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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
Rfam
 
Resource Report
Resource Website
1000+ mentions
Rfam (RRID:SCR_007891) Rfam, RFAM service resource, production service resource, data analysis service, data or information resource, analysis service resource, database The Rfam database is a collection of RNA families, each represented by multiple sequence alignments, consensus secondary structures and covariance models (CMs). The families in Rfam break down into three broad functional classes: Non-coding RNA genes, structured cis-regulatory elements and self-splicing RNAs. Typically these functional RNAs often have a conserved secondary structure which may be better preserved than the RNA sequence. The CMs used to describe each family are a slightly more complicated relative of the profile hidden Markov models (HMMs) used by Pfam. CMs can simultaneously model RNA sequence and the structure in an elegant and accurate fashion. Rfam is also available via FTP. You can find data in Rfam in various ways... * Analyze your RNA sequence for Rfam matches * View Rfam family annotation and alignments * View Rfam clan details * Query Rfam by keywords * Fetch families or sequences by NCBI taxonomy * Enter any type of accession or ID to jump to the page for a Rfam family, sequence or genome family, genome, clan, structure, non-coding rna, FASEB list has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom Howard Hughes Medical Institute ;
University of Manchester; Manchester; United Kingdom ;
Wellcome Trust WT077044/Z/05/Z
PMID:21062808 http://rfam.sanger.ac.uk/ SCR_007891 RFAM, Rfam database 2026-08-06 09:27:01 3693
Wellcome Trust Sanger Institute; Hinxton; United Kingdom
 
Resource Report
Resource Website
500+ mentions
Wellcome Trust Sanger Institute; Hinxton; United Kingdom (RRID:SCR_011784) WTSI, Sanger institution Non profit research organization for genome sequences to advance understanding of biology of humans and pathogens in order to improve human health globally. Provides data which can be translated for diagnostics, treatments or therapies including over 100 finished genomes, which can be downloaded. Data are publicly available on limited basis, and provided more extensively upon request. research, genome, sequence, human, health, project, global, data, treatment, therapy is listed by: re3data.org
is affiliated with: Open Targets
is related to: Clonalframe
is related to: ClonalOrigin
is related to: TraCeR
is parent organization of: ILLUMINUS
is parent organization of: ARNIE
is parent organization of: Sequence Search and Alignment by Hashing Algorithm
is parent organization of: Sequencing of Idd regions in the NOD mouse genome
is parent organization of: CAROL
is parent organization of: DINDEL
is parent organization of: Wellcome Trust Case Control Consortium
is parent organization of: OLORIN
is parent organization of: Exomiser
is parent organization of: COSMIC - Catalogue Of Somatic Mutations In Cancer
is parent organization of: GeneDB
is parent organization of: Breast Cancer Somatic Genetics Study
is parent organization of: Artemis: Genome Browser and Annotation Tool
is parent organization of: ACT: Artemis Comparison Tool
is parent organization of: Alien hunter
is parent organization of: Pfam
is parent organization of: DNAPlotter
is parent organization of: VAGrENT
is parent organization of: SMALT
is parent organization of: LookSeq
is parent organization of: ZMP
is parent organization of: Deciphering Developmental Disorders
is parent organization of: Sanger Mouse Resources Portal
is parent organization of: SpliceDB
is parent organization of: DECIPHER
is parent organization of: 1000 Genomes: A Deep Catalog of Human Genetic Variation
is parent organization of: Genes to Cognition: Neuroscience Research Programme
is parent organization of: MEROPS
is parent organization of: Rfam
is parent organization of: VEGA
is parent organization of: Bacterial Genomes
is parent organization of: Caenorhabditis Genome Sequencing Projects
is parent organization of: D. rerio Blast Server
is parent organization of: Fungi Sequencing Projects
is parent organization of: PEER
is parent organization of: Alfresco - FRont-End for Sequence COmparison
is parent organization of: AutoCSA (Automatic Comparative Sequence Analysis)
is parent organization of: AceDB
is parent organization of: CnD
is parent organization of: Genomics of Drug Sensitivity in Cancer
is parent organization of: Zebrafish Genome Project
is parent organization of: Tree families database
is parent organization of: Ensembl
is parent organization of: BamView
is parent organization of: SVMerge
is parent organization of: RetroSeq
is parent organization of: Consensus CDS
is parent organization of: WormBase
is parent organization of: Belvu
is parent organization of: Bio-tradis
is parent organization of: Blixem
is parent organization of: Dotter
is parent organization of: Exonerate
is parent organization of: Fastaq
is parent organization of: Gubbins
is parent organization of: CellPhoneDB
is parent organization of: Ensembl Metazoa
is parent organization of: Scmap
is parent organization of: Scfind
is parent organization of: Recognition of Errors in Assemblies using Paired Reads
is parent organization of: SAMTOOLS
is parent organization of: Cell Model Passports
Wellcome Trust ISNI: 0000 0004 0606 5382, nlx_91258, grid.10306.34, Wikidata: Q1142544 https://ror.org/05cy4wa09 SCR_011784 Wellcome Trust Sanger Institute, Genome Research Limited, The Wellcome Sanger Institute, Sanger Institute, Wellcome Trust Sanger Institute Genome Research Limited 2026-08-01 12:04:18 527

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