4.7 Article

The Sleipnir library for computational functional genomics

期刊

BIOINFORMATICS
卷 24, 期 13, 页码 1559-1561

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btn237

关键词

-

资金

  1. NHGRI NIH HHS [T32 HG003284] Funding Source: Medline
  2. NIGMS NIH HHS [R01 GM071966, P50 GM071508] Funding Source: Medline

向作者/读者索取更多资源

Motivation: Biological data generation has accelerated to the point where hundreds or thousands of whole-genome datasets of various types are available for many model organisms. This wealth of data can lead to valuable biological insights when analyzed in an integrated manner, but the computational challenge of managing such large data collections is substantial. In order to mine these data efficiently, it is necessary to develop methods that use storage, memory and processing resources carefully. Results: The Sleipnir C library implements a variety of machine learning and data manipulation algorithms with a focus on heterogeneous data integration and efficiency for very large biological data collections. Sleipnir allows microarray processing, functional ontology mining, clustering, Bayesian learning and inference and support vector machine tasks to be performed for heterogeneous data on scales not previously practical. In addition to the library, which can easily be integrated into new computational systems, prebuilt tools are provided to perform a variety of common tasks. Many tools are multithreaded for parallelization in desktop or high-throughput computing environments, and most tasks can be performed in minutes for hundreds of datasets using a standard personal computer.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据