This glossary contains a number of definitions from the following publication:
J. M. Cock; Tessmar-Raible, K.; Boyen, C.; Viard, F. (Eds.), Introduction to Marine Genomics, vol. 1, 1st ed., Advances in Marine Genomics Vol. (Springer, 2010). Available from: http://www.springer.com/life+
Term | Definition |
---|---|
PTM |
Post-transcriptional modification. Alterations made to pre-mRNA before it leaves the nucleus and becomes mature mRNA. |
Pyrosequencing |
Massively parallel DNA sequencing technique without the requirement of a prior cloning of the DNA. |
Q-PCR, qPCR or qRT-PCR |
Quantitative real-time reverse-transcription PCR. A PCR-based assay, which involves the direct measurment of the incorportation of a fluorescent dye into the PCR product. The level of fluorescence is a direct reflection on the amount of prduct present. By comparing the point in the PCR reaction where the reaction enters the log phase of replication for a control and a treated sample and determining the difference between the two, a measure of the change in relative gene expression caused by the treatment is determined. |
QTL |
Quantitative Trait Loci; A region of a chromosome that is associated with a particular measurable trait (see also eQTL). |
RAPD |
Random Amplification of Polymorphic DNA; DNA fragments randomly amplified by PCR from genomic DNA with short primers (8-12 nucleotides) of arbitrary nucleotide sequence. |
RAST |
Rapid Annotation using Subsystem Technology. |
Replicate |
A repetition of the same experimental measurement, The replicate can either be technical, where the same biological extract is analyzed twice, eg. by using the same mRNA for multiple microarrays; or it can be a biological replicate, when for example sample material is harvested from different individuals grown under the same conditions. |
Reporter/Probe |
An oligonucleotide attached to the surface of a microarray. |
RNA interference (RNAI) |
A genetic mechanism in which double-stranded RNA is cleaved into small fragments and acts a signal to either initiate the degradation of a complementary messenger RNA or to interfere with its translation. |
ROS |
Reactive Oxygen species; Small molecules or ions formed by the incomplete one-electron reduction of oxygen; ROS contribute to oxidative stress/damage of DNA, lipids (oxidations of polydesaturated fatty acids), proteins (oxidations of amino acids) and inactivate specific enzymes (oxidation of co-factors). |
SAGE |
Serial Analysis of Gene Expression. A high-throughput method to measure gene-expression by sequencing. Short fragments (tags) are generated from cDNA, which are then ligated to form long concatenated sequences, and, sequenced. |
Scatter-plot |
A two-dimensional plot where each measurement value is depicted by a single dot. Scatter-plots are often used to inspect data distributions. |
SDS-PAGE |
Sodium dodecylsulphate - polyacrylamide gel electrophoresis; method used to separate proteins involving electrophoresis on an acrylamide gel. |
Seaweed Brown |
Red or green macroalgae. |
Secondary endosymbiosis |
An event in which a eukaryotic cell enslaves another eukaryotic cell that possesses a plastid derived from a primary endosymbiosis (see also endosymbiosis and primary endosymbiosis). |
Sequence trace file |
Raw sequence data in the form of a chromatogram from a Sanger sequencing reaction. The NCBI Trace Archive (http://www.ncbi.nlm.nih.gov.gate1.inist.fr/Traces/home/) and the Ensembl Trace Server (http://trace.ensembl.org/) are a public repositories for this sort of data. |
Short Read Archive (SRA) |
An NCBI database that stores raw data from sequencing platforms such as the Roche 454 System. |
Singleton |
A single EST sequence that does not cluster with other ESTs. |
SNP |
Single-nucleotide polymorphism; particular sites (base pairs) in a sequence that are polymorphic and can be used as markers. |
SOM |
Self Organizing Maps. |