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Satellite DNA
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Satellite DNA consists of highly repetitive
DNA, and is so called because repetitive DNA sequences tend to have a
relatively high frequency of the nucleotides Adenine and Thymine, and thus
have lower density - such that they form a second 'satellite' band when
genomic DNA is separated along a density gradient.
Definition
from:
"Satellite DNA." Wikipedia, The Free Encyclopedia
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A portion of the DNA that differs enough in
base composition so that it forms a distinct band on cesium chloride
gradient centrifugation; usually contains highly repetitive DNA sequences
Definition
from:
http://www.kumc.edu/gec/gloss.html
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DNA that forms a separate band in a bouyant
density gradient because of its different nucleotide composition (A:T rich
DNAs are less dense than G:C rich DNAs). Highly repetitive eukaryotic DNA
primarily located around centromeres. Satellite DNA usually has a
different buoyant density than the rest of the cell's DNA.
Definition
from:
http://www.biochem.northwestern.edu/holmgren/Glossary/Definitions/Def-S/satellite_DNA.html
SCAR (
Sequence characterised amplified region )
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A locus representing a single RAPD fragment
which has been sequenced. Primers specific to the locus can be designed
and used in PCR amplification.
Definition
from:
Hypermedia Glossary Of Genetic Terms
SINE (
Short interspersed element )
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A type of small dispersed repetitive DNA
sequence (eg Alu family in the human genome) found throughout a eukaryotic
genome.
Definition
from:
http://www.biochem.northwestern.edu/holmgren/Glossary/Definitions/Def-S/SINE.html
SNP ( Single
nucleotide polymorphism )
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Sequence polymorphism differing in a single
base pair.
Definition
from:
Hypermedia Glossary Of Genetic Terms
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A type of polymorphism in which two
chromosomes differ in a given segment by the identity of a single base
pair.
Definition
from:
Mouse Genome Informatics
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DNA sequence variations that occur when a
single nucleotide (A, T, C, or G) in the genome sequence is altered. Each
individual has many single nucleotide polymorphisms that together create a
unique DNA pattern for that person. SNPs promise to significantly advance
our ability to understand and treat human disease.
Definition
from:
http://www.biochem.northwestern.edu/holmgren/Glossary/Definitions/Def-S/SNP.html
spacer DNA
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Regions of non-transcribed DNA between
transcribed repeated genes such as ribosomal RNA genes in eukaryotes. Its
function is probably to do with ensuring the high rates of transcription
associated with these genes.
Definition
from:
http://www.biochem.northwestern.edu/holmgren/Glossary/Definitions/Def-S/spacer_DNA.html
SPAR ( Single primer amplification reaction
)
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A PCR technique using core motifs of
microsatellite DNA
Definition
from:
Hypermedia Glossary Of Genetic Terms
SSCP
( Single stranded conformational
polymorphism )
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A method for distinguishing between similar
sized DNA fragments according to the mobility of the single-stranded DNA
under polyacrylamide gel electrophoresis
Definition
from:
Hypermedia Glossary Of Genetic Terms
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A type of mutation scanning; the
identification of abnormally migrating single-stranded DNA segments on
gel
electrophoresis
Definition
from:
Genetests
STMS
(Sequence tagged microsatellite)
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Primers constructed from the flanking
regions of microsatellite DNA which can be used in PCR reactions to
amplify the repeat region.
Definition
from:
Hypermedia Glossary Of Genetic Terms
STR (
Short Tandem Repeats )
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Multiple copies of an identical DNA sequence
arranged in direct succession in a particular region of a chromosome.
Definition
from:
Genetics/DNA
Glossary
STS ( Sequence
tagged site )
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Any site in a chromosome or genome that is
identified by a known unique DNA sequence. STSs can be used to form
genetic maps by standard mapping procedures
Definition
from:
http://www.biochem.northwestern.edu/holmgren/Glossary/Definitions/Def-S/sequence_tagged_site.html
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A short segment of unique sequence derived
from genomic DNA. A large collection of STSs can be used to assemble a
physical map of the genome from a collection of genomic clones (e.g., BACs
or YACs) by testing each clone for the presence of each STS. Two clones
that contain one or more STSs in common must overlap
Definition
from:
Mouse Genome Informatics
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Short (200 to 500 base pairs) sequence of
genomic DNA 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.
Definition
from:
Hypermedia Glossary Of Genetic Terms
Substitution
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In genetics, a type of mutation
due to replacement of one nucleotide in a DNA sequence by another
nucleotide or replacement of one amino acid in a protein by another amino
acid.
Definition
from:
Genome Glossary
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