Registered trials

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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.