K-FluDB: A Novel K-Mer Based Database for Enhanced Genomic Surveillance of Influenza A Viruses

Abstract Motivation Influenza A viruses frequently cause seasonal outbreaks and pandemics due to their genetic diversity and reassortment potential. Existing genomic surveillance tools face challenges with redundant databases, delaying subtype identification and obscuring reassortment dynamics. K-FluDB, a novel k-mer-based database, addresses these issues by enhancing subtype identification, capturing genomic diversity, and assisting in the detection of reassortment events critical for understanding viral evolution and improving outbreak proactive measures. Results K-FluDB provides a comprehensive pangenome for Influenza A, including complete and subtype-specific subsequences from 50 subtype combinations across all 18 hemagglutinin (HA) and 11 neuraminidase (NA) subtypes. Achieving 99.64% compression, K-FluDB eliminates redundancy while preserving essential information. Validation with real-world datasets showed high recovery indices (up to 96.24%) and correct subtype prediction ratios (exceeding 99% for HA and NA). K-FluDB also assists in the detection of reassortment events. Availability and implementation Three versions of K-FluDB, optimized for read lengths of 75, 150, and 300 nucleotides, are freely available at https://zenodo.org/records/17203072, and the source code is available at https://github.com/usjunco/pangen.

Authors

Institutions

Publication Details

Journal
Bioinformatics Advances
Published
2025-10-09
DOI
https://doi.org/10.1093/bioadv/vbaf254
Primary Topic
Machine Learning in Bioinformatics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

K-FluDB: A Novel K-Mer Based Database for Enhanced Genomic Surveillance of Influenza A Viruses

Blanca Taboada, Lorena Díaz‐González, Alejandro Uscanga Junco
Bioinformatics Advances
Machine Learning in Bioinformatics
article

K-FluDB: A Novel K-Mer Based Database for Enhanced Genomic Surveillance of Influenza A Viruses

Blanca Taboada, Lorena Díaz‐González, Alejandro Uscanga Junco
article en

Abstract

Abstract Motivation Influenza A viruses frequently cause seasonal outbreaks and pandemics due to their genetic diversity and reassortment potential. Existing genomic surveillance tools face challenges with redundant databases, delaying subtype identification and obscuring reassortment dynamics. K-FluDB, a novel k-mer-based database, addresses these issues by enhancing subtype identification, capturing genomic diversity, and assisting in the detection of reassortment events critical for understanding viral evolution and improving outbreak proactive measures. Results K-FluDB provides a comprehensive pangenome for Influenza A, including complete and subtype-specific subsequences from 50 subtype combinations across all 18 hemagglutinin (HA) and 11 neuraminidase (NA) subtypes. Achieving 99.64% compression, K-FluDB eliminates redundancy while preserving essential information. Validation with real-world datasets showed high recovery indices (up to 96.24%) and correct subtype prediction ratios (exceeding 99% for HA and NA). K-FluDB also assists in the detection of reassortment events. Availability and implementation Three versions of K-FluDB, optimized for read lengths of 75, 150, and 300 nucleotides, are freely available at https://zenodo.org/records/17203072, and the source code is available at https://github.com/usjunco/pangen.

Bioinformatics Advances
Universidad Autónoma del Estado de Morelos (MX), Universidad Nacional Autónoma de México (MX)
Openalex Percentile: Top 75%
Machine Learning in Bioinformatics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.