LDNFSGB: prediction of long non-coding rna and disease association using network feature similarity and gradient boosting.

Abstract:

BACKGROUND:A large number of experimental studies show that the mutation and regulation of long non-coding RNAs (lncRNAs) are associated with various human diseases. Accurate prediction of lncRNA-disease associations can provide a new perspective for the diagnosis and treatment of diseases. The main function of many lncRNAs is still unclear and using traditional experiments to detect lncRNA-disease associations is time-consuming. RESULTS:In this paper, we develop a novel and effective method for the prediction of lncRNA-disease associations using network feature similarity and gradient boosting (LDNFSGB). In LDNFSGB, we first construct a comprehensive feature vector to effectively extract the global and local information of lncRNAs and diseases through considering the disease semantic similarity (DISSS), the lncRNA function similarity (LNCFS), the lncRNA Gaussian interaction profile kernel similarity (LNCGS), the disease Gaussian interaction profile kernel similarity (DISGS), and the lncRNA-disease interaction (LNCDIS). Particularly, two methods are used to calculate the DISSS (LNCFS) for considering the local and global information of disease semantics (lncRNA functions) respectively. An autoencoder is then used to reduce the dimensionality of the feature vector to obtain the optimal feature parameter from the original feature set. Furthermore, we employ the gradient boosting algorithm to obtain the lncRNA-disease association prediction. CONCLUSIONS:In this study, hold-out, leave-one-out cross-validation, and ten-fold cross-validation methods are implemented on three publicly available datasets to evaluate the performance of LDNFSGB. Extensive experiments show that LDNFSGB dramatically outperforms other state-of-the-art methods. The case studies on six diseases, including cancers and non-cancers, further demonstrate the effectiveness of our method in real-world applications.

journal_name

BMC Bioinformatics

journal_title

BMC bioinformatics

authors

Zhang Y,Ye F,Xiong D,Gao X

doi

10.1186/s12859-020-03721-0

subject

Has Abstract

pub_date

2020-09-03 00:00:00

pages

377

issue

1

issn

1471-2105

pii

10.1186/s12859-020-03721-0

journal_volume

21

pub_type

杂志文章
  • MPAgenomics: an R package for multi-patient analysis of genomic markers.

    abstract:BACKGROUND:Last generations of Single Nucleotide Polymorphism (SNP) arrays allow to study copy-number variations in addition to genotyping measures. RESULTS:MPAgenomics, standing for multi-patient analysis (MPA) of genomic markers, is an R-package devoted to: (i) efficient segmentation and (ii) selection of genomic ma...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-014-0394-y

    authors: Grimonprez Q,Celisse A,Blanck S,Cheok M,Figeac M,Marot G

    更新日期:2014-12-14 00:00:00

  • A computational diffusion model to study antibody transport within reconstructed tumor microenvironments.

    abstract:BACKGROUND:Antibodies revolutionized cancer treatment over the past decades. Despite their successfully application, there are still challenges to overcome to improve efficacy, such as the heterogeneous distribution of antibodies within tumors. Tumor microenvironment features, such as the distribution of tumor and othe...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-020-03854-2

    authors: Cartaxo AL,Almeida J,Gualda EJ,Marsal M,Loza-Alvarez P,Brito C,Isidro IA

    更新日期:2020-11-17 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

  • Detection of biological switches using the method of Gröebner bases.

    abstract:BACKGROUND:Bistability and ability to switch between two stable states is the hallmark of cellular responses. Cellular signaling pathways often contain bistable switches that regulate the transmission of the extracellular information to the nucleus where important biological functions are executed. RESULTS:In this wor...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-019-3155-0

    authors: Arkun Y

    更新日期:2019-11-28 00:00:00

  • Identifications of conserved 7-mers in 3'-UTRs and microRNAs in Drosophila.

    abstract:BACKGROUND:MicroRNAs (miRNAs) are a class of endogenous regulatory small RNAs which play an important role in posttranscriptional regulations by targeting mRNAs for cleavage or translational repression. The base-pairing between the 5'-end of miRNA and the target mRNA 3'-UTRs is essential for the miRNA:mRNA recognition....

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-432

    authors: Gu J,Fu H,Zhang X,Li Y

    更新日期:2007-11-08 00:00:00

  • Francisella tularensis novicida proteomic and transcriptomic data integration and annotation based on semantic web technologies.

    abstract:BACKGROUND:This paper summarises the lessons and experiences gained from a case study of the application of semantic web technologies to the integration of data from the bacterial species Francisella tularensis novicida (Fn). Fn data sources are disparate and heterogeneous, as multiple laboratories across the world, us...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-10-S10-S3

    authors: Anwar N,Hunt E

    更新日期:2009-10-01 00:00:00

  • TPMS: a set of utilities for querying collections of gene trees.

    abstract:BACKGROUND:The information in large collections of phylogenetic trees is useful for many comparative genomic studies. Therefore, there is a need for flexible tools that allow exploration of such collections in order to retrieve relevant data as quickly as possible. RESULTS:In this paper, we present TPMS (Tree Pattern-...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-14-109

    authors: Bigot T,Daubin V,Lassalle F,Perrière G

    更新日期:2013-03-27 00:00:00

  • A Web-based and Grid-enabled dChip version for the analysis of large sets of gene expression data.

    abstract:BACKGROUND:Microarray techniques are one of the main methods used to investigate thousands of gene expression profiles for enlightening complex biological processes responsible for serious diseases, with a great scientific impact and a wide application area. Several standalone applications had been developed in order t...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-480

    authors: Corradi L,Fato M,Porro I,Scaglione S,Torterolo L

    更新日期:2008-11-13 00:00:00

  • IILLS: predicting virus-receptor interactions based on similarity and semi-supervised learning.

    abstract:BACKGROUND:Viral infectious diseases are the serious threat for human health. The receptor-binding is the first step for the viral infection of hosts. To more effectively treat human viral infectious diseases, the hidden virus-receptor interactions must be discovered. However, current computational methods for predicti...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-019-3278-3

    authors: Yan C,Duan G,Wu FX,Wang J

    更新日期:2019-12-27 00:00:00

  • Variable cellular decision-making behavior in a constant synthetic network topology.

    abstract:BACKGROUND:Modules of interacting components arranged in specific network topologies have evolved to perform a diverse array of cellular functions. For a network with a constant topological structure, its function within a cell may still be tuned by changing the number of instances of a particular component (e.g., gene...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-019-2866-6

    authors: Shah NA,Sarkar CA

    更新日期:2019-05-14 00:00:00

  • Effective automated pipeline for 3D reconstruction of synapses based on deep learning.

    abstract:BACKGROUND:The locations and shapes of synapses are important in reconstructing connectomes and analyzing synaptic plasticity. However, current synapse detection and segmentation methods are still not adequate for accurately acquiring the synaptic connectivity, and they cannot effectively alleviate the burden of synaps...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-018-2232-0

    authors: Xiao C,Li W,Deng H,Chen X,Yang Y,Xie Q,Han H

    更新日期:2018-07-13 00:00:00

  • PIGS: improved estimates of identity-by-descent probabilities by probabilistic IBD graph sampling.

    abstract::Identifying segments in the genome of different individuals that are identical-by-descent (IBD) is a fundamental element of genetics. IBD data is used for numerous applications including demographic inference, heritability estimation, and mapping disease loci. Simultaneous detection of IBD over multiple haplotypes has...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-16-S5-S9

    authors: Park DS,Baran Y,Hormozdiari F,Eng C,Torgerson DG,Burchard EG,Zaitlen N

    更新日期:2015-01-01 00:00:00

  • Nonparametric relevance-shifted multiple testing procedures for the analysis of high-dimensional multivariate data with small sample sizes.

    abstract:BACKGROUND:In many research areas it is necessary to find differences between treatment groups with several variables. For example, studies of microarray data seek to find a significant difference in location parameters from zero or one for ratios thereof for each variable. However, in some studies a significant deviat...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-54

    authors: Frömke C,Hothorn LA,Kropf S

    更新日期:2008-01-27 00:00:00

  • MiRFinder: an improved approach and software implementation for genome-wide fast microRNA precursor scans.

    abstract:BACKGROUND:MicroRNAs (miRNAs) are recognized as one of the most important families of non-coding RNAs that serve as important sequence-specific post-transcriptional regulators of gene expression. Identification of miRNAs is an important requirement for understanding the mechanisms of post-transcriptional regulation. Hu...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-8-341

    authors: Huang TH,Fan B,Rothschild MF,Hu ZL,Li K,Zhao SH

    更新日期:2007-09-17 00:00:00

  • The tumor as an organ: comprehensive spatial and temporal modeling of the tumor and its microenvironment.

    abstract:BACKGROUND:Research related to cancer is vast, and continues in earnest in many directions. Due to the complexity of cancer, a better understanding of tumor growth dynamics can be gleaned from a dynamic computational model. We present a comprehensive, fully executable, spatial and temporal 3D computational model of the...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-016-1168-5

    authors: Bloch N,Harel D

    更新日期:2016-08-24 00:00:00

  • A weighted string kernel for protein fold recognition.

    abstract:BACKGROUND:Alignment-free methods for comparing protein sequences have proved to be viable alternatives to approaches that first rely on an alignment of the sequences to be compared. Much work however need to be done before those methods provide reliable fold recognition for proteins whose sequences share little simila...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-017-1795-5

    authors: Nojoomi S,Koehl P

    更新日期:2017-08-25 00:00:00

  • Accurate prediction of protein-lncRNA interactions by diffusion and HeteSim features across heterogeneous network.

    abstract:BACKGROUND:Identifying the interactions between proteins and long non-coding RNAs (lncRNAs) is of great importance to decipher the functional mechanisms of lncRNAs. However, current experimental techniques for detection of lncRNA-protein interactions are limited and inefficient. Many methods have been proposed to predi...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-018-2390-0

    authors: Deng L,Wang J,Xiao Y,Wang Z,Liu H

    更新日期:2018-10-11 00:00:00

  • R2R--software to speed the depiction of aesthetic consensus RNA secondary structures.

    abstract:BACKGROUND:With continuing identification of novel structured noncoding RNAs, there is an increasing need to create schematic diagrams showing the consensus features of these molecules. RNA structural diagrams are typically made either with general-purpose drawing programs like Adobe Illustrator, or with automated or i...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-12-3

    authors: Weinberg Z,Breaker RR

    更新日期:2011-01-04 00:00:00

  • Efficient computation of absent words in genomic sequences.

    abstract:BACKGROUND:Analysis of sequence composition is a routine task in genome research. Organisms are characterized by their base composition, dinucleotide relative abundance, codon usage, and so on. Unique subsequences are markers of special interest in genome comparison, expression profiling, and genetic engineering. Relat...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-9-167

    authors: Herold J,Kurtz S,Giegerich R

    更新日期:2008-03-26 00:00:00

  • Ontological representation, integration, and analysis of LINCS cell line cells and their cellular responses.

    abstract:BACKGROUND:Aiming to understand cellular responses to different perturbations, the NIH Common Fund Library of Integrated Network-based Cellular Signatures (LINCS) program involves many institutes and laboratories working on over a thousand cell lines. The community-based Cell Line Ontology (CLO) is selected as the defa...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-017-1981-5

    authors: Ong E,Xie J,Ni Z,Liu Q,Sarntivijai S,Lin Y,Cooper D,Terryn R,Stathias V,Chung C,Schürer S,He Y

    更新日期:2017-12-21 00:00:00

  • PanACEA: a bioinformatics tool for the exploration and visualization of bacterial pan-chromosomes.

    abstract:BACKGROUND:Bacterial pan-genomes, comprised of conserved and variable genes across multiple sequenced bacterial genomes, allow for identification of genomic regions that are phylogenetically discriminating or functionally important. Pan-genomes consist of large amounts of data, which can restrict researchers ability to...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-018-2250-y

    authors: Clarke TH,Brinkac LM,Inman JM,Sutton G,Fouts DE

    更新日期:2018-06-27 00:00:00

  • Homology modeling, molecular docking, and molecular dynamics simulations elucidated α-fetoprotein binding modes.

    abstract:BACKGROUND:An important mechanism of endocrine activity is chemicals entering target cells via transport proteins and then interacting with hormone receptors such as the estrogen receptor (ER). α-Fetoprotein (AFP) is a major transport protein in rodent serum that can bind and sequester estrogens, thus preventing entry ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-14-S14-S6

    authors: Shen J,Zhang W,Fang H,Perkins R,Tong W,Hong H

    更新日期:2013-01-01 00:00:00

  • Shared data science infrastructure for genomics data.

    abstract:BACKGROUND:Creating a scalable computational infrastructure to analyze the wealth of information contained in data repositories is difficult due to significant barriers in organizing, extracting and analyzing relevant data. Shared data science infrastructures like Boag is needed to efficiently process and parse data co...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-019-2967-2

    authors: Bagheri H,Muppirala U,Masonbrink RE,Severin AJ,Rajan H

    更新日期:2019-08-22 00:00:00

  • A theorem proving approach for automatically synthesizing visualizations of flow cytometry data.

    abstract:BACKGROUND:Polychromatic flow cytometry is a popular technique that has wide usage in the medical sciences, especially for studying phenotypic properties of cells. The high-dimensionality of data generated by flow cytometry usually makes it difficult to visualize. The naive solution of simply plotting two-dimensional g...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-017-1662-4

    authors: Raj S,Hussain F,Husein Z,Torosdagli N,Turgut D,Deo N,Pattanaik S,Chang CJ,Jha SK

    更新日期:2017-06-07 00:00:00

  • Menoci: lightweight extensible web portal enhancing data management for biomedical research projects.

    abstract:BACKGROUND:Biomedical research projects deal with data management requirements from multiple sources like funding agencies' guidelines, publisher policies, discipline best practices, and their own users' needs. We describe functional and quality requirements based on many years of experience implementing data managemen...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-020-03928-1

    authors: Suhr M,Lehmann C,Bauer CR,Bender T,Knopp C,Freckmann L,Öst Hansen B,Henke C,Aschenbrandt G,Kühlborn LK,Rheinländer S,Weber L,Marzec B,Hellkamp M,Wieder P,Sax U,Kusch H,Nussbeck SY

    更新日期:2020-12-17 00:00:00

  • Texture based skin lesion abruptness quantification to detect malignancy.

    abstract:BACKGROUND:Abruptness of pigment patterns at the periphery of a skin lesion is one of the most important dermoscopic features for detection of malignancy. In current clinical setting, abrupt cutoff of a skin lesion determined by an examination of a dermatologist. This process is subjective, nonquantitative, and error-p...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-017-1892-5

    authors: Erol R,Bayraktar M,Kockara S,Kaya S,Halic T

    更新日期:2017-12-28 00:00:00

  • Detecting intergene correlation changes in microarray analysis: a new approach to gene selection.

    abstract:BACKGROUND:Microarray technology is commonly used as a simple screening tool with a focus on selecting genes that exhibit extremely large differential expressions between different phenotypes. It lacks the ability to select genes that change their relationships with other genes in different biological conditions (diffe...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-10-20

    authors: Hu R,Qiu X,Glazko G,Klebanov L,Yakovlev A

    更新日期:2009-01-15 00:00:00

  • Big data analysis for evaluating bioinvasion risk.

    abstract:BACKGROUND:Global maritime trade plays an important role in the modern transportation industry. It brings significant economic profit along with bioinvasion risk. Species translocate and establish in a non-native area through ballast water and biofouling. Aiming at aquatic bioinvasion issue, people proposed various sug...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-018-2272-5

    authors: Wang S,Wang C,Wang S,Ma L

    更新日期:2018-08-13 00:00:00

  • ATMAD: robust image analysis for Automatic Tissue MicroArray De-arraying.

    abstract:BACKGROUND:Over the last two decades, an innovative technology called Tissue Microarray (TMA), which combines multi-tissue and DNA microarray concepts, has been widely used in the field of histology. It consists of a collection of several (up to 1000 or more) tissue samples that are assembled onto a single support - ty...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/s12859-018-2111-8

    authors: Nguyen HN,Paveau V,Cauchois C,Kervrann C

    更新日期:2018-04-19 00:00:00

  • Knowledge discovery of drug data on the example of adverse reaction prediction.

    abstract:BACKGROUND:Antibiotics are the widely prescribed drugs for children and most likely to be related with adverse reactions. Record on adverse reactions and allergies from antibiotics considerably affect the prescription choices. We consider this a biomedical decision-making problem and explore hidden knowledge in survey ...

    journal_title:BMC bioinformatics

    pub_type: 杂志文章

    doi:10.1186/1471-2105-15-S6-S7

    authors: Yildirim P,Majnarić L,Ekmekci O,Holzinger A

    更新日期:2014-01-01 00:00:00