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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
genehunter-imprinting
 
Resource Report
Resource Website
1+ mentions
genehunter-imprinting (RRID:SCR_009104) GENEHUNTER-TWOLOCUS software application, software resource Resource no longer in service. Documented on February 23,2021.Software tool as modification of GENEHUNTER software package . Allows for parametric multi-marker linkage analysis of dichotomous traits caused by imprinted genes. By specification of two heterozygote penetrance parameters, paternal and maternal origin of the disease allele can be treated differently in terms of probability of expression of the trait. gene, genetic, genomic, c, unix, sunos, solaris, osf, hpux, aix, ultrix, linux, ms-windows, bio.tools is listed by: Genetic Analysis Software
is listed by: Debian
is listed by: bio.tools
DOI:10.1086/302911 Resource no longer in service. Documented on February 23,2021 nlx_154199, biotools:genehunter-imprinting https://bio.tools/genehunter-imprinting http://www.staff.uni-marburg.de/~strauchk/software.html SCR_009104 GENEHUNTER-MODSCORE, GENEHUNTER-PLUS, GENEHUNTER, GENEHUNTER-IMPRINTING 2026-07-26 09:04:44 1
CCREL
 
Resource Report
Resource Website
CCREL (RRID:SCR_009142) CCREL software application, software resource Software program for case-control genetic analysis that takes relatedness between individuals into account. It will perform single-marker and haplotypic tests, however it will only work with SNP or other biallelic markers. (entry from Genetic Analysis Software) gene, genetic, genomic, r, perl, c, unix, linux, bio.tools is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
biotools:ccrel, nlx_154261 https://bio.tools/ccrel SCR_009142 Case-Control association analysis with RELlated individuals 2026-07-26 09:04:52 0
HS-TDT
 
Resource Report
Resource Website
1+ mentions
HS-TDT (RRID:SCR_009240) HS-TDT software application, software resource Software application for testing association using tightly linked markers in nuclear pedigrees (entry from Genetic Analysis Software) gene, genetic, genomic, unix, ms-windows, bio.tools is listed by: Genetic Analysis Software
is listed by: bio.tools
is listed by: Debian
nlx_154401, biotools:hs-tdt https://bio.tools/hs-tdt SCR_009240 Haplotype Sharing Transmission Disequilibrium Test 2026-07-26 09:04:55 4
SNPAAMapper
 
Resource Report
Resource Website
SNPAAMapper (RRID:SCR_002012) SNPAAMapper software application, software resource, data processing software THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 19,2025. A downstream variant annotation program that can effectively classify variants by region (e.g. exon, intron, etc), predict amino acid change type (e.g. synonymous, non-synonymous mutation, etc), and prioritize mutation effects (e.g. CDS versus 5?UTR, etc). Major features: * The pipeline accepts the VCF (Variant Call Format) input file in tab-delimited format and processes the vcf input file containing all cases (G5, lowFreq, and novel) * The variant mapping step has the option of letting users select whether they want to report the bp distance between each identified intron variant and its nearby exon * The pipeline can deal with VCF files called by different SAMTools versions (0.1.18 and older ones) and also offers flexibility in dealing with vcf input files generated using SAMTools with two or three samples * The spreadsheet result file contains full protein sequences for both ref and alt alleles, which makes it easier for downstream protein structure/function analysis tools to take single nucleotide polymorphism, amino acid, variant, annotation, exon, intron, mutation, next-generation sequencing, perl, downstream analysis, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Michigan Medical School; Michigan; USA
PMID:24250114 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01922, biotools:snpaamapper https://bio.tools/snpaamapper SCR_002012 SNPAAMapper - A SNP Amino Acid Mapping tool 2026-07-26 09:03:08 0
HTqPCR
 
Resource Report
Resource Website
50+ mentions
HTqPCR (RRID:SCR_003375) HTqPCR software application, software resource, data processing software Software package for the analysis of Ct values from high throughput quantitative real-time PCR (qPCR) assays across multiple conditions or replicates. The input data can be from spatially-defined formats such ABI TaqMan Low Density Arrays or OpenArray; LightCycler from Roche Applied Science; the CFX plates from Bio-Rad Laboratories; conventional 96- or 384-well plates; or microfluidic devices such as the Dynamic Arrays from Fluidigm Corporation. HTqPCR handles data loading, quality assessment, normalization, visualization and parametric or non-parametric testing for statistical significance in Ct values between features (e.g. genes, microRNAs). data import, differential expression, gene expression, microtitre plate assay, multiple comparison, preprocessing, quality control, visualization, qpcr, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
has parent organization: European Bioinformatics Institute
PMID:19808880 Free, Available for download, Freely available biotools:htqpcr, OMICS_02314 https://bio.tools/htqpcr SCR_003375 HTqPCR - Automated analysis of high-throughput qPCR data 2026-07-26 09:03:25 74
NanoStringNorm
 
Resource Report
Resource Website
100+ mentions
NanoStringNorm (RRID:SCR_003382) NanoStringNorm software application, software resource, data processing software Software package for normalizing, diagnostics and visualization of NanoString nCounter data. Key features include an extensible environment for method comparison and new algorithm development, integrated gene and sample diagnostics, and facilitated downstream statistical analysis. normalization, nanostring ncounter, mirna, mrna, r, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Ontario Institute for Cancer Research
PMID:22513995 Free, Available for download, Freely available OMICS_02308, biotools:nanostringnorm https://www.rdocumentation.org/packages/NanoStringNorm/versions/1.2.1.1/topics/NanoStringNorm SCR_003382 NanoStringNorm: Normalize NanoString miRNA and mRNA data 2026-07-26 09:03:25 134
skewer
 
Resource Report
Resource Website
10+ mentions
skewer (RRID:SCR_001151) skewer software application, software resource, data processing software Software program for adapter trimming that is specially designed for processing Illumina paired-end sequences. illumina, unix/linux, c++, adapter trimming, paired-end, sequence, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:24925680 Free, Available for download, Freely available OMICS_02106, biotools:skewer https://bio.tools/skewer, https://sources.debian.org/src/skewer/, https://github.com/relipmoc/skewer SCR_001151 skewer - A fast and sensitive adapter trimmer for illumina paired-end sequences 2026-07-26 09:03:01 11
COILS: Prediction of Coiled Coil Regions in Proteins
 
Resource Report
Resource Website
100+ mentions
COILS: Prediction of Coiled Coil Regions in Proteins (RRID:SCR_008440) software application, software resource, data processing software COILS is a program that compares a sequence to a database of known parallel two-stranded coiled-coils and derives a similarity score. By comparing this score to the distribution of scores in globular and coiled-coil proteins, the program then calculates the probability that the sequence will adopt a coiled-coil conformation. software, prediction, database, sequence, coil, globular, protein, probability, bio.tools, FASEB list is listed by: 3DVC
is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
DOI:10.1126/science.252.5009.1162 biotools:ncoils, OMICS_07850, nif-0000-30263 https://bio.tools/ncoils, https://sources.debian.org/src/ncoils/ https://sources.debian.org/src/ncoils/ SCR_008440 COILS Server 2026-07-26 09:04:39 164
SeqExpress
 
Resource Report
Resource Website
SeqExpress (RRID:SCR_007075) software application, software resource, data processing software A comprehensive analysis and visualization software package for gene expression experiments that provides: a number of clustering and analysis techniques; integrated gene expression and analysis result visualizations, integration with the Gene Expression Omnibus; and an optional data sharing architecture. GO is used to assign functional enrichment scores to clusters, using a combination of specially developed techniques and general statistical methods. These results can be explored using the in built ontology browsing tool or through the generated web pages. SeqExpress also supports numerous data transformation, projection, visualization, file export/import, searching, integration (with R), and clustering options. gene, gene expression, function, analysis, visualization, statistical analysis, windows, c#, gene function, chromosome location, bio.tools is listed by: Gene Ontology Tools
is listed by: bio.tools
is listed by: Debian
is related to: Gene Ontology
is related to: Gene Expression Omnibus
PMID:14988116 Free nlx_149285, biotools:seqexpress https://bio.tools/seqexpress SCR_007075 2026-07-26 09:04:28 0
epigenomix
 
Resource Report
Resource Website
1+ mentions
epigenomix (RRID:SCR_006407) epigenomix software application, software resource, data processing software Software package for the integrative analysis of microarray based gene expression and histone modification data obtained by ChIP-seq. The package provides methods for data preprocessing and matching as well as methods for fitting bayesian mixture models in order to detect genes with differences in both data types. epigenetic, gene expression, microarray, histone modification, chip-seq, classification, differential expression, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
PMID:24403540 GNU Lesser General Public License, v3 biotools:epigenomix, OMICS_02205 https://bio.tools/epigenomix SCR_006407 epigenomix - Epigenetic and gene expression data normalization and integration with mixture models 2026-07-26 09:04:16 2
SOAPaligner/soap2
 
Resource Report
Resource Website
100+ mentions
SOAPaligner/soap2 (RRID:SCR_005503) SOAPaligner, SOAP2 software application, software resource, data processing software THIS RESOURCE IS NO LONGER IN SERVICE. Documented on April 12,2024. Updated version of SOAP software for short oligonucleotide alignment that features in super fast and accurate alignment for huge amounts of short reads generated by Illumina/Solexa Genome Analyzer., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. next generation sequencing, alignment, short read, oligonucleotide, single-read, pair-end, resequencing, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SOAP
PMID:19497933
DOI:10.1093/bioinformatics/btn025
THIS RESOURCE IS NO LONGER IN SERVICE biotools:soap2 https://bio.tools/soap2, https://sources.debian.org/src/soapaligner/ SCR_005503 2026-07-26 09:03:57 322
Subread
 
Resource Report
Resource Website
1000+ mentions
Subread (RRID:SCR_009803) software application, software resource, data processing software Software package for high-performance read alignment, quantification and mutation discovery.General purpose read aligner which can be used to map both genomic DNA-seq reads and RNA-seq reads. Subread aligner as fast, accurate and scalable read mapping by seed-and-vote.These programs were also implemented in Bioconductor R package Rsubread. read alignment, DNA-seq reads mapping, RNA-seq reads mapping, mutation discovery, , bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
is related to: Rsubread
has parent organization: University of Melbourne; Victoria; Australia
Australian National Health and Medical Research Council ;
Victorian State Government Operational Infrastructure Support ;
Australian Government
PMID:23558742 Free, Freely available OMICS_01255, biotools:subread https://bio.tools/subread, https://sources.debian.org/src/subread/ SCR_009803 2026-07-26 09:05:12 1854
GSA-SNP
 
Resource Report
Resource Website
10+ mentions
GSA-SNP (RRID:SCR_013109) GSA-SNP software application, software resource, data processing software A tool for the gene-set (or pathway) analysis of a genome-wide association study result. It accepts a genome-wide list of SNPs and their association P-values. It summarizes the SNP P-values into nearby genes. The gene-by-gene summary results are then further summarized by gene-sets such as Gene Ontology, KEGG pathways, or user-created gene-sets. Various standardization and statistical tests can be performed and the resulting gene-sets that pass a significance level after multiple-testing correction are reported. The tool is written in Java and is available as a standalone version. clinical neuroinformatics, computational neuroscience, imaging genomics, bio.tools is listed by: NeuroImaging Tools and Resources Collaboratory (NITRC)
is listed by: Debian
is listed by: bio.tools
has parent organization: Soongsil University; Seoul; South Korea
PMID:20501604 GNU General Public License v2 nlx_155765, biotools:gsa-snp https://bio.tools/gsa-snp SCR_013109 2026-07-26 09:05:49 18
Trim Galore
 
Resource Report
Resource Website
5000+ mentions
Rating or validation data
Trim Galore (RRID:SCR_011847) Trim Galore! software application, software resource, data processing software Software tool to automate quality and adapter trimming as well as quality control, with some added functionality to remove biased methylation positions for RRBS sequence files for directional, non-directional or paired-end sequencing. Wrapper around Cutadapt and FastQC to consistently apply adapter and quality trimming to FastQ files, with extra functionality for Reduced Representation Bisulfite Sequencing data. Automate, quality, adapter, trimming, remove, biased, methylation, position, RRBS, reduced, representation, bisulfite, data, sequence, wrapper, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Babraham Institute
works with: cutadapt
Free, Available for download, Freely available biotools:trim_galore, OMICS_01096, SCR_016946 https://github.com/FelixKrueger/TrimGalore, https://bio.tools/trim_galore, https://sources.debian.org/src/trim-galore/ SCR_011847 TrimGalore 2026-07-26 09:05:32 6255
docker4seq
 
Resource Report
Resource Website
1+ mentions
docker4seq (RRID:SCR_017006) software application, software resource, data processing software Software R package to execute next generation sequencing computing applications, e.g. reads mapping and counting, wrapped in docker containers. next, generation, sequencing, computing, application, read, mapping, count, docker, container, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: University of Turin;Turin;Italy
Free, Available for download, Freely available biotools:docker4seq https://kendomaniac.github.io/docker4seq/index.html, https://bio.tools/docker4seq SCR_017006 2026-07-26 09:06:54 5
ProCon - PROteomics CONversion
 
Resource Report
Resource Website
1+ mentions
ProCon - PROteomics CONversion (RRID:SCR_016363) ProCon software application, software resource, data processing software Java based conversion tool for conversion of data from Proteomics files or a LIMS (Laboratory Information Management System) database into standard formats. Used to support wet-lab scientists in creating proteomics data files ready for upload into the public repositories. data, proteomics, conversion, file, laboratory, information, management, system, database, standard, format, , bio.tools is listed by: Debian
is listed by: bio.tools
is related to: Ruhr University Bochum; North Rhine-Westphalia; Germany
European Union Projects ProDac ;
European Union Projects ProteomeXchange ;
the German Federal Ministry of Education and Research BMBF
PMID:26182917 Free, Available for download, Freely available biotools:procon https://bio.tools/procon SCR_016363 PROteomics CONversion 2026-07-26 09:06:43 1
ScaffMatch
 
Resource Report
Resource Website
1+ mentions
ScaffMatch (RRID:SCR_017025) software application, software resource, data processing software Software tool as scaffolding algorithm based on maximum weight matching able to produce high quality scaffolds from next generation sequencing data (reads and contigs). Able to handle reads with both short and long insert sizes. scaffolding, algorithm, maximum, weight, matching, next, generation, sequencing, data, read, contig, bio.tools uses: Python Programming Language
is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Georgia State University; Georgia; USA
NSF IIS 0916401 PMID:25890305 Free, Available for download, Freely available biotools:scaffmatch, OMICS_08198 http://alan.cs.gsu.edu/NGS/?q=content/scaffmatch, https://bio.tools/scaffmatch SCR_017025 2026-07-26 09:06:54 1
Racon
 
Resource Report
Resource Website
100+ mentions
Racon (RRID:SCR_017642) software application, software resource, data processing software Software tool as de novo genome assembly from long uncorrected reads. Used to correct raw contigs generated by rapid assembly methods which do not include consensus step. Supports data produced by Pacific Biosciences and Oxford Nanopore Technologies. Assembly, de novo, long, uncorrected, read, raw, contig, consensus, step, data, sequence, bio.tools is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
Croatian Science Foundation ;
Croatian Academy of Sciences and Arts ;
A*STAR ;
Singapore
DOI:10.1101/068122 Free, Available for download, Freely available OMICS_25714, biotools:Racon, BioTools:Racon https://bio.tools/Racon, https://sources.debian.org/src/racon/ SCR_017642 2026-07-26 09:07:03 149
CiLiQuant
 
Resource Report
Resource Website
CiLiQuant (RRID:SCR_019319) software application, software resource, data processing software Software tool to separate junction reads based on their linear or circular origin. Only non ambiguous junction reads are used to compare relative linear and circular transcript abundance. RNA, splicing, circular origin, separate junction reads, circular transcript abundance, linear transcript abundance, compare, bio.tools is listed by: bio.tools
is listed by: Debian
FWO ;
Special Research Fund UGent ;
Stichting Tegen Kanker ;
Kom Op Tegen Kanker (Stand Up To Cancer) ;
European Union's Horizon 2020
Free, Available for download, Freely available biotools:ciliquant https://bio.tools/ciliquant SCR_019319 2026-07-26 09:07:34 0
FlowCal
 
Resource Report
Resource Website
1+ mentions
FlowCal (RRID:SCR_018140) software application, software resource, 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 2026-07-26 09:07:12 5

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