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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
ToppGene Suite
 
Resource Report
Resource Website
1000+ mentions
ToppGene Suite (RRID:SCR_005726) analysis service resource, data analysis service, data or information resource, database, portal, production service resource, resource, service resource ToppGene Suite is a one-stop portal for gene list enrichment analysis and candidate gene prioritization based on functional annotations and protein interactions network. ToppGene Suite is a one-stop portal for (i) gene list functional enrichment, (ii) candidate gene prioritization using either functional annotations or network analysis and (iii) identification and prioritization of novel disease candidate genes in the interactome. Functional annotation-based disease candidate gene prioritization uses a fuzzy-based similarity measure to compute the similarity between any two genes based on semantic annotations. The similarity scores from individual features are combined into an overall score using statistical meta-analysis. gene portal, enrichment analysis, functional annotation, gene prioritization, protein interaction, bio.tools, FASEB list is listed by: Gene Ontology Tools
is listed by: NIDDK Information Network (dkNET)
is listed by: GUDMAP Ontology
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
is related to: ToppCluster
State of Ohio Computational Medicine Center ODD TECH 04-042;
NIDDK 1U01DK70219;
NIDDK P30DK078392
PMID:19465376 Free for academic use nlx_149183, biotools:toppgene_suite https://bio.tools/toppgene_suite SCR_005726 ToppGene 2026-09-05 06:25:40 1131
TMAJ
 
Resource Report
Resource Website
10+ mentions
TMAJ (RRID:SCR_005601) TMAJ software resource Open-source software to support information and images related to tissue micro-arrays. It contains support for multiple organ systems, multiple users, image analysis, and is designed to be compliant with HIPPA regulations. Patients, specimens, blocks, slides, cores, images, and scores can all be stored and viewed. Features include advanced security, custom dynamic fields, and an image analysis program. tissue microarray, java, java swing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Johns Hopkins University; Maryland; USA
has parent organization: SourceForge
GNU General Public License, v3 biotools:tmaj, OMICS_00823 https://bio.tools/tmaj SCR_005601 TMAJ Software Project 2026-09-05 06:25:38 10
GoFish
 
Resource Report
Resource Website
1+ mentions
GoFish (RRID:SCR_005682) GoFish analysis service resource, data analysis service, production service resource, service resource, software resource, source code Software program, available as a Java applet online or to download, allows the user to select a subset of Gene Ontology (GO) attributes, and ranks genes according to the probability of having all those attributes., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. gene, ontology or annotation browser, java, windows, mac os x, linux, unix, bio.tools is listed by: Gene Ontology Tools
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
has parent organization: University of Toronto; Ontario; Canada
has parent organization: Harvard Medical School; Massachusetts; USA
Aventis Pharmaceuticals ;
Howard Hughes Medical Institute ;
NHGRI
PMID:12691998 THIS RESOURCE IS NO LONGER IN SERVICE biotools:gofish, nlx_149126, OMICS_02272 http://llama.mshri.on.ca/Software.html, https://bio.tools/gofish SCR_005682 2026-09-05 06:25:40 1
Maqview
 
Resource Report
Resource Website
Maqview (RRID:SCR_005632) MaqView data processing software, data visualization software, software application, software resource A graphical read alignment viewer specifically designed for the Maq alignment file and allows you to see the mismatches, base qualities and mapping qualities. It is highly efficient in speed, memory and disk usage. Maqview is based on OpenGL and is known to work on both Mac OS X and Linux. Porting to Windows is in principle easy. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
DOI:10.1101/gr.078212.108 GNU General Public License OMICS_00889, biotools:maqview https://bio.tools/maqview, https://sources.debian.org/src/maqview/ SCR_005632 Mapping and Assembly with Qualities Viewer, M.A.Q Viewer 2026-09-05 06:25:39 0
Staden Package
 
Resource Report
Resource Website
50+ mentions
Staden Package (RRID:SCR_005629) software resource A fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin) for Unix, Linux, MacOSX and MS Windows. c, unix/linux, sequence assembly, dna/protein analysis, spin, sequence alignment, genome, genome viewer, c++, fortran, tcl, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:20513662
DOI:10.1093/bioinformatics/btq268
BSD License OMICS_00894, biotools:staden https://bio.tools/staden, https://sources.debian.org/src/staden/ SCR_005629 Staden Package 2026-09-05 06:25:39 87
FunCluster
 
Resource Report
Resource Website
1+ mentions
FunCluster (RRID:SCR_005774) FunCluster data analysis software, data processing software, software application, software resource FunCluster is a genomic data analysis algorithm which performs functional analysis of gene expression data obtained from cDNA microarray experiments. Besides automated functional annotation of gene expression data, FunCluster functional analysis aims to detect co-regulated biological processes through a specially designed clustering procedure involving biological annotations and gene expression data. FunCluster''''s functional analysis relies on Gene Ontology and KEGG annotations and is currently available for three organisms: Homo Sapiens, Mus Musculus and Saccharomyces Cerevisiae. FunCluster is provided as a standalone R package, which can be run on any operating system for which an R environment implementation is available (Windows, Mac OS, various flavors of Linux and Unix). Download it from the FunCluster website, or from the worldwide mirrors of CRAN. FunCluster is provided freely under the GNU General Public License 2.0. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible genomic, gene, functional analysis, gene expression, cdna microarray, cdna, microarray, function, cluster, annotation, biological process, statistical analysis, bio.tools is listed by: Gene Ontology Tools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
has parent organization: Cordelier Research Center
PMID:17007070
PMID:16506959
PMID:16046292
Free for academic use, GNU General Public License, v2 nlx_149242, biotools:funcluster https://bio.tools/funcluster SCR_005774 FunCluster R Package, FunCluster Algorithm 2026-09-05 06:25:41 2
InterProScan
 
Resource Report
Resource Website
5000+ mentions
InterProScan (RRID:SCR_005829) analysis service resource, data access protocol, data analysis service, data analysis software, data processing software, production service resource, service resource, software application, software resource, web service Software package for functional analysis of sequences by classifying them into families and predicting presence of domains and sites. Scans sequences against InterPro's signatures. Characterizes nucleotide or protein function by matching it with models from several different databases. Used in large scale analysis of whole proteomes, genomes and metagenomes. Available as Web based version and standalone Perl version and SOAP Web Service. functional, analysis, sequence, protein, nucleotide, predict, presence, domain, site, proteome, genome, metagenome, bio.tools is listed by: Gene Ontology Tools
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
is related to: Gene Ontology
is related to: RARTF
is related to: InterPro
is related to: LegumeIP
is related to: UniProtKB
has parent organization: European Bioinformatics Institute
Biotechnology and Biological Sciences Research Council ;
EMBL ;
European Union
PMID:15980438
PMID:17202162
PMID:24451626
Free, Available for download, Freely available OMICS_01479, biotools:interproscan_4, nlx_149337 https://www.ebi.ac.uk/interpro/download.html, https://bio.tools/interproscan_4 SCR_005829 InterProScan Sequence Search, InterProScan 2, InterProScan 3, InterProScan 4, InterProScan 5 2026-09-05 06:25:42 7512
ccPDB - Compilation and Creation of datasets from PDB
 
Resource Report
Resource Website
1+ mentions
ccPDB - Compilation and Creation of datasets from PDB (RRID:SCR_005870) ccPDB data access protocol, data or information resource, database, software resource, web service ccPDB (Compilation and Creation of datasets from PDB) is designed to provide service to scientific community working in the field of function or structure annoation of proteins. This database of datasets is based on Protein Data Bank (PDB), where all datasets were derived from PDB. ccPDB have four modules; i) compilation of datasets, ii) creation of datasets, iii) web services and iv) Important links. * Compilation of Datasets: Datasets at ccPDB can be classified in two categories, i) datasets collected from literature and ii) datasets compiled from PDB. We are in process of collecting PDB datasetsfrom literature and maintaining at ccPDB. We are also requesting community to suggest datasets. In addition, we generate datasets from PDB, these datasets were generated using commonly used standard protocols like non-redundant chains, structures solved at high resolution. * Creation of datasets: This module developed for creating customized datasets where user can create a dataset using his/her conditions from PDB. This module will be useful for those users who wish to create a new dataset as per ones requirement. This module have six steps, which are described in help page. * Web Services: We integrated following web services in ccPDB; i) Analyze of PDB ID service allows user to submit their PDB on around 40 servers from single point, ii) BLAST search allows user to perform BLAST search of their protein against PDB, iii) Structural information service is designed for annotating a protein structure from PDB ID, iv) Search in PDB facilitate user in searching structures in PDB, v)Generate patterns service facility to generate different types of patterns required for machine learning techniques and vi) Download useful information allows user to download various types of information for a given set of proteins (PDB IDs). * Important Links: One of major objectives of this web site is to provide links to web servers related to functional annotation of proteins. In first phase we have collected and compiled these links in different categories. In future attempt will be made to collect as many links as possible. secondary structure, nucleic acid interaction, ligand interaction, structure, nucleic acid, interaction, ligand, data set, function, protein, annotate, tight-turn, nucleotide interacting residue, metals interacting residue, dna/rna binding residue, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
has parent organization: Institute of Microbial Technology; Chandigarh; India
OSDD ;
DBT ;
Council of Scientific and Industrial Research; New Delhi; India
PMID:22139939 biotools:ccpdb, nlx_149416 https://bio.tools/ccpdb SCR_005870 Compilation and Creation of datasets from PDB, ccPDB - Compilation Creation of datasets from PDB 2026-09-05 06:25:43 2
UTRdb/UTRsite
 
Resource Report
Resource Website
10+ mentions
UTRdb/UTRsite (RRID:SCR_005868) data or information resource, portal, topical portal UTRdb/UTRsite is a portal to other databases, including Nucleotide Sequence Databases, Protein Sequence Databases, other Sequence databanks, Untranslated Nucleotide Sequence Databases, Mitochondrial Databases, Mutation Databases, and others. The site also allows users to start long-term permanent projects or just to do quick searches, depending on the user''s needs. bio.tools, FASEB list is listed by: bio.tools
is listed by: Debian
biotools:utrdb, nif-0000-03619 https://bio.tools/utrdb http://bighost.area.ba.cnr.it/srs6/ SCR_005868 UTRdb/UTRsite 2026-09-05 06:25:43 41
GWAMA
 
Resource Report
Resource Website
100+ mentions
GWAMA (RRID:SCR_006624) GWAMA data analysis software, data processing software, software application, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 28,2023. Software tool for meta analysis of whole genome association data. meta, analysis, genome, association, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Wellcome Trust Centre for Human Genetics
PMID:20509871
DOI:10.1186/1471-2105-11-288
THIS RESOURCE IS NO LONGER IN SERVICE biotools:gwama, OMICS_00235 https://bio.tools/gwama, https://sources.debian.org/src/gwama/ http://www.well.ox.ac.uk/GWAMA/ SCR_006624 Genome-Wide Association Meta Analysis 2026-09-05 06:25:57 177
casper
 
Resource Report
Resource Website
100+ mentions
casper (RRID:SCR_006613) casper software resource Software to infer alternative splicing from paired-end RNA-seq data. The model is based on counting paths across exons, rather than pairwise exon connections, and estimates the fragment size and start distributions non-parametrically, which improves estimation precision. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
GNU General Public License, v2 or greater biotools:casper, OMICS_01270 https://bio.tools/casper SCR_006613 casper - Characterization of Alternative Splicing based on Paired-End Reads, Characterization of Alternative Splicing based on Paired-End Reads 2026-09-05 06:25:57 152
MIRIAM Resources
 
Resource Report
Resource Website
1+ mentions
MIRIAM Resources (RRID:SCR_006697) catalog, data access protocol, data or information resource, database, narrative resource, software resource, standard specification, web service A set of online services created in support of MIRIAM, a set of guidelines for the annotation and curation of computational models. The core of MIRIAM Resources is a catalogue of data types (namespaces corresponding to controlled vocabularies or databases), their URIs and the corresponding physical URLs or resources. Access to this data is made available via exports (XML) and Web Services (SOAP). MIRIAM Resources are developed and maintained under the BioModels.net initiative, and are free for use by all. MIRIAM Resources are composed of four components: a database, some Web Services, a Java library and this web application. * Database: The core of the system is a MySQL database. It allows us to store the data types (which can be controlled vocabularies or databases), their URIs and the corresponding physical URLs, and other details such as documentation and resource identifier patterns. Each entry contains a diverse set of details about the data type: official name and synonyms, root URI, pattern of identifiers, documentation, etc. Moreover, each data type can be associated with several resources (or physical locations). * Web Services: Programmatic access to the data is available via Web Services (based on Apache Axis and SOAP messages). In addition, REST-based services are currently being developed. This API allows one to not only resolve model annotations, but also to generate appropriate URIs, based upon the provision of a resource name and accession number. A list of available web services, and a WSDL are provided. A browser-based online demonstration of the Web Services is also available to try. * Java Library: A Java library is provided to access the Web Services. The documentation explains where to download it, its dependencies, and how to use it. * Web Application: A Web application, using an Apache Tomcat server, offers access to the whole data set via a Web browser. It is possible to browse by data type names as well as browse by tags. A search engine is also provided. life science, bio.tools is used by: Identifiers.org
is listed by: bio.tools
is listed by: Debian
has parent organization: European Bioinformatics Institute
PMID:22140103
PMID:18078503
Free nlx_69582, biotools:miriam https://bio.tools/miriam SCR_006697 MIRIAM Registry 2026-09-05 06:25:59 1
Immune Epitope Database and Analysis Resource (IEDB)
 
Resource Report
Resource Website
500+ mentions
Immune Epitope Database and Analysis Resource (IEDB) (RRID:SCR_006604) IEDB analysis service resource, data analysis service, data repository, production service resource, service resource, storage service resource Repository contains antibody/B cell and T cell epitope information and epitope prediction and analysis tools. Immune epitopes are defined as molecular structures recognized by specific antigen receptors of the immune system, namely antibodies, B cell receptors, and T cell receptors. Immune epitopes from infectious diseases, excluding HIV, and immune-mediated diseases and the accompanying biological information are included. human, non-human primate, rodent, pig, cat, non-human animal, t cell, b cell, epitope, infectious disease, major histocompatibility complex, bio.tools, FASEB list is listed by: NIH Data Sharing Repositories
is listed by: Debian
is listed by: bio.tools
is affiliated with: AIRR Knowledge Commons
has parent organization: NIAID
has organization facet: La Jolla Institute for Immunology
niad PMID:39558162 open nif-0000-03017, biotools:iedb, r3d100012702 https://nextgen-tools.iedb.org/, https://doi.org/10.17616/R3X217 SCR_006604 Immune Epitope Database and Analysis Resource, , IEDB 2026-09-05 06:25:57 622
SpliceTrap
 
Resource Report
Resource Website
10+ mentions
SpliceTrap (RRID:SCR_006728) SpliceTrap software resource A statistic tool for quantifying exon inclusion ratios in paired-end RNA-seq data, with broad applications for the study of alternative splicing. SpliceTrap approaches to exon inclusion level estimation as a Bayesian inference problem. For every exon it quantifies the extent to which it is included, skipped or subjected to size variations due to alternative 3?/5? splice sites or Intron Retention. In addition, SpliceTrap can quantify alternative splicing within a single cellular condition, with no need of a background set of reads. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Galaxy
has parent organization: Cold Spring Harbor Laboratory
PMID:21896509 biotools:splicetrap, OMICS_01292 https://bio.tools/splicetrap SCR_006728 2026-09-05 06:25:59 16
BEDTools
 
Resource Report
Resource Website
10000+ mentions
BEDTools (RRID:SCR_006646) BEDTools software resource A powerful toolset for genome arithmetic allowing one to address common genomics tasks such as finding feature overlaps and computing coverage. Bedtools allows one to intersect, merge, count, complement, and shuffle genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF. While each individual tool is designed to do a relatively simple task (e.g., intersect two interval files), quite sophisticated analyses can be conducted by combining multiple bedtools operations on the UNIX command line. genomics, bed, sam, bam, overlap, sequencing, intersect, coverage, gff, vcf, bedgraph, interval, genome arithmetic, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
is related to: Hydra
is related to: pybedtools
is required by: SL-quant
PMID:20110278
DOI:10.1093/bioinformatics/btq033
GNU General Public License, v2, Acknowledgement requested OMICS_01159, biotools:bedtools https://code.google.com/p/bedtools/, https://bio.tools/bedtools, https://sources.debian.org/src/bedtools/ SCR_006646 bedtools - a swiss army knife for genome arithmetic, bedtools: a flexible suite of utilities for comparing genomic features 2026-09-05 06:25:58 11365
Dictyostelium discoideum genome database
 
Resource Report
Resource Website
100+ mentions
Dictyostelium discoideum genome database (RRID:SCR_006643) dictyBase, dictyBase gene name, dictyBase REF, DictyBase biomaterial supply resource, material resource, organism supplier Model organism database for the social amoeba Dictyostelium discoideum that provides the biomedical research community with integrated, high quality data and tools for Dictyostelium discoideum and related species. dictyBase houses the complete genome sequence, ESTs, and the entire body of literature relevant to Dictyostelium. This information is curated to provide accurate gene models and functional annotations, with the goal of fully annotating the genome to provide a ''''reference genome'''' in the Amoebozoa clade. They highlight several new features in the present update: (i) new annotations; (ii) improved interface with web 2.0 functionality; (iii) the initial steps towards a genome portal for the Amoebozoa; (iv) ortholog display; and (v) the complete integration of the Dicty Stock Center with dictyBase. The Dicty Stock Center currently holds over 1500 strains targeting over 930 different genes. There are over 100 different distinct amoebozoan species. In addition, the collection contains nearly 600 plasmids and other materials such as antibodies and cDNA libraries. The strain collection includes: * strain catalog * natural isolates * MNNG chemical mutants * tester strains for parasexual genetics * auxotroph strains * null mutants * GFP-labeled strains for cell biology * plasmid catalog The Dicty Stock Center can accept Dictyostelium strains, plasmids, and other materials relevant for research using Dictyostelium such as antibodies and cDNA or genomic libraries. genome, sequence, est, literature, gene model, functional annotation, reference genome, gene, antibody, cdna, bacteria, dictyostelium discoideum, dictyostelium purpureum, dictyostelium fasciculatum, polysphondylium pallidium, bio.tools is used by: NIF Data Federation
is listed by: One Mind Biospecimen Bank Listing
is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: AmiGO
is related to: Textpresso
has parent organization: Northwestern University; Illinois; USA
has parent organization: Baylor University; Texas; USA
has parent organization: University of Cologne; Cologne; Germany
is parent organization of: Dictyostelium Discoideum Anatomy Ontology
is parent organization of: Dictyostelium Anatomy Ontology
is parent organization of: dictyBase - Teaching Tools Using Dictyostelium discoideum
European Union ;
NHGRI HG0022;
NIGMS GM087371;
NIGMS GM64426
PMID:23172289
PMID:21087999
PMID:18974179
PMID:14681427
PMID:16381903
biotools:dictybase, nif-0000-20974, SCR_008149, nif-0000-02751, OMICS_03158 https://bio.tools/dictybase http://genome.imb-jena.de/dictyostelium/ SCR_006643 dictyBase gene name, dictyBase REF, Dicty, dictyBase, Dictyostelium discoideum 2026-09-05 06:25:58 315
Descriptions of Plant Viruses
 
Resource Report
Resource Website
10+ mentions
Descriptions of Plant Viruses (RRID:SCR_006656) data or information resource, database, portal, topical portal DPVweb provides a central source of information about viruses, viroids and satellites of plants, fungi and protozoa. Comprehensive taxonomic information, including brief descriptions of each family and genus, and classified lists of virus sequences are provided. The database also holds detailed, curated, information for all sequences of viruses, viroids and satellites of plants, fungi and protozoa that are complete or that contain at least one complete gene. For comparative purposes, it also contains a single representative sequence of all other fully sequenced virus species with an RNA or single-stranded DNA genome. The start and end positions of each feature (gene, non-translated region and the like) have been recorded and checked for accuracy. As far as possible, nomenclature for genes and proteins are standardized within genera and families. Sequences of features (either as DNA or amino acid sequences) can be directly downloaded from the website in FASTA format. The sequence information can also be accessed via client software for PC computers (freely downloadable from the website) that enable users to make an easy selection of sequences and features of a chosen virus for further analyses. The public sequence databases contain vast amounts of data on virus genomes but accessing and comparing the data, except for relatively small sets of related viruses can be very time consuming. The procedure is made difficult because some of the sequences on these databases are incorrectly named, poorly annotated or redundant. The NCBI Reference Sequence project (1) provides a comprehensive, integrated, non-redundant set of sequences, including genomic DNA, transcript (RNA) and protein products, for major research organisms. This now includes curated information for a single sequence of each fully sequenced virus species. While this is a welcome development, it can only deal with complete sequences. An important feature of DPV is the opportunity to access genes (and other features) of multiple sequences quickly and accurately. Thus, for example, it is easy to obtain the nucleotide or amino acid sequences of all the available accessions of the coat protein gene of a given virus species or for a group of viruses. To increase its usefulness further, DPVweb also contains a single representative sequence of all other fully sequenced virus species with an RNA or single-stranded DNA (ssDNA) genome. Sponsors: This site is supported by the Association of Applied Biologists and the Zhejiang Academy of Agricultural Sciences, Hangzhou, People''s Republic of China. family, fungi, gene, amino acid, comparative, development, dna, genome, genomic, genus, nomenclature, non-translated, nucleotide, organism, plant, product, protein, protozoa, region, rna, satellite, sequence, single, specie, taxonomic, transcript, viral databases, viroid, virus, bio.tools is listed by: bio.tools
is listed by: Debian
nif-0000-21127, biotools:dpvweb https://bio.tools/dpvweb SCR_006656 DPV 2026-09-05 06:25:58 15
BarraCUDA
 
Resource Report
Resource Website
1+ mentions
BarraCUDA (RRID:SCR_006881) BarraCUDA software resource A sequence mapping software that utilizes the massive parallelism of graphics processing units to accelerate the inexact alignment of short sequence reads to a particular location on a reference genome. It can align a paired-end library containing 14 million pairs of 76bp reads to the Human genome in about 27 minutes (from fastq files to SAM alignment) using a ��380 NVIDIA Geforce GTX 680*. The alignment throughput can be boosted further by using multiple GPUs (up to 8) at the same time. Being based on BWA (http://bio-bwa.sf.net) from the Sanger Institute, BarraCUDA delivers a high level of alignment fidelity and is comparable to other mainstream alignment programs. It can perform gapped alignment with gap extensions, in order to minimise the number of false variant calls in re-sequencing studies. gpu/cuda, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Cambridge; Cambridge; United Kingdom
has parent organization: SourceForge
PMID:22244497
PMID:19451168
Acknowledgement requested OMICS_00650, biotools:barracuda https://bio.tools/barracuda SCR_006881 2026-09-05 06:26:03 5
PeptideAtlas
 
Resource Report
Resource Website
500+ mentions
PeptideAtlas (RRID:SCR_006783) PeptideAtlas data or information resource, data repository, database, service resource, storage service resource Multi-organism, publicly accessible compendium of peptides identified in a large set of tandem mass spectrometry proteomics experiments. Mass spectrometer output files are collected for human, mouse, yeast, and several other organisms, and searched using the latest search engines and protein sequences. All results of sequence and spectral library searching are subsequently processed through the Trans Proteomic Pipeline to derive a probability of correct identification for all results in a uniform manner to insure a high quality database, along with false discovery rates at the whole atlas level. The raw data, search results, and full builds can be downloaded for other uses. All results of sequence searching are processed through PeptideProphet to derive a probability of correct identification for all results in a uniform manner ensuring a high quality database. All peptides are mapped to Ensembl and can be viewed as custom tracks on the Ensembl genome browser. The long term goal of the project is full annotation of eukaryotic genomes through a thorough validation of expressed proteins. The PeptideAtlas provides a method and a framework to accommodate proteome information coming from high-throughput proteomics technologies. The online database administers experimental data in the public domain. You are encouraged to contribute to the database. proteomics, peptide, mass spectrometry, annotation, eukaryotic, genome, peptide sequence, high-throughput mass spectrometry, ensembl, peptideprophet, protein sequence, blood plasma, protein, eukaryotic cell, dna, bio.tools, FASEB list is used by: NIF Data Federation
is used by: ProteomeXchange
is recommended by: NIDDK Information Network (dkNET)
is recommended by: National Library of Medicine
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: Biositemaps
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: Ensembl
is related to: ProteomeXchange
is related to: NIH Data Sharing Repositories
is related to: Integrated Manually Extracted Annotation
has parent organization: Institute for Systems Biology; Washington; USA
NCI ;
NHGRI ;
NIGMS
PMID:20013378
PMID:23215161
PMID:16381952
PMID:15642101
Public, The community can contribute to this resource, Acknowledgement requested nif-0000-03266, r3d100010889, biotools:peptideatlas https://bio.tools/peptideatlas, https://doi.org/10.17616/R3BK61 SCR_006783 Peptide Atlas, PeptideAtlas 2026-09-05 06:26:01 511
Ensembl Genomes
 
Resource Report
Resource Website
100+ mentions
Ensembl Genomes (RRID:SCR_006773) data access protocol, data or information resource, database, software resource, web service Database portal offering integrated access to genome-scale data from non-vertebrate species of scientific interest, developed using the Ensembl genome annotation and visualization platform. Ensembl Genomes consists of five sub-portals (for bacteria, protists, fungi, plants and invertebrate metazoa) designed to complement the availability of vertebrate genomes in Ensembl. Many of the databases supporting the portal have been built in close collaboration with the scientific community - essential for maintaining the accuracy and usefulness of the resource. A common set of user interfaces (which include a graphical genome browser, FTP, BLAST search, a query optimized data warehouse, programmatic access, and a Perl API) is provided for all domains. Data types incorporated include annotation of (protein and non-protein coding) genes, cross references to external resources, and high throughput experimental data (e.g. data from large scale studies of gene expression and polymorphism visualized in their genomic context). Additionally, extensive comparative analysis has been performed, both within defined clades and across the wider taxonomy, and sequence alignments and gene trees resulting from this can be accessed through the site. genome, gold standard, bio.tools, FASEB list is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is related to: Ensembl
is related to: Ensembl
is related to: g:Profiler
has parent organization: European Bioinformatics Institute
European Molecular Biology Laboratory ;
European Union FELICS 021902 (RII3);
BBSRC BB/F019793/1
PMID:24163254
PMID:19884133
r3d100011197, OMICS_01648, biotools:ensembl_genomes, nlx_65207 https://bio.tools/ensembl_genomes, https://doi.org/10.17616/R3MW6M SCR_006773 Ensembl Genomes: Extending Ensembl across the taxonomic space, EnsemblGenomes, Ensembl Genome 2026-09-05 06:26:00 320

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