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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 Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
Cake
 
Resource Report
Resource Website
10+ mentions
Cake (RRID:SCR_002133) software resource A bioinformatics software pipeline that integrates four publicly available somatic variant-calling algorithms to identify single nucleotide variants with higher sensitivity and accuracy than any one algorithm alone. standalone software, unix/linux, mac os x, perl, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:23803469 Free, Available for download, Freely available OMICS_03613, biotools:cake https://bio.tools/cake SCR_002133 2026-02-14 02:00:18 11
SBARS
 
Resource Report
Resource Website
SBARS (RRID:SCR_002371) software resource Bioinformatics tool for searching different types of long repeats in sequences comparable by size with chromosomes. linux, windows, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:24532721 OMICS_03432, biotools:sbars https://bio.tools/sbars SCR_002371 S.B.A.R.S, S.B.A.R.S., S.B.A.R.S - Spectral-Based Approach for Repeats Search, Spectral-Based Approach for Repeats Search 2026-02-14 02:00:16 0
CAMERA - Collection of annotation related methods for mass spectrometry data
 
Resource Report
Resource Website
1+ mentions
CAMERA - Collection of annotation related methods for mass spectrometry data (RRID:SCR_002466) CAMERA software resource A Bioconductor package integrating algorithms to extract compound spectra, annotate isotope and adduct peaks, and propose the accurate compound mass even in highly complex data. standalone software, mac os x, unix/linux, windows, r, spectra, extraction, annotation, liquid chromatography, mass spectrometry, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Bioconductor
PMID:22111785 Free, Available for download, Freely available biotools:camera, OMICS_03366 https://bio.tools/camera SCR_002466 CAMERA - Collection of annotation related methods for mass spectrometry data 2026-02-14 02:00:17 4
Ensembl
 
Resource Report
Resource Website
10000+ mentions
Ensembl (RRID:SCR_002344) data or information resource, database Collection of genome databases for vertebrates and other eukaryotic species with DNA and protein sequence search capabilities. Used to automatically annotate genome, integrate this annotation with other available biological data and make data publicly available via web. Ensembl tools include BLAST, BLAT, BioMart and the Variant Effect Predictor (VEP) for all supported species. collection, genome, dataset, database, vertebrate, eukaryotic, DNA, protein, sequence, search, automaticly, annotate, data, bio.tools, FASEB list is used by: NIF Data Federation
is used by: Animal QTLdb
is used by: ChannelPedia
is used by: Blueprint Epigenome
is used by: HmtPhenome
lists: Ensembl Covid-19
is listed by: OMICtools
is listed by: Biositemaps
is listed by: re3data.org
is listed by: LabWorm
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
is related to: Ensembl Genomes
is related to: GermOnline
is related to: CandiSNPer
is related to: Human Splicing Finder
is related to: NGS-SNP
is related to: Sanger Mouse Resources Portal
is related to: DECIPHER
is related to: Ensembl Genomes
is related to: PeptideAtlas
is related to: AnimalTFDB
is related to: Bgee: dataBase for Gene Expression Evolution
is related to: FlyMine
is related to: Rat Gene Symbol Tracker
is related to: UniParc at the EBI
is related to: go-db-perl
is related to: UniParc
is related to: g:Profiler
is related to: RIKEN integrated database of mammals
is related to: VBASE2
is related to: p300db
is related to: ShinyGO
has parent organization: European Bioinformatics Institute
has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom
is parent organization of: Ensembl Metazoa
is parent organization of: Ensembl Variation
is parent organization of: Pre Ensembl
is parent organization of: Variant Effect Predictor
is parent organization of: Ensembl Bacteria
is parent organization of: Ensembl Plants
is parent organization of: Ensembl Fungi
is parent organization of: Ensembl Protists
is parent organization of: Ensembl Genome Browser
works with: Genotate
works with: CellPhoneDB
works with: Open Regulatory Annotation Database
works with: Database of genes related to Repeat Expansion Diseases
works with: TarBase
Wellcome Trust ;
EMBL ;
European Union ;
FP7 ;
FP6 ;
MRC ;
NHGRI ;
BBSRC
PMID:24316576
PMID:23203987
nif-0000-21145, OMICS_01647, biotools:ensembl, r3d100010228 https://bio.tools/ensembl
https://sources.debian.org/src/ensembl/
https://doi.org/10.17616/R39K5B
SCR_002344 ENSEMBL 2026-02-14 02:00:23 11652
PolyPhred
 
Resource Report
Resource Website
100+ mentions
PolyPhred (RRID:SCR_002337) PolyPhred software resource Software program that compares fluorescence-based sequences across traces obtained from different individuals to identify heterozygous sites for single nucleotide substitutions. Its functions are integrated with the use of three other programs: Phred (Brent Ewing and Phil Green), Phrap (Phil Green), and Consed (David Gordon and Phil Green). PolyPhred identifies potential heterozygotes using the base calls and peak information provided by Phred and the sequence alignments provided by Phrap. Potential heterozygotes identified by PolyPhred are marked for rapid inspection using the Consed tool. windows, sequence, nucleotide substitution, heterozygote, polymorphic, genotype, single nucleotide polymorphism, fluorescence, single nucleotide substitution, polymorphism, insertion, deletion, indel, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Washington; Seattle; USA
PMID:17115056
PMID:16493422
PMID:9207020
Free for academic use, Commercial use requires a license biotools:polyphred, OMICS_01815 https://bio.tools/polyphred SCR_002337 2026-02-14 02:00:16 123
Iterative Signature Algorithm
 
Resource Report
Resource Website
Iterative Signature Algorithm (RRID:SCR_002327) isa2, ISA software resource A biclustering algorithm that finds modules in an input matrix. A module or bicluster is a block of the reordered input matrix. standalone software, mac os x, unix/linux, windows, r, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: CRAN
PMID:12689096 Creative Commons Attribution-NonCommercial-ShareAlike License, v3 biotools:isa, OMICS_03487 https://bio.tools/isa SCR_002327 isa2: The Iterative Signature Algorithm 2026-02-14 02:00:22 0
CUDA-EC
 
Resource Report
Resource Website
1+ mentions
CUDA-EC (RRID:SCR_001090) CUDA-EC software resource A fast parallel error correction tool for short reads. c, gpu/cuda, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: SourceForge
PMID:20426693 Free, Available for download, Freely available OMICS_01100, biotools:cuda-ec https://bio.tools/cuda-ec SCR_001090 Compute Unified Device Architecture 2026-02-14 01:59:55 1
GimmeMotifs
 
Resource Report
Resource Website
1+ mentions
GimmeMotifs (RRID:SCR_001146) GimmeMotifs software resource Software that provides a de novo motif prediction pipeline, especially suited for ChIP-seq datasets. It incorporates several existing motif prediction algorithms in an ensemble method to predict motifs and clusters these motifs using the WIC similarity scoring metric., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. linux, chip-seq, motif, cluster, python, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Radboud University; Nijmegen; The Netherlands
PMID:21081511 THIS RESOURCE IS NO LONGER IN SERVICE biotools:gimmemotifs, OMICS_02150 https://bio.tools/gimmemotifs SCR_001146 GimmeMotifs: a systematic de novo motif prediction pipeline 2026-02-14 02:00:00 4
rbsurv
 
Resource Report
Resource Website
1+ mentions
rbsurv (RRID:SCR_001175) rbsurv software resource Software package that selects genes associated with survival. microarray, gene, survival, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Bioconductor
Free, Available for download, Freely available biotools:rbsurv, BioTools:rbsurv, OMICS_02088 https://bio.tools/rbsurv
https://bio.tools/rbsurv
https://bio.tools/rbsurv
SCR_001175 rbsurv - Robust likelihood-based survival modeling with microarray data 2026-02-14 01:59:56 1
Sherman
 
Resource Report
Resource Website
100+ mentions
Sherman (RRID:SCR_001294) Sherman software resource Software tool to simulate FastQ files for high-throughput sequencing experiments. It allows the user to introduce various "contaminants" into the sequences, such as basecall errors, SNPs, adapter fragments etc., in order to evaluate the influence of common problems observed in many Next-Gen Sequencing experiments. perl, bisulfite sequencing, high-throughput sequencing, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Babraham Institute
Free, Available for download, Freely available biotools:sherman, OMICS_02041 http://www.bioinformatics.babraham.ac.uk/projects/sherman/ SCR_001294 Sherman - bisulfite-treated Read FastQ Simulator 2026-02-14 02:00:00 122
GenomicTools
 
Resource Report
Resource Website
GenomicTools (RRID:SCR_001205) GenomicTools software resource A flexible computational platform, comprising both a command-line set of tools and a C++ API, for the analysis and manipulation of high-throughput sequencing data such as DNA-seq, RNA-seq, ChIP-seq and MethylC-seq. It implements a variety of mathematical operations between sets of genomic regions thereby enabling the prototyping of computational pipelines that can address tasks from preprocessing and quality control to meta-analyses. The user can create average read profiles across transcriptional start sites or enhancer sites, quickly prototype customized peak discovery methods for ChIP-seq experiments, perform genome-wide statistical tests such as enrichment analyses, design controls via appropriate randomization schemes, among other applications. In addition to enabling rapid prototyping, the platform is designed to analyze large-datasets in a single-pass fashion in order to minimize memory and intermediate file requirements. The platform supports the widely used BED format to facilitate visualization as well as integration with existing platforms and pipelines such as Galaxy or BioConductor. high-throughput sequencing, rna-seq, chip-seq, genomics, sequencing, hi-c, epigenetics, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Google Code
PMID:22113082 Free, Available for download, Freely available biotools:genomictools, OMICS_02144 https://bio.tools/genomictools SCR_001205 GenomicTools: a computational platform for developing high-throughput analytics in genomics. 2026-02-14 02:00:02 0
PARalyzer
 
Resource Report
Resource Website
1+ mentions
PARalyzer (RRID:SCR_001208) PARalyzer software resource Software tool to generate a high resolution map of interaction sites between RNA-binding proteins and their targets. The algorithm utilizes the deep sequencing reads generated by the newly developed PAR-CLIP (Photoactivatable-Ribonucleoside-Enhanced Crosslinking and Immunoprecipitation) protocol. The use of photoactivatable nucleotides in the PAR-CLIP protocol results in a more efficient crosslinking between the RNA-binding protein and its target relative to other CLIP methods; in addition a nucleotide substitution occurs at the site of crosslinking during Illumina library preparation. PARalyzer utilizes this nucleotide substition in a kernel density estimate classifier to generate the high resolution set of Protein-RNA interaction sites. interaction, rna-binding protein, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Duke University; North Carolina; USA
PMID:21851591 THIS RESOURCE IS NO LONGER IN SERVICE biotools:paralyzer, OMICS_02137 https://bio.tools/paralyzer SCR_001208 PAR-CLIP data analyzer, PARalyzer (PAR-CLIP data analyzer) 2026-02-14 01:59:55 6
ProbRNA
 
Resource Report
Resource Website
1+ mentions
ProbRNA (RRID:SCR_001288) ProbRNA software resource Software for computational identification of protein binding sites on RNAs using high-throughput RNA structure-probing data. high-throughput sequencing, probe, rna structure, rna, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Chinese University of Hong Kong; Hong Kong; China
PMID:24376038 THIS RESOURCE IS NO LONGER IN SERVICE biotools:probrna, OMICS_02195 https://bio.tools/probrna SCR_001288 2026-02-14 02:00:00 1
Sequedex
 
Resource Report
Resource Website
1+ mentions
Sequedex (RRID:SCR_001233) Sequedex software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 18,2025.Software to classify the function and phylogeny of reads as short as 30 bp. It is flexible, which can utilize multiple data modules and downstream analysis scripts. It is fast, reading in signature lists of 5-500 million peptide signatures in 1-15 minutes, and subsequently processes genomic fragments at the rate of 6 Gbp/hr. It parallelizes without significant increase in memory requirements until I/O bound on multiple input files; parallelization works well on 64 processors. phylogenetic, function, profile, metagenomics, synthetic, dna sequence, classification, java, linux, mac os, genomic analysis, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Los Alamos National Laboratory
PMID:22925230 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02110, biotools:sequedex https://bio.tools/sequedex SCR_001233 2026-02-14 02:00:03 1
PeakAnalyzer
 
Resource Report
Resource Website
1+ mentions
PeakAnalyzer (RRID:SCR_001194) PeakAnalyzer software resource A set of standalone software programs for the automated processing of any genomic loci, with an emphasis on datasets consisting of ChIP-derived signal peaks. The software is able to identify individual binding / modification sites from enrichment loci, retrieve peak region sequences for motif discovery, and integrate experimental data with different classes of annotated elements throughout the genome. PeakAnalyzer requires a peak file and a feature annotation file in BED or GTF format. Complete annotation files for the current builds of the human (HG19) and mouse (MM9) genomes are provided with the software distribution. genome, chip, signal peak, binding site, modification site, enrichment loci, peak region, sequence, motif, chip-seq, chip-chip, c++, java, linux, mac os x, windows, bed, gtf, annotation, r, high-throughput sequencing, chromatin binding, modification loci, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: European Bioinformatics Institute
PMID:20691053 Free, Available for download, Freely available biotools:peakanalyzer, OMICS_02156 https://bio.tools/peakanalyzer SCR_001194 2026-02-14 01:59:57 3
BreakSeq
 
Resource Report
Resource Website
1+ mentions
BreakSeq (RRID:SCR_001186) BreakSeq software resource Software for scanning reads from short-read sequenced genomes against a human breakpoint library to accurately identify structural variants (SVs). The library of breakpoints at nucleotide resolution were assembled from collating and standardizing ~2,000 published structural variants (SVs). For each breakpoint, its ancestral state (through comparison to primate genomes) was inferred and its mechanism of formation (e.g., nonallelic homologous recombination, NAHR). structural variant, breakpoint, nucleotide, fasta, gff, bowtie, genomic variation, junction mapping, insertion sequence, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Yale University; Connecticut; USA
PMID:20037582 THIS RESOURCE IS NO LONGER IN SERVICE biotools:breakseq, OMICS_02168 https://bio.tools/breakseq SCR_001186 Breakpoint Library and BreakSeq 2026-02-14 01:59:55 1
SLOPE
 
Resource Report
Resource Website
SLOPE (RRID:SCR_001185) SLOPE software resource Software that consists of two command-line utilities, slope_align (which finds the best split-read alignments to the reference genome) and slope_cluster (which clusters and outputs the alignments)., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. c++, alignment, cluster, command-line, reference genome, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Utah; Utah; USA
PMID:20876606 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02169, biotools:slope https://bio.tools/slope SCR_001185 2026-02-14 01:59:57 0
Genometa
 
Resource Report
Resource Website
Genometa (RRID:SCR_001181) Genometa software resource A Java based bioinformatics program which allows rapid analysis of metagenomic short read datasets. Millions of short reads can be accurately analysed within minutes and visualised in the browser component. A large database of diverse bacteria and archaea has been constructed as a reference sequence. The approach is based upon the established open source visualisation tool IGB and supported by the rapid alignment program bowtie. The Picard toolset for SAM files is also made use of. metagenomic, classify, windows, linux, java, bio.tools, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Hannover Medical School; Lower Saxony; Germany
PMID:22927906 Free, Available for download, Freely available biotools:genometa, OMICS_02175 https://bio.tools/genometa SCR_001181 Genometa - Rapid analysis of metagenomic short reads 2026-02-14 01:59:55 0
piCALL
 
Resource Report
Resource Website
1+ mentions
piCALL (RRID:SCR_001242) piCALL software resource Software to detect short insertion / deletion variants (and SNPs) from population sequence data, i.e. sequence reads generated from a population of individuals. It uses a probabilistic model to utilize sequence reads from a population of individuals to automatically account for context-specific sequencing errors associated with indels. piCALL is implemented in C for use on Linux platforms and can be applied to sequence data from different sequencing platforms. However, the method requires each individual in a dataset to be sequenced using the same platform. The reads for each individual should be aligned to the same reference genome sequence. Note that the program will not be able to call indels from individual sequence datasets or data from a small number of individuals. c, genotyping, indel, population, high-throughput sequencing, insertion, deletion, variant, single nucleotide polymorphism, linux, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: Scripps Research Institute
PMID:21653520 OMICS_02098, biotools:picall https://bio.tools/picall http://polymorphism.scripps.edu/~vbansal/software/piCALL/ SCR_001242 2026-02-14 01:59:58 1
mapDamage
 
Resource Report
Resource Website
100+ mentions
mapDamage (RRID:SCR_001240) mapDamage software resource Software for tracking and quantifying DNA damage patterns among ancient DNA sequencing reads generated by Next-Generation Sequencing platforms. python, r, illumina, windows, perl, dna damage, dna sequencing, next-generation sequencing, dna, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Copenhagen; Copenhagen; Denmark
PMID:23613487
PMID:21659319
DOI:10.1093/bioinformatics/btt193
Free, Available for download, Freely available OMICS_02099, biotools:mapdamage https://bio.tools/mapdamage
https://sources.debian.org/src/mapdamage/
SCR_001240 mapDamage 2.0, mapDamage: tracking and quantifying damage patterns in ancient DNA sequences, mapDamage2.0 2026-02-14 01:59:58 363

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