Evidence map›Paper›PMID 42620161›Full record

ArticlebioRxiv : the preprint server for biology2026

TDKC (Target Distilled K-mer Classifier): Ultrafast and Memory-Efficient Sequence Classification for Target Pathogen Diagnostics.

Seungmo Lee, Vivek Agarwal, William O'Brien, Eleazar Eskin

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Seungmo LeeDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA .ORCID 0009-0004-7831-8251
Vivek AgarwalDepartment of Computational Medicine, University of California, Los Angeles, Los Angeles, CA, USA .
William O'BrienDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA .
Eleazar EskinDepartment of Computer Science, University of California, Los Angeles, Los Angeles, CA, USA .ORCID 0000-0003-1149-4758

Funding

Expanding Swabseq sequencing technology to enable readiness for emerging pathogensR01AI177859 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Valerie A Arboleda, ELEAZAR ESKIN · 2023 to 2026
$2.3M
NIAID NIH HHS R01 AI177859
6 · The paper itself

Abstract

Metagenomic sequencing can identify pathogens from clinical samples without prior knowledge of the causative agent. Yet, as sequencing workflows scale to process thousands of multiplexed samples simultaneously, classifying these samples against massive reference databases creates a significant computational bottleneck. Furthermore, large-scale applications such as screening public sequence repositories remain computationally challenging. Existing metagenomic classifiers are designed for full-taxon classification, where the goal is to identify all organisms in a sample. However, many diagnostic applications focus on detecting a specific set of clinically relevant pathogens. This constraint can be exploited to significantly lower computational costs. Here we present TDKC (

Indexed as

alignment-free methodsclinical metagenomicsmemory-efficient algorithmsmetagenomic classificationpathogen detection

Identifiers

PMID42620161
PMCPMC13484499

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.