| STS |
A short DNA sequence with a known chromosomal location that occurs once within the human genome.
Ãâó: www.genpromag.com/Glossary~LETTER~S.html
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| STS |
A short fragment of DNA whose exact sequence is found nowhere else in the genome; typically about 200 to 300 bp. Polymerase chain reaction can be used to amplify the known sequences, which can serve as physical landmarks for mapping.
Ãâó: www.kumc.edu/gec/gloss.html
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| STS |
A short stretch of DNA whose sequence occurs once in the genome and whose location is known. It serves as a landmark used in the mapping and assembly of a genome.
Ãâó: www.bscs.org/onco/glossary.htm
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| STS |
Short (200 to 500 base pairs) DNA sequence that has a single occurrence in the human genome and whose location and base sequence are known. Detectable by polymerase chain reaction, STSs are useful for localizing and orienting the mapping and sequence data reported from many different laboratories and serve as landmarks on the developing physical map of the human genome. Expressed sequence tags (ESTs) are STSs derived from cDNAs.
Ãâó: www.ornl.gov/sci/techresources/Human_Genome/public...
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| STS |
single trusted system
Ãâó: www.fas.org/irp/doddir/army/ar380-19/glossary.htm
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