Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

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.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Related Resources:bio.tools (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

1,667 Results - per page

Show More Columns | Download Top 1000 Results

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
NEMBASE
 
Resource Report
Resource Website
10+ mentions
NEMBASE (RRID:SCR_006070) NEMBASE analysis service resource, data analysis service, data or information resource, database, production service resource, service resource NEMBASE is a comprehensive Nematode Transcriptome Database including 63 nematode species, over 600,000 ESTs and over 250,000 proteins. Nematode parasites are of major importance in human health and agriculture, and free-living species deliver essential ecosystem services. The genomics revolution has resulted in the production of many datasets of expressed sequence tags (ESTs) from a phylogenetically wide range of nematode species, but these are not easily compared. NEMBASE4 presents a single portal into extensively functionally annotated, EST-derived transcriptomes from over 60 species of nematodes, including plant and animal parasites and free-living taxa. Using the PartiGene suite of tools, we have assembled the publicly available ESTs for each species into a high-quality set of putative transcripts. These transcripts have been translated to produce a protein sequence resource and each is annotated with functional information derived from comparison with well-studied nematode species such as Caenorhabditis elegans and other non-nematode resources. By cross-comparing the sequences within NEMBASE4, we have also generated a protein family assignment for each translation. The data are presented in an openly accessible, interactive database. An example of the utility of NEMBASE4 is that it can examine the uniqueness of the transcriptomes of major clades of parasitic nematodes, identifying lineage-restricted genes that may underpin particular parasitic phenotypes, possible viral pathogens of nematodes, and nematode-unique protein families that may be developed as drug targets. nematode, transcriptome, expressed sequence tag, protein, cluster, library, sequence, peptide prediction, functional annotation, gene family, gene, annotation, pathway, genome, partigene, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: nematodes.org
Wellcome Trust ;
Hospital for Sick Children ;
BBSRC ;
MRC ;
NERC
PMID:21550347
PMID:14681449
Public nlx_151476, biotools:nembase4 https://bio.tools/nembase4 SCR_006070 NEMBASE4, NEMBASE4 - Nematode Transcriptome Analyses 2026-09-03 04:48:24 25
HFV Database
 
Resource Report
Resource Website
1+ mentions
HFV Database (RRID:SCR_006017) HFV Database analysis service resource, data analysis service, data or information resource, database, production service resource, service resource The Hemorrhagic Fever Viruses (HFV) sequence database collects and stores sequence data and provides a user-friendly search interface and a large number of sequence analysis tools, following the model of the highly regarded and widely used Los Alamos HIV database. The database uses an algorithm that aligns each sequence to a species-wide reference sequence. The NCBI RefSeq database is used for this; if a reference sequence is not available, a Blast search finds the best candidate. Using this method, sequences in each genus can be retrieved pre-aligned. Hemorrhagic fever viruses (HFVs) are a diverse set of over 80 viral species, found in 10 different genera comprising five different families: arena-, bunya-, flavi-, filo- and togaviridae. All these viruses are highly variable and evolve rapidly, making them elusive targets for the immune system and for vaccine and drug design. About 55,000 HFV sequences exist in the public domain today. A central website that provides annotated sequences and analysis tools will be helpful to HFV researchers worldwide. gene, hemorrhagic fever virus, biothreat, virus, sequence, nucleotide sequence, reference sequence, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: RefSeq
has parent organization: HIV Databases
United States Department of Defense contract HDTRA B084498I PMID:22064861 biotools:hfv, nlx_151408 https://bio.tools/hfv SCR_006017 HFV Sequence Database, Hemorrhagic Fever Viruses Database, Hemorrhagic Fever Viruses (HFV) Database, LANL hemorrhagic fever virus database, Hemorrhagic Fever Viruses (HFV) Database Project 2026-09-03 04:48:28 1
BLESS
 
Resource Report
Resource Website
10+ mentions
BLESS (RRID:SCR_005963) BLESS algorithm resource, data analysis software, data processing software, sequence analysis software, software application, software resource Software tool for Bloom-filter-based error correction for next-generation sequencing (NGS) reads. The algorithm produces accurate correction results with much less memory. c++, next-generation sequencing, bloom-filter, error correction, ngs, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:24451628 GNU General Public License v3 OMICS_02246, biotools:bless https://bio.tools/bless SCR_005963 BLoom-filter-based Error correction Solution for high-throughput Sequencing reads, BLESS - Bloom-filter-based Error Correction Tool for NGS reads 2026-09-03 04:48:21 46
GWASdb
 
Resource Report
Resource Website
10+ mentions
GWASdb (RRID:SCR_006015) GWASdb data access protocol, data or information resource, database, software resource, web service Combines collections of genetic variants (GVs) from GWAS and their comprehensive functional annotations, as well as disease classifications. Used to maximize utilility of GWAS data to gain biological insights through integrative, multi-dimensional functional annotation portal. In addition to all GVs annotated in NHGRI GWAS Catalog, we manually curate GVs that are marginally significant (P value < 10-3) by looking into supplementary materials of each original publication and provide extensive functional annotations for these GVs. GVs are manually classified by diseases according to Disease Ontology Lite and HPO (Human Phenotype Ontology) for easy access. Database can also conduct gene based pathway enrichment and PPI network association analysis for those diseases with sufficient variants. SOAP services are available. You may Download GWASdb SNP. (This file contains all of the significant SNP in GWASdb. In the pvalue column, 0 means this P-value is not reported in the study but it is significant SNP. In the source column, GWAS:A represents the original data in GWAS catalog, while GWAS:B is our curation data which P-value < 10-3) genetic variant, genome-wide association study, functional annotation, disease classification, snp, gene, chromosome region, annotation, pathway, protein-protein interaction, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: GWASrap
is related to: Human Phenotype Ontology
is related to: IKMB GWAS Association Testing Pipeline
is related to: GWAS Quality Control Pipeline
is related to: Human Disease Ontology
University of Hong Kong Small Project Fund 201007176262;
Research Grants Council of Hong Kong 781511M;
Research Grants Council of Hong Kong 778609M;
Research Grants Council of Hong Kong N_HKU752/10;
Food and Health Bureau of Hong Kong 10091262;
NCI
PMID:22139925 biotools:gwasdb, nlx_151404 https://bio.tools/gwasdb SCR_006015 2026-09-03 04:48:13 43
eQuilibrator
 
Resource Report
Resource Website
100+ mentions
eQuilibrator (RRID:SCR_006011) data or information resource, database, software resource, web application Web interface designed for thermodynamic analysis of biochemical systems. eQuilibrator enables free-text search for biochemical compounds and reactions and provides thermodynamic estimates for both in a variety of conditions. It can provide estimates for compounds in the KEGG database, and individual compounds and enzymes can be searched for by their common names (water, glucosamine, hexokinase). Reactions can be entered in a free-text format that eQuilibrator parses automatically. eQuilibrator also allows manipulation of the conditions of a reaction - pH, ionic strength, and reactant and product concentrations. web interface, thermodynamics, biochemical system, bio.tools, FASEB list is listed by: Debian
is listed by: bio.tools
is related to: KEGG
Azrieli Foundation ;
Israel Academy of Sciences and Humanities ;
European Research Council 260392 - SYMPAC
PMID:22064852 Open source nlx_151400, biotools:equilibrator https://bio.tools/equilibrator SCR_006011 eQuilibrator - biochemical thermodynamics calculator 2026-09-03 04:48:15 118
OMPdb
 
Resource Report
Resource Website
OMPdb (RRID:SCR_006221) OMPdb analysis service resource, data analysis service, data or information resource, database, production service resource, service resource A database of Beta-barrel outer membrane proteins from Gram-negative bacteria. The web interface of OMPdb offers the user the ability not only to view the available data, but also to submit advanced queries for text search within the database''s protein entries or run BLAST searches against the database. The most up-to-date version of the database (as well as all past versions) can be downloaded in various formats (flat text, XML format or raw FASTA sequences). For constructing OMPdb, multiple freely accessible resources were combined and a detailed literature search was performed. The classification of OMPdb''s protein entries into families is based mainly on structural and functional criteria. Information included in the database consists of sequence data, as well as annotation for structural characteristics (such as the transmembrane segments), literature references and links to other public databases, features that are unique worldwide. Along with the database, a collection of profile Hidden Markov Models that were shown to be characteristic for Beta-barrel outer membrane proteins was also compiled. This set, when used in combination with our previously developed algorithms (PRED-TMBB, MCMBB and ConBBPRED) will serve as a powerful tool in matters of discrimination and classification of novel Beta-barrel proteins and whole-genome analyses., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. beta-barrel, outer membrane protein, gram-negative bacteria, protein, protein sequence, transmembrane, annotation, genome-wide analyses, comparative genomics, sequence, structure, blast, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: University of Athens Biophysics and Bioinformatics Laboratory
PMID:20952406 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01611, biotools:ompdb, nlx_151768 https://bio.tools/ompdb SCR_006221 OMPdb - A database of Beta-barrel outer membrane proteins from Gram-negative bacteria 2026-09-03 04:48:20 0
deepSNV
 
Resource Report
Resource Website
10+ mentions
deepSNV (RRID:SCR_006214) deepSNV software resource Software package that provides quantitative variant callers for detecting subclonal mutations in ultra-deep (>=100x coverage) sequencing experiments. The algorithm is used for a comparative setup with a control experiment of the same loci and uses a beta-binomial model and a likelihood ratio test to discriminate sequencing errors and subclonal SNVs (single nucleotide variants). data import, genetic variability, genetics, snp, sequencing, single nucleotide variant, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
PMID:24443148 GNU General Public License, v3 OMICS_02239, biotools:deepsnv https://bio.tools/deepsnv SCR_006214 deepSNV - Detection of subclonal SNVs in deep sequencing experiments 2026-09-03 04:48:22 34
PHYLIP
 
Resource Report
Resource Website
1000+ mentions
PHYLIP (RRID:SCR_006244) PHYLIP data processing software, software application, software resource, source code A free package of software programs for inferring phylogenies (evolutionary trees). The source code is distributed (in C), and executables are also distributed. In particular, already-compiled executables are available for Windows (95/98/NT/2000/me/xp/Vista), Mac OS X, and Linux systems. Older executables are also available for Mac OS 8 or 9 systems. phylogeny prediction, evolutionary tree, bio.tools is listed by: bio.tools
is listed by: Debian
is listed by: OMICtools
is listed by: SoftCite
has parent organization: University of Washington; Seattle; USA
works with: PAML
NSF ;
NIGMS ;
DOE
Free nif-0000-06708, OMICS_04240, biotools:phylip https://bio.tools/phylip, https://sources.debian.org/src/phylip/ SCR_006244 PHYLogeny Inference Package 2026-09-03 04:48:29 3544
ScerTF
 
Resource Report
Resource Website
10+ mentions
ScerTF (RRID:SCR_006121) ScerTF analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Catalog of over 1,200 position weight matrices (PWMs) for 196 different yeast transcription factors (TFs). They've curated 11 literature sources, benchmarked the published position-specific scoring matrices against in-vivo TF occupancy data and TF deletion experiments, and combined the most accurate models to produce a single collection of the best performing weight matrices for Saccharomyces cerevisiae. ScerTF is useful for a wide range of problems, such as linking regulatory sites with transcription factors, identifying a transcription factor based on a user-input matrix, finding the genes bound/regulated by a particular TF, and finding regulatory interactions between transcription factors. Enter a TF name to find the recommended matrix for a particular TF, or enter a nucleotide sequence to identify all TFs that could bind a particular region. binding site, transcription factor, regulatory site, gene, regulation, regulatory interaction, matrix, nucleotide sequence, dna sequence, yeast, position weight matrix, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA
NIGMS R01 GM078222;
NHGRI HG00249
PMID:22140105 biotools:scertf, nlx_151599, OMICS_00542 http://ural.wustl.edu/ScerTF, https://bio.tools/scertf http://ural.wustl.edu/TFDB/ SCR_006121 2026-09-03 04:48:27 19
SitEx
 
Resource Report
Resource Website
1+ mentions
SitEx (RRID:SCR_006122) SitEx analysis service resource, data analysis service, data or information resource, database, production service resource, service resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 19,2019. Analyzing protein structure projection on exon-intron structure of corresponding gene through years led to several fundamental conclusions about structural and functional organization of the protein. According to these results we decided to map the protein functional sites. So we created the database SitEx that keep the information about this mapping and included the BLAST search and 3D similar structure search using PDB3DScan for the polypeptide encoded by one exon, participating in organizing the functional site. This will help: # to study the positions of the functional sites in exon structure; # to make the complex analysis of the protein function; # to exposure the exons that took part in exon shuffling and came from bacterial genomes; # to study the peculiarities of coding the polypeptide structures. Currently, SitEx contains information about 9994 functional sites presented in 2021 proteins described in proteomes of 17 organisms. projection, protein, functional site, exon, blast, structure, function, gene, amino acid, encoding gene, proteome, ligand, data set, bio.tools is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
has parent organization: Institute of Cytology and Genetics of the Siberian Branch of the RAS; Novosibirsk; Russia
Ministry of Science and Education 14.740.11.0001;
Ministry of Science and Education 07.514.11.4003;
Interdisciplinary Integrative Project 35 of SB RAS ;
Russian Foundation for Basic Research 11-04-92712;
EU-FP7 260429;
Program of RAS ;
DAAD Leonard Euler Program Grant
PMID:22139920 THIS RESOURCE IS NO LONGER IN SERVICE. biotools:sitex, nlx_151602 https://bio.tools/sitex SCR_006122 SitEx Database 2026-09-03 04:48:32 1
Predictive Networks
 
Resource Report
Resource Website
Predictive Networks (RRID:SCR_006110) PN analysis service resource, data analysis service, data or information resource, database, production service resource, service resource, software resource, source code A flexible, open-source, web-based application and data services framework that enables the integration, navigation, visualization and analysis of gene interaction networks. The primary goal of PN is to allow biomedical researchers to evaluate experimentally derived gene lists in the context of large-scale gene interaction networks. The PN analytical pipeline involves two key steps. The first is the collection of a comprehensive set of known gene interactions derived from a variety of publicly available sources. The second is to use these ''known'' interactions together with gene expression data to infer robust gene networks. The regression-based network inference algorithm creates a graph of gene interactions in which cycles may be present (but no self-loops). Based on information-theoretic techniques, a causal gene interaction network is inferred from both prior knowledge (interactions extracted from biomedical literature and structured biological databases) and gene expression data. A prediction model is fitted for each gene, given its parents, enabling assessment of the predictive ability of the network model. gene interaction network, gene, interaction, gene expression, graph, visualization, gene interaction, gene network, predictive network analysis, model, bio.tools is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
has parent organization: Dana-Farber Cancer Institute
has parent organization: SourceForge
NLM 1R01LM010129 PMID:22096235 Apache License, v2 nlx_151582, biotools:predictivenetworks https://bio.tools/predictivenetworks SCR_006110 2026-09-03 04:48:48 0
SpliceDisease
 
Resource Report
Resource Website
1+ mentions
SpliceDisease (RRID:SCR_006130) SpliceDisease data or information resource, data repository, database, service resource, storage service resource Curated database of experimentally supported data of RNA Splicing mutation and disease. The RNA Splicing mutations include cis-acting mutations that disrupt splicing and trans-acting mutations that affecting RNA-dependent functions that cause disease. Information such as EntrezGeneID, gene genomic sequence, mutation (nucleotide substitutions, deletions and insertions), mutation location within the gene, organism, detailed description of the splicing mutation and references are also given. Users are able to submit new entries to the database. This database integrating RNA splicing and disease associations would be helpful for understanding not only the RNA splicing but also its contribution to disease. In SpliceDisease database, they manually curated 2337 splicing mutation disease entries involving 303 genes and 370 diseases, which have been supported experimentally in 898 publications. The SpliceDisease database provides information including the change of the nucleotide in the sequence, the location of the mutation on the gene, the reference PubMed ID and detailed description for the relationship among gene mutations, splicing defects and diseases. They standardized the names of the diseases and genes and provided links for these genes to NCBI and UCSC genome browser for further annotation and genomic sequences. For the location of the mutation, they give direct links of the entry to the respective position/region in the genome browser. rna splicing, mutation, disease, gene, genomic sequence, nucleotide substitution, deletion, insertion, mutation location, splicing mutation, nucleotide, disease association, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: Peking University; Beijing; China
National Natural Science Foundation of China 81001481 PMID:22139928 The community can contribute to this resource biotools:splicedisease_db, nlx_151614 https://bio.tools/splicedisease_db SCR_006130 Splice Disease, SpliceDisease Database Site, Splice Disease Database, SpliceDisease Database 2026-09-03 04:48:27 2
ChemSpider
 
Resource Report
Resource Website
1000+ mentions
ChemSpider (RRID:SCR_006360) ChemSpider data access protocol, data or information resource, database, mobile app, service resource, software application, software resource, web service Collection of chemical structures. Provides access to structures, properties and associated information from hundreds of data sources to find compounds of interest and provides services to improve this data by curation and annotation and to integrate it with users applications. collection, chemical, structure, property, data, compound, bio.tools, FASEB list is used by: Open PHACTS
is used by: GEROprotectors
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
has parent organization: Royal Society of Chemistry
GGA Software Services ;
Waters
Free, Freely available, Registration required for some sites nlx_152101, biotools:chemspider, r3d100010205 https://bio.tools/chemspider, https://doi.org/10.17616/R38P4P SCR_006360 2026-09-03 04:48:36 2112
QCGWAS
 
Resource Report
Resource Website
1+ mentions
QCGWAS (RRID:SCR_006408) QCGWAS software resource Software tools for (automated and manual) quality control of the results of Genome Wide Association Studies. quality control, genome wide association study, windows, os x, r, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:24395754 GNU General Public License, v3 or later OMICS_02203, biotools:qcgwas https://bio.tools/qcgwas SCR_006408 QCGWAS: Quality Control of Genome Wide Association Study results, Quality Control of Genome Wide Association Study 2026-09-03 04:48:29 7
IsoEM
 
Resource Report
Resource Website
10+ mentions
IsoEM (RRID:SCR_009993) IsoEM software resource Software package that can be used to infer isoform and gene expression levels from high-throughput transcriptome sequencing (RNA-Seq) data. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Connecticut; Connecticut; USA
biotools:isoem, OMICS_01278 https://bio.tools/isoem SCR_009993 2026-09-03 04:50:13 10
BitSeq
 
Resource Report
Resource Website
10+ mentions
BitSeq (RRID:SCR_009904) BitSeq software resource A software application for inferring expression levels of individual transcripts from sequencing (RNA-Seq) data and estimating differential expression (DE) between conditions. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
DOI:10.1093/bioinformatics/btv483
DOI:10.1093/bioinformatics/bts260
, OMICS_01269, biotools:bitseq https://bio.tools/bitseq, https://sources.debian.org/src/bitseq/, SCR_009904 2026-09-03 04:50:18 20
BEAST
 
Resource Report
Resource Website
5000+ mentions
BEAST (RRID:SCR_010228) data analysis software, data processing software, sequence analysis software, software application, software repository, software resource A cross-platform software program for Bayesian MCMC analysis of molecular sequences. It is entirely orientated towards rooted, time-measured phylogenies inferred using strict or relaxed molecular clock models. It can be used as a method of reconstructing phylogenies but is also a framework for testing evolutionary hypotheses without conditioning on a single tree topology. BEAST uses MCMC to average over tree space, so that each tree is weighted proportional to its posterior probability. We include a simple to use user-interface program for setting up standard analyses and a suit of programs for analysing the results. bio.tools is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
is related to: TempEst
is related to: BEAST2
is related to: PhyDyn
has parent organization: University of Edinburgh; Scotland; United Kingdom
DOI:10.1186/1471-2148-7-214 nlx_156859, OMICS_04233, biotools:beast, SCR_015988 http://www.nitrc.org/projects/beast-library, https://bio.tools/beast, https://sources.debian.org/src/beast-mcmc/ http://beast.bio.ed.ac.uk/Main_Page SCR_010228 BEaST Segmentation Library, Beast Software 2026-09-03 04:50:19 6777
WEBLOGO
 
Resource Report
Resource Website
1000+ mentions
WEBLOGO (RRID:SCR_010236) data access protocol, service resource, software resource, web service Web application to generate sequence logos, graphical representations of patterns within multiple sequence alignment. Designed to make generation of sequence logos easy. Sequence logo generator. Generate sequence logo, pattern graphical representation, multiple sequence alignment, sequence logo generator, amino acid sequence alignment, nucleic acid sequence alignment, sequence alignment representation, bio.tools is listed by: Debian
is listed by: bio.tools
is listed by: SoftCite
has parent organization: University of California at Berkeley; Berkeley; USA
NHGRI K22 HG00056;
NIGMS P50 GM62412;
Searle Scholars program
PMID:15173120 Free, Available for download, Freely available nlx_156853, biotools:weblogo_3 http://weblogo.threeplusone.com/, https://bio.tools/weblogo_3 SCR_010236 WebLogo Version 2.8.2, WebLogo3, WebLogo 2026-09-03 04:50:06 3980
MaSuRCA
 
Resource Report
Resource Website
100+ mentions
MaSuRCA (RRID:SCR_010691) MaSuRCA software resource A whole genome assembly software that combines the efficiency of the de Bruijn graph and Overlap-Layout-Consensus (OLC) approaches., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Maryland; Maryland; USA
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00020, biotools:masurca https://bio.tools/masurca SCR_010691 2026-09-03 04:50:48 468
Pathema
 
Resource Report
Resource Website
1+ mentions
Pathema (RRID:SCR_010585) Pathema analysis service resource, data analysis service, data or information resource, database, production service resource, service resource Pathema is one of the eight Bioinformatics Resource Centers designed to serve as a core resource for the bio-defense and infectious disease research community. Pathema strives to support basic research and accelerate scientific progress for understanding, detecting, diagnosing and treating an established set of six target NIAID Category A-C pathogens: Category A priority pathogens; Bacillus anthracis and Clostridium botulinum, and Category B priority pathogens; Burkholderia mallei, Burkholderia pseudomallei, Clostridium perfringens and Entamoeba histolytica. Each target pathogen is represented in one of four distinct clade-specific Pathema web resources and underlying databases developed to target the specific data and analysis needs of each scientific community. All publicly available complete genome projects of phylogenetically related organisms are also represented, providing a comprehensive collection of organisms for comparative analyses. Pathema facilitates the scientific exploration of genomic and related data through its integration with web-based analysis tools, customized to obtain, display, and compute results relevant to ongoing pathogen research. Pathema serves the bio-defense and infectious disease research community by disseminating data resulting from pathogen genome sequencing projects and providing access to the results of inter-genomic comparisons for these organisms. The Pathema BRC contract ends in December 2009. At that time JCVI will cease maintenance of the Pathema web resource and data. The PATRIC team, located at the Virginia Bioinformatics Institute, created and maintains a consolidated BRC for all of the NIAID category A-C priority pathogenic bacteria. The EuPathDB team at the University of Pennsylvania will support all eukaryotic pathogens. Pathema transferred all data and software to PATRIC and EuPathDB for incorporation into their new Web-based bioinformatics resource. bacillus anthracis, clostridium botulinum, burkholderia mallei, burkholderia pseudomallei, clostridium perfringens, entamoeba histolytica, bio.tools is listed by: Debian
is listed by: bio.tools
has parent organization: J. Craig Venter Institute
NIAID contract HHSN266200400038C PMID:19843611 biotools:pathema, nlx_45829 https://bio.tools/pathema SCR_010585 Pathema Genome Resource, Pathema Bioinformatics Resource Center 2026-09-03 04:50:32 6

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. Neuroscience Information Framework Resources

    Welcome to the NIF Resources search. From here you can search through a compilation of resources used by NIF and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that NIF has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on NIF then you can log in from here to get additional features in NIF such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into NIF you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.