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Bookmark or Share- A Brief Guide to Genomics - National Human Genome Research InstituteLast updated: August 16, 2022. Genomics is the study of all of a person's genes (the genome), including interactions of those genes with each other and with the person's environment.
- DNA sequencing at 40: past, present and future | NatureMajor categories of the application of DNA sequencing include de novo genome assembly, individual genome resequencing, clinical applications such as non-invasive prenatal testing, and using...
- DNA sequencing (article) | Biotechnology | Khan AcademyDNA sequencing is the process of determining the sequence of nucleotide bases (As, Ts, Cs, and Gs) in a piece of DNA. Today, with the right equipment and materials, sequencing a short piece of DNA is relatively straightforward. Sequencing an entire genome (all of an organism’s DNA) remains a complex task.
- Whole-Genome Sequencing (WGS) - IlluminaWhole-genome sequencing (WGS) is a comprehensive method for analyzing entire genomes. Genomic information has been instrumental in identifying inherited disorders, characterizing the mutations that drive cancer progression, and tracking disease outbreaks.
- DNA Sequencing Fact Sheet - National Human Genome Research InstituteSequencing DNA means determining the order of the four chemical building blocks - called "bases" - that make up the DNA molecule. The sequence tells scientists the kind of genetic information that is carried in a particular DNA segment. For example, scientists can use sequence information to determine which stretches of DNA contain genes and ...
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