Suppr超能文献

基于读取的基因剪接算法调查。

Survey of gene splicing algorithms based on reads.

机构信息

a Department of Computer Science & Technology , Heilongjiang University , Harbin , China.

b Shandong Aerospace Institute of Electronic Technology , Yantai , China.

出版信息

Bioengineered. 2017 Nov 2;8(6):750-758. doi: 10.1080/21655979.2017.1373538. Epub 2017 Sep 21.

Abstract

Gene splicing is the process of assembling a large number of unordered short sequence fragments to the original genome sequence as accurately as possible. Several popular splicing algorithms based on reads are reviewed in this article, including reference genome algorithms and de novo splicing algorithms (Greedy-extension, Overlap-Layout-Consensus graph, De Bruijn graph). We also discuss a new splicing method based on the MapReduce strategy and Hadoop. By comparing these algorithms, some conclusions are drawn and some suggestions on gene splicing research are made.

摘要

基因拼接是将大量无序的短序列片段尽可能准确地组装到原始基因组序列中的过程。本文综述了几种基于读取的流行拼接算法,包括参考基因组算法和从头拼接算法(贪婪扩展、重叠布局共识图、De Bruijn 图)。我们还讨论了一种基于 MapReduce 策略和 Hadoop 的新拼接方法。通过比较这些算法,得出了一些结论,并对基因拼接研究提出了一些建议。

相似文献

1
Survey of gene splicing algorithms based on reads.基于读取的基因剪接算法调查。
Bioengineered. 2017 Nov 2;8(6):750-758. doi: 10.1080/21655979.2017.1373538. Epub 2017 Sep 21.
2
Assembly of long error-prone reads using de Bruijn graphs.使用德布鲁因图组装长易错读段。
Proc Natl Acad Sci U S A. 2016 Dec 27;113(52):E8396-E8405. doi: 10.1073/pnas.1604560113. Epub 2016 Dec 12.
8
Genome sequence assembly algorithms and misassembly identification methods.基因组序列组装算法和错误组装识别方法。
Mol Biol Rep. 2022 Nov;49(11):11133-11148. doi: 10.1007/s11033-022-07919-8. Epub 2022 Sep 23.

引用本文的文献

本文引用的文献

1
The challenge of small-scale repeats for indel discovery.小尺度重复序列对插入缺失(indel)检测的挑战。
Front Bioeng Biotechnol. 2015 Jan 26;3:8. doi: 10.3389/fbioe.2015.00008. eCollection 2015.
3
Genotyping in the cloud with Crossbow.使用Crossbow在云端进行基因分型。
Curr Protoc Bioinformatics. 2012 Sep;Chapter 15:15.3.1-15.3.15. doi: 10.1002/0471250953.bi1503s39.
4
A survey of error-correction methods for next-generation sequencing.下一代测序错误纠正方法综述。
Brief Bioinform. 2013 Jan;14(1):56-66. doi: 10.1093/bib/bbs015. Epub 2012 Apr 6.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验