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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
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MIPS Ustilago maydis Database Resource Report Resource Website 1+ mentions |
MIPS Ustilago maydis Database (RRID:SCR_007563) | data or information resource, database | The MIPS Ustilago maydis Genome Database aims to present information on the molecular structure and functional network of the entirely sequenced, filamentous fungus Ustilago maydis. The underlying sequence is the initial release of the high quality draft sequence of the Broad Institute. The goal of the MIPS database is to provide a comprehensive genome database in the Genome Research Environment in parallel with other fungal genomes to enable in depth fungal comparative analysis. The specific aims are to: 1. Generate and assemble Whole Genome Shotgun sequence reads yielding 10X coverage of the U. maydis genome 2. Integrate the genomic sequence assembly with physical maps generated by Bayer CropScience 3. Perform automated annotation of the sequence assembly 4. Align the strain 521 assembly with the FB1 assembly provided by Exelixis 5. Release the sequence assembly and results of our annotation and analysis to public Ustilago maydis is a basidiomycete fungal pathogen of maize and teosinte. The genome size is approximately 20 Mb. The fungus induces tumors on host plants and forms masses of diploid teliospores. These spores germinate and form haploid meiotic products that can be propagated in culture as yeast-like cells. Haploid strains of opposite mating type fuse and form a filamentous, dikaryotic cell type that invades plant tissue to reinitiate infection. Ustilago maydis is an important model system for studying pathogen-host interactions and has been studied for more than 100 years by plant pathologists. Molecular genetic research with U. maydis focuses on recombination, the role of mating in pathogenesis, and signaling pathways that influence virulence. Recently, the fungus has emerged as an excellent experimental model for the molecular genetic analysis of phytopathogenesis, particularly in the characterization of infection-specific morphogenesis in response to signals from host plants. Ustilago maydis also serves as an important model for other basidiomycete plant pathogens that are more difficult to work with in the laboratory, such as the rust and bunt fungi. Genomic sequence of U. maydis will also be valuable for comparative analysis of other fungal genomes, especially with respect to understanding the host range of fungal phytopathogens. The analysis of U. maydis would provide a framework for studying the hundreds of other Ustilago species that attack important crops, such as barley, wheat, sorghum, and sugarcane. Comparisons would also be possible with other basidiomycete fungi, such as the important human pathogen C. neoformans. Commercially, U. maydis is an excellent model for the discovery of antifungal drugs. In addition, maize tumors caused by U. maydis are prized in Hispanic cuisine and there is interest in improving commercial production. The complete putative gene set of the Broad Institute''s second release is loaded into the database and in addition all deviating putative genes from a putative gene set produced by MIPS with different gene prediction parameters are also loaded. The complete dataset will then be analysed, gene predictions will be manually corrected due to combined information derived from different gene prediction algorithms and, more important, protein and EST comparisons. Gene prediction will be restricted to ORFs larger than 50 codons; smaller ORFs will be included only if similarities to other proteins or EST matches confirm their existence or if a coding region was postulated by all prediction programs used. The resulting proteins will be annotated. They will be classified according to the MIPS classification catalogue receiving appropriate descriptions. All proteins with a known, characterized homolog will be automatically assigned to functional categories using the MIPS functional catalog. All extracted proteins are in addition automatically analysed and annotated by the PEDANT suite. | drug, environment, filamentous, functional, fungal, fungal genome databases, fungus, gene, genetic, basidiomycete, cell, codon, culture, dikaryotic, diploid, genome, genomic, germinate, haploid, host, human, infection, maize, mating, meiotic, model, molecular, morphogenesis, network, orf, pathogen, pathologist, phytopathogen, phytopathogenesis, plant, protein, recombination, sequence, signal, spore, strain, structure, teliospore, teosinte, tissue, tumor, ustilago maydis, virulence, yeast | nif-0000-21276 | SCR_007563 | MUMDB | 2026-08-29 11:29:53 | 9 | ||||||||||
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Olfactory Bulb Odor Map DataBase (OdorMapDB) Resource Report Resource Website |
Olfactory Bulb Odor Map DataBase (OdorMapDB) (RRID:SCR_007287) | OdorMapDB | atlas, data or information resource, database | OdorMapDB is designed to be a database to support the experimental analysis of the molecular and functional organization of the olfactory bulb and its basis for the perception of smell. It is primarily concerned with archiving, searching and analyzing maps of the olfactory bulb generated by different methods. The first aim is to facilitate comparison of activity patterns elicited by odor stimulation in the glomerular layer obtained by different methods in different species. It is further aimed at facilitating comparison of these maps with molecular maps of the projections of olfactory receptor neuron subsets to different glomeruli, especially for gene targeted animals and for antibody staining. The main maps archived here are based on original studies using 2-deoxyglucose and on current studies using high resolution fMRI in mouse and rat. Links are also provided to sites containing maps by other laboratories. OdorMapDB thus serves as a nodal point in a multilaboratory effort to construct consensus maps integrating data from different methodological approaches. OdorMapDB is integrated with two other databases in SenseLab: ORDB, a database of olfactory receptor genes and proteins, and OdorDB, a database of odor molecules that serve as ligands for the olfactory receptor proteins. The combined use of the three integrated databases allows the user to identify odor ligands that activate olfactory receptors that project to specific glomeruli that are involved in generating the odor activity maps. | odor, male, urine, mouse, methyl anisole, patchone, indole, helional, butyrophenone, fenchone, olfactory bulb, fmri, rat, odor ligand, olfactory receptor, smell |
is used by: NIF Data Federation has parent organization: Yale University; Connecticut; USA |
Aging | The Human Brain Project ; NIMH ; NIA ; NICD ; NINDS ; Multidisciplinary University Research Initiative ; NIDCD RO1 DC 009977 |
PMID:15067166 | nif-0000-00057 | SCR_007287 | OdorMap DB, Odor Map Database | 2026-08-29 11:29:51 | 0 | |||||
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POOLSCORE Resource Report Resource Website |
POOLSCORE (RRID:SCR_007514) | software application, software resource | Software program for analysis of case-control genetic association studies using allele frequency measurements on DNA pools (entry from Genetic Analysis Software) | gene, genetic, genomic, r | is listed by: Genetic Analysis Software | SCR_009373, nlx_154595, nlx_154087 | SCR_007514 | R/POOLSCORE | 2026-08-29 11:30:00 | 0 | |||||||||
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ChromDB- the chromatin database Resource Report Resource Website 50+ mentions |
ChromDB- the chromatin database (RRID:SCR_007597) | data or information resource, database | ChromDB is a chromatin database. Three types of sequences are included in the database: genomic-based (predominantly plant sequences); transcript-based (EST contigs or cDNAs for plants lacking a sequenced genome); and NCBI RefSeq sequences for a variety of model animal organisms. The Gene Record Page for any sequence indicates the type of sequence. The broad mission of ChromDB is display, annotate, and curate sequences of two broad functional classes of biologically important proteins: chromatin-associated proteins (CAPs) and RNA interference-associated proteins. Plant proteins are the major focus of the work support by The Plant Genome Research Program (PGRP) of the National Science Foundation. Our intent is to produce intensively curated sequence information and make it available to the research and teaching community in support of comparative analyses toward understanding the chromatin proteome in plants, especially in important crop species. In order to do a comparative analysis, it is necessary to include non-plant proteins in the database. Non-plant genes are not curated to the degree carried out for plants and to automate the process of data import, our non-plant genes are from the RefSeq database of NCBI. We reason that the inclusion of non-plant, model organisms will broaden the relevance and usefulness of ChromDB to the entire chromatin community and will provide a more complete data set for phylogenetic analyses in support of the evolution of the plant chromatin proteome. ChromDB is funded by a grant from the National Science Foundation Plant Genome Research Project(#DBI-0421679). | chromatin, chromatin-associated protein, crop species chromatin, plant chromatin proteome, plant protein, rna interference-associated proteins, FASEB list | has parent organization: University of Arizona; Arizona; USA | nif-0000-02661 | SCR_007597 | ChromDB | 2026-08-29 11:30:02 | 62 | |||||||||
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Ciliate IES-MDS database Resource Report Resource Website 1+ mentions |
Ciliate IES-MDS database (RRID:SCR_007599) | data or information resource, database | IES-MDS DB is a database of macronuclear and micronuclear genes in spirotrichous ciliates. The database contains information on 440 MDS pairs (each pair composed of the MIC and the MAC version of a given MDS), 392 IES and 361 pointer triples (each pointer has two active copies in the MIC and one copy in the MAC) (7). Out of the 440 MDSs, 235 are scrambled, and 65 are in the opposite strand in the MIC. A total of 320 IESs and 202 pointers are scrambled. For each pair of genes in the database the user can see the micronuclear and macronuclear organization and has the option to see all the MDS, IES and pointer sequences. Another option is to download the MIC sequence with the MDSs and pointers in uppercase and the IESs in lowercase. It is also possible to graphically compare the organization of several genes. | macronuclear gene, micronuclear gene, spirotrichous ciliate | has parent organization: Princeton University; New Jersey; USA | nif-0000-02663 | SCR_007599 | IES-MDS DB | 2026-08-29 11:29:55 | 1 | |||||||||
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ChemDB: The UC Irvine ChemDB Resource Report Resource Website 10+ mentions |
ChemDB: The UC Irvine ChemDB (RRID:SCR_007594) | data or information resource, database | A database of general chemical information. The datasets are comprised of various available chemical datasets annotated with interesting properties to train and test machine-learning prediction and searching methods. Tools provided include ChemicalSearch, Virtual Chemical Space, Reaction Explorer, Datasets, and supplemental material. ChemicalSearch is a tool that allows users to find a chemical by basic criteria like molecular weight and predicted logP, or by the more abstract notion of structural similarity. Virtual Chemical Space is a tool which lets users interactively deconstruct target compounds into component precursors and reconstruct similar building-blocks into combinatorial libraries representing the virtual chemical space near the target compound. Reaction Explorer is a synthesis explorer and mechanism explorer. It provides an interactive system for learning and practicing reactions, syntheses and mechanisms in organic chemistry, with advanced support for the automatic generation of random problems, curved-arrow mechanism diagrams, and inquiry-based learning. | chemical, chemical property, chemical reaction, chemistry, compound, organic chemistry, synthesis, software |
is listed by: 3DVC has parent organization: University of California at Irvine; California; USA |
nif-0000-02657 | SCR_007594 | ChemDB | 2026-08-29 11:30:02 | 14 | |||||||||
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Atlas of Genetics and Cytogenetics in Oncology and Haematology Resource Report Resource Website 10+ mentions |
Atlas of Genetics and Cytogenetics in Oncology and Haematology (RRID:SCR_007199) | atlas, data or information resource, database | Online journal and database devoted to genes, cytogenetics, and clinical entities in cancer, and cancer-prone diseases. Its aim is to cover the entire field under study and it presents concise and updated reviews (cards) or longer texts (deep insights) concerning topics in cancer research and genomics. | gene, cytogenetic, cancer, cancer research, genomic, online journal, bio.tools, FASEB list |
is listed by: Debian is listed by: bio.tools |
PMID:23161685 | Freely available, Available to the scientific community | nif-0000-30129, biotools:atlasgeneticsoncology | https://bio.tools/atlasgeneticsoncology | SCR_007199 | Genetics and Cytogenetics Atlas | 2026-08-29 11:29:57 | 43 | ||||||
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Chicken Variation Database Resource Report Resource Website 1+ mentions |
Chicken Variation Database (RRID:SCR_007595) | data or information resource, database | ChickVD hosts high-quality sequence variation data, variation analysis in the context of chicken genes, cDNAs, chicken orthologs of human disease genes, genetic markers, quantitative trait loci (QTLs) etc . All data are uniquely mapped onto the RJF draft genome and graphically represented in MapView, an efficient visualization tool that allows users to browse sequence variations in the genomic and functional context. The sub-viewer TraceView assists users to view the vivid graphics of the original traces around the detected SNP. Users may query the data by the online search tool and define concrete limitations to extract records that are best suited to their research needs. For the convenience of data presentation in ChickVD, different types of sequence variations (substitutions, insertions or deletions) are all referred as ???SNPs''. ChickVD is updated constantly as more data generated and is under the continued improvement for its content and functionality | chicken, chicken cdna, chicken gene, chicken genetics, chicken genome, chicken ortholog of human gene, chicken quantitative trait loci, genome visualization, mapview, traceview | has parent organization: BGI; Shenzhen; China | nif-0000-02658 | SCR_007595 | ChickVD | 2026-08-29 11:29:51 | 4 | |||||||||
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Cleansed EST Database Resource Report Resource Website 1+ mentions |
Cleansed EST Database (RRID:SCR_007587) | data or information resource, database | A database to provide cleansed EST sequences of classified dbEST libraries. All dbEST libraries were classified according to organism, sequencing center, and eVOC ontologies (for human libraries). For each dbEST library, we provide three different EST sequences: raw, pre-cleansed, and user-cleansed. pre-cleansed ESTs are obtained from major contamination databases and cleaned of contaminated sequences. User-cleansed ESTs, however, involve the use of an automatic user-cleansing pipeline, in which sequences in a user-selected library are cleansed on-the-fly according to user-input options. CleanEST contains 62,008,259 EST sequences (24,000 libraries) with contamination information. | est, cleansed est sequence, contamination database, dbest | nif-0000-02666 | SCR_007587 | CleanEST | 2026-08-29 11:29:51 | 1 | ||||||||||
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COPE: Cytokines and Cells Online Pathfinder Encyclopaedia Resource Report Resource Website 100+ mentions |
COPE: Cytokines and Cells Online Pathfinder Encyclopaedia (RRID:SCR_007187) | data or information resource, database | COPE is an encyclopedia of cytokines and has fully integrated subdictionaries on Angiogenesis, Apoptosis, Bacterial Modulins, CD Antigens, Cell lines, Eukaryotic cell types, Chemokines, CytokineTopics, Cytokine Concentrations in Body Fluids, Cytokine Inter-Species Reactivities, Dual identity proteins, Hematology, Innate Immunity Defense Proteins, Metalloproteinases, Protein domains, Regulatory peptide factors, Virokines, Viroceptors, and Virulence Factors. Most entries have a description as well as references. | FASEB list | has parent organization: COPE | nif-0000-00783 | SCR_007187 | Cytokines and Cells Online Pathfinder Encyclopedia, COPE | 2026-08-29 11:29:49 | 162 | |||||||||
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CATH: Protein Structure Classification Resource Report Resource Website 100+ mentions |
CATH: Protein Structure Classification (RRID:SCR_007583) | data or information resource, database | CATH is a hierarchical classification of protein domain structures, which clusters proteins at four major levels: Class (C), Architecture (A), Topology (T) and Homologous superfamily (H). The boundaries and assignments for each protein domain are determined using a combination of automated and manual procedures which include computational techniques, empirical and statistical evidence, literature review and expert analysis Users can search CATH by ID/Sequence/text. They can also browse CATH from the top of the hierarchy, or download CATH data. | architecture, class, homologous superfamily, protein cluster, protein domain structure, topology, bio.tools, FASEB list |
is listed by: bio.tools is listed by: Debian is related to: FunTree has parent organization: University College London; London; United Kingdom |
nif-0000-02640, r3d100012629, biotools:cath | https://bio.tools/cath, https://doi.org/10.17616/R32Z1F | SCR_007583 | CATH | 2026-08-29 11:29:54 | 306 | ||||||||
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Combinatorial Extension (CE) Resource Report Resource Website 1+ mentions |
Combinatorial Extension (CE) (RRID:SCR_007585) | CE | data or information resource, database | CE is a databases of alignments for all polypeptide chains. A representative set of proteins is available and kept current with the PDB, a method for calculating pairwise structure alignments. CE aligns two polypeptide chains using characteristics of their local geometry as defined by vectors between C alpha positions. Matches are termed aligned fragment pairs (AFPs). Heuristics are used in defining a set of optimal paths joining AFPs with gaps as needed. The path with the best RMSD is subject to dynamic programming to achieve an optimal alignment. For specific families of proteins additional characteristics are used to weight the alignment. Complete details are described in the paper (PDF format). Databases of alignments for all polypeptide chains and a representative set of proteins is available and kept current with the PDB | polypeptide, polypeptide chain, protein, protein alignment, protein structure |
is listed by: 3DVC is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB) has parent organization: University of California at San Diego; California; USA |
nif-0000-02648 | http://cl.sdsc.edu/ce.html | SCR_007585 | Combinatorial extension | 2026-08-29 11:30:01 | 5 | |||||||
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SDSC Biology Workbench Resource Report Resource Website 10+ mentions |
SDSC Biology Workbench (RRID:SCR_007188) | data or information resource, database, service resource | The Biology WorkBench is a web-based tool for biologists. The WorkBench allows biologists to search many popular protein and nucleic acid sequence databases. Database searching is integrated with access to a wide variety of analysis and modeling tools, all within a point and click interface that eliminates file format compatibility problems. Register for a free account. | has parent organization: University of California at San Diego; California; USA | nlx_28496 | SCR_007188 | Biology Workbench | 2026-08-29 11:29:50 | 12 | ||||||||||
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CASRDB- Calcium Sensing Receptor Database Resource Report Resource Website 10+ mentions |
CASRDB- Calcium Sensing Receptor Database (RRID:SCR_007581) | data or information resource, database | CASRdb is a calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia. The information can be searched by mutation, genotype-phenotype, clinical data, in vitro analyses, and authors of publications describing the mutations. CASRdb is regularly updated for new mutations and it also provides a mutation submission form to ensure up-to-date information. The home page of this database provides links to different web pages that are relevant to the CASR, as well as disease clinical pages, sequence of the CASR gene exons, and position of mutations in the CASR. The CASRdb will help researchers to better understand and analyze the mutations, and aid in structure-function analyses. | familial hypocalciuric hypercalcemia, benign hypocalciuric hypercalcemia, calcium-sensing, hypocalciuric hypercalcemia, mutation causing hypocalciuric hypercalcemia | has parent organization: McGill University; Montreal; Canada | r3d100012040, nif-0000-02638 | https://doi.org/10.17616/R3X07T | SCR_007581 | CASRDB | 2026-08-29 11:29:54 | 21 | ||||||||
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Bath Information and Data Services Resource Report Resource Website 1+ mentions |
Bath Information and Data Services (RRID:SCR_007184) | data or information resource, database | BIDS provided bibliographic database services to the academic community in the UK. Their mission is to provide, on a not-for-profit basis, the highest possible level of service to allow UK Academic institutions and their members access to bibliographic data, scholarly publications and research data. BIDS is believed to have been a world first - a national service providing widespread network access to commercially supplied bibliographic databases, free at the point of delivery. BIDS academic and scholarly journals services are now incorporated into IngentaConnect www.ingentaconnect.com If you are a student, researcher or member of staff at a UK higher or further education institution you can access any of the services to which your institution has subscribed. In addition, there are some services which can be searched without a subscription. These include ingentaJournals and Medline. You can discover which services are available to you by logging in to BIDS with your Athens username and password. All available services will be highlighted in the service selection page. | database, academic, scholarly, journal, education, research | JISC | nif-0000-30162 | SCR_007184 | BIDS | 2026-08-29 11:29:57 | 1 | |||||||||
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Next-Gen Sequencing Resource Report Resource Website |
Next-Gen Sequencing (RRID:SCR_007245) | Next-Gen Sequencing | blog, data or information resource, narrative resource | A working guide to the rapidly developing world of Next-Generation DNA sequencing, with an emphasis on bioinformatics. | is listed by: OMICtools | OMICS_01717 | SCR_007245 | 2026-08-29 11:29:50 | 0 | ||||||||||
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psychometric Resource Report Resource Website 1+ mentions |
psychometric (RRID:SCR_024295) | software resource, software toolkit | Software R package for measurement theory, meta-analysis, reliability, item analysis, inter-rater reliability, classical utility, and correlation | psychometric theory, measurement theory, meta-analysis, reliability, item analysis, inter-rater reliability, classical utility, correlation | is listed by: Debian | Free, Available for download, Freely available, | https://sources.debian.org/src/r-cran-psychometric/ | SCR_024295 | Applied Psychometric Theory | 2026-08-29 11:29:10 | 1 | ||||||||
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rniftilib Resource Report Resource Website |
rniftilib (RRID:SCR_024296) | software resource, software toolkit | Software R package provides R-interface to the NIfTI reference implementation the niftilib C-library. | R-interface, NIfTI reference implementation, niftilib C-library, | is listed by: Debian | Free, Available for download, Freely available, | https://sources.debian.org/src/r-cran-rniftilib/ | SCR_024296 | 2026-08-29 11:29:11 | 0 | |||||||||
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SimpleITK Resource Report Resource Website 50+ mentions |
SimpleITK (RRID:SCR_024693) | software library, software resource, software toolkit | Open source software library for multi dimensional image analysis in Python, R, Java, C#, Lua, Ruby, TCL and C++. New interface to Insight Segmentation and Registration Toolkit (ITK) designed to facilitate rapid prototyping, education and scientific activities via high level programming languages. Provides easy to use and simplified interface to ITK's algorithms. | multi dimensional image analysis, Insight Segmentation and Registration Toolkit, | is related to: Insight Segmentation and Registration Toolkit | NLM | PMID:24416015 | Free, Available for download, Freely available | https://github.com/SimpleITK/SimpleITK | SCR_024693 | Simple Insight Segmentation and Registration Toolkit | 2026-08-29 11:29:13 | 69 | ||||||
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rook Resource Report Resource Website |
rook (RRID:SCR_024298) | software resource, software toolkit | Web server for R with documented API to interface between R and the server. The documentation contains the Rook specification and details for building and running Rook applications. | web server for R, building and running Rook applications, | is listed by: Debian | Free, Available for download, Freely available, | https://sources.debian.org/src/r-cran-rook/ | SCR_024298 | 2026-08-29 11:29:01 | 0 |
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