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T-IDBA: A de novo Iterative de Bruijn Graph Assembler for Transcriptome (Extended Abstract)

机译:T-IDBA:用于转录组的从头开始的Bruijn迭代图汇编程序(扩展摘要)

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摘要

RNA-seq data produced by next-generation sequencing technology is a useful tool for analyzing transcriptomes. However, existing de novo transcriptome assemblers do not fully utilize the properties of transcriptomes and may result in short contigs because of the splicing nature (shared exons) of the genes. We propose the T-IDBA algorithm to reconstruct expressed isoforms without reference genome. By using pair-end information to solve the problem of long repeats in different genes and branching in the same gene due to alternative splicing, the graph can be decomposed into small components, each corresponds to a gene. The most possible isoforms with sufficient support from the pair-end reads will be found heuristically. In practice, our de novo transcriptome assembler, T-IDBA, outperforms Abyss substantially in terms of sensitivity and precision for both simulated and real data.
机译:下一代测序技术产生的RNA-seq数据是分析转录组的有用工具。但是,由于基因的剪接性质(共有的外显子),现有的从头转录组组装者不能充分利用转录组的特性,并且可能导致短重叠群。我们提出了T-IDBA算法来重建没有参考基因组的表达的同工型。通过使用端对端信息来解决不同基因中的长重复序列以及由于交替剪接而在同一基因中分支的问题,该图可以分解成小的组件,每个组件对应一个基因。可以从试探法中找到最可能的同工型,其具有来自对端读取的足够支持。在实践中,我们的从头转录组汇编程序T-IDBA在模拟和真实数据的灵敏度和精度方面都大大优于Abyss。

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