BioinformaticsBioinformaticsPeer-reviewed journal article
Sigmoni: classification of nanopore signal with a compressed pangenome index
Vikram S. ShivakumariD, Omar Y. AhmediD, Sam KovakaiD, Mohsen ZakeriiD, Ben LangmeadiD
Abstract
Improvements in nanopore sequencing necessitate efficient classification methods, including pre-filtering and adaptive sampling algorithms that enrich for reads of interest. Signal-based approaches circumvent the computational bottleneck of basecalling. But past methods for signal-based classification do not scale efficiently to large, repetitive references like pangenomes, limiting their utility to partial references or individual genomes. We introduce Sigmoni: a rapid, multiclass classification method based on the r-index that scales to references of hundreds of Gbps. Sigmoni quantizes nanopore signal into a discrete alphabet of picoamp ranges. It performs rapid, approximate matching using matching statistics, classifying reads based on distributions of picoamp matching statistics and co-linearity statistics. Sigmoni is 10-100x faster than previous methods for adaptive sampling in host depletion experiments with improved accuracy, and can query reads against large microbial or human pangenomes.
- assay: long-read sequencing
- research focus: clustering
- research focus: cell type annotation
- research focus: variant calling
- approach: statistical model
- Citations
- 23
- FWCI
- 3.14
- Field percentile
- top 6%
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