TransPS:一种用于组装高质量基因组的转录组后支架方法。

Computational biology journal Pub Date : 2014-01-01 Epub Date: 2014-05-28 DOI:10.1155/2014/961823
Mingming Liu, Zach N Adelman, Liqing Zhang
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引用次数: 14

摘要

动机:随着高通量测序技术的发展,转录组测序可以以低价格和高效率进行。序列组装方法已经更新,以满足新的测序技术的新要求。对于需要组装实验中生成的转录组的生物学家来说,组装策略是重要的。然而,一些现代从头组装策略由于序列变化而产生大量冗余组,这极大地影响了下游的分析和实验。本工作提出了TransPS,一种生成高质量转录组的转录组后支架方法。结果:TransPS在测试转录组数据集上显示出令人鼓舞的结果,其中冗余度大大降低了至少50%,而覆盖率也得到了显着提高。可用性:web服务器和源代码可在https://bioinformatics.cs.vt.edu/zhanglab/transps/上获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

TransPS: A Transcriptome Post Scaffolding Method for Assembling High Quality Contigs.

TransPS: A Transcriptome Post Scaffolding Method for Assembling High Quality Contigs.

Motivation: As the development of the high throughput sequencing technologies, transcriptome can be sequenced with a low price and high efficiency. Sequence assembly approaches have been renewed to meet the new requirements from new sequencing technologies. Assembly strategies are important for biologists who need to assemble the transcriptome generated in their experiments. However, some modern de novo assembly strategies generate a large section of redundant contigs due to sequence variations, which greatly affect downstream analysis and experiments. This work proposed TransPS, a post transcriptome scaffolding method to generate high quality transcriptomes.

Results: TransPS shows promising results on the test transcriptome data sets where the redundancy is greatly reduced by at least 50%, while the coverage is improved considerately.

Availability: The web server and source code are available at https://bioinformatics.cs.vt.edu/zhanglab/transps/.

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