Predicting peptide presentation by major histocompatibility complex class I: an improved machine learning approach to the immunopeptidome.

Abstract:

BACKGROUND:To further our understanding of immunopeptidomics, improved tools are needed to identify peptides presented by major histocompatibility complex class I (MHC-I). Many existing tools are limited by their reliance upon chemical affinity data, which is less biologically relevant than sampling by mass spectrometry, and other tools are limited by incomplete exploration of machine learning approaches. Herein, we assemble publicly available data describing human peptides discovered by sampling the MHC-I immunopeptidome with mass spectrometry and use this database to train random forest classifiers (ForestMHC) to predict presentation by MHC-I. RESULTS:As measured by precision in the top 1% of predictions, our method outperforms NetMHC and NetMHCpan on test sets, and it outperforms both these methods and MixMHCpred on new data from an ovarian carcinoma cell line. We also find that random forest scores correlate monotonically, but not linearly, with known chemical binding affinities, and an information-based analysis of classifier features shows the importance of anchor positions for our classification. The random-forest approach also outperforms a deep neural network and a convolutional neural network trained on identical data. Finally, we use our large database to confirm that gene expression partially determines peptide presentation. CONCLUSIONS:ForestMHC is a promising method to identify peptides bound by MHC-I. We have demonstrated the utility of random forest-based approaches in predicting peptide presentation by MHC-I, assembled the largest known database of MS binding data, and mined this database to show the effect of gene expression on peptide presentation. ForestMHC has potential applicability to basic immunology, rational vaccine design, and neoantigen binding prediction for cancer immunotherapy. This method is publicly available for applications and further validation.

journal_name

BMC Bioinformatics

journal_title

BMC bioinformatics

authors

Boehm KM,Bhinder B,Raja VJ,Dephoure N,Elemento O

doi

10.1186/s12859-018-2561-z

subject

Has Abstract

pub_date

2019-01-05 00:00:00

pages

7

issue

1

issn

1471-2105

pii

10.1186/s12859-018-2561-z

journal_volume

20

pub_type

杂志文章
  • Construction of phylogenetic trees by kernel-based comparative analysis of metabolic networks.

    abstract:BACKGROUND:To infer the tree of life requires knowledge of the common characteristics of each species descended from a common ancestor as the measuring criteria and a method to calculate the distance between the resulting values of each measure. Conventional phylogenetic analysis based on genomic sequences provides inf...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-7-284

    authors: Oh SJ,Joung JG,Chang JH,Zhang BT

    更新日期:2006-06-06 00:00:00

  • Predikin and PredikinDB: a computational framework for the prediction of protein kinase peptide specificity and an associated database of phosphorylation sites.

    abstract:BACKGROUND:We have previously described an approach to predicting the substrate specificity of serine-threonine protein kinases. The method, named Predikin, identifies key conserved substrate-determining residues in the kinase catalytic domain that contact the substrate in the region of the phosphorylation site and so ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-245

    authors: Saunders NF,Brinkworth RI,Huber T,Kemp BE,Kobe B

    更新日期:2008-05-26 00:00:00

  • A novel computational model for predicting potential LncRNA-disease associations based on both direct and indirect features of LncRNA-disease pairs.

    abstract:BACKGROUND:Accumulating evidence has demonstrated that long non-coding RNAs (lncRNAs) are closely associated with human diseases, and it is useful for the diagnosis and treatment of diseases to get the relationships between lncRNAs and diseases. Due to the high costs and time complexity of traditional bio-experiments, ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-020-03906-7

    authors: Xiao Y,Xiao Z,Feng X,Chen Z,Kuang L,Wang L

    更新日期:2020-12-02 00:00:00

  • GeneLibrarian: an effective gene-information summarization and visualization system.

    abstract:BACKGROUND:Abundant information about gene products is stored in online searchable databases such as annotation or literature. To efficiently obtain and digest such information, there is a pressing need for automated information-summarization and functional-similarity clustering of genes. RESULTS:We have developed a n...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-7-392

    authors: Chiang JH,Shin JW,Liu HH,Chin CL

    更新日期:2006-08-29 00:00:00

  • LSX: automated reduction of gene-specific lineage evolutionary rate heterogeneity for multi-gene phylogeny inference.

    abstract:BACKGROUND:Lineage rate heterogeneity can be a major source of bias, especially in multi-gene phylogeny inference. We had previously tackled this issue by developing LS3, a data subselection algorithm that, by removing fast-evolving sequences in a gene-specific manner, identifies subsets of sequences that evolve at a r...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-019-3020-1

    authors: Rivera-Rivera CJ,Montoya-Burgos JI

    更新日期:2019-08-13 00:00:00

  • Normalized N50 assembly metric using gap-restricted co-linear chaining.

    abstract:BACKGROUND:For the development of genome assembly tools, some comprehensive and efficiently computable validation measures are required to assess the quality of the assembly. The mostly used N50 measure summarizes the assembly results by the length of the scaffold (or contig) overlapping the midpoint of the length-orde...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-13-255

    authors: Mäkinen V,Salmela L,Ylinen J

    更新日期:2012-10-03 00:00:00

  • Reverse engineering gene regulatory networks: coupling an optimization algorithm with a parameter identification technique.

    abstract:BACKGROUND:To infer gene regulatory networks from time series gene profiles, two important tasks that are related to biological systems must be undertaken. One task is to determine a valid network structure that has topological properties that can influence the network dynamics profoundly. The other task is to optimize...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-S15-S8

    authors: Hsiao YT,Lee WP

    更新日期:2014-01-01 00:00:00

  • SAMSA: a comprehensive metatranscriptome analysis pipeline.

    abstract:BACKGROUND:Although metatranscriptomics-the study of diverse microbial population activity based on RNA-seq data-is rapidly growing in popularity, there are limited options for biologists to analyze this type of data. Current approaches for processing metatranscriptomes rely on restricted databases and a dedicated comp...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-016-1270-8

    authors: Westreich ST,Korf I,Mills DA,Lemay DG

    更新日期:2016-09-29 00:00:00

  • Automated peptide mapping and protein-topographical annotation of proteomics data.

    abstract:BACKGROUND:In quantitative proteomics, peptide mapping is a valuable approach to combine positional quantitative information with topographical and domain information of proteins. Quantitative proteomic analysis of cell surface shedding is an exemplary application area of this approach. RESULTS:We developed ImproViser...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-207

    authors: Videm P,Gunasekaran D,Schröder B,Mayer B,Biniossek ML,Schilling O

    更新日期:2014-06-19 00:00:00

  • Accuracy of RNA-Seq and its dependence on sequencing depth.

    abstract:BACKGROUND:The cost of DNA sequencing has undergone a dramatical reduction in the past decade. As a result, sequencing technologies have been increasingly applied to genomic research. RNA-Seq is becoming a common technique for surveying gene expression based on DNA sequencing. As it is not clear how increased sequencin...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-13-S13-S5

    authors: Cai G,Li H,Lu Y,Huang X,Lee J,Müller P,Ji Y,Liang S

    更新日期:2012-01-01 00:00:00

  • Random generalized linear model: a highly accurate and interpretable ensemble predictor.

    abstract:BACKGROUND:Ensemble predictors such as the random forest are known to have superior accuracy but their black-box predictions are difficult to interpret. In contrast, a generalized linear model (GLM) is very interpretable especially when forward feature selection is used to construct the model. However, forward feature ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-14-5

    authors: Song L,Langfelder P,Horvath S

    更新日期:2013-01-16 00:00:00

  • Is EC class predictable from reaction mechanism?

    abstract:BACKGROUND:We investigate the relationships between the EC (Enzyme Commission) class, the associated chemical reaction, and the reaction mechanism by building predictive models using Support Vector Machine (SVM), Random Forest (RF) and k-Nearest Neighbours (kNN). We consider two ways of encoding the reaction mechanism ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-13-60

    authors: Nath N,Mitchell JB

    更新日期:2012-04-24 00:00:00

  • Identification of markers associated with global changes in DNA methylation regulation in cancers.

    abstract::DNA methylation exhibits different patterns in different cancers. DNA methylation rates at different genomic loci appear to be highly correlated in some samples but not in others. We call such phenomena conditional concordant relationships (CCRs). In this study, we explored DNA methylation patterns in 12 common cancer...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-13-S13-S7

    authors: Qiu P,Zhang L

    更新日期:2012-01-01 00:00:00

  • On pairwise distances and median score of three genomes under DCJ.

    abstract::In comparative genomics, the rearrangement distance between two genomes (equal the minimal number of genome rearrangements required to transform them into a single genome) is often used for measuring their evolutionary remoteness. Generalization of this measure to three genomes is known as the median score (while a re...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-13-S19-S1

    authors: Aganezov S Jr,Alekseyev MA

    更新日期:2012-01-01 00:00:00

  • The PowerAtlas: a power and sample size atlas for microarray experimental design and research.

    abstract:BACKGROUND:Microarrays permit biologists to simultaneously measure the mRNA abundance of thousands of genes. An important issue facing investigators planning microarray experiments is how to estimate the sample size required for good statistical power. What is the projected sample size or number of replicate chips need...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-7-84

    authors: Page GP,Edwards JW,Gadbury GL,Yelisetti P,Wang J,Trivedi P,Allison DB

    更新日期:2006-02-22 00:00:00

  • Redundancy in electronic health record corpora: analysis, impact on text mining performance and mitigation strategies.

    abstract:BACKGROUND:The increasing availability of Electronic Health Record (EHR) data and specifically free-text patient notes presents opportunities for phenotype extraction. Text-mining methods in particular can help disease modeling by mapping named-entities mentions to terminologies and clustering semantically related term...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-14-10

    authors: Cohen R,Elhadad M,Elhadad N

    更新日期:2013-01-16 00:00:00

  • Investigating the concordance of Gene Ontology terms reveals the intra- and inter-platform reproducibility of enrichment analysis.

    abstract:BACKGROUND:Reliability and Reproducibility of differentially expressed genes (DEGs) are essential for the biological interpretation of microarray data. The microarray quality control (MAQC) project launched by US Food and Drug Administration (FDA) elucidated that the lists of DEGs generated by intra- and inter-platform...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-14-143

    authors: Zhang L,Zhang J,Yang G,Wu D,Jiang L,Wen Z,Li M

    更新日期:2013-04-29 00:00:00

  • Meta-analysis of breast cancer microarray studies in conjunction with conserved cis-elements suggest patterns for coordinate regulation.

    abstract:BACKGROUND:Gene expression measurements from breast cancer (BrCa) tumors are established clinical predictive tools to identify tumor subtypes, identify patients showing poor/good prognosis, and identify patients likely to have disease recurrence. However, diverse breast cancer datasets in conjunction with diagnostic cl...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-63

    authors: Smith DD,Saetrom P,Snøve O Jr,Lundberg C,Rivas GE,Glackin C,Larson GP

    更新日期:2008-01-28 00:00:00

  • Quantitative prediction of the effect of genetic variation using hidden Markov models.

    abstract:BACKGROUND:With the development of sequencing technologies, more and more sequence variants are available for investigation. Different classes of variants in the human genome have been identified, including single nucleotide substitutions, insertion and deletion, and large structural variations such as duplications and...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-5

    authors: Liu M,Watson LT,Zhang L

    更新日期:2014-01-09 00:00:00

  • Protein subcellular localization prediction based on compartment-specific features and structure conservation.

    abstract:BACKGROUND:Protein subcellular localization is crucial for genome annotation, protein function prediction, and drug discovery. Determination of subcellular localization using experimental approaches is time-consuming; thus, computational approaches become highly desirable. Extensive studies of localization prediction h...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-330

    authors: Su EC,Chiu HS,Lo A,Hwang JK,Sung TY,Hsu WL

    更新日期:2007-09-08 00:00:00

  • RocSampler: regularizing overlapping protein complexes in protein-protein interaction networks.

    abstract:BACKGROUND:In recent years, protein-protein interaction (PPI) networks have been well recognized as important resources to elucidate various biological processes and cellular mechanisms. In this paper, we address the problem of predicting protein complexes from a PPI network. This problem has two difficulties. One is r...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-017-1920-5

    authors: Maruyama O,Kuwahara Y

    更新日期:2017-12-06 00:00:00

  • ConEVA: a toolbox for comprehensive assessment of protein contacts.

    abstract:BACKGROUND:In recent years, successful contact prediction methods and contact-guided ab initio protein structure prediction methods have highlighted the importance of incorporating contact information into protein structure prediction methods. It is also observed that for almost all globular proteins, the quality of co...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-016-1404-z

    authors: Adhikari B,Nowotny J,Bhattacharya D,Hou J,Cheng J

    更新日期:2016-12-07 00:00:00

  • Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment.

    abstract:BACKGROUND:Many Bioinformatics studies begin with a multiple sequence alignment as the foundation for their research. This is because multiple sequence alignment can be a useful technique for studying molecular evolution and analyzing sequence structure relationships. RESULTS:In this paper, we have proposed a Vertical...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-12-353

    authors: Naznin F,Sarker R,Essam D

    更新日期:2011-08-25 00:00:00

  • ElliPro: a new structure-based tool for the prediction of antibody epitopes.

    abstract:BACKGROUND:Reliable prediction of antibody, or B-cell, epitopes remains challenging yet highly desirable for the design of vaccines and immunodiagnostics. A correlation between antigenicity, solvent accessibility, and flexibility in proteins was demonstrated. Subsequently, Thornton and colleagues proposed a method for ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-514

    authors: Ponomarenko J,Bui HH,Li W,Fusseder N,Bourne PE,Sette A,Peters B

    更新日期:2008-12-02 00:00:00

  • Network-based group variable selection for detecting expression quantitative trait loci (eQTL).

    abstract:BACKGROUND:Analysis of expression quantitative trait loci (eQTL) aims to identify the genetic loci associated with the expression level of genes. Penalized regression with a proper penalty is suitable for the high-dimensional biological data. Its performance should be enhanced when we incorporate biological knowledge o...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-12-269

    authors: Wang W,Zhang X

    更新日期:2011-06-30 00:00:00

  • GenomeBlast: a web tool for small genome comparison.

    abstract:BACKGROUND:Comparative genomics has become an essential approach for identifying homologous gene candidates and their functions, and for studying genome evolution. There are many tools available for genome comparisons. Unfortunately, most of them are not applicable for the identification of unique genes and the inferen...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-7-S4-S18

    authors: Lu G,Jiang L,Helikar RM,Rowley TW,Zhang L,Chen X,Moriyama EN

    更新日期:2006-12-12 00:00:00

  • CorrelaGenes: a new tool for the interpretation of the human transcriptome.

    abstract:BACKGROUND:The amount of gene expression data available in public repositories has grown exponentially in the last years, now requiring new data mining tools to transform them in information easily accessible to biologists. RESULTS:By exploiting expression data publicly available in the Gene Expression Omnibus (GEO) d...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-S1-S6

    authors: Cremaschi P,Rovida S,Sacchi L,Lisa A,Calvi F,Montecucco A,Biamonti G,Bione S,Sacchi G

    更新日期:2014-01-01 00:00:00

  • Identifying metabolic enzymes with multiple types of association evidence.

    abstract:BACKGROUND:Existing large-scale metabolic models of sequenced organisms commonly include enzymatic functions which can not be attributed to any gene in that organism. Existing computational strategies for identifying such missing genes rely primarily on sequence homology to known enzyme-encoding genes. RESULTS:We pres...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-7-177

    authors: Kharchenko P,Chen L,Freund Y,Vitkup D,Church GM

    更新日期:2006-03-29 00:00:00

  • ArrayIDer: automated structural re-annotation pipeline for DNA microarrays.

    abstract:BACKGROUND:Systems biology modeling from microarray data requires the most contemporary structural and functional array annotation. However, microarray annotations, especially for non-commercial, non-traditional biomedical model organisms, are often dated. In addition, most microarray analysis tools do not readily acce...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-10-30

    authors: van den Berg BH,Konieczka JH,McCarthy FM,Burgess SC

    更新日期:2009-01-23 00:00:00

  • Multi-scale structural community organisation of the human genome.

    abstract:BACKGROUND:Structural interaction frequency matrices between all genome loci are now experimentally achievable thanks to high-throughput chromosome conformation capture technologies. This ensues a new methodological challenge for computational biology which consists in objectively extracting from these data the structu...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-017-1616-x

    authors: Boulos RE,Tremblay N,Arneodo A,Borgnat P,Audit B

    更新日期:2017-04-11 00:00:00