Upload your assembled genome and start a conversation. Real bioinformatics analysis. Real science. No external dependencies.
Powered by independent k-mer profiling, sequence-based AMR/virulence detection, MLST typing, and plasmid replicon identification — all running in your browser.
Real bioinformatics, not simulations. Every result is traceable to validated methods.
K-mer compositional profiling + GC/size matching. 8 ESKAPE+ Tier 1 priority pathogens.
N50/L50/N90, GC analysis, ORF prediction, quality scoring per QUAST standards.
24+ resistance gene markers. Beta-lactamases, MRSA, VRE, carbapenemases, colistin resistance.
30+ virulence markers. Toxins, adhesins, invasion factors, immune evasion, biofilm genes.
7 MLST schemes with 40+ known STs. Epidemiological context for each clone.
15+ replicon types. Conjugation assessment, transfer risk, associated resistance.
GenoVox uses the same principles as established bioinformatics tools
Method: Compositional analysis: GC content + genome size + tetranucleotide frequency signatures + diagnostic markers
References: Karlin & Burge (1995) Trends Genet; Ondov et al. (2016) Genome Biol — same principles as Mash/Kraken2
Method: Conserved diagnostic marker subsequence search on forward and reverse complement strands
References: Alcock et al. (2023) CARD; Bortolaia et al. (2020) ResFinder; Feldgarden et al. (2019) AMRFinderPlus
Method: Curated VF marker sequence matching with category-based pathogenicity scoring
References: Liu et al. (2022) VFDB; Joensen et al. (2014) VirulenceFinder
Method: Conserved primer-region marker detection for MLST loci + allelic profile matching
References: Jolley et al. (2018) PubMLST; Seemann T — mlst tool
Method: Replicon marker sequence identification on assembled contigs
References: Carattoli et al. (2014) PlasmidFinder; Robertson & Nash (2018) MOB-suite
Scientific Disclaimer
GenoVox provides computational predictions based on genomic markers. Results are for research purposes. Phenotypic antimicrobial susceptibility testing (AST) is essential for clinical decision-making. Genotype does not always predict phenotype.
WHO priority + ESKAPE pathogens — covering ~80% of hospital-acquired infections
E. coli
Escherichia coli
UTI, sepsis, ESBL
K. pneumoniae
Klebsiella pneumoniae
CRE, hvKp
S. aureus
Staphylococcus aureus
MRSA
P. aeruginosa
Pseudomonas aeruginosa
MDR, CF
A. baumannii
Acinetobacter baumannii
XDR, ICU
E. faecium
Enterococcus faecium
VRE
S. enterica
Salmonella enterica
Typhoid, iNTS
M. tuberculosis
Mycobacterium tuberculosis
MDR-TB, XDR-TB
Upload your FASTA file and get scientifically-grounded characterization
Assembled bacterial genome in FASTA format
Drop your FASTA file here or click to browse
.fasta, .fa, .fna — assembled contigs or complete genome