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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
V-Phaser 2
 
Resource Report
Resource Website
1+ mentions
V-Phaser 2 (RRID:SCR_005212) V-Phaser 2 software resource A software tool to call variants in genetically heterogeneous populations from ultra-deep sequence data. It combines information regarding the covariation (i.e. phasing) between observed variants to increase sensitivity and an expectation maximization algorithm that iteratively recalibrates base quality scores to increase specificity. V-Phaser can reliably detect rare variants in diverse populations that occur at frequencies of <1%. V-Phaser 2 is a complete rewrite of the original V-Phaser. It contains a new model for length polymorphisms (indels) and incorporates paired end read information in its phasing model. The data access and probability computation sections of the code have also been highly optimized, resulting in substantial improvements in running time and memory usage. variant, polymorphism, indel, virus, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Broad Institute
NIAID PMID:24088188 Free for academic use, Non-commercial, Http://www.broadinstitute.org/scientific-community/science/projects/viral-genomics/viral-genomics-software-license-v-phaser-2 biotools:v-phaser, OMICS_00232 https://bio.tools/v-phaser SCR_005212 2026-08-01 12:02:50 2
GOEx - Gene Ontology Explorer
 
Resource Report
Resource Website
10+ mentions
GOEx - Gene Ontology Explorer (RRID:SCR_005779) GOEx software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented July 5, 2018. Gene Ontology Explorer (GOEx) combines data from protein fold changes with GO over-representation statistics to help draw conclusions in proteomic experiments. It is tightly integrated within the PatternLab for Proteomics project and, thus, lies within a complete computational environment that provides parsers and pattern recognition tools designed for spectral counting. GOEx offers three independent methods to query data: an interactive directed acyclic graph, a specialist mode where key words can be searched, and an automatic search. A recent hack included in GOEx is to load the sparse matrix index file directly into GOEx, instead of going through the report generation using the AC/T-fold methods. This makes it easy for GOEx to analyze any list of proteins as long as the list follows the index file format (described in manuscript) . Please note that if using this alternative strategy, there will be no protein fold information. Platform: Windows compatible proteomics, visualization, statistical analysis, gene ontology, parse, pattern recognition, spectral counting, analysis, protein fold is listed by: Gene Ontology Tools
is related to: Gene Ontology
has parent organization: Scripps Research Institute
CNPq ;
CAPES ;
FAPERJ BBP grant ;
PAPES ;
PDTIS ;
Ary Frauzino Foundation ;
NIAID ;
NIH ;
genesis molecular biology laboratory ;
Fiocruz-INCA collaboration ;
NIAID UCSD/MCB0237059;
NCRR P41RR011823;
NIMH 5R01 MH067880
PMID:19239707 THIS RESOURCE IS NO LONGER IN SERVICE nlx_149249 http://pcarvalho.com/patternlab/goex.shtml SCR_005779 Gene Ontology Explorer, GO Explorer 2026-08-01 12:02:59 26
Xenopus laevis Research Resource for Immunobiology (XLRR)
 
Resource Report
Resource Website
1+ mentions
Xenopus laevis Research Resource for Immunobiology (XLRR) (RRID:SCR_014354) XLRR biomaterial supply resource, material resource A comprehensive resource specializing in the use of the amphibian Xenopus laevis (the African clawed frog) for biomedical and immunological research. Several genetically-defined inbred strains and clones are available for study. The facility also maintains and develops research tools such as transgenic animals, monoclonal antibodies, cell lines, DNA libraries, and molecular probes. XLRR includes a satellite facility devoted to study infectious diseases caused by iridovirus. Technical assistance, education, and training are also provided. Immunology, cancer, inbred frog, cloned frog, monoclonal antibody, xenopus laevis, lymphoid tumor cell lines NIAID SCR_014354 Xenopus laevis Research Resource, Xenopus laevis Research Resource for Immunobiology 2026-08-01 12:10:56 4
ReBATE
 
Resource Report
Resource Website
ReBATE (RRID:SCR_017139) software toolkit, software resource Open source software Python package to compare relief based feature selection algorithms used in data mining. Used for feature selection in any bioinformatics problem with potentially predictive features and target outcome variable, to detect feature interactions without examination of all feature combinations, to detect features involved in heterogeneous patterns of association such as genetic heterogeneity . compare, relief, feature, algorithm, data, mining, variable, heterogeneous, pattern, genetic has parent organization: University of Pennsylvania; Philadelphia; USA NIAID AI116794;
NIDDK DK112217;
NIEHS ES013508;
NEI EY022300;
NHLBI HL134015;
NLM LM009012;
NLM LM010098;
NLM LM011360;
NCATS TR001263;
Warren Center for Network and Data Science
PMID:30030120 Free, Available for download, Freely available https://epistasislab.github.io/ReBATE/ SCR_017139 Relief Based Algorithm Training Environment 2026-08-02 09:07:35 0
MaAsLin2
 
Resource Report
Resource Website
100+ mentions
MaAsLin2 (RRID:SCR_023241) software toolkit, software resource SoftwareR package that identifies microbial taxa correlated with factors of interest using generalized linear models and mixed models.Used for efficiently determining multivariable association between clinical metadata and microbial meta'omic features. Microbiome Multivariable Associations with Linear Models, NSF DEB-2028280;
NIAID U19AI110820;
NHGRI R01HG005220;
NIDDK R24DK110499;
NIDDK U54DK102557
DOI:10.1371/journal.pcbi.1009442 Free, Available for download, Freely available https://huttenhower.sph.harvard.edu/maaslin/ SCR_023241 2026-08-02 09:08:54 170
Hepatitis C Virus Database (HCVdb)
 
Resource Report
Resource Website
1+ mentions
Hepatitis C Virus Database (HCVdb) (RRID:SCR_005718) HCVdb, production service resource, data analysis service, data or information resource, database, analysis service resource, service resource The Hepatitis C Virus Database (HCVdb) is a cooperative project of several groups with the mission of providing to the scientific community studying the hepatitis C virus a comprehensive battery of informational and analytical tools. The Viral Bioinformatics Resource Center (VBRC), the Immune Epitope Database and Analysis Resource (IEDB), the Broad Institute Microbial Sequencing Center (MSC), and the Los Alamos HCV Sequence Database (HCV-LANL) are combining forces to acquire and annotate data on Hepatitis C virus, and to develop and utilize new tools to facilitate the study of this group of organisms. hepatitis c, hepatitis c virus, genome, gene, virus, ortholog comparison, ortholog has parent organization: VBRC Hepatitis C virus NIAID contract HHSN266200400036C nlx_149175 SCR_005718 Hepatitis C Viral Database 2026-08-03 09:32:55 4
VBRC
 
Resource Report
Resource Website
10+ mentions
VBRC (RRID:SCR_005971) VBRC data repository, production service resource, data analysis service, service resource, database, storage service resource, analysis service resource, data or information resource One of eight Bioinformatics Resource Centers nationwide providing comprehensive web-based genomics resources including a relational database and web application supporting data storage, annotation, analysis, and information exchange to support scientific research directed at viruses belonging to the Arenaviridae, Bunyaviridae, Filoviridae, Flaviviridae, Paramyxoviridae, Poxviridae, and Togaviridae families. These centers serve the scientific community and conduct basic and applied research on microorganisms selected from the NIH/NIAID Category A, B, and C priority pathogens that are regarded as possible bioterrorist threats or as emerging or re-emerging infectious diseases. The VBRC provides a variety of analytical and visualization tools to aid in the understanding of the available data, including tools for genome annotation, comparative analysis, whole genome alignments, and phylogenetic analysis. Each data release contains the complete genomic sequences for all viral pathogens and related strains that are available for species in the above-named families. In addition to sequence data, the VBRC provides a curation for each virus species, resulting in a searchable, comprehensive mini-review of gene function relating genotype to biological phenotype, with special emphasis on pathogenesis. virus, arenaviridae, bunyaviridae, filoviridae, flaviviridae, paramyxoviridae, poxviridae, togaviridae, blast, ortholog, variation, sequence analysis, genome, gene, epidemiology, bioinformatics resource center, phenotype, pathogenesis, pathogen, annotation, genomics has parent organization: University of Alabama at Birmingham; Alabama; USA
has parent organization: University of Victoria; British Columbia; Canada
is parent organization of: Hepatitis C Virus Database (HCVdb)
NIAID contract HHSN266200400036C r3d100012088, nif-0000-03632 https://doi.org/10.17616/R31M1P SCR_005971 Viral Bioinformatics Resource Center 2026-08-03 09:32:58 18
Autoimmune Lymphoproliferative Syndrome Information
 
Resource Report
Resource Website
1+ mentions
Autoimmune Lymphoproliferative Syndrome Information (RRID:SCR_006451) NIAID ALPS topical portal, data or information resource, portal, disease-related portal A disease-related portal about Autoimmune Lymphoproliferative Syndrome (ALPS) including research in the following categories: Medical and Genetic Description, Database of Mutations, Database of ALPS-FAS Mutations, and Molecular Pathways. Autoimmune Lymphoproliferative Syndrome (ALPS) is a recently recognized disease in which a genetic defect in programmed cell death, or apoptosis, leads to breakdown of lymphocyte homeostasis and normal immunologic tolerance. It is an inherited disorder of the immune system that affects both children and adults. In ALPS, unusually high numbers of white blood cells called lymphocytes accumulate in the lymph nodes, liver, and spleen, which can lead to enlargement of these organs. Database of Mutations * All existing ALPS-FAS mutations (NIH Web site) * ALPS-FAS * ALPS Type Ia (most common type) ** Reported FAS (TNFRSF6) mutations causing ALPS ** Distribution of FAS (TNFRSF6) mutations ** FAS (TNFRSF6) polymorphisms * ALPS Type II apoptosis, autoimmune lymphoproliferative syndrome, double negative t cell, lymphocyte, pathway, immune system, clinical trial, child, adult, mutation Autoimmune Lymphoproliferative Syndrome NIAID nif-0000-02542 http://research.nhgri.nih.gov/ALPS/ SCR_006451 NIAID Autoimmune Lymphoproliferative Syndrome (ALPS), NIAID Autoimmune Lymphoproliferative Syndrome, ALPSbase, Autoimmune Lymphoproliferative Syndrome (ALPS) 2026-08-03 09:33:01 1
Influenza Research Database (IRD)
 
Resource Report
Resource Website
10+ mentions
Influenza Research Database (IRD) (RRID:SCR_006641) IRD data repository, production service resource, data analysis service, service resource, database, storage service resource, analysis service resource, data or information resource The Influenza Research Database (IRD) serves as a public repository and analysis platform for flu sequence, experiment, surveillance and related data. avian, clinical, genomic, host, influenza, isolate, mammalian, nonhuman, phenotypic, preventive, proteomic, repository, strain, epitope, surveillance, treatment, virus, protein sequence, immune, 3d protein structure, align, blast, short peptide, flu protein, sequence variation, snp, phylogenetic tree, human, 3d spacial image, image, clinical data, clinical, genomic, proteomic, phenotype is recommended by: NIDDK Information Network (dkNET)
is listed by: DataCite
is listed by: re3data.org
is listed by: FAIRsharing
is related to: Los Alamos National Laboratory
is related to: University of California at Davis; California; USA
is related to: Sage Analytica
is related to: J. Craig Venter Institute
has parent organization: University of Texas Southwestern Medical Center; Texas; USA
has parent organization: Los Alamos National Laboratory
has parent organization: Sage Analytica
Influenza virus, Influenza NIAID PMID:17965094 Acknowledgement requested, The community can contribute to this resource DOI:10.25504/FAIRsharing.ws7cgw, nif-0000-21222, DOI:10.35094, DOI:10.17616/R3S634, r3d100011558 https://www.fludb.org/, https://doi.org/10.17616/R3S634, https://doi.org/10.17616/r3s634, https://doi.org/10.35094/, https://dx.doi.org/10.35094/, https://fairsharing.org/10.25504/FAIRsharing.ws7cgw, https://doi.org/10.17616/R3S634 http://www.fludb.org/brc/home.do?decorator=influenza SCR_006641 , Influenza Research Database, IRD 2026-08-03 09:33:06 28
Autoimmunity Centers of Excellence
 
Resource Report
Resource Website
Autoimmunity Centers of Excellence (RRID:SCR_006510) ACE portal, disease-related portal, resource, topical portal, research forum portal, data or information resource Nine centers that conduct clinical trials and basic research on new immune-based therapies for autoimmune diseases. This program enhances interactions between scientists and clinicians in order to accelerate the translation of research findings into medical applications. By promoting better coordination and communication, and enabling limited resources to be pooled, ACEs is one of NIAID''''s primary vehicles for both expanding our knowledge and improving our ability to effectively prevent and treat autoimmune diseases. This coordinated approach incorporates key recommendations of the NIH Autoimmune Diseases Research Plan and will ensure progress in identifying new and highly effective therapies for autoimmune diseases. ACEs is advancing the search for effective treatments through: * Diverse Autoimmunity Expertise Medical researchers at ACEs include rheumatologists, neurologists, gastroenterologists, and endocrinologists who are among the elite in their respective fields. * Strong Mechanistic Foundation ACEs augment each clinical trial with extensive basic studies designed to enhance understanding of the mechanisms responsible for tolerance initiation, maintenance, or loss, including the role of cytokines, regulatory T cells, and accessory cells, to name a few. * Streamlined Patient Recruitment The cooperative nature of ACEs helps scientists recruit patients from distinct geographical areas. The rigorous clinical and basic science approach of ACEs helps maintain a high level of treatment and analysis, enabling informative comparisons between patient groups. immune system, infection, clinical trial, clinical, basic research is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
Type 1 diabetes, Diabetes, Autoimmune disease, Systematic lupus erythematosus, Rheumatoid arthritis, Sjogren's syndrome, Multiple sclerosis, Chronic inflammatory bowel disease, Pemphigus vulgaris, Scleroderma NIAID ;
NIDDK ;
NIH Office of Research on Womens Health
nlx_152751 SCR_006510 2026-08-03 09:33:09 0
Nonhuman Primate Transplantation Tolerance Cooperative Study Group
 
Resource Report
Resource Website
Nonhuman Primate Transplantation Tolerance Cooperative Study Group (RRID:SCR_006847) NHPCSG portal, disease-related portal, resource, topical portal, research forum portal, data or information resource Cooperative program for research on nonhuman primate models of kidney, islet, heart, and lung transplantation evaluating the safety and efficacy of existing and new treatment regimens that promote the immune system''''s acceptance of a transplant and to understand why the immune system either rejects or does not reject a transplant. This program bridges the critical gap between small-animal research and human clinical trials. The program supports research into the immunological mechanisms of tolerance induction and development of surrogate markers for the induction, maintenance, and loss of tolerance. transplantation, clinical, kidney, islet, tolerance, heart, lung, treatment, immune system, tolerance induction is related to: NIDDK Information Network (dkNET) Kidney transplantation, Islet transplantation, Heart transplantation, Lung transplantation NIDDK ;
NIAID
nlx_152728 http://www.niddk.nih.gov/fund/diabetesspecialfunds/consortia/NHP.pdf SCR_006847 Non-human Primate Transplantation Tolerance Cooperative Study Group 2026-08-03 09:33:11 0
Pathosystems Resource Integration Center
 
Resource Report
Resource Website
1000+ mentions
Pathosystems Resource Integration Center (RRID:SCR_004154) PATRIC production service resource, data analysis service, service resource, bioinformatics resource center, database, analysis service resource, data or information resource A Bioinformatics Resource Center bacterial bioinformatics database and analysis resource that provides researchers with an online resource that stores and integrates a variety of data types (e.g. genomics, transcriptomics, protein-protein interactions (PPIs), three-dimensional protein structures and sequence typing data) and associated metadata. Datatypes are summarized for individual genomes and across taxonomic levels. All genomes, currently more than 10 000, are consistently annotated using RAST, the Rapid Annotations using Subsystems Technology. Summaries of different data types are also provided for individual genes, where comparisons of different annotations are available, and also include available transcriptomic data. PATRIC provides a variety of ways for researchers to find data of interest and a private workspace where they can store both genomic and gene associations, and their own private data. Both private and public data can be analyzed together using a suite of tools to perform comparative genomic or transcriptomic analysis. PATRIC also includes integrated information related to disease and PPIs. The PATRIC project includes three primary collaborators: the University of Chicago, the University of Manchester, and New City Media. The University of Chicago is providing genome annotations and a PATRIC end-user genome annotation service using their Rapid Annotation using Subsystem Technology (RAST) system. The National Centre for Text Mining (NaCTeM) at the University of Manchester is providing literature-based text mining capability and service. New City Media is providing assistance in website interface development. An FTP server and download tool are available. genomics, genome, transcriptomics, protein-protein interaction, sequence typing, proteobacteria, brucella, rickettsia, coxiella, coronavirus, calicivirus, lyssavirus, virus, hepatitis a, hepatitis e, pathway, proteome, metabolic pathway, drug, vaccine, diagnostics, FASEB list is listed by: OMICtools
has parent organization: Virginia Polytechnic Institute and State University; Virginia; USA
NIAID PMID:24225323
PMID:17142235
Free, Public, Acknowledgement requested r3d100010142, OMICS_01658, nlx_17476 http://patricbrc.vbi.vt.edu/portal/portal/patric/Home, https://doi.org/10.17616/R3WS3X http://patric.vbi.vt.edu/ SCR_004154 PathoSystems Resource Integration Center, PATRIC, Pathosystems Resource Integration Center 2026-08-03 09:32:37 1083
HCV Databases
 
Resource Report
Resource Website
50+ mentions
HCV Databases (RRID:SCR_002863) HCV Databases topical portal, data or information resource, portal, disease-related portal The Hepatitis C Virus (HCV) Database Project strives to present HCV-associated genetic and immunologic data in a user-friendly way, by providing access to the central database via web-accessible search interfaces and supplying a number of analysis tools. hcv, hepatitis c virus, hepatitis c, database, data analysis service, sequence, immunology, annotation, FASEB list has parent organization: HIV Databases
is parent organization of: HCV Sequence Database
is parent organization of: HCV Immunology Database
Hepatitis C NIAID Free, Freely available nif-0000-02944 SCR_002863 Hepatitis C Virus Database, Hepatitis C Virus Database Project, HCV Database, Hepatitis C Virus Databases, Hepatitis C Virus (HCV) Database Project 2026-08-03 09:31:52 66
JCVI CMR
 
Resource Report
Resource Website
10+ mentions
JCVI CMR (RRID:SCR_005398) JCVI_CMR, JCVI CMR, TIGR_CMR, TIGR CMR production service resource, data analysis service, service resource, database, analysis service resource, data or information resource Database of all of the publicly available, complete prokaryotic genomes. In addition to having all of the organisms on a single website, common data types across all genomes in the CMR make searches more meaningful, and cross genome analysis highlight differences and similarities between the genomes. CMR offers a wide variety of tools and resources, all of which are available off of our menu bar at the top of each page. Below is an explanation and link for each of these menu options. * Genome Tools: Find organism lists as well as summary information and analyses for selected genomes. * Searches: Search CMR for genes, genomes, sequence regions, and evidence. * Comparative Tools: Compare multiple genomes based on a variety of criteria, including sequence homology and gene attributes. SNP data is also found under this menu. * Lists: Select and download gene, evidence, and genomic element lists. * Downloads: Download gene sequences or attributes for CMR organisms, or go to our FTP site. * Carts: Select genome preferences from our Genome Cart or download your Gene Cart genes. The Omniome is the relational database underlying the CMR and it holds all of the annotation for each of the CMR genomes, including DNA sequences, proteins, RNA genes and many other types of features. Associated with each of these DNA features in the Omniome are the feature coordinates, nucleotide and protein sequences (where appropriate), and the DNA molecule and organism with which the feature is associated. Also available are evidence types associated with annotation such as HMMs, BLAST, InterPro, COG, and Prosite, as well as individual gene attributes. In addition, the database stores identifiers from other centers such as GenBank and SwissProt, as well as manually curated information on each genome or each DNA molecule including website links. Also stored in the Omniome are precomputed homology data, called All vs All searches, used throughout the CMR for comparative analysis. microbial, prokaryotic, genome, annotation, dna sequence, protein, rna gene, blast, FASEB list is used by: NIF Data Federation
is related to: AmiGO
has parent organization: J. Craig Venter Institute
is parent organization of: JCVI GenProp
NSF ;
NIAID ;
DOE
Free nif-0000-03555 SCR_005398 JCVI Comprehensive Microbial Resource, J. Craig Venter Institute Comprehensive Microbial Resource, CMR, Comprehensive Microbial Resource 2026-08-03 09:32:50 37
EVidenceModeler
 
Resource Report
Resource Website
1000+ mentions
EVidenceModeler (RRID:SCR_014659) EVM sequence analysis software, software application, data processing software, data analysis software, software resource Software tool for automated eukaryotic gene structure annotation that reports eukaryotic gene structures as weighted consensus of all available evidence. Used to combine ab intio gene predictions and protein and transcript alignments into weighted consensus gene structures. Inputs include genome sequence, gene predictions, and alignment data (in GFF3 format). sequence analysis software, framework, ab intio gene, gene prediction, protein alignment, transcript alignment, consensus gene structure NIAID N01 AI30071;
NLM R01 LM006845
PMID:18190707 Free, Available for download, Freely available SCR_017649 SCR_014659 2026-08-03 09:35:47 1135
NIAID Overview of Coronaviruses
 
Resource Report
Resource Website
1+ mentions
NIAID Overview of Coronaviruses (RRID:SCR_018290) funding resource, topical portal, data or information resource, portal Information about coronaviruses, including COVID-19. NIAID provides research funding and resources for scientific community to facilitate development of vaccines, therapeutics, and diagnostics for infectious diseases, including those caused by coronaviruses. Coronavirus, COVID-19, data, infectious disease, NIAID is listed by: Data and Computational Resources to Address COVID-19
is related to: NIAID
COVID-19 NIAID Free, Freely available SCR_018290 2026-08-03 09:37:00 3
Nonhuman Primate Reagent Resource
 
Resource Report
Resource Website
100+ mentions
Nonhuman Primate Reagent Resource (RRID:SCR_012986) NHPRR antibody supplier, material resource, reagent supplier Center that facilitates the optimal use of nonhuman primate models in biomedical research by identifying, developing, characterizing and producing reagents for monitoring or modulating immune responses. They distribute non-human primate-specific antibodies for in vitro diagnostics, as well as develop and produce primate recombinant antibodies for in vivo cell depletion or modulating immune responses. anti-ig, antibody, biomedical, cell, depletion, diagnostic, immune, immunoglobulin, in vitro, in vivo, macaque, monkey, nonhuman, primate, reagent, recombinant, research, response, specie NIH Office of the Director R24 OD010976;
NIH HHSN272200900037C;
NIH HHSN286200400101C;
NIH HHSN2722001300031C;
NIAID AI126683;
NCRR RR016001;
NIAID AI040101;
NIH 272200900037C;
NIH 286200400101C;
NIH AI-126683;
NIH OD-010976;
NIH RR-016001;
NIH 2722001300031C;
NIH 272201300031C;
NIH AI-040101;
NIH NHPRR
nif-0000-24368 https://orip.nih.gov/comparative-medicine/programs/vertebrate-models, http://www.nhpreagents.org/NHP/contact.aspx http://nhpreagents.bidmc.harvard.edu/NHP/default.aspx SCR_012986 nhp reagents, Nonhuman Primate Reagent Resources, Non-human primate repository, Non human Primate Reagent Resources, NHP Reagent Resource, nhpreagents, NIH Nonhuman Primate Reagent Resource, NHP Reagent, nhpreagent, Non-human Primate Reagent Resources 2026-08-03 09:35:07 221
CytoMAP
 
Resource Report
Resource Website
10+ mentions
CytoMAP (RRID:SCR_021227) software toolkit, software application, data analytics software, data processing software, data analysis software, software resource Software tool as spatial analysis software for whole tissue sections.Utilizes information on cell type and position to phenotype local neighborhoods and reveal how their spatial distribution leads to generation of global tissue architecture.Used to make advanced data analytic techniques accessible for single cell data with position information. Histo cytometric multidimensional, analysis pipeline, whole tissue sections, spatial analysis, single cell data with position information, phenotype local neighborhoods, global tissue architecture has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA NIAID R01 AI134713;
NIAID R21 AI142667;
NIAID R01 AI134246;
NIAID R01 AI076327;
NIAID U19 AI135976;
NIAID T32 AI10667;
NIGMS T32 GM007270;
NICHD T32 HD007233;
NSF DGE 1762114
PMID:32320656 Free, Available for download, Freely available SCR_021227 Histo-Cytometric Multidimensional Analysis Pipeline 2026-08-03 09:37:23 22
SpiecEasi
 
Resource Report
Resource Website
10+ mentions
SpiecEasi (RRID:SCR_022712) SpiecEasi software resource, data processing software, software application, data analysis software Software R package for microbiome network analysis. Used for inference of microbial ecological networks from amplicon sequencing datasets. Combines data transformations developed for compositional data analysis with graphical model inference framework that assumes underlying ecological association network is sparse. microbiome network analysis, amplicon sequencing datasets, microbial ecological networks inference NIAID AI007180;
NIDDK DK103358;
NIGMS GM63270;
Simons Foundation
PMID:25950956 Free, Available for download, Freely available SCR_022712 SParse InversE Covariance Estimation for Ecological Association Inference 2026-08-03 09:38:06 15
FlowCal
 
Resource Report
Resource Website
1+ mentions
FlowCal (RRID:SCR_018140) software resource, software application, data processing software Open source software tool for automatically converting flow cytometry data from arbitrary to calibrated units. Can be run using intuitive Microsoft Excel interface, or customizable Python scripts. Software accepts Flow Cytometry Standard (FCS) files as inputs and is compatible with different calibration particles, fluorescent probes, and cell types. Automatically gates data, calculates common statistics, and produces plots. Converting flow cytometry data, arbitrary unit, calibrated unit, data gating, statistic, plot, data, bio.tools is listed by: Debian
is listed by: bio.tools
NSF EFRI 1137266;
NSF MCB 1244135;
Office of Naval Research MURI N000141310074;
Office of Naval Research YIP N000141410487;
NIAID R21 AI115014;
Welch Foundation ;
NSF Graduate Research Fellowship DGE 0940902;
NDSEG Fellowship
PMID:27110723 Free, Available for download, Freely available biotools:flowcal https://bio.tools/flowcal SCR_018140 Python Flow Cytometry Calibration Library 2026-08-03 09:36:52 5

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