Author: Gardner, Paul P.; Daub, Jennifer; Tate, John G.; Nawrocki, Eric P.; Kolbe, Diana L.; Lindgreen, Stinus; Wilkinson, Adam C.; Finn, Robert D.; Griffiths-Jones, Sam; Eddy, Sean R.; Bateman, Alex
Title: Rfam: updates to the RNA families database Document date: 2008_10_25
ID: wj7yonjw_19
Snippet: A new version of Infernal (v1.0) is now available (http://infernal.janelia.org) and we plan to use this 0 Sequence conservation latest version to prepare the next major release of Rfam. Testing suggests that, compared with the version used for Rfam 9 (v0.72), v1.0 is faster and slightly more sensitive, whilst introducing for the first time E-values for hits returned from database searches. Although the speed increase will not be sufficient to obv.....
Document: A new version of Infernal (v1.0) is now available (http://infernal.janelia.org) and we plan to use this 0 Sequence conservation latest version to prepare the next major release of Rfam. Testing suggests that, compared with the version used for Rfam 9 (v0.72), v1.0 is faster and slightly more sensitive, whilst introducing for the first time E-values for hits returned from database searches. Although the speed increase will not be sufficient to obviate the need for BLAST filters in the Rfam production pipeline, this remains a major goal for Infernal development. Importantly, Infernal v1.0 is not compatible with the Rfam 9 CM files. Rfam/Infernal users may wish to generate new CMs from Rfam 9 SEED or FULL alignment files. We have mapped a subset of three-dimensional RNA structures found in the Protein DataBank (PDB) (25) (primarily SRP and ribosomal RNAs) to corresponding sequences in Rfam. In an initial feasibility study, we have demonstrated that RNA sequences can be retrieved from PDB files and mapped to Rfam sequences reliably. The mapping is currently performed using BLAT (26) to detect local regions of high similarity with high specificity. The positions of matches to Rfam entries are transferred to the PDB sequences, allowing us to colour threedimensional structures as in Figure 3 . We intend to rollout this mapping across all Rfam families and PDB entries using both local similarities and global matches to Rfam models. This sequence-to-structure mapping will allow us to use determined tertiary structures to calculate secondary structure as a quality control for existing families, and catalogue interactions between RNA-RNA and RNAprotein families.
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