Compressing and Indexing Aligned Readsets

T. Gagie, Garance Gourdel, G. Manzini
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引用次数: 4

Abstract

In this paper we show how to use one or more assembled or partially assembled genome as the basis for a compressed full-text index of its readset. Specifically, we build a labelled tree by taking the assembled genome as a trunk and grafting onto it the reads that align to it, at the starting positions of their alignments. Next, we compute the eXtended Burrows-Wheeler Transform (XBWT) of the resulting labelled tree and build a compressed full-text index on that. Although this index can occasionally return false positives, it is usually much more compact than the alternatives. Following the established practice for datasets with many repetitions, we compare different full-text indices by looking at the number of runs in the transformed strings. For a human Chr19 readset our preliminary experiments show that eliminating separators characters from the EBWT reduces the number of runs by 19\%, from 220 million to 178 million, and using the XBWT reduces it by a further 15\%, to 150 million.
压缩和索引对齐的Readsets
在本文中,我们展示了如何使用一个或多个组装或部分组装的基因组作为其readset压缩全文索引的基础。具体地说,我们通过将组装好的基因组作为树干,并将与之对齐的reads嫁接到树干上,在它们对齐的起始位置上,构建一个标记树。接下来,我们计算结果标记树的扩展Burrows-Wheeler变换(XBWT),并在其上构建压缩的全文索引。虽然这个索引偶尔会返回假阳性,但它通常比其他选择要紧凑得多。按照具有多次重复的数据集的惯例,我们通过查看转换后的字符串中的运行次数来比较不同的全文索引。对于一个人类Chr19 readset,我们的初步实验表明,从EBWT中去除分隔符字符可以减少19%的运行次数,从2.2亿次减少到1.78亿次,使用XBWT可以减少15%,到1.5亿次。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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