Identification of mathematical patterns in genomic spectrograms linked to variant classification in complete
Ana Guerrero-Tamayo1, Borja Sanz Urquijo2, María-Dolores Moragues Tosantos3
1Faculty of Engineering, University of Deusto, 48007, Bilbao, Biscay, Spain. ana.guerrero@deusto.es.
Mathematical patterns in viral genomes, like SARS-CoV-2, can define characteristics. This study used genomic spectrograms and transfer learning to classify variants, revealing key patterns for identification.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- Previous studies identified mathematical patterns in viral genomes.
- These patterns may determine viral characteristics.
- Hypothesis: Inherent genomic mathematical patterns dictate viral features.
Purpose of the Study:
- Explore mathematical patterns in SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) variant classification.
- Develop a methodology for variant identification using genomic data.
- Investigate the role of specific nucleotide frequencies in variant differentiation.
Main Methods:
- Genomic spectrograms generation from viral sequences.
- Two-stage transfer learning approach using pre-trained Convolutional Neural Networks (CNNs).
- Two-step explainability for identifying significant genomic regions and patterns.
Main Results:
- Identified distinct mathematical patterns characterizing specific SARS-CoV-2 variants.
- Highlighted the genomic region from the S gene to 3'UTR as crucial for variant identification.
- Nucleotide frequencies, particularly G and C, were key identifiers, with shared patterns in Omicron and pre-VOC lineages.
Conclusions:
- Mathematical patterns are significantly associated with SARS-CoV-2 variant classification.
- These patterns represent an additional layer of genomic information for efficient virus characterization.
- Findings suggest potential phylogenetic connections or evolutionary pathways within SARS-CoV-2 lineages.
More Related Videos
11:02Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
Published on: October 18, 2013
07:15Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
Published on: January 16, 2019
Related Concept Videos
Modern Molecular Taxonomy
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Evolutionary Relationships through Genome Comparisons
Single Nucleotide Polymorphisms-SNPs
Genome-wide Association Studies-GWAS
GWAS does not require the identification of the target gene involved in...
