Biosciences and Informatics, Keio University, 3-14-1 Hiyoshi, Yokohama, Japan.
Bioinformatics. 2012 May 1;28(9):1276-7. doi: 10.1093/bioinformatics/bts122. Epub 2012 Mar 13.
Existing SAM visualization tools like 'samtools tview' (Li et al., 2009) are limited to a small region of the genome, and tools like Tablet (Milne et al., 2010) are limited to a relatively small number of reads and may fail outright on large datasets. We need to visualize complex ChIP-Seq and RNA-Seq features such as polarity as well as coverage across whole 3 Gbp genomes such as Human. We have addressed these problems in a lightweight visualization system called SAMSCOPE accelerated by OpenGL. The extensive pre-processing and fast OpenGL interface of SAMSCOPE provides instantaneous and intuitive browsing of complex data at all levels of detail across multiple experiments.
The SAMSCOPE software, implemented in C++ for Linux, with source code, binary packages and documentation are freely available from http://samscope.dna.bio.keio.ac.jp.
现有的 SAM 可视化工具,如“samtools tview”(Li 等人,2009),只能用于基因组的一小部分区域,而像 Tablet(Milne 等人,2010)这样的工具则限于相对较少的读取次数,并且在大型数据集上可能会直接失败。我们需要可视化复杂的 ChIP-Seq 和 RNA-Seq 特征,如极性以及覆盖整个 3Gbp 基因组,如人类基因组。我们已经在一个名为 SAMSCOPE 的轻量级可视化系统中解决了这些问题,该系统由 OpenGL 加速。SAMSCOPE 的广泛预处理和快速 OpenGL 接口提供了在多个实验中各个细节层次上的复杂数据的即时直观浏览。
SAMSCOPE 软件是用 C++编写的 Linux 系统,源代码、二进制包和文档均可从 http://samscope.dna.bio.keio.ac.jp 免费获得。