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Sketching and sampling approaches for fast and accurate long read classification
1Department of Computer Science, Johns Hopkins University, Baltimore, MD, 21218, USA. arun.das@jhu.edu.
BMC Bioinformatics
|November 1, 2022
Summary
Accurately identifying the source of sequencing reads is vital for metagenomics and contamination detection, especially for error-prone long reads. Sampling and sketching methods offer an efficient and accurate alternative to traditional alignment-based tools.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- Accurate read source identification is critical in sequencing, particularly for metagenomics and distinguishing contaminants.
- Long reads present challenges due to high error rates, complicating origin determination.
- Existing alignment-based tools often suffer from significant time and space overheads.
Purpose of the Study:
- To investigate the effectiveness of sampling and sketching approaches for read classification.
- To provide an efficient and accurate method for identifying the source of sequencing reads, especially long reads.
- To compare these novel methods against existing read classification tools.
Main Methods:
- Exploration of various sampling and sketching algorithms, including uniform sampling, MinHash variants, and a novel clustering-based approach.
- Generation of a reduced representation (screen) of potential source genomes for query readsets.
- Classification of reads based on their similarity to the generated screen.
Main Results:
- Sampling and sketching methods demonstrate high accuracy in identifying microbial genomes from metagenomic data.
- These techniques effectively distinguish between reads from target organisms and contaminants.
- The investigated approaches offer a viable alternative to traditional alignment and index-based methods.
Conclusions:
- Sampling and sketching techniques provide an effective and efficient solution for read classification.
- These methods are suitable for both metagenomic analysis and contaminant detection in sequencing data.
- A reference implementation is available, facilitating the adoption of these approaches.
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