Genomics Terms
Genomics studies whole genomes, all of an organism's DNA at once, rather than one gene at a time. These terms cover sequencing methods, genetic variation such as SNPs, genome-wide association studies, and the tools used to analyze the data.
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- BioinformaticsBioinformaticsBioinformatics is the science of using computers to gather, store, analyze and share biological data, especially DNA, RNA and protein sequences.
- BLASTBioinformaticsBLAST is a widely used program that searches databases for DNA or protein sequences similar to a query and ranks the matches by statistical significance.
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- GenBankBioinformaticsGenBank is the public database of DNA and RNA sequences run by the US National Center for Biotechnology Information, with annotated records free to use.
- GeneGeneticsA gene is a stretch of DNA that carries the instructions for making a protein or a working RNA molecule, and is the basic unit of heredity.
- Genetic linkageGeneticsGenetic linkage is the tendency of genes that lie close together on the same chromosome to be inherited together rather than sorted independently.
- GenomeGenomicsA genome is the complete set of DNA in an organism or cell, including all of its genes and the stretches of DNA between them.
- Genome annotationGenomicsGenome annotation is the process of identifying where genes and other features lie in a genome sequence and describing what each of them does.
- Genome-wide association studyGenomicsA genome-wide association study (GWAS) scans the genomes of many people to find genetic variants that are more common in those with a trait or disease.
- GenotypeGeneticsA genotype is the genetic makeup of an organism, either at one locus, such as Aa, or across its whole genome, including alleles it does not express.
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- MetagenomicsGenomicsMetagenomics is the study of all the DNA recovered directly from a sample, such as soil, seawater or stool, to reveal its whole community of microbes.
- MicrobiomeMicrobiologyA microbiome is the community of bacteria, fungi, viruses and other microbes, with their genes, that lives in a particular place, such as the human gut.
- Minimal genomeSynthetic BiologyA minimal genome is the smallest set of genes that allows a cell to grow and divide on its own under defined laboratory conditions.
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- Sanger sequencingGenomicsSanger sequencing is a method for reading the order of bases in DNA that uses chain-terminating nucleotides, developed by Frederick Sanger in the 1970s.
- Single nucleotide polymorphismGenomicsA single nucleotide polymorphism (SNP) is a position in the genome where people differ by a single DNA base, the most common kind of genetic variation.
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