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Asterias: A Parallelized Web-based Suite for the Analysis of Expression and aCGH Data

机译:Asterias:基于并行Web的套件用于分析表达和aCGH数据

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摘要

The analysis of expression and CGH arrays plays a central role in the study of complex diseases, especially cancer, including finding markers for early diagnosis and prognosis, choosing an optimal therapy, or increasing our understanding of cancer development and metastasis. Asterias () is an integrated collection of freely-accessible web tools for the analysis of gene expression and aCGH data. Most of the tools use parallel computing (via MPI) and run on a server with 60 CPUs for computation; compared to a desktop or server-based but not parallelized application, parallelization provides speed ups of factors up to 50. Most of our applications allow the user to obtain additional information for user-selected genes (chromosomal location, PubMed ids, Gene Ontology terms, etc.) by using clickable links in tables and/or figures. Our tools include: normalization of expression and aCGH data (DNMAD); converting between different types of gene/clone and protein identifiers (IDconverter/IDClight); filtering and imputation (preP); finding differentially expressed genes related to patient class and survival data (Pomelo II); searching for models of class prediction (Tnasas); using random forests to search for minimal models for class prediction or for large subsets of genes with predictive capacity (GeneSrF); searching for molecular signatures and predictive genes with survival data (SignS); detecting regions of genomic DNA gain or loss (ADaCGH). The capability to send results between different applications, access to additional functional information, and parallelized computation make our suite unique and exploit features only available to web-based applications.
机译:表达和CGH阵列的分析在复杂疾病(尤其是癌症)的研究中起着核心作用,包括寻找早期诊断和预后的标志物,选择最佳疗法或加深我们对癌症发展和转移的了解。 Asterias()是可免费访问的网络工具的集成集合,用于分析基因表达和aCGH数据。大多数工具使用并行计算(通过MPI),并在具有60个CPU的服务器上运行;与基于桌面或服务器但未并行化的应用程序相比,并行化可将速度提高50倍。我们的大多数应用程序都允许用户获得用户选择的基因的其他信息(染色体位置,PubMed ID,基因本体论术语,等等),方法是使用表格和/或图表中的可点击链接。我们的工具包括:表达和aCGH数据标准化(DNMAD);在不同类型的基因/克隆和蛋白质标识符之间进行转换(IDconverter / IDClight);过滤和插补(preP);寻找与患者分类和生存数据相关的差异表达基因(Pomelo II);搜索班级预测模型(Tnasas);使用随机森林搜索用于类别预测的最小模型或具有预测能力的基因大子集(GeneSrF);搜索具有生存数据(SignS)的分子标记和预测基因;检测基因组DNA得失(ADaCGH)区域。在不同应用程序之间发送结果,访问其他功能信息以及并行化计算的功能使我们的套件具有独特性,并且仅针对基于Web的应用程序提供利用功能。

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