Pith. sign in

REVIEW

Enhancing Downstream Analysis in Genome Sequencing: Species Classification While Basecalling

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2504.07065 v1 pith:VUOZ7PYC submitted 2025-04-09 q-bio.GN cs.LG

classification q-bio.GNcs.LG
keywords basecallingspeciesclassificationaccuracygenomeaccuracieshigheridentifying
verification ladder T0 review T1 audit T2 compute T3 formal

Signed reviews

No signed human review yet.

0 comments
read the original abstract

The ability to quickly and accurately identify microbial species in a sample, known as metagenomic profiling, is critical across various fields, from healthcare to environmental science. This paper introduces a novel method to profile signals coming from sequencing devices in parallel with determining their nucleotide sequences, a process known as basecalling, via a multi-objective deep neural network for simultaneous basecalling and multi-class genome classification. We introduce a new loss strategy where losses for basecalling and classification are back-propagated separately, with model weights combined for the shared layers, and a pre-configured ranking strategy allowing top-K species accuracy, giving users flexibility to choose between higher accuracy or higher speed at identifying the species. We achieve state-of-the-art basecalling accuracies, while classification accuracies meet and exceed the results of state-of-the-art binary classifiers, attaining an average of 92.5%/98.9% accuracy at identifying the top-1/3 species among a total of 17 genomes in the Wick bacterial dataset. The work presented here has implications for future studies in metagenomic profiling by accelerating the bottleneck step of matching the DNA sequence to the correct genome.

Discussion (0). Continue with ORCID to comment.

Pith tools