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A Computational Approach for Gene Assembly and Exon Annotation Based on BLAST

机译:基于爆炸的基因组装与外显子注释的计算方法

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Accurate gene assembly and precise exon annotations are two of the key goals of Human Genome Project. Existing gene reference sequences and exon annotations are far from perfection. This paper introduces a new greedy algorithm which makes use of mRNA reference sequence and BLAST tools from NCBI (National Center for Biotechnology Information) to effectively assemble and annotate gene structures. Four pipelined components are included in this approach. 1. Blast Parser: extract mRNA-DNA local alignment pairs. 2. Chain Finder: transform local alignments to spliced alignment. 3. Assembler: assemble multiple DNA sequences of into a continuous DNA sequence based on their spliced alignments with a given mRNA sequence. 4. Annotator: resolve exon-intron boundary based on splicing signals. Test results on one sample set of human genes show that gene assembly and exon annotation using the proposed approach is significantly better than contig references from NCBI. The software is available upon request.
机译:准确的基因组装和精确的外显子注释是人类基因组项目的两个关键目标。现有的基因参考序列和外显子注释远非完美。本文介绍了一种新的贪婪算法,它利用来自NCBI的MRNA参考序列和BLAST工具,从NCBI(国家生物技术信息中心)有效地组装和注释基因结构。这种方法包括四个流水线组件。 1.爆炸解析器:提取mRNA-DNA局部对准对。 2.链式查找器:将局部对齐转换为拼接对准。 3.汇编器:基于与给定mRNA序列的拼接对准组装在连续DNA序列中的多个DNA序列。 4.注释器:基于拼接信号解析外显子边界。在一个样本集的人类基因上的测试结果表明,使用所提出的方法的基因组装和外显子注释明显优于来自NCBI的COTIG参考。可根据要求提供该软件。

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