Related Experiment Video
Updated: Aug 28, 2025

10:34
Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
Published on: December 9, 2022
4.4K
Tracking mutational semantics of SARS-CoV-2 genomes
Rohan Singh1, Sunil Nagpal2,3,4, Nishal K Pinna1
1TCS Research, Tata Consultancy Services Ltd, Pune, 411013, India.
Scientific Reports
|September 20, 2022
Summary
Natural language processing (NLP) models analyze SARS-CoV-2 genomic data to reveal viral evolution and mutation patterns. This approach uncovers mutation relevance to patient health, identifying key mutations of concern.
Area of Science:
- Computational Biology
- Genomics
- Bioinformatics
Background:
- Genomic datasets, like those from SARS-CoV-2, are sequential and dynamic, presenting unique analytical challenges.
- Traditional methods may not fully capture the temporal evolution and complex associations within viral genomes.
Purpose of the Study:
- To apply Natural Language Processing (NLP) algorithms to SARS-CoV-2 genomic data.
- To reveal viral characteristics and evolutionary patterns.
- To identify mutations relevant to patient health outcomes.
Main Methods:
- Utilized fundamental NLP algorithms for processing SARS-CoV-2 genome sequences and mutations.
- Employed dynamic topic modeling to probe temporal mutational signatures.
- Applied semantic drift analysis to trace mutation associations in genomic records.
Main Results:
- Demonstrated NLP's applicability in analyzing viral evolution and mutation dynamics.
- Successfully traced mutation associations and semantic drift within genomic data.
- Identified potential links between specific mutations and patient health status.
Conclusions:
- NLP offers a novel framework for understanding viral evolution and mutation impact.
- The approach can identify significant mutations and their relevance to disease.
- This methodology aids in detecting mutations of concern and understanding their clinical relevance.
Related Concept Videos
Viral Mutations
32.8K
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...
32.8K
Point and Frameshift Mutations
66
Point mutations are genetic alterations involving the change of a single nucleotide base pair in DNA. Depending on how the alteration affects protein synthesis, they can lead to various consequences.Point mutations fall into the following types:Silent mutations occur when a nucleotide change does not alter the amino acid sequence due to the redundancy of the genetic code. For instance, changing ACC to ACA still encodes threonine, leaving the protein function unaffected. This occurs because...
66
Mutations in Microorganisms
58
Mutations are heritable changes in an organism’s genome involving alterations in the base sequence of DNA or RNA. These changes can influence cellular processes and phenotypic traits, potentially transforming the unaltered wild type into a mutant form. Such changes, termed forward mutations, are pivotal in shaping the genetic diversity of organisms.RNA viruses exhibit the highest mutation rates due to the absence of robust proofreading mechanisms during genome replication. In contrast,...
58
Single Nucleotide Polymorphisms-SNPs
15.6K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.6K
Mutations
84.2K
Overview
84.2K
Leaky Scanning
5.2K
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...
5.2K

