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Updated: Jun 26, 2026

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
Published on: August 3, 2018
ReadChop: a high-performance demultiplexer for long-read sequencing data
1Department of Biochemistry, Key Laboratory of Gene Engineering of the Ministry of Education, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510275, China.
Summary:
Long-read sequencing (LRS) platforms offer extended read lengths but present computational challenges due to high error rates and frequent insertion-deletion (indel) artifacts. While sample multiplexing is essential for cost-efficiency, existing demultiplexing solutions face a dichotomy: vendor-provided tools (e.g., Dorado) often lack the structural flexibility required for highly non-canonical designs, while open-source tools (e.g., Cutadapt) often lack the speed or algorithmic robustness to handle custom, high-complexity barcode designs. Here, we present ReadChop, a high-performance demultiplexer implemented in Rust. ReadChop leverages Myers' bit-parallel algorithm to efficiently model indel-rich error profiles and employs a streaming architecture to ensure low memory footprint. Benchmarking demonstrates that ReadChop achieves classification precision exceeding 99.99% on both simulated datasets-even under ultra-high multiplexing conditions (e.g., 13 824-plex)-and empirical SARS-CoV-2 amplicons. Furthermore, it excels in filtering in silico chimeras (0.1% miss rate) and exhibits linear computational scalability on ultra-long templates (up to 100 kb). Crucially, it significantly accelerates execution speeds-being >6 times faster than Dorado, >2 times faster than Nanoplexer, and >30 times faster than Cutadapt-with memory usage consistently below 200 MB. ReadChop provides a flexible, robust solution for processing massive LRS datasets with non-canonical experimental designs.
Availability And Implementation:
Source code and documentation are freely available under the MIT license at https://github.com/cherryamme/ReadChop.
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