Powerful, privacy-focused DNA analysis using advanced ML algorithms designed for both researchers and individuals.
Our cutting-edge technology provides unparalleled accuracy and insights while keeping your data secure.
Your genetic data never leaves your device. All computation is performed locally using our advanced on-device ML models.
Identify open reading frames, high coverage regions, protein sequences, and transcription factor binding sites with precision.
Our cutting-edge neural networks provide insights and pattern recognition beyond traditional analytics capabilities.
A simple three-step process to analyze your DNA sequences
Upload your DNA sequence file in FASTA or FASTQ format. Your data stays on your device.
Choose from a variety of analysis options, including codon detection, coverage analysis, and protein prediction.
Receive detailed insights with visualizations and downloadable reports for your research.
Comprehensive tools designed for researchers, students, and enthusiasts
Scans DNA for start and stop codons to identify protein-coding sequences (open reading frames). Recognizes canonical start codons (e.g., ATG) and stop codons to pinpoint the locations of putative proteins within a genome.
Locates high coverage (GC-rich) regions in the DNA, often associated with gene-dense areas and promoter regions. Flags GC-rich stretches to help identify potential regulatory regions.
Scans for known core promoter motifs in the DNA sequence, such as the TATA box, BRE, INR, and DPE motifs. Detecting these elements can indicate the presence of gene promoters, helping you locate potential gene start sites.
Join thousands of researchers and scientists using DNAnalyzer for their genetic analysis needs.
Limitation of Liability: The DNAnalyzer tool is intended for research, educational, and informational purposes only. The machine learning-based DNA analysis provides computational predictions that should not be used for medical diagnosis, clinical interpretation, or treatment decisions. DNAnalyzer is not a substitute for professional medical advice, diagnosis, or treatment.
Analysis Limitations: DNAnalyzer's computational analysis, including open reading frame identification, GC-rich region detection, and promoter element identification, is based on algorithmic predictions using machine learning models trained on public datasets. Results may vary in accuracy depending on the quality of input data, sequence type, and other biological factors. The absence of identified genomic features does not rule out their presence, and the identification of features does not guarantee their biological relevance or function.
Privacy Notice: While DNAnalyzer processes DNA sequences locally on your device to maximize privacy, users should exercise caution when uploading sensitive genetic information. We recommend against uploading human genomic data with identifiable personal information. DNAnalyzer is not responsible for any privacy implications resulting from user actions.
Research Use Only: Results generated by DNAnalyzer should be experimentally validated before being used in research publications or academic work. Citations of DNAnalyzer should acknowledge its computational nature and inherent limitations.
No Warranty: DNAnalyzer is provided "as is" without warranty of any kind, express or implied. The creators and contributors of DNAnalyzer disclaim all warranties, including but not limited to accuracy, reliability, and fitness for a particular purpose. In no event shall the creators, contributors, or copyright holders be liable for any claim, damages, or other liability arising from the use of this software.