Dataset Information

MacroSEQUEST: efficient candidate-centric searching and high-resolution correlation analysis for large-scale proteomics data sets.

ABSTRACT: Modern mass spectrometers are now capable of producing tens of thousands of tandem mass (MS/MS) spectra per hour of operation, resulting in an ever-increasing burden on the computational tools required to translate these raw MS/MS spectra into peptide sequences. In the present work, we describe our efforts to improve the performance of one of the earliest and most commonly used algorithms, SEQUEST, through a wholesale redesign of its processing architecture. We call this new program MacroSEQUEST, which exhibits a dramatic improvement in processing speed by transiently indexing the array of MS/MS spectra prior to searching FASTA databases. We demonstrate the performance of MacroSEQUEST relative to a suite of other programs commonly encountered in proteomics research. We also extend the capability of SEQUEST by implementing a parameter in MacroSEQUEST that allows for scalable sparse arrays of experimental and theoretical spectra to be implemented for high-resolution correlation analysis and demonstrate the advantages of high-resolution MS/MS searching to the sensitivity of large-scale proteomics data sets.

SUBMITTER: Faherty BK

PROVIDER: S-EPMC2925463 | biostudies-literature | 2010 Aug

REPOSITORIES: biostudies-literature

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MacroSEQUEST: efficient candidate-centric searching and high-resolution correlation analysis for large-scale proteomics data sets.

Faherty Brendan K BK Gerber Scott A SA

Analytical chemistry 20100801 16

Modern mass spectrometers are now capable of producing tens of thousands of tandem mass (MS/MS) spectra per hour of operation, resulting in an ever-increasing burden on the computational tools required to translate these raw MS/MS spectra into peptide sequences. In the present work, we describe our efforts to improve the performance of one of the earliest and most commonly used algorithms, SEQUEST, through a wholesale redesign of its processing architecture. We call this new program MacroSEQUEST ...[more]

PMID: 20684545

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Project description:MotivationWe have proposed a mixture model based approach to the concordant integrative analysis of multiple large-scale two-sample expression datasets. Since the mixture model is based on the transformed differential expression test P-values (z-scores), it is generally applicable to the expression data generated by either microarray or RNA-seq platforms. The mixture model is simple with three normal distribution components for each dataset to represent down-regulation, up-regulation and no differential expression. However, when the number of datasets increases, the model parameter space increases exponentially due to the component combination from different datasets.ResultsIn this study, motivated by the well-known generalized estimating equations (GEEs) for longitudinal data analysis, we focus on the concordant components and assume that the proportions of non-concordant components follow a special structure. We discuss the exchangeable, multiset coefficient and autoregressive structures for model reduction, and their related expectation-maximization (EM) algorithms. Then, the parameter space is linear with the number of datasets. In our previous study, we have applied the general mixture model to three microarray datasets for lung cancer studies. We show that more gene sets (or pathways) can be detected by the reduced mixture model with the exchangeable structure. Furthermore, we show that more genes can also be detected by the reduced model. The Cancer Genome Atlas (TCGA) data have been increasingly collected. The advantage of incorporating the concordance feature has also been clearly demonstrated based on TCGA RNA sequencing data for studying two closely related types of cancer.Availability and implementationAdditional results are included in a supplemental file. Computer program R-functions are freely available at http://home.gwu.edu/?ylai/research/Concordance.Contactylai@gwu.edu.Supplementary informationSupplementary data are available at Bioinformatics online.

Dataset Information

MacroSEQUEST: efficient candidate-centric searching and high-resolution correlation analysis for large-scale proteomics data sets.

Publications

MacroSEQUEST: efficient candidate-centric searching and high-resolution correlation analysis for large-scale proteomics data sets.

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