QAlign: aligning nanopore reads accurately using current-level modeling.
QAlign: aligning nanopore reads accurately using current-level modeling.
复制标题
QAlign:使用电流水平建模准确对齐纳米孔读数。
DOI:
10.1093/bioinformatics/btaa875
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发表时间:
2021
期刊:
影响因子:
--
通讯作者:
Diggavi,Suhas
中科院分区:
文献类型:
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作者:
Joshi,Dhaivat;Mao,Shunfu;Kannan,Sreeram;Diggavi,Suhas
MotivationEfficient and accurate alignment of DNA/RNA sequence reads to each other or to a reference genome/transcriptome is an important problem in genomic analysis. Nanopore sequencing has emerged as a major sequencing technology and many long-read aligners have been designed for aligning nanopore reads. However, the high error rate makes accurate and efficient alignment difficult. Utilizing the noise and error characteristics inherent in the sequencing process properly can play a vital role in constructing a robust aligner. In this article, we design QAlign, a pre-processor that can be used with any long-read aligner for aligning long reads to a genome/transcriptome or to other long reads. The key idea in QAlign is to convert the nucleotide reads into discretized current levels that capture the error modes of the nanopore sequencer before running it through a sequence aligner.ResultsWe show that QAlign is able to improve alignment rates from aroundup towith nanopore reads when aligning to the genome. We also show that QAlign improves the average overlap quality byandin three real datasets for read-to-read alignment. Read-to-transcriptome alignment rates are improved from% toand% toin two real datasets.Availability and implementationhttps://github.com/joshidhaivat/QAlign.git.Supplementary informationSupplementary data are available atBioinformaticsonline.