DeepQA: improving the estimation of single protein model quality with deep belief networks.

Abstract:

BACKGROUND:Protein quality assessment (QA) useful for ranking and selecting protein models has long been viewed as one of the major challenges for protein tertiary structure prediction. Especially, estimating the quality of a single protein model, which is important for selecting a few good models out of a large model pool consisting of mostly low-quality models, is still a largely unsolved problem. RESULTS:We introduce a novel single-model quality assessment method DeepQA based on deep belief network that utilizes a number of selected features describing the quality of a model from different perspectives, such as energy, physio-chemical characteristics, and structural information. The deep belief network is trained on several large datasets consisting of models from the Critical Assessment of Protein Structure Prediction (CASP) experiments, several publicly available datasets, and models generated by our in-house ab initio method. Our experiments demonstrate that deep belief network has better performance compared to Support Vector Machines and Neural Networks on the protein model quality assessment problem, and our method DeepQA achieves the state-of-the-art performance on CASP11 dataset. It also outperformed two well-established methods in selecting good outlier models from a large set of models of mostly low quality generated by ab initio modeling methods. CONCLUSION:DeepQA is a useful deep learning tool for protein single model quality assessment and protein structure prediction. The source code, executable, document and training/test datasets of DeepQA for Linux is freely available to non-commercial users at http://cactus.rnet.missouri.edu/DeepQA/ .

journal_name

BMC Bioinformatics

journal_title

BMC bioinformatics

authors

Cao R,Bhattacharya D,Hou J,Cheng J

doi

10.1186/s12859-016-1405-y

subject

Has Abstract

pub_date

2016-12-05 00:00:00

pages

495

issue

1

issn

1471-2105

pii

10.1186/s12859-016-1405-y

journal_volume

17

pub_type

杂志文章
  • How to decide which are the most pertinent overly-represented features during gene set enrichment analysis.

    abstract:BACKGROUND:The search for enriched features has become widely used to characterize a set of genes or proteins. A key aspect of this technique is its ability to identify correlations amongst heterogeneous data such as Gene Ontology annotations, gene expression data and genome location of genes. Despite the rapid growth ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-332

    authors: Barriot R,Sherman DJ,Dutour I

    更新日期:2007-09-11 00:00:00

  • Membrane protein orientation and refinement using a knowledge-based statistical potential.

    abstract:BACKGROUND:Recent increases in the number of deposited membrane protein crystal structures necessitate the use of automated computational tools to position them within the lipid bilayer. Identifying the correct orientation allows us to study the complex relationship between sequence, structure and the lipid environment...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-14-276

    authors: Nugent T,Jones DT

    更新日期:2013-09-18 00:00:00

  • TreeDyn: towards dynamic graphics and annotations for analyses of trees.

    abstract:BACKGROUND:Analyses of biomolecules for biodiversity, phylogeny or structure/function studies often use graphical tree representations. Many powerful tree editors are now available, but existing tree visualization tools make little use of meta-information related to the entities under study such as taxonomic descriptio...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-7-439

    authors: Chevenet F,Brun C,Bañuls AL,Jacq B,Christen R

    更新日期:2006-10-10 00:00:00

  • A CoD-based stationary control policy for intervening in large gene regulatory networks.

    abstract:BACKGROUND:One of the most important goals of the mathematical modeling of gene regulatory networks is to alter their behavior toward desirable phenotypes. Therapeutic techniques are derived for intervention in terms of stationary control policies. In large networks, it becomes computationally burdensome to derive an o...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-12-S10-S10

    authors: Ghaffari N,Ivanov I,Qian X,Dougherty ER

    更新日期:2011-10-18 00:00:00

  • Identifying overrepresented concepts in gene lists from literature: a statistical approach based on Poisson mixture model.

    abstract:BACKGROUND:Large-scale genomic studies often identify large gene lists, for example, the genes sharing the same expression patterns. The interpretation of these gene lists is generally achieved by extracting concepts overrepresented in the gene lists. This analysis often depends on manual annotation of genes based on c...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-11-272

    authors: He X,Sarma MS,Ling X,Chee B,Zhai C,Schatz B

    更新日期:2010-05-20 00:00:00

  • Deconvolution of gene expression from cell populations across the C. elegans lineage.

    abstract:BACKGROUND:Knowledge of when and in which cells each gene is expressed across multicellular organisms is critical in understanding both gene function and regulation of cell type diversity. However, methods for measuring expression typically involve a trade-off between imaging-based methods, which give the precise locat...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-14-204

    authors: Burdick JT,Murray JI

    更新日期:2013-06-22 00:00:00

  • Prediction of dinucleotide-specific RNA-binding sites in proteins.

    abstract:BACKGROUND:Regulation of gene expression, protein synthesis, replication and assembly of many viruses involve RNA-protein interactions. Although some successful computational tools have been reported to recognize RNA binding sites in proteins, the problem of specificity remains poorly investigated. After the nucleotide...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-12-S13-S5

    authors: Fernandez M,Kumagai Y,Standley DM,Sarai A,Mizuguchi K,Ahmad S

    更新日期:2011-01-01 00:00:00

  • CGHpower: exploring sample size calculations for chromosomal copy number experiments.

    abstract:BACKGROUND:Determining a suitable sample size is an important step in the planning of microarray experiments. Increasing the number of arrays gives more statistical power, but adds to the total cost of the experiment. Several approaches for sample size determination have been developed for expression array studies, but...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-11-331

    authors: Scheinin I,Ferreira JA,Knuutila S,Meijer GA,van de Wiel MA,Ylstra B

    更新日期:2010-06-17 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

  • Comparison of methods to detect copy number alterations in cancer using simulated and real genotyping data.

    abstract:BACKGROUND:The detection of genomic copy number alterations (CNA) in cancer based on SNP arrays requires methods that take into account tumour specific factors such as normal cell contamination and tumour heterogeneity. A number of tools have been recently developed but their performance needs yet to be thoroughly asse...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-13-192

    authors: Mosén-Ansorena D,Aransay AM,Rodríguez-Ezpeleta N

    更新日期:2012-08-07 00:00:00

  • Assembly-free genome comparison based on next-generation sequencing reads and variable length patterns.

    abstract:BACKGROUND:With the advent of Next-Generation Sequencing technologies (NGS), a large amount of short read data has been generated. If a reference genome is not available, the assembly of a template sequence is usually challenging because of repeats and the short length of reads. When NGS reads cannot be mapped onto a r...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-S9-S1

    authors: Comin M,Schimd M

    更新日期:2014-01-01 00:00:00

  • Predicting MoRFs in protein sequences using HMM profiles.

    abstract:BACKGROUND:Intrinsically Disordered Proteins (IDPs) lack an ordered three-dimensional structure and are enriched in various biological processes. The Molecular Recognition Features (MoRFs) are functional regions within IDPs that undergo a disorder-to-order transition on binding to a partner protein. Identifying MoRFs i...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-016-1375-0

    authors: Sharma R,Kumar S,Tsunoda T,Patil A,Sharma A

    更新日期:2016-12-22 00:00:00

  • Fast and robust group-wise eQTL mapping using sparse graphical models.

    abstract:BACKGROUND:Genome-wide expression quantitative trait loci (eQTL) studies have emerged as a powerful tool to understand the genetic basis of gene expression and complex traits. The traditional eQTL methods focus on testing the associations between individual single-nucleotide polymorphisms (SNPs) and gene expression tra...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-014-0421-z

    authors: Cheng W,Shi Y,Zhang X,Wang W

    更新日期:2015-01-16 00:00:00

  • KinMap: a web-based tool for interactive navigation through human kinome data.

    abstract:BACKGROUND:Annotations of the phylogenetic tree of the human kinome is an intuitive way to visualize compound profiling data, structural features of kinases or functional relationships within this important class of proteins. The increasing volume and complexity of kinase-related data underlines the need for a tool tha...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-016-1433-7

    authors: Eid S,Turk S,Volkamer A,Rippmann F,Fulle S

    更新日期:2017-01-05 00:00:00

  • MATLIGN: a motif clustering, comparison and matching tool.

    abstract:BACKGROUND:Sequence motifs representing transcription factor binding sites (TFBS) are commonly encoded as position frequency matrices (PFM) or degenerate consensus sequences (CS). These formats are used to represent the characterised TFBS profiles stored in transcription factor databases, as well as to represent the po...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-189

    authors: Kankainen M,Löytynoja A

    更新日期:2007-06-08 00:00:00

  • svapls: an R package to correct for hidden factors of variability in gene expression studies.

    abstract:BACKGROUND:Hidden variability is a fundamentally important issue in the context of gene expression studies. Collected tissue samples may have a wide variety of hidden effects that may alter their transcriptional landscape significantly. As a result their actual differential expression pattern can be potentially distort...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-14-236

    authors: Chakraborty S,Datta S,Datta S

    更新日期:2013-07-24 00:00:00

  • Method to represent the distribution of QTL additive and dominance effects associated with quantitative traits in computer simulation.

    abstract:BACKGROUND:Computer simulation is a resource which can be employed to identify optimal breeding strategies to effectively and efficiently achieve specific goals in developing improved cultivars. In some instances, it is crucial to assess in silico the options as well as the impact of various crossing schemes and breedi...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-016-0906-z

    authors: Sun X,Mumm RH

    更新日期:2016-02-06 00:00:00

  • A semi-parametric statistical model for integrating gene expression profiles across different platforms.

    abstract:BACKGROUND:Determining differentially expressed genes (DEGs) between biological samples is the key to understand how genotype gives rise to phenotype. RNA-seq and microarray are two main technologies for profiling gene expression levels. However, considerable discrepancy has been found between DEGs detected using the t...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-015-0847-y

    authors: Lyu Y,Li Q

    更新日期:2016-01-11 00:00:00

  • HapSolo: an optimization approach for removing secondary haplotigs during diploid genome assembly and scaffolding.

    abstract:BACKGROUND:Despite marked recent improvements in long-read sequencing technology, the assembly of diploid genomes remains a difficult task. A major obstacle is distinguishing between alternative contigs that represent highly heterozygous regions. If primary and secondary contigs are not properly identified, the primary...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-020-03939-y

    authors: Solares EA,Tao Y,Long AD,Gaut BS

    更新日期:2021-01-06 00:00:00

  • An iterative block-shifting approach to retention time alignment that preserves the shape and area of gas chromatography-mass spectrometry peaks.

    abstract:BACKGROUND:Metabolomics, petroleum and biodiesel chemistry, biomarker discovery, and other fields which rely on high-resolution profiling of complex chemical mixtures generate datasets which contain millions of detector intensity readings, each uniquely addressed along dimensions of time (e.g., retention time of chemic...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-S9-S15

    authors: Chae M,Shmookler Reis RJ,Thaden JJ

    更新日期:2008-08-12 00:00:00

  • Metabolite coupling in genome-scale metabolic networks.

    abstract:BACKGROUND:Biochemically detailed stoichiometric matrices have now been reconstructed for various bacteria, yeast, and for the human cardiac mitochondrion based on genomic and proteomic data. These networks have been manually curated based on legacy data and elementally and charge balanced. Comparative analysis of thes...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-7-111

    authors: Becker SA,Price ND,Palsson BØ

    更新日期:2006-03-06 00:00:00

  • A unifying model of genome evolution under parsimony.

    abstract:BACKGROUND:Parsimony and maximum likelihood methods of phylogenetic tree estimation and parsimony methods for genome rearrangements are central to the study of genome evolution yet to date they have largely been pursued in isolation. RESULTS:We present a data structure called a history graph that offers a practical ba...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-206

    authors: Paten B,Zerbino DR,Hickey G,Haussler D

    更新日期:2014-06-19 00:00:00

  • Principal components analysis based methodology to identify differentially expressed genes in time-course microarray data.

    abstract:BACKGROUND:Time-course microarray experiments are being increasingly used to characterize dynamic biological processes. In these experiments, the goal is to identify genes differentially expressed in time-course data, measured between different biological conditions. These differentially expressed genes can reveal the ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-267

    authors: Jonnalagadda S,Srinivasan R

    更新日期:2008-06-06 00:00:00

  • Bayesian mixture regression analysis for regulation of Pluripotency in ES cells.

    abstract:BACKGROUND:Observed levels of gene expression strongly depend on both activity of DNA binding transcription factors (TFs) and chromatin state through different histone modifications (HMs). In order to recover the functional relationship between local chromatin state, TF binding and observed levels of gene expression, r...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-019-3331-2

    authors: Aflakparast M,Geeven G,de Gunst MCM

    更新日期:2020-01-02 00:00:00

  • Extended analysis of benchmark datasets for Agilent two-color microarrays.

    abstract:BACKGROUND:As part of its broad and ambitious mission, the MicroArray Quality Control (MAQC) project reported the results of experiments using External RNA Controls (ERCs) on five microarray platforms. For most platforms, several different methods of data processing were considered. However, there was no similar consid...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-371

    authors: Kerr KF

    更新日期:2007-10-03 00:00:00

  • Toward an interactive article: integrating journals and biological databases.

    abstract:BACKGROUND:Journal articles and databases are two major modes of communication in the biological sciences, and thus integrating these critical resources is of urgent importance to increase the pace of discovery. Projects focused on bridging the gap between journals and databases have been on the rise over the last five...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-12-175

    authors: Rangarajan A,Schedl T,Yook K,Chan J,Haenel S,Otis L,Faelten S,DePellegrin-Connelly T,Isaacson R,Skrzypek MS,Marygold SJ,Stefancsik R,Cherry JM,Sternberg PW,Müller HM

    更新日期:2011-05-19 00:00:00

  • Prioritizing disease genes with an improved dual label propagation framework.

    abstract:BACKGROUND:Prioritizing disease genes is trying to identify potential disease causing genes for a given phenotype, which can be applied to reveal the inherited basis of human diseases and facilitate drug development. Our motivation is inspired by label propagation algorithm and the false positive protein-protein intera...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-018-2040-6

    authors: Zhang Y,Liu J,Liu X,Fan X,Hong Y,Wang Y,Huang Y,Xie M

    更新日期:2018-02-08 00:00:00

  • IRSS: a web-based tool for automatic layout and analysis of IRES secondary structure prediction and searching system in silico.

    abstract:BACKGROUND:Internal ribosomal entry sites (IRESs) provide alternative, cap-independent translation initiation sites in eukaryotic cells. IRES elements are important factors in viral genomes and are also useful tools for bi-cistronic expression vectors. Most existing RNA structure prediction programs are unable to deal ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-10-160

    authors: Wu TY,Hsieh CC,Hong JJ,Chen CY,Tsai YS

    更新日期:2009-05-27 00:00:00

  • Algebraic comparison of metabolic networks, phylogenetic inference, and metabolic innovation.

    abstract:BACKGROUND:Comparison of metabolic networks is typically performed based on the organisms' enzyme contents. This approach disregards functional replacements as well as orthologies that are misannotated. Direct comparison of the structure of metabolic networks can circumvent these problems. RESULTS:Metabolic networks a...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-7-67

    authors: Forst CV,Flamm C,Hofacker IL,Stadler PF

    更新日期:2006-02-14 00:00:00

  • REW-ISA: unveiling local functional blocks in epi-transcriptome profiling data via an RNA expression-weighted iterative signature algorithm.

    abstract:BACKGROUND:Recent studies have shown that N6-methyladenosine (m6A) plays a critical role in numbers of biological processes and complex human diseases. However, the regulatory mechanisms of most methylation sites remain uncharted. Thus, in-depth study of the epi-transcriptomic patterns of m6A may provide insights into ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-020-03787-w

    authors: Zhang L,Chen S,Zhu J,Meng J,Liu H

    更新日期:2020-10-09 00:00:00