ISRN bioinformatics最新文献_第2页

Transcriptome Analysis of Spermophilus lateralis and Spermophilus tridecemlineatus Liver Does Not Suggest the Presence of Spermophilus-Liver-Specific Reference Genes. 侧边嗜精鱼和三头嗜精鱼肝脏的转录组分析不表明存在嗜精鱼肝脏特异性参考基因。

ISRN bioinformatics Pub Date : 2013-05-25 eCollection Date: 2013-01-01 DOI: 10.1155/2013/361321

Bryan M H Keng, Oliver Y W Chan, Sean S J Heng, Maurice H T Ling

{"title":"Transcriptome Analysis of Spermophilus lateralis and Spermophilus tridecemlineatus Liver Does Not Suggest the Presence of Spermophilus-Liver-Specific Reference Genes.","authors":"Bryan M H Keng, Oliver Y W Chan, Sean S J Heng, Maurice H T Ling","doi":"10.1155/2013/361321","DOIUrl":"https://doi.org/10.1155/2013/361321","url":null,"abstract":"The expressions of reference genes used in gene expression studies are assumed to be stable under most circumstances. However, studies had demonstrated that genes assumed to be stably expressed in a species are not necessarily stably expressed in other organisms. This study aims to evaluate the likelihood of genus-specific reference genes for liver using comparable microarray datasets from Spermophilus lateralis and Spermophilus tridecemlineatus. The coefficient of variance (CV) of each probe was calculated and there were 178 probes common between the lowest 10% CV of both datasets (n = 1258). All 3 lists were analysed by NormFinder. Our results suggest that the most invariant probe for S. tridecemlineatus was 02n12, while that for S. lateralis was 24j21. However, our results showed that Probes 02n12 and 24j21 are ranked 8644 and 926 in terms of invariancy for S. lateralis and S. tridecemlineatus respectively. This suggests the lack of common liver-specific reference probes for both S. lateralis and S. tridecemlineatus. Given that S. lateralis and S. tridecemlineatus are closely related species and the datasets are comparable, our results do not support the presence of genus-specific reference genes. ","PeriodicalId":90877,"journal":{"name":"ISRN bioinformatics","volume":"2013 ","pages":"361321"},"PeriodicalIF":0.0,"publicationDate":"2013-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/361321","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33272170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 6

IsoPlotter(+): A Tool for Studying the Compositional Architecture of Genomes. IsoPlotter(+):一个研究基因组组成结构的工具。

ISRN bioinformatics Pub Date : 2013-04-18 eCollection Date: 2013-01-01 DOI: 10.1155/2013/725434

Eran Elhaik, Dan Graur

{"title":"IsoPlotter(+): A Tool for Studying the Compositional Architecture of Genomes.","authors":"Eran Elhaik, Dan Graur","doi":"10.1155/2013/725434","DOIUrl":"https://doi.org/10.1155/2013/725434","url":null,"abstract":"Eukaryotic genomes, particularly animal genomes, have a complex, nonuniform, and nonrandom internal compositional organization. The compositional organization of animal genomes can be described as a mosaic of discrete genomic regions, called \"compositional domains,\" each with a distinct GC content that significantly differs from those of its upstream and downstream neighboring domains. A typical animal genome consists of a mixture of compositionally homogeneous and nonhomogeneous domains of varying lengths and nucleotide compositions that are interspersed with one another. We have devised IsoPlotter, an unbiased segmentation algorithm for inferring the compositional organization of genomes. IsoPlotter has become an indispensable tool for describing genomic composition and has been used in the analysis of more than a dozen genomes. Applications include describing new genomes, correlating domain composition with gene composition and their density, studying the evolution of genomes, testing phylogenomic hypotheses, and detect regions of potential interbreeding between human and extinct hominines. To extend the use of IsoPlotter, we designed a completely automated pipeline, called IsoPlotter(+) to carry out all segmentation analyses, including graphical display, and built a repository for compositional domain maps of all fully sequenced vertebrate and invertebrate genomes. The IsoPlotter(+) pipeline and repository offer a comprehensive solution to the study of genome compositional architecture. Here, we demonstrate IsoPlotter(+) by applying it to human and insect genomes. The computational tools and data repository are available online. ","PeriodicalId":90877,"journal":{"name":"ISRN bioinformatics","volume":"2013 ","pages":"725434"},"PeriodicalIF":0.0,"publicationDate":"2013-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393066/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33272129","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 6

HMEC: A Heuristic Algorithm for Individual Haplotyping with Minimum Error Correction. HMEC:个体单倍型最小纠错的启发式算法。

ISRN bioinformatics Pub Date : 2013-01-28 eCollection Date: 2013-01-01 DOI: 10.1155/2013/291741

Md Shamsuzzoha Bayzid, Md Maksudul Alam, Abdullah Mueen, Md Saidur Rahman

引用次数: 8

CallSim: Evaluation of Base Calls Using Sequencing Simulation. CallSim:基于序列模拟的基调用评估。

ISRN bioinformatics Pub Date : 2012-12-12 eCollection Date: 2012-01-01 DOI: 10.5402/2012/371718

Jarrett D Morrow, Brandon W Higgs

{"title":"CallSim: Evaluation of Base Calls Using Sequencing Simulation.","authors":"Jarrett D Morrow, Brandon W Higgs","doi":"10.5402/2012/371718","DOIUrl":"https://doi.org/10.5402/2012/371718","url":null,"abstract":"Accurate base calls generated from sequencing data are required for downstream biological interpretation, particularly in the case of rare variants. CallSim is a software application that provides evidence for the validity of base calls believed to be sequencing errors and it is applicable to Ion Torrent and 454 data. The algorithm processes a single read using a Monte Carlo approach to sequencing simulation, not dependent upon information from any other read in the data set. Three examples from general read correction, as well as from error-or-variant classification, demonstrate its effectiveness for a robust low-volume read processing base corrector. Specifically, correction of errors in Ion Torrent reads from a study involving mutations in multidrug resistant Staphylococcus aureus illustrates an ability to classify an erroneous homopolymer call. In addition, support for a rare variant in 454 data for a mixed viral population demonstrates \"base rescue\" capabilities. CallSim provides evidence regarding the validity of base calls in sequences produced by 454 or Ion Torrent systems and is intended for hands-on downstream processing analysis. These downstream efforts, although time consuming, are necessary steps for accurate identification of rare variants. ","PeriodicalId":90877,"journal":{"name":"ISRN bioinformatics","volume":"2012 ","pages":"371718"},"PeriodicalIF":0.0,"publicationDate":"2012-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393072/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33272805","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1

Electric LAMP: Virtual Loop-Mediated Isothermal AMPlification. 电灯:虚拟环路介导的等温放大。

ISRN bioinformatics Pub Date : 2012-11-21 eCollection Date: 2012-01-01 DOI: 10.5402/2012/696758

Nelson R Salinas, Damon P Little

引用次数: 15

Classifying multigraph models of secondary RNA structure using graph-theoretic descriptors. 利用图论描述符对二级RNA结构的多图模型进行分类。

ISRN bioinformatics Pub Date : 2012-11-11 eCollection Date: 2012-01-01 DOI: 10.5402/2012/157135

Debra Knisley, Jeff Knisley, Chelsea Ross, Alissa Rockney

{"title":"Classifying multigraph models of secondary RNA structure using graph-theoretic descriptors.","authors":"Debra Knisley, Jeff Knisley, Chelsea Ross, Alissa Rockney","doi":"10.5402/2012/157135","DOIUrl":"https://doi.org/10.5402/2012/157135","url":null,"abstract":"The prediction of secondary RNA folds from primary sequences continues to be an important area of research given the significance of RNA molecules in biological processes such as gene regulation. To facilitate this effort, graph models of secondary structure have been developed to quantify and thereby characterize the topological properties of the secondary folds. In this work we utilize a multigraph representation of a secondary RNA structure to examine the ability of the existing graph-theoretic descriptors to classify all possible topologies as either RNA-like or not RNA-like. We use more than one hundred descriptors and several different machine learning approaches, including nearest neighbor algorithms, one-class classifiers, and several clustering techniques. We predict that many more topologies will be identified as those representing RNA secondary structures than currently predicted in the RAG (RNA-As-Graphs) database. The results also suggest which descriptors and which algorithms are more informative in classifying and exploring secondary RNA structures. ","PeriodicalId":90877,"journal":{"name":"ISRN bioinformatics","volume":"2012 ","pages":"157135"},"PeriodicalIF":0.0,"publicationDate":"2012-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5402/2012/157135","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33173868","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 9

A robust topology-based algorithm for gene expression profiling. 基于拓扑的基因表达谱鲁棒算法。

ISRN bioinformatics Pub Date : 2012-11-11 eCollection Date: 2012-01-01 DOI: 10.5402/2012/381023

Lars Seemann, Jason Shulman, Gemunu H Gunaratne

{"title":"A robust topology-based algorithm for gene expression profiling.","authors":"Lars Seemann, Jason Shulman, Gemunu H Gunaratne","doi":"10.5402/2012/381023","DOIUrl":"https://doi.org/10.5402/2012/381023","url":null,"abstract":"Early and accurate diagnoses of cancer can significantly improve the design of personalized therapy and enhance the success of therapeutic interventions. Histopathological approaches, which rely on microscopic examinations of malignant tissue, are not conducive to timely diagnoses. High throughput genomics offers a possible new classification of cancer subtypes. Unfortunately, most clustering algorithms have not been proven sufficiently robust. We propose a novel approach that relies on the use of statistical invariants and persistent homology, one of the most exciting recent developments in topology. It identifies a sufficient but compact set of genes for the analysis as well as a core group of tightly correlated patient samples for each subtype. Partitioning occurs hierarchically and allows for the identification of genetically similar subtypes. We analyzed the gene expression profiles of 202 tumors of the brain cancer glioblastoma multiforme (GBM) given at the Cancer Genome Atlas (TCGA) site. We identify core patient groups associated with the classical, mesenchymal, and proneural subtypes of GBM. In our analysis, the neural subtype consists of several small groups rather than a single component. A subtype prediction model is introduced which partitions tumors in a manner consistent with clustering algorithms but requires the genetic signature of only 59 genes. ","PeriodicalId":90877,"journal":{"name":"ISRN bioinformatics","volume":"2012 ","pages":"381023"},"PeriodicalIF":0.0,"publicationDate":"2012-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393071/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33173870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 10

Hybrid-controlled neurofuzzy networks analysis resulting in genetic regulatory networks reconstruction. 通过混合控制神经模糊网络分析，重建基因调控网络。

ISRN bioinformatics Pub Date : 2012-11-01 eCollection Date: 2012-01-01 DOI: 10.5402/2012/419419

Roozbeh Manshaei, Pooya Sobhe Bidari, Mahdi Aliyari Shoorehdeli, Amir Feizi, Tahmineh Lohrasebi, Mohammad Ali Malboobi, Matthew Kyan, Javad Alirezaie

{"title":"Hybrid-controlled neurofuzzy networks analysis resulting in genetic regulatory networks reconstruction.","authors":"Roozbeh Manshaei, Pooya Sobhe Bidari, Mahdi Aliyari Shoorehdeli, Amir Feizi, Tahmineh Lohrasebi, Mohammad Ali Malboobi, Matthew Kyan, Javad Alirezaie","doi":"10.5402/2012/419419","DOIUrl":"10.5402/2012/419419","url":null,"abstract":"Reverse engineering of gene regulatory networks (GRNs) is the process of estimating genetic interactions of a cellular system from gene expression data. In this paper, we propose a novel hybrid systematic algorithm based on neurofuzzy network for reconstructing GRNs from observational gene expression data when only a medium-small number of measurements are available. The approach uses fuzzy logic to transform gene expression values into qualitative descriptors that can be evaluated by using a set of defined rules. The algorithm uses neurofuzzy network to model genes effects on other genes followed by four stages of decision making to extract gene interactions. One of the main features of the proposed algorithm is that an optimal number of fuzzy rules can be easily and rapidly extracted without overparameterizing. Data analysis and simulation are conducted on microarray expression profiles of S. cerevisiae cell cycle and demonstrate that the proposed algorithm not only selects the patterns of the time series gene expression data accurately, but also provides models with better reconstruction accuracy when compared with four published algorithms: DBNs, VBEM, time delay ARACNE, and PF subjected to LASSO. The accuracy of the proposed approach is evaluated in terms of recall and F-score for the network reconstruction task. ","PeriodicalId":90877,"journal":{"name":"ISRN bioinformatics","volume":"2012 ","pages":"419419"},"PeriodicalIF":0.0,"publicationDate":"2012-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393070/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"33173871","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Dynamic clustering of gene expression. 基因表达的动态聚类

ISRN bioinformatics Pub Date : 2012-10-16 eCollection Date: 2012-01-01 DOI: 10.5402/2012/537217

Lingling An, R W Doerge

引用次数: 0

Differential Expression Analysis for RNA-Seq Data. RNA-Seq数据的差异表达分析

ISRN bioinformatics Pub Date : 2012-09-20 eCollection Date: 2012-01-01 DOI: 10.5402/2012/817508

Rashi Gupta, Isha Dewan, Richa Bharti, Alok Bhattacharya

引用次数: 33