Clan is a group of families that either share a common ancestor but are too divergent to be reasonably aligned or a group of families that could be aligned, but have distinct functions.
A general purpose multiple sequence alignment program for DNA (RNA) which we use while building our SEED alignments. See the Clustal web server.
A secondary structure profile for a RNA structural alignment (also called profile stochastic context-free grammars).
A group of RNA sequences which we believe are evolutionarily related in sequence or secondary structure.
An alignment of the set of related sequences which score higher than the manually set threshold values for the CMs of a particular Rfam family.
The bit score gathering threshold (GA cutoff), set by Rfam curators when building the family. All sequences that score at or above this threshold will be included in the full alignment and are believed to be true homologs to the model. For more information see Nawrocki et al., 2015.
Infernal is the core software that enables us to make consensus RNA secondary structure profiles (covariance models (CMs)) for our families. We also use Infernal for searching sequence databases for homologous RNAs. See the Infernal website for more details.
RNA structure prediction algorithm which utilises minimum free energy information. See the MFOLD website.
RNA folding software which folds alignments using a Stochastic Context-Free Grammars (SCFG) trained on rRNA alignments. It takes an alignment of RNA sequences as input and predicts a common structure for all sequences. See the Pfold website.
Folds pre-computed alignments using a combination of free-energy and covariation measures. Part of the Vienna package.
R-scape is a method for testing whether covariation analysis supports the presence of a conserved RNA secondary structure in a multiple sequence alignment. R-scape is used to create and improve Rfam families, and R-scape visualisations are shown on the secondary structure tab for each family (for example, SAM riboswitch).
A manually curated sample of representative sequences for a family. These sequences are aligned and annotated with a consensus secondary structure. This alignment is used to build the covariance model for the family.
A single segment of nucleotide sequence in our alignments. Multiple sequence regions from a single EMBL sequence may be in the same family.
A multiple sequence alignment format used by Rfam (and Pfam) for the dissemination of protein and RNA sequence alignments. For more information see the Wikipedia article on Stockholm format.
A simple functional classification used to organise Rfam families. This is our own ontology and does not current directly relate to the ontologies used by other databases. For a full list of RNA types in our current ontology see the Search by entry type section.