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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
NetMHCpan Server
 
Resource Report
Resource Website
100+ mentions
NetMHCpan Server (RRID:SCR_018182) data access protocol, software resource, web service Web server for quantitative prediction of peptide binding to any MHC molecule of known sequence using artificial neural networks. Characterizes binding specificity of given major histocompatibility complex molecule and predicts peptide length profile and peptide binding affinity. NetMHCpan 3.0 is improved prediction of binding to MHC class I molecules integrating information from multiple receptor and peptide length data sets. NetMHCpan 4.0 is trained on naturally eluted ligands and on peptide binding affinity data. NetMHCpan-4.1 server predicts binding of peptides to any MHC molecule of known sequence using artificial neural networks (ANNs). Quantitative prediction, peptide binding, MHC molecule, artificial neural network, Major Histocompatibilty Complex, peptide length, peptide binding affinity, data, bio.tools is listed by: bio.tools
is listed by: Debian
Agencia Nacional de Promoción Científica y Tecnológica ;
Argentina ;
NIAID
PMID:19002680
PMID:28978689
Free, Available for download, Freely Available biotools:netmhcpan https://bio.tools/netmhcpan, https://services.healthtech.dtu.dk/services/NetMHCpan-4.1/ SCR_018182 NetMHCpan 1.0, NetMHCpan 3.0, NetMHCpan 2.0, NetMHCpan 4.1, NetMHCpan 4.0, NetMHCpan 2026-08-04 09:44:18 138
4See
 
Resource Report
Resource Website
1+ mentions
4See (RRID:SCR_018014) data processing software, data visualization software, software application, software resource Software tool to visualize 4C data. Visualize, 4C data, bio.tools is listed by: bio.tools
is listed by: Debian
DOI:10.3389/fgene.2019.01372 Free, Available for download, Freely available biotools:4see https://bio.tools/4see SCR_018014 2026-08-04 09:44:16 1
Online Peri-Event Time Histogram for Open Ephys
 
Resource Report
Resource Website
1+ mentions
Online Peri-Event Time Histogram for Open Ephys (RRID:SCR_018022) OPETH data processing software, data visualization software, software application, software resource Software tool to enable flexible online visualization of action potential alignment to external events. Performs spike detection based on raw Open Ephys data exported via ZeroMQ. Requires triggers from Open Ephys for histogram display as spikes are detected around them. Open source, open ephys, optogenetics, behavior, electrophysiology data, neuroscience experiment, spike detection, behavior tagging, neuron, histogram, bio.tools is listed by: Debian
is listed by: bio.tools
Hungarian Academy of Sciences Lendület Program LP2015-2/2015;
European Research Council Starting Grant 715043;
Generalitat Valenciana Postdoctoral Fellowship Program APOSTD/2019/003
DOI:10.1101/783688 Free, Available for download, Freely available biotools:OPEtH https://bio.tools/OPETH SCR_018022 Online Peri-Event Time Histogram 2026-08-04 09:44:16 4
biobambam
 
Resource Report
Resource Website
50+ mentions
biobambam (RRID:SCR_003308) data processing software, software application, software resource Software tools for read pair collation based algorithms on BAM files including * bamcollate2: reads BAM and writes BAM reordered such that alignment or collated by query name * bammarkduplicates: reads BAM and writes BAM with duplicate alignments marked using the BAM flags field * bammaskflags: reads BAM and writes BAM while masking (removing) bits from the flags column * bamrecompress: reads BAM and writes BAM with a defined compression setting. This tool is capable of multi-threading. * bamsort: reads BAM and writes BAM resorted by coordinates or query name * bamtofastq: reads BAM and writes FastQ; output can be collated or uncollated by query name standalone software, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
DOI:10.1186/1751-0473-9-13 Free, Available for download, Freely available biotools:biobambam, OMICS_04664 https://bio.tools/biobambam, https://sources.debian.org/src/biobambam2/ SCR_003308 2026-08-04 09:40:52 58
SeqTrace
 
Resource Report
Resource Website
50+ mentions
SeqTrace (RRID:SCR_005580) SeqTrace data processing software, software application, software resource A software application for viewing and processing DNA sequencing chromatograms (trace files) that makes it easy to quickly generate high-quality finished sequences from a large number of trace files. SeqTrace can automatically identify, align, and compute consensus sequences from matching forward and reverse traces, filter low-quality base calls, and perform end trimming of finished sequences. The finished DNA sequences can then be exported to common sequence file formats, such as FASTA. SeqTrace also includes a full-featured trace file viewer and editor. You can view your sequencing chromatograms at a variety of scales and zoom levels, simultaneously view matching forward and reverse traces, edit the called bases, and export individual DNA sequences as well as forward/reverse alignments. SeqTrace supports popular trace file formats, including ABIF, SCF, and ZTR. dna sequencing trace file, dna sequencing, trace file, trace, python, gtk, chromatogram, graphic, sequence analysis, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Google Code
has parent organization: University of Colorado Boulder; Colorado; USA
PMID:22942788 GNU General Public License, v3 OMICS_01021, biotools:seqtrace https://bio.tools/seqtrace SCR_005580 Seqtrace - User-friendly software for viewing and processing DNA sequencing trace files 2026-08-04 09:41:23 62
Mammalian Gene Collection
 
Resource Report
Resource Website
10+ mentions
Mammalian Gene Collection (RRID:SCR_007024) MGC cell repository, material resource, biomaterial supply resource NIH initiative project to provide full-length open reading frame (FL-ORF) clones for human, mouse, and rat genes, cow. MGC cDNA clones were obtained by screening of cDNA libraries, by transcript-specific RT-PCR cloning, and by DNA synthesis of cDNA inserts. All MGC sequences are deposited in GenBank and clones can be purchased from distributors of IMAGE consortium. With conclusion of MGC project in March 2009, GenBank records of MGC sequences will be frozen, without further updates. Since definition of what constitutes full-length coding region for some of genes and transcripts for which they have MGC clones will likely change in future, users planning to order MGC clones will need to monitor for these changes. Users can make use of genome browsers and gene-specific databases, such as the UCSC Genome browser, NCBI's Map Viewer, and Entrez Gene, to view relevant regions of genome (browsers) or gene-related information (Entrez Gene). cell line, cdna, frozen, clone, vector, gene, open reading frame, sequence, expressed sequence tag, bio.tools, FASEB list is listed by: One Mind Biospecimen Bank Listing
is listed by: bio.tools
is listed by: Debian
is related to: One Mind Biospecimen Bank Listing
is related to: NIDDK Information Network (dkNET)
is related to: ATCC
is related to: GenBank
is related to: Invitrogen Clones
is related to: Open Biosystems
is related to: Zebrafish Gene Collection
has parent organization: National Cancer Institute
NIH Blueprint for Neuroscience Research Free, Freely available biotools:mammalian_gene_collection, nif-0000-00195 https://bio.tools/mammalian_gene_collection SCR_007024 Mammalian Gene Collection 2026-08-04 09:41:44 46
Sickle
 
Resource Report
Resource Website
1000+ mentions
Sickle (RRID:SCR_006800) Sickle data processing software, software application, software resource Software tool for windowed adaptive trimming for fastq files using quality. Supports quality values like Illumina, Solexa, and Sanger. Takes the quality values and slides a window across them whose length is 0.1 times the length of the read. bio.tools, windowed, adaptive, trimming, FASTQ, quality, value, read is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
Free, Available for download, Freely available OMICS_01077, biotools:sickle, SCR_016901 https://bio.tools/sickle, https://sources.debian.org/src/sickle/ SCR_006800 sickle - A windowed adaptive trimming tool for FASTQ files using quality 2026-08-04 09:41:42 1422
Trimmomatic
 
Resource Report
Resource Website
10000+ mentions
Trimmomatic (RRID:SCR_011848) Trimmomatic data processing software, software application, software resource Software Java pipeline for trimming tasks for Illumina paired end and single ended data. Flexible Trimmer for Illumina Sequence Data. Pair aware preprocessing tool optimized for Illumina next generation sequencing data. Includes several processing steps for read trimming and filtering. Operating systems Unix/Linux, Mac OS, Windows. trimming, task, paired, end, single, data, next, generation, sequencing, filtering, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
is related to: shovill
BLE/BMELV Verbundprojekt ;
BMBF
PMID:24695404
DOI:10.1093/bioinformatics/btu170
biotools:trimmomatic, OMICS_01097 https://omictools.com/trimmomatic-tool, https://bio.tools/trimmomatic, https://sources.debian.org/src/trimmomatic/ SCR_011848 Trimmomatic v 0.32 2026-08-04 09:42:52 21028
Open Babel
 
Resource Report
Resource Website
50+ mentions
Open Babel (RRID:SCR_014920) data processing software, software application, software resource, data analytics software Software toolbox that is used to convert, analyze, or store data from molecular modeling, chemistry, biochemistry and other related areas. This software is used to read, write, and convert into over 110 chemical file formats. toolbox, conversion, analysis, molecular model, chemistry, biochemistry, chemical file, bio.tools is listed by: bio.tools
is listed by: Debian
Open source biotools:open_babel https://bio.tools/open_babel SCR_014920 2026-08-04 09:43:32 81
xia2 pipeline
 
Resource Report
Resource Website
10+ mentions
xia2 pipeline (RRID:SCR_015746) data processing software, software application, software resource Data processing software that performs X-ray diffraction data processing. It handles multi-pass, multi-wavelength data sets and supports remote access to synchrotron facilities. xray, diffraction, data processing, synchrotron, mmulti-pass, multi-wavelength, bio.tools is listed by: bio.tools
is listed by: Debian
PMID:23793152 Open Source, Available for download biotools:xia2 https://bio.tools/xia2 SCR_015746 2026-08-04 09:43:43 34
PASTEClassifier
 
Resource Report
Resource Website
10+ mentions
PASTEClassifier (RRID:SCR_017645) PASTEC data processing software, software application, software resource Software tool for automatic transposable element classification. Used for searching for structural features and similarity to classify transposable elements. Automatic, transposable, element, classification, bio.tools, bio.tools is listed by: Debian
is listed by: bio.tools
French National Research Agency PMID:24786468 Free, Available for download, Freely available biotools:PAStEClassifier https://urgi.versailles.inra.fr/download/repet/PASTEClassifier-1.0.tar.gz, https://bio.tools/repet, https://bio.tools/PASTEClassifier SCR_017645 Pseudo Agent System for Transposable Elements Classification, PASTEC 2026-08-04 09:44:10 11
Sniffles
 
Resource Report
Resource Website
50+ mentions
Sniffles (RRID:SCR_017619) data processing software, software application, software resource Software tool as structural variation caller using third generation sequencing (PacBio or Oxford Nanopore). It detects all types of SVs (10bp+) using evidence from split-read alignments, high-mismatch regions, and coverage analysis. Used to avoid single molecule long read sequencing high error rates. Structural, variation, caller, third, generation, sequencing, SV, split, read, alignment, mismatch, region, analysis, error, bio.tools is listed by: bio.tools
is listed by: Debian
NHGRI R01 HG006677;
NHGRI UM1 HG008898
PMID:29713083 Free, Available for download, Freely available biotools:sniffles https://bio.tools/sniffles SCR_017619 2026-08-04 09:44:10 59
TGS-GapCloser
 
Resource Report
Resource Website
10+ mentions
TGS-GapCloser (RRID:SCR_017633) data processing software, software application, software resource Software tool that uses long reads to enhance genome assembly. Fast and accurate gap closing software tool that uses low coverage of error-prone long reads generated by third generation sequence techniques (Pacbio, Oxford Nanopore, etc.) or preassembled contigs for large genomes. Error, prone, third, generation, sequencing, long, read, gap, closing, genome, assembly, contig, bio.tools is listed by: Debian
is listed by: bio.tools
Free, Available for download, Freely available biotools:tGS-GapCloser https://bio.tools/TGS-GapCloser SCR_017633 2026-08-04 09:44:15 35
rnaQUAST
 
Resource Report
Resource Website
1+ mentions
rnaQUAST (RRID:SCR_016994) data processing software, software application, software resource Software tool for evaluating RNA-Seq assembly quality and benchmarking transcriptome assemblers using reference genome and gene database. Capable to estimate gene database coverage by raw reads and de novo quality assessment using third party software. evaluation, quality, RNA-Seq, assembly, data, transcriptome, assembler, reference, genome, gene, database, raw, read, , bio.tools uses: BUSCO
is listed by: Debian
is listed by: bio.tools
is related to: rnaSPAdes
is related to: Python Programming Language
is related to: SPAdes
EMC Research and Development Department ;
St. Petersburg State University ;
Russia
PMID:27153654 Free, Available for download, Freely available biotools:rnaQUASt https://bio.tools/rnaQUAST SCR_016994 2026-08-04 09:44:02 3
parSMURF
 
Resource Report
Resource Website
1+ mentions
parSMURF (RRID:SCR_017560) data processing software, software application, software resource Open source software package as high performance computing imbalance aware machine learning tool for genome wide detection of pathogenic variants. High, performance, computing, imbalance, aware, machine, learning, genome, wide, detection, pathogenic, variant, bio.tools is listed by: bio.tools
is listed by: Debian
Free, Available for download, Freely available biotools:parsmurf https://bio.tools/parsmurf SCR_017560 2026-08-04 09:44:14 1
MEGAHIT
 
Resource Report
Resource Website
1000+ mentions
MEGAHIT (RRID:SCR_018551) data processing software, software application, software resource Software tool as Next Generation Sequencing assembler. Optimized for metagenomes, but also works well on generic single genome assembly (small or mammalian size) and single cell assembly. Can assemble genome sequences from metagenomic datasets of hundreds of Giga base-pairs in time and memory efficient manner on single server. NGS metagenome, Next Generation Sequencing assembler, metagenome, genome assembly, genome sequence, metagenomic dataset, giga base pairs, bio.tools is listed by: bio.tools
is listed by: Debian
is listed by: OMICtools
Hong Kong GRF ;
Innovation and Technology Fund
PMID:25609793
PMID:27012178
Free, Available for download, Freely available OMICS_07234, biotools:megahit https://bio.tools/megahit, https://sources.debian.org/src/megahit/ SCR_018551 MEGAHIT v0.1 2026-08-04 09:44:22 1451
rna-stability
 
Resource Report
Resource Website
1+ mentions
rna-stability (RRID:SCR_019259) data processing software, software application, software resource Software tool as parallel processing framework for large scale generation of secondary RNA structures and folding statistics for transcriptome of any species. Secondary RNA structures generation, large scale generation, RNA structures, transcriptome folding statistics, , bio.tools is listed by: bio.tools
is listed by: Debian
Free, Freely available biotools:rna-stability https://bio.tools/rna-stability SCR_019259 2026-08-04 09:44:31 1
mosdepth
 
Resource Report
Resource Website
10+ mentions
mosdepth (RRID:SCR_018929) data processing software, software application, software resource Software command line tool for rapidly calculating genome wide sequencing coverage. Measures depth from BAM or CRAM files at either each nucleotide position in genome or for sets of genomic regions. Used for fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing quick coverage calculation for genomes and exomes. Calculating genome, wide sequencing coverage, depth measurement, BAM file, CRAM file, nucleotide position, genome, genomic region set, WGS exom, targeted sequencing, coverage calculation, exom, bio.tools is listed by: Debian
is listed by: bio.tools
is listed by: OMICtools
NHGRI R01 HG006693;
NHGRI R01 HG009141;
NIGMS R01 GM124355;
NCI U24 CA209999
PMID:29096012 Free, Available for download, Freely available OMICS_20873, biotools:mosdepth https://bio.tools/mosdepth, https://sources.debian.org/src/mosdepth/ SCR_018929 2026-08-04 09:44:29 38
EHRtemporalVariability
 
Resource Report
Resource Website
1+ mentions
EHRtemporalVariability (RRID:SCR_018663) data processing software, software application, software resource Software R package for delineating temporal dataset shifts in electronic health records. Functions to delineate temporal dataset shifts in electronic health records through projection and visualization of dissimilarities among data temporal batches.Enables exploration and identification of dataset shifts, contributing to broadly examine and repurpose large, longitudinal datasets. Used to help ensure reliable data reuse to biomedical data users. Delineating temporal data set shift, data set shift, electronic health record, temporal variability, delineate temporal data set shift, data dissimilarities, reliable data reuse, examine data set, biomedical data reuse, bio.tools is listed by: Debian
is listed by: bio.tools
is related to: CRAN
is related to: Shiny
DOI:10.1101/2020.04.07.20056564 Free, Available for download, Freely available biotools:ehrtemporalvariability https://cran.r-project.org/web/packages/EHRtemporalVariability/readme/README.html, https://bio.tools/ehrtemporalvariability SCR_018663 Electronic Health Records temporal variability 2026-08-04 09:44:22 3
OmicsOffice for NGS SeqSolve
 
Resource Report
Resource Website
OmicsOffice for NGS SeqSolve (RRID:SCR_001222) OmicsOffice for NGS commercial organization, software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 18,2025. Software for secondary and tertiary analysis of Next Generation Sequencing (NGS) data. next-generation sequencing, rna-seq, chip-seq, transcript, alternative splicing, variant, mirna, non-coding rna expression, genome, differential expression, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:20671709 THIS RESOURCE IS NO LONGER IN SERVICE biotools:seqsolve, OMICS_02111 https://bio.tools/seqsolve SCR_001222 OmicsOffice for NGS (SeqSolve), SeqSolve 2026-08-04 09:40:20 0

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