基于Cygwin实现生物信息学软件从Unix/Linux向Windows移植

Cygwin可在Windows环境下提供对Unix/Linux环境的模拟与支持,具有较为完善的Unix/Linux工具包和编程环境。利用Cygwin对常用的生物信息学数据分析软件如Sim4、FASTA、Phred/Phrap/RepeatMasker、EMBOSS、HMMER和ClustalW等进行重新编译,发现通过该方式能够获得可在Windows环境下运行的可执行代码,为利用Windows环境优势的同时进行跨平台生物信息学数据分析平台的开发提供重要参考价值。     

Building chromosome-wide LD maps

SUMMARY: BMapBuilder builds maps of pairwise linkage disequilibrium (LD) in either two or three dimensions. The optimized resolution allows for graphical display of LD for single nucleotide polymorphisms (SNPs) in a whole chromosome. AVAILABILITY: The program is coded in Java, which runs on all relevant operating systems, including Windows, Mac and Unix/Linux, and is available from http://bios.ugr.es/BMapBuilder.     

CAPS: coevolution analysis using protein sequences

Coevolution Analysis using Protein Sequences (CAPS) is a PERL based software that identifies co-evolution between amino acid sites. Blosum-corrected amino acid distances are used to identify amino acid co-variation. The phylogenetic sequence relationships are used to remove the phylogenetic and stochastic dependencies between sites. The 3D protein structure is used to identify the nature of the dependencies between co-evolving amino acid sites. Friendly interpretable output files are generated. AVAILABILITY: CAPS version 1 is available at http://bioinf.gen.tcd.ie/~faresm/software/caps/. Distribution versions for Linux/Unix, Mac OS X and Windows operating systems are available, including manual and example files.     

基于核酸测序流程的信息管理系统

通过分析研究核酸测序实验室的工作流程和管理体系,采用Java技术开发了一套基于实验流程管理的测序实验室的信息管理系统。系统为B／S体系,采用轻量级J2EE系统的分层架构,层次清晰、安全可靠,易于维护和扩展。系统实现了对实验流程的全方位跟踪管理,实现了对数据的采集、存储、整合、查询、导出等功能。系统的实施应用极大地提高了实验室的工作效率和管理水平。同时可为今后分子生物学、医学及其他学科的实验室信息管理系统的建设提供参考。     

QTLNetwork: mapping and visualizing genetic architecture of complex traits in experimental populations

SUMMARY: QTLNetwork is a software package for mapping and visualizing the genetic architecture underlying complex traits for experimental populations derived from a cross between two inbred lines. It can simultaneously map quantitative trait loci (QTL) with individual effects, epistasis and QTL-environment interaction. Currently, it is able to handle data from F(2), backcross, recombinant inbred lines and double-haploid populations, as well as populations from specific mating designs (immortalized F(2) and BC(n)F(n) populations). The Windows version of QTLNetwork was developed with a graphical user interface. Alternatively, the command-line versions have the facility to be run in other prevalent operating systems, such as Linux, Unix and MacOS. AVAILABILITY: http://ibi.zju.edu.cn/software/qtlnetwork.     

GeneSyn: a tool for detecting conserved gene order across genomes

SUMMARY: GeneSyn is a software tool that allows automatic detection of conserved gene order from annotated genomes. AVAILABILITY: Available free of charge for Unix/Linux/Cygwin platforms at ftp://159.149.110.11/pub/GeneSyn_1.0/ SUPPLEMENTARY INFORMATION: ftp://159.149.110.11/pub/GeneSyn_1.0/     

MorphoJ: an integrated software package for geometric morphometrics

Increasingly, data on shape are analysed in combination with molecular genetic or ecological information, so that tools for geometric morphometric analysis are required. Morphometric studies most often use the arrangements of morphological landmarks as the data source and extract shape information from them by Procrustes superimposition. The MorphoJ software combines this approach with a wide range of methods for shape analysis in different biological contexts. The program offers an integrated and user-friendly environment for standard multivariate analyses such as principal components, discriminant analysis and multivariate regression as well as specialized applications including phylogenetics, quantitative genetics and analyses of modularity in shape data. MorphoJ is written in Java and versions for the Windows, Macintosh and Unix/Linux platforms are freely available from http://www.flywings.org.uk/MorphoJ_page.htm.     

ACGT-a comparative genomics tool

SUMMARY: ACGT (a comparative genomics tool) is a genomic DNA sequence comparison viewer and analyzer. It can read a pair of DNA sequences in GenBank, Embl or Fasta formats, with or without a comparison file, and provide users with many options to view and analyze the similarities between the input sequences. It is written in Java and can be run on Unix, Linux and Windows platforms. AVAILABILITY: The ACGT program is freely available with documentation and examples at website: http://db.systemsbiology.net/projects/local/mhc/acgt/     

Clann: investigating phylogenetic information through supertree analyses

SUMMARY: Clann has been developed in order to provide methods of investigating phylogenetic information through the application of supertrees. AVAILABILITY: Clann has been precompiled for Linux, Apple Macintosh and Windows operating systems and is available from http://bioinf.may.ie/software/clann. Source code is available on request from the authors. SUPPLEMENTARY INFORMATION: Clann has been written in the C programming language. Source code is available on request.     

Genview and Gencode : a pair of programs to test theories of genetic code evolution

GENVIEW: and GENCODE: are tools for testing the adaptive nature of a genetic code under different assumptions about patterns of genetic error and the nature of amino acid similarity. GENVIEW: provides a user friendly, point-and-click interface by which a user may reproduce and extend analysis of the adaptive properties of the standard genetic code or any of its secondary derivatives. GENVIEW: is a graphical user interface (GUI) program which runs on Linux, Unix and Microsoft Windows platforms and is based on the GTKf + toolkit. GENVIEW: outputs ASCII configuration files which are interpreted by GENCODE: to perform an analysis. GENCODE: is available for the same platforms as GENVIEW.     

IPeak: An open source tool to combine results from multiple MS/MS search engines

Liquid chromatography coupled tandem mass spectrometry (LC‐MS/MS) is an important technique for detecting peptides in proteomics studies. Here, we present an open source software tool, termed IPeak, a peptide identification pipeline that is designed to combine the Percolator post‐processing algorithm and multi‐search strategy to enhance the sensitivity of peptide identifications without compromising accuracy. IPeak provides a graphical user interface (GUI) as well as a command‐line interface, which is implemented in JAVA and can work on all three major operating system platforms: Windows, Linux/Unix and OS X. IPeak has been designed to work with the mzIdentML standard from the Proteomics Standards Initiative (PSI) as an input and output, and also been fully integrated into the associated mzidLibrary project, providing access to the overall pipeline, as well as modules for calling Percolator on individual search engine result files. The integration thus enables IPeak (and Percolator) to be used in conjunction with any software packages implementing the mzIdentML data standard. IPeak is freely available and can be downloaded under an Apache 2.0 license at https://code.google.com/p/mzidentml‐lib/ .     

famoz: a software for parentage analysis using dominant,codominant and uniparentally inherited markers

famoz (an acronym for father/mother) is a software useful in reconstructing parentage for dominant, codominant and uniparentally inherited markers. It is written in C and TclTk languages and is available for Unix, Linux and Windows systems at http://www.pierroton.inra.fr/genetics/labo/Software/Famoz/index.html . Parameters and assumptions used in the calculations are few and simple. Exclusion and identity probabilities, log‐likelihoods of any genetic relationship, potential father and parent or parent pair, half‐ and full‐sibship are calculated based on real or simulated data. Error rates for genotypic mistyping can be introduced. Simulations can be done to build statistical tests for parentage assignment.     

Clustal W and Clustal X version 2.0

SUMMARY: The Clustal W and Clustal X multiple sequence alignment programs have been completely rewritten in C++. This will facilitate the further development of the alignment algorithms in the future and has allowed proper porting of the programs to the latest versions of Linux, Macintosh and Windows operating systems. AVAILABILITY: The programs can be run on-line from the EBI web server: http://www.ebi.ac.uk/tools/clustalw2. The source code and executables for Windows, Linux and Macintosh computers are available from the EBI ftp site ftp://ftp.ebi.ac.uk/pub/software/clustalw2/     

burial (version 1.0): a method for testing genetic similarity within small groups of individuals using fragmentary data sets

Biologists are frequently facing the problem of dealing with data sets with a small amount of data and a high proportion of missing information. We were particularly interested in analysing fragmentary data sets generated by the application of molecular methods in palaeoanthropology in order to determine whether individuals are genetically related. In this note, we announce the release of the software burial (version 1.0) to test the null hypothesis that the observed grouping of individuals at a particular burial site reflects random placement of genotypes. The proposed test, however, can also be applied to data sets whose objects can be grouped according to nongenetic criteria such as the style of clothing, the kind of burial gifts or cultural artefacts. The C + + source code and binary executables for Windows and Linux are available for download at: http://www.uni‐tuebingen.de/uni/bcm/BURIAL/index.html .     

An efficient Monte Carlo method for estimating Ne from temporally spaced samples using a coalescent-based likelihood

This article presents an efficient importance-sampling method for computing the likelihood of the effective size of a population under the coalescent model of Berthier et al. Previous computational approaches, using Markov chain Monte Carlo, required many minutes to several hours to analyze small data sets. The approach presented here is orders of magnitude faster and can provide an approximation to the likelihood curve, even for large data sets, in a matter of seconds. Additionally, confidence intervals on the estimated likelihood curve provide a useful estimate of the Monte Carlo error. Simulations show the importance sampling to be stable across a wide range of scenarios and show that the N(e) estimator itself performs well. Further simulations show that the 95% confidence intervals around the N(e) estimate are accurate. User-friendly software implementing the algorithm for Mac, Windows, and Unix/Linux is available for download. Applications of this computational framework to other problems are discussed.     

Windows下16S rRNA基因扩增子测序数据分析的简易流程

微生物组数据分析需要掌握Linux系统操作,这对缺乏计算机知识的生物研究人员是一个很大的障碍。为此我们设计了一套在Windows的Linux子系统(WSL)下分析16S rRNA基因扩增子高通量测序数据的简易流程。本流程整合常用的开源软件VSEARCH与QIIME等,能对16S rRNA测序数据进行质量控制、OTU聚类、多样性分析及结果可视化呈现。以唾液微生物组分析为例,详细介绍从原始数据到多样性统计分析过程的参数和命令,及结果解读。教学实践证明,此流程易于学习,并有助于掌握微生物组的基本概念与方法。利用Windows系统最新的WSL功能,本流程方便Windows用户使用大量在Linux上运行的生物信息工具,有助于促进微生物组研究的发展。流程的安装程序与测序数据可从网址(http://www. ligene. cn/win16s/)免费下载使用。     

An efficient approach to the deployment of complex open source information systems

Complex open source information systems are usually implemented as component-based software to inherit the available functionality of existing software packages developed by third parties. Consequently, the deployment of these systems not only requires the installation of operating system, application framework and the configuration of services but also needs to resolve the dependencies among components. The problem becomes more challenging when the application must be installed and used on different platforms such as Linux and Windows. To address this, an efficient approach using the virtualization technology is suggested and discussed in this paper. The approach has been applied in our project to deploy a web-based integrated information system in molecular genetics labs. It is a low-cost solution to benefit both software developers and end-users.     

Voroprot: an interactive tool for the analysis and visualization of complex geometric features of protein structure

We present Voroprot, an interactive cross-platform software tool that provides a unique set of capabilities for exploring geometric features of protein structure. Voroprot allows the construction and visualization of the Apollonius diagram (also known as the additively weighted Voronoi diagram), the Apollonius graph, protein alpha shapes, interatomic contact surfaces, solvent accessible surfaces, pockets and cavities inside protein structure. AVAILABILITY: Voroprot is available for Windows, Linux and Mac OS X operating systems and can be downloaded from http://www.ibt.lt/bioinformatics/voroprot/.