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Related Concept Videos

Viral Mutations00:36

Viral Mutations

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A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
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Viral Structure00:56

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Viruses are extraordinarily diverse in shape and size, but they all have several structural features in common. All viruses have a core that contains a DNA- or RNA-based genome. The core is surrounded by a protective coat of proteins called the capsid. The capsid is composed of subunits called capsomeres. The capsid and genome-containing core are together known as the nucleocapsid.
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Viral Recombination00:57

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Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
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Evolutionary Relationships through Genome Comparisons02:54

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Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
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Classification of Leukocytes01:30

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Leukocytes are classified into two groups based on the presence or absence of cytoplasmic granules. Granular leukocytes, which contain granules, belong to the myeloid lineage and are divided into three subtypes: neutrophils, eosinophils, and basophils. These cells are roughly spherical and characterized by the granules in their cytoplasm.
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Leaky Scanning

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During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
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Updated: May 11, 2025

Unbiased Deep Sequencing of RNA Viruses from Clinical Samples
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Unbiased Deep Sequencing of RNA Viruses from Clinical Samples

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Alignment-free viral sequence classification at scale.

Daniel J van Zyl1,2, Marcel Dunaiski3, Houriiyah Tegally4

  • 1Centre for Epidemic Response and Innovation (CERI), School of Data Science and Computational Thinking, Stellenbosch University, Stellenbosch, South Africa. danielvanzyl@sun.ac.za.

BMC Genomics
|April 18, 2025
PubMed
Summary
This summary is machine-generated.

Alignment-free methods offer a scalable and rapid alternative for viral sequence classification. These techniques achieve high accuracy on large datasets, outperforming traditional alignment-based approaches.

Keywords:
Alignment-freeBiological sequencesFeature extractionMachine learningVirus classification

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Next-generation sequencing (NGS) generates vast amounts of nucleotide data, necessitating efficient sequence comparison tools.
  • Traditional alignment-based methods (e.g., BLAST) struggle with scalability for massive datasets.
  • Alignment-free (AF) methods present a promising, computationally efficient alternative for sequence analysis.

Purpose of the Study:

  • To evaluate the efficacy of AF methods for large-scale viral sequence classification.
  • To identify AF techniques that balance accuracy and computational efficiency.
  • To assess the performance of AF methods across diverse viral datasets.

Main Methods:

  • Six established AF techniques were utilized to generate feature vectors from viral genomes.
  • Random Forest classifiers were trained using these feature vectors.
  • Models were validated on extensive SARS-CoV-2, dengue, and HIV sequence datasets.

Main Results:

  • AF classifiers achieved high accuracy: 97.8% for SARS-CoV-2, 99.8% for dengue, and 89.1% for HIV.
  • Word-based AF methods effectively represent viral sequences, even with high dimensionality.
  • Demonstrated robustness and scalability across different viral genomic datasets.

Conclusions:

  • AF methods provide a practical and efficient solution for viral sequence classification.
  • These techniques offer significant speed advantages over alignment-based methods.
  • AF approaches enable sequence classification using limited computational resources.