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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
flowUtils
 
Resource Report
Resource Website
1+ mentions
flowUtils (RRID:SCR_001879) software resource Software that provides utilities for flow cytometry data. software package, mac os x, unix/linux, windows, r, cell based assay, flow cytometry, decision tree, infrastructure is listed by: OMICtools
has parent organization: Bioconductor
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_05614 SCR_001879 flowUtils - Utilities for flow cytometry 2026-07-25 12:05:12 6
TEMP
 
Resource Report
Resource Website
100+ mentions
TEMP (RRID:SCR_001788) software resource Software package for detecting transposable elements (TEs) insertions and excisions from pooled high-throughput sequencing data. standalone software, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Massachusetts Medical School; Massachusetts; USA
PMID:24753423 Free, Available for download, Freely available OMICS_03821, biotools:temp https://bio.tools/temp SCR_001788 2026-07-25 12:05:13 211
EXTREME
 
Resource Report
Resource Website
10+ mentions
EXTREME (RRID:SCR_001821) software resource A motif discovery algorithm designed to find DNA-binding motifs in ChIP-Seq and DNase-Seq data. java, perl, python is listed by: OMICtools PMID:24532725 Free, Available for download, Freely available OMICS_03428 SCR_001821 2026-07-25 12:05:13 28
GLiMMPS
 
Resource Report
Resource Website
1+ mentions
GLiMMPS (RRID:SCR_001787) GLiMMPS software resource Software to characterize the genetic variation of alternative splicing using a robust statistical method for detecting splicing quantitative trait loci (sQTLs) from RNA-seq data. It takes into account the individual variation in sequencing coverage and the noise prevalent in RNA-seq data. alternative splicing, rna-seq, genetic variation, splicing quantitative trait loci is listed by: OMICtools
has parent organization: University of California at Los Angeles; California; USA
PMID:23876401 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01947 SCR_001787 2026-07-25 12:05:10 2
flowTrans
 
Resource Report
Resource Website
1+ mentions
flowTrans (RRID:SCR_002093) software resource Software for profile maximum likelihood estimation of parameters for flow cytometry data transformations. software package, mac os x, unix/linux, windows, r, flow cytometry is listed by: OMICtools
has parent organization: Bioconductor
PMID:21050468 Free, Available for download, Freely available OMICS_05612 SCR_002093 flowTrans - Parameter Optimization for Flow Cytometry Data Transformation 2026-07-25 12:05:16 4
AffyPipe
 
Resource Report
Resource Website
1+ mentions
AffyPipe (RRID:SCR_002032) software resource An open-source software pipeline for Affymetrix Axiom genotyping workflow. affymetrix, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
Italian Ministry of Education University and Research 505/Ric;
project GenHome ;
European Union FP7 project Gene2Farm 289592
PMID:25028724 Free, Available for download, Freely available biotools:affypipe, OMICS_05203 https://bio.tools/affypipe SCR_002032 AffyPipe: an open-source pipeline for Affymetrix Axiom genotyping workflow 2026-07-25 12:05:15 5
CanSNPer
 
Resource Report
Resource Website
10+ mentions
CanSNPer (RRID:SCR_001980) software resource Software that is a hierarchical genotype classifier of clonal pathogens. python, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:24574113 Free, Available for download, Freely available biotools:cansnper, OMICS_03706 https://bio.tools/cansnper SCR_001980 2026-07-25 12:05:14 18
DMET-Analyzer
 
Resource Report
Resource Website
1+ mentions
DMET-Analyzer (RRID:SCR_002030) DMET-Analyzer software resource Software tool for the automatic association analysis among the variation of the patient genomes and the clinical conditions of patients, i.e. the different response to drugs. The system allows: (i) to automatize the workflow of analysis of DMET (drug metabolism enzymes and transporters)-SNP (Single Nucleotide Polymorphism) data avoiding the use of multiple tools; (ii) the automatic annotation of DMET-SNP data and the search in existing databases of SNPs (e.g. dbSNP), (iii) the association of SNP with pathway through the search in PharmaKGB, a major knowledge base for pharmacogenomic studies. It has a simple graphical user interface that allows users (doctors/biologists) to upload and analyze DMET files produced by Affymetrix DMET-Console in an interactive way. drug, metabolism, enzyme, transporter, affymetrix, variation, genome, clinical, affymetrix dmet, single nucleotide polymorphism, annotation, analysis, pharmacogenomic, pathway is listed by: OMICtools
has parent organization: SourceForge
PMID:23035929 Free, Available for download, Freely available OMICS_01920 SCR_002030 DMETANALYZER, DMETANALYZER - A tool for supporting pharmacogenomics data analysis 2026-07-25 12:05:18 1
Ray
 
Resource Report
Resource Website
1+ mentions
Ray (RRID:SCR_001916) Ray software resource Software that assembles reads obtained with new sequencing technologies (Illumina, 454, SOLiD) using MPI 2.2. mpi, bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: SourceForge
PMID:20958248
DOI:10.1089/cmb.2009.0238
Free, Available for download, Freely available OMICS_00027, biotools:ray https://bio.tools/ray, https://sources.debian.org/src/ray/ SCR_001916 Ray - a de novo assembler using MPI 2.2, Ray - Parallel genome assemblies for parallel DNA sequencing 2026-07-25 12:05:12 1
PyroHMMvar
 
Resource Report
Resource Website
1+ mentions
PyroHMMvar (RRID:SCR_002073) PyroHMMvar software resource A software program to call short indels and SNPs for Ion Torrent and 454 data. is listed by: OMICtools
has parent organization: Google Code
PMID:23995392 Free, Available for download, Freely available OMICS_00069 https://code.google.com/p/pyrohmmvar/ SCR_002073 2026-07-25 12:05:15 1
NIMBL
 
Resource Report
Resource Website
1+ mentions
NIMBL (RRID:SCR_000482) NIMBL software resource MATLAB code to quality control and prioritize differentially methylated markers from illumina infinium arrays. quality control, illumina, infinium array, dna methylation, biomarker, dna methylation array, dna methylome, infinium 450k, biomarker discovery, differential methylation, epigenetics, epigenomics is listed by: OMICtools
has parent organization: University of Nottingham; Nottingham; United Kingdom
PMID:22936948 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02305 SCR_000482 NIMBL: Numerical Identification of Methylation Biomarker Lists, Numerical Identification of Methylation Biomarker Lists 2026-07-25 12:04:47 1
iBMQ
 
Resource Report
Resource Website
iBMQ (RRID:SCR_000481) software resource Software for integrated Bayesian Modeling of eQTL data. It implements a joint hierarchical Bayesian model where all genes and SNPs are modeled concurrently. standalone software, mac os x, unix/linux, windows, r, gene expression, microarray, preprocessing, snp is listed by: OMICtools
has parent organization: Bioconductor
PMID:23958729 Free, Available for download, Freely available OMICS_04601 SCR_000481 iBMQ - integrated Bayesian Modeling of eQTL data 2026-07-25 12:04:46 0
fourSig
 
Resource Report
Resource Website
fourSig (RRID:SCR_000516) software resource A suite of software programs for analyzing and visualizing 4C-seq data. standalone software, perl, r is listed by: OMICtools
has parent organization: SourceForge
PMID:24561615 Free, Available for download, Freely available OMICS_02628 SCR_000516 2026-07-25 12:04:46 0
SAMBLASTER
 
Resource Report
Resource Website
10+ mentions
SAMBLASTER (RRID:SCR_000468) software resource Software tool to mark duplicates and extract discordant and split reads from SAM files. This fast and flexible program for marking duplicates in read-id grouped paired-end SAM files can also optionally output discordant read pairs and/or split read mappings to separate SAM files, and/or unmapped/clipped reads to a separate FASTQ file. When marking duplicates, samblaster will require approximately 20MB of memory per 1M read pairs. standalone software, c++, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of Virginia; Virginia; USA
PMID:24812344
DOI:10.1093/bioinformatics/btu314
Free, Available for download, Freely available biotools:samblaster, OMICS_04682 https://bio.tools/samblaster, https://sources.debian.org/src/samblaster/ SCR_000468 2026-07-25 12:04:46 18
TAPyR
 
Resource Report
Resource Website
1+ mentions
TAPyR (RRID:SCR_000588) software resource An efficient software tool for the local alignment of pyrosequencing reads produced by the GS FLX (454) Genome Analyzer technology against a reference genome sequence. The approach explores the characteristics of the data in re-sequencing applications and uses state of the art BWT-based indexing techniques combined with a flexible seed-based approach, leading to a fast and accurate algorithm which needs very little user parameterization. Although initially developed having this specific technology in mind, this software performs equally well on any other platform that can return its sequencing reads in the FASTA, FASTQ or SFF formats, including Illumina, Ion Torrent and Pacific Biosciences technologies. gs flx, genome analyzer, bwt, fasta, fastq, sff formats, pyrosequencing reads, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
PMID:21672185 THIS RESOURCE IS NO LONGER IN SERVICE biotools:tapyr, OMICS_00693 https://bio.tools/tapyr SCR_000588 Tool for Alignment of Pyrosequencing Reads 2026-07-25 12:04:48 1
TOPPAS
 
Resource Report
Resource Website
1+ mentions
TOPPAS (RRID:SCR_000533) software resource A graphical user interface (GUI) for rapid composition of HPLC-MS analysis workflows. Workflow construction is reduced to drag-and-drop of analysis tools and adding connections in between. gui, graphical user interface, analysis, hplc-ms, workflow is listed by: OMICtools
has parent organization: SourceForge
PMID:22583024 THIS RESOURCE IS NO LONGER IN SERVICE OMICS_02640 http://open-ms.sourceforge.net/workflow-integration/toppasworkflows/ SCR_000533 The OpenMS Proteomics Pipeline Assistant, TOPP Pipeline Assistant 2026-07-25 12:04:47 1
GERP
 
Resource Report
Resource Website
50+ mentions
GERP (RRID:SCR_000563) GERP software resource Software that identifies constrained elements in multiple alignments by quantifying substitution deficits. These deficits represent substitutions that would have occurred if the element were neutral DNA, but did not occur because the element has been under functional constraint. We refer to these deficits as Rejected Substitutions. Rejected substitutions are a natural measure of constraint that reflects the strength of past purifying selection on the element. GERP estimates constraint for each alignment column; elements are identified as excess aggregations of constrained columns. A false-positive rate (which is user-settable) is calculated using "shuffled" alignments in which the order of columns is randomized., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. genomic, evolution, rate profiling is listed by: OMICtools
is listed by: Debian
has parent organization: Stanford University; Stanford; California
PMID:15965027
PMID:21152010
THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00174 https://sources.debian.org/src/gerp++/ SCR_000563 Genomic Evolutionary Rate Profiling, GERP++, Genomic Evolutionary Rate Profiling: GERP, GERP2 2026-07-25 12:04:47 53
MuTect
 
Resource Report
Resource Website
50+ mentions
MuTect (RRID:SCR_000559) MuTect software resource Software for the reliable and accurate identification of somatic point mutations in next generation sequencing data of cancer genomes. next-generation sequencing, somatic mutation, tumor, normal, genome, bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
is listed by: SoftCite
has parent organization: Broad Institute
Cancer PMID:23396013 THIS RESOURCE IS NO LONGER IN SERVICE biotools:mutect, OMICS_00087 https://bio.tools/mutect SCR_000559 Mutect 2026-07-25 12:04:48 91
MetaDrug
 
Resource Report
Resource Website
1+ mentions
MetaDrug (RRID:SCR_000461) MetaDrug commercial organization A leading systems pharmacology solution that incorporates extensive manually curated information on biological effects of small molecule compounds. Predictive and analytical algorithms look at chemical compounds from different angles in one integrated workflow are available for: * Individual previously described compounds to look up their known information and predict currently unknown properties * Individual newly synthesized or isolated compounds to predict their properties from its structures * Compound libraries to extract known and predict new properties of individual compounds and perform their comparison and prioritization pharmacology, compound, pathway, target, metabolite, prediction, toxicity, indication, metabolism, gene, protein, analysis, drug effect is listed by: OMICtools THIS RESOURCE IS NO LONGER IN SERVICE OMICS_01584 SCR_000461 2026-07-25 12:04:46 1
Reprever
 
Resource Report
Resource Website
Reprever (RRID:SCR_000463) Reprever software resource Software that identifies (a) the insertion breakpoints where the extra duplicons inserted into the donor genome and (b) the actual sequence of the duplicon for any genomic regions that are increased in copy number. genomics, genomic region, insertion breakpoint, insertion, breakpoint, duplicon, genome is listed by: OMICtools
has parent organization: SourceForge
has parent organization: University of California at San Diego; California; USA
PMID:23658221 Free, Available for download, Freely available OMICS_01561 SCR_000463 Reprever: resolving low-copy duplicated sequences using template drive 2026-07-25 12:04:45 0

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