CARE 2.0: Reducing False-positive Sequencing Error Corrections Using Machine Learning
Overview
Affiliations
Background: Next-generation sequencing pipelines often perform error correction as a preprocessing step to obtain cleaned input data. State-of-the-art error correction programs are able to reliably detect and correct the majority of sequencing errors. However, they also introduce new errors by making false-positive corrections. These correction mistakes can have negative impact on downstream analysis, such as k-mer statistics, de-novo assembly, and variant calling. This motivates the need for more precise error correction tools.
Results: We present CARE 2.0, a context-aware read error correction tool based on multiple sequence alignment targeting Illumina datasets. In addition to a number of newly introduced optimizations its most significant change is the replacement of CARE 1.0's hand-crafted correction conditions with a novel classifier based on random decision forests trained on Illumina data. This results in up to two orders-of-magnitude fewer false-positive corrections compared to other state-of-the-art error correction software. At the same time, CARE 2.0 is able to achieve high numbers of true-positive corrections comparable to its competitors. On a simulated full human dataset with 914M reads CARE 2.0 generates only 1.2M false positives (FPs) (and 801.4M true positives (TPs)) at a highly competitive runtime while the best corrections achieved by other state-of-the-art tools contain at least 3.9M FPs and at most 814.5M TPs. Better de-novo assembly and improved k-mer analysis show the applicability of CARE 2.0 to real-world data.
Conclusion: False-positive corrections can negatively influence down-stream analysis. The precision of CARE 2.0 greatly reduces the number of those corrections compared to other state-of-the-art programs including BFC, Karect, Musket, Bcool, SGA, and Lighter. Thus, higher-quality datasets are produced which improve k-mer analysis and de-novo assembly in real-world datasets which demonstrates the applicability of machine learning techniques in the context of sequencing read error correction. CARE 2.0 is written in C++/CUDA for Linux systems and can be run on the CPU as well as on CUDA-enabled GPUs. It is available at https://github.com/fkallen/CARE .
Moon Y, Hong C, Kim Y, Kim J, Ye S, Kang E Int J Mol Sci. 2025; 25(24.
PMID: 39769013 PMC: 11678496. DOI: 10.3390/ijms252413250.
A survey of k-mer methods and applications in bioinformatics.
Moeckel C, Mareboina M, Konnaris M, Chan C, Mouratidis I, Montgomery A Comput Struct Biotechnol J. 2024; 23:2289-2303.
PMID: 38840832 PMC: 11152613. DOI: 10.1016/j.csbj.2024.05.025.
CAREx: context-aware read extension of paired-end sequencing data.
Kallenborn F, Schmidt B BMC Bioinformatics. 2024; 25(1):186.
PMID: 38730374 PMC: 11088031. DOI: 10.1186/s12859-024-05802-w.
MAC-ErrorReads: machine learning-assisted classifier for filtering erroneous NGS reads.
Sami A, El-Metwally S, Rashad M BMC Bioinformatics. 2024; 25(1):61.
PMID: 38321434 PMC: 10848413. DOI: 10.1186/s12859-024-05681-1.
Illumina reads correction: evaluation and improvements.
Dlugosz M, Deorowicz S Sci Rep. 2024; 14(1):2232.
PMID: 38278837 PMC: 11222498. DOI: 10.1038/s41598-024-52386-9.