Global Discriminative Learning for Higher-Accuracy Computational Gene Prediction 英文参考文献.docVIP
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Global Discriminative Learning for Higher-Accuracy Computational Gene Prediction 英文参考文献
GlobalDiscriminativeLearningforHigher-
AccuracyComputationalGenePrediction
Axel Bernal1*,Koby Crammer1,Artemis Hatzigeorgiou2,Fernando Pereira1
1DepartmentofComputerandInformationScience,UniversityofPennsylvania,Philadelphia,Pennsylvania,UnitedStatesofAmerica,2DepartmentofGenetics,University
ofPennsylvania,Philadelphia,Pennsylvania,UnitedStatesofAmerica
Most ab initio gene predictors use a probabilistic sequence model, typically a hidden Markov model, to combine
separately trained models of genomic signals and content. By combining separate models of relevant genomic
features,suchgenepredictorscanexploitsmalltrainingsets andincomplete annotations,andcanbetrainedfairly
efficiently. However, that type of piecewise training does not optimize prediction accuracy and has difficulty in
accounting for statistical dependencies among different parts of the gene model. With genomic information being
createdatanever-increasingrate,itisworthinvestigatingalternativeapproachesinwhichmanydifferenttypesof
genomicevidence, with complex statistical dependencies, canbe integratedby discriminative learningto maximize
annotation accuracy. Among discriminative learning methods, large-margin classifiers have become prominent
because of the success of support vector machines (SVM) in many classification tasks. We describe CRAIG, a new
programforabinitiogenepredictionbasedonaconditionalrandomfieldmodelwithsemi-Markovstructurethatis
trainedwithanonlinelarge-marginalgorithmrelatedtomulticlassSVMs.Ourexperimentsonbenchmarkvertebrate
datasets and on regions from the ENCODE project show significant improvements in prediction accuracy over
publishedgenepredictorsthatuseintrinsicfeaturesonly,particularlyatthegenelevelandongeneswithlongintrons.
Citation:BernalA,CrammerK,HatzigeorgiouA,PereiraF(2007)Globaldiscriminativelearningforhigher-accuracycomputationalgeneprediction.PLoSComputBiol3(3):
e54.doi:10.1371/journal.pcbi.0030054
regions represent more than 95% of the total number of
genesinmos
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