Significance of Genome sequencing
Genome sequencing is the process of determining the complete DNA sequence of an organism's genome. It is essential for identifying genetic variants linked to diseases, understanding viral evolution and its pathogenicity, and conducting epidemiological studies of viruses. This comprehensive analysis helps scientists gain insights into genetics and viral behaviors, improving disease prediction and management. Overall, genome sequencing plays a pivotal role in advancing our knowledge of both human and viral genomes.
Synonyms: Dna sequencing, Genome mapping, Nucleotide sequencing, Genomic sequencing, Gene sequencing, Dna analysis
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The concept of Genome sequencing in scientific sources
Genome sequencing involves determining the complete DNA sequence of a viral genome, which is crucial for epidemiological studies. This process helps track virus transmission and evolution, thereby aiding in public health responses and disease management.
From: The Malaysian Journal of Medical Sciences
(1) Genome sequencing, also known as whole genome sequencing, can be affected by the presence of ecDNA, potentially leading to discrepancies in the ascertainment of chromosomal sequences if ecDNA is not accounted for.[1] (2) This is a method used by researchers to gain a deep understanding of MRSA epidemiology, innovation, and genetic content.[2] (3) The provided text mentions the process of genome sequencing in the context of characterizing and analyzing various bacteriophages, indicating that this process is used to determine the genetic makeup of these viruses.[3] (4) The process of determining the complete DNA sequence of an organism's genome, which is crucial for identifying genetic variants associated with diseases.[4]