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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
QSRA
 
Resource Report
Resource Website
1+ mentions
QSRA (RRID:SCR_010733) QSRA software resource A quality-value guided de novo short read assembler. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
OMICS_00026, biotools:qsra https://bio.tools/qsra SCR_010733 2026-08-08 11:59:35 1
rSW-seq
 
Resource Report
Resource Website
1+ mentions
rSW-seq (RRID:SCR_010825) rSW-seq software resource Designed to identify CNVs between two genomes. is listed by: OMICtools PMID:20718989 OMICS_00351 SCR_010825 2026-08-08 11:59:37 4
SegSeq
 
Resource Report
Resource Website
10+ mentions
SegSeq (RRID:SCR_010826) SegSeq software resource An algorithm to identify chromosomal breakpoints using massively parallel next generation sequence data. is listed by: OMICtools
has parent organization: Broad Institute
OMICS_00352 SCR_010826 2026-08-08 11:59:37 20
miRDeep
 
Resource Report
Resource Website
100+ mentions
miRDeep (RRID:SCR_010829) miRDeep2 sequence analysis software, software resource, software application, data analysis software, data processing software Software tool to identify known and novel miRNA genes in seven animal clades by analyzing sequenced RNAs. Used for discovering known and novel miRNAs from small RNA sequencing data. miRNA, gene, animal, clade, analysis, sequence, RNA, data is listed by: OMICtools Helmholtz-Alliance on Systems Biology ;
Helmholtz Association ;
German Ministry of Education and Research ;
Senate of Berlin ;
China Scholarship Council ;
Max Delbrück Centrum Systems Biology Network
PMID:18392026
PMID:21911355
Free, Available for download, Freely available OMICS_00373 https://github.com/rajewsky-lab/mirdeep2 SCR_010829 2026-08-08 11:59:37 182
SAPRED
 
Resource Report
Resource Website
1+ mentions
SAPRED (RRID:SCR_010785) SAPRED software resource Offers the researchers an automatic pipeline to predict the disease-association of SAPs. is listed by: OMICtools
has parent organization: Peking University; Beijing; China
PMID:17384424 OMICS_00161 SCR_010785 SAP Disease-Association Predictor 2026-08-08 11:59:36 4
SNAP - Effects of Single Amino Acid Substitutions on Protein Function
 
Resource Report
Resource Website
10+ mentions
SNAP - Effects of Single Amino Acid Substitutions on Protein Function (RRID:SCR_010786) SNAP production service resource, software resource, data analysis service, analysis service resource, service resource A method for evaluating effects of single amino acid substitutions on protein function. is listed by: OMICtools
has parent organization: Columbia University; New York; USA
PMID:17526529 Acknowledgement requested OMICS_00162 SCR_010786 2026-08-08 11:59:24 38
TransFIC
 
Resource Report
Resource Website
10+ mentions
TransFIC (RRID:SCR_010788) TransFIC production service resource, software resource, data analysis service, software application, analysis service resource, data analysis software, service resource, data processing software A method to transform Functional Impact scores taking into account the differences in basal tolerance to germline SNVs of genes that belong to different functional classes. is listed by: OMICtools
has parent organization: Pompeu Fabra University; Barcelona; Spain
Cancer OMICS_00164 SCR_010788 TRANSformed Functional Impact for Cancer 2026-08-08 11:59:36 14
JointSLM
 
Resource Report
Resource Website
1+ mentions
JointSLM (RRID:SCR_010823) JointSLM software resource Copy number estimation from read depth information. is listed by: OMICtools OMICS_00346 SCR_010823 2026-08-08 11:59:37 2
EMINIM
 
Resource Report
Resource Website
1+ mentions
EMINIM (RRID:SCR_010790) EMINIM software resource A software tool for imputation of unobserved genotypes using a set of reference haplotype panel at a higher-density SNP set such as HapMap, and lower-density genotypes of a target individual using such as genotyping arrays. is listed by: OMICtools
has parent organization: University of California at Los Angeles; California; USA
OMICS_00196 SCR_010790 Expectation-Maximized INtegreative Imputation, Expectation-Maximized INtegreative IMputation (EMINIM) 2026-08-08 11:59:24 1
HARSH
 
Resource Report
Resource Website
10+ mentions
HARSH (RRID:SCR_010792) HARSH software resource Software that provides a method to infer the haplotype using haplotype reference panel and high throughput sequencing data. bio.tools is listed by: OMICtools
is listed by: bio.tools
is listed by: Debian
has parent organization: University of California at Los Angeles; California; USA
OMICS_00199, biotools:harsh https://bio.tools/harsh SCR_010792 HAplotype inference using Reference and Sequencing tecHnology 2026-08-08 11:59:36 15
HapFABIA
 
Resource Report
Resource Website
1+ mentions
HapFABIA (RRID:SCR_010793) HapFABIA software resource Software that identifies short identity by descent (IBD) segments that are tagged by rare variants in large sequencing data. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
has parent organization: Johannes Kepler University of Linz; Linz; Austria
PMID:24174545 biotools:hapfabia, OMICS_00203 https://bio.tools/hapfabia SCR_010793 HapFABIA: Identification of very short segments of identity by descent characterized by rare variants in large sequencing data 2026-08-08 11:59:24 3
C-mii
 
Resource Report
Resource Website
1+ mentions
C-mii (RRID:SCR_010839) C-mii software resource A software tool for plant miRNA and target identification. C-mii pipelines are based on combined steps and criteria from previous studies and also incorporated with several tools such as standalone BLAST and UNAFold and pre-installed databases including miRBase, UniProt, and Rfam. C-mii provides following distinguished features. First, it comes with graphical user interfaces of well-defined pipelines for both miRNA and target identifications with reliable results. Second, it provides a set of filters allowing users to reduce the number of results corresponding to the recently proposed constraints in plant miRNA and target biogenesis. Third, it extends the standard computational steps of miRNA target identification with miRNA-target folding module and GO annotation. Fourth, it supplies the bird eye views of the identification results with info-graphics and grouping information. Fifth, it provides helper functions for database update and auto-recovery to ease system usage and maintenance. Finally, it supports the multi-project and multi-thread management to improve the computational speed. ubuntu linux, windows is listed by: OMICtools PMID:23281648 GNU General Public License OMICS_00394 SCR_010839 C-mii: A software for Computational miRNA identificaion, C-mii (A software for Computational miRNA identificaion) 2026-08-08 11:59:38 4
Pedimap
 
Resource Report
Resource Website
10+ mentions
Pedimap (RRID:SCR_010796) Pedimap software resource A software tool for visualizing phenotypic and genotypic data for related individuals linked in pedigrees. bio.tools is listed by: OMICtools
is listed by: Debian
is listed by: bio.tools
PMID:23087384 OMICS_00214, biotools:pedimap https://bio.tools/pedimap SCR_010796 2026-08-08 11:59:36 11
Phylogeny Programs
 
Resource Report
Resource Website
10+ mentions
Phylogeny Programs (RRID:SCR_010797) Phylogeny Programs data or information resource, production service resource, software resource, data analysis service, topical portal, analysis service resource, service resource, portal 392 phylogeny software packages and 54 free web servers describing all known software for inferring phylogenies (evolutionary trees). Submissions are welcome. Programs are listed by methods available, by computer systems on which they work, cross-referenced by method and by computer system, by ones which analyze particular kinds of data, to show the most recent listings, or to show ones most recently changed. phylogeny is listed by: OMICtools
has parent organization: University of Washington; Seattle; USA
NSF Free, The community can contribute to this resource OMICS_00219 SCR_010797 Felsenstein''s website 2026-08-08 11:59:24 13
NHLBI Grand Opportunity Exome Sequencing Project
 
Resource Report
Resource Website
10+ mentions
NHLBI Grand Opportunity Exome Sequencing Project (RRID:SCR_010798) NHLBI GO ESP, GO ESP knowledge environment Project focused on understanding the contribution of rare genetic variation to heart, lung and blood disorders through the sequencing of well-phenotyped populations. next-generation sequencing, protein coding region, human, genome, phenotype, exome sequencing is listed by: OMICtools
has parent organization: University of Washington; Seattle; USA
NHLBI RC2 HL-103010;
NHLBI RC2 HL-102923;
NHLBI RC2 HL-102924;
NHLBI RC2 HL-102925;
NHLBI RC2 HL-102926
OMICS_00277 SCR_010798 NHLBI Grand Opportunity Exome Sequencing Project (ESP), NHLBI GO Exome Sequencing Project (ESP) 2026-08-08 11:59:36 35
miRspring
 
Resource Report
Resource Website
1+ mentions
miRspring (RRID:SCR_010832) miRspring software resource Pipeline scripts for creating a miRspring (miRNA sequence profiling) document, a new way of sharing and analysing sequencing data for small RNA. is listed by: OMICtools
has parent organization: Victor Chang Cardiac Research Institute; New South Wales; Australia
OMICS_00382 SCR_010832 miRNA sequence profiling (miRspring) document, miRspring document, miRNA sequence profiling 2026-08-08 11:59:37 1
ShortStack
 
Resource Report
Resource Website
100+ mentions
ShortStack (RRID:SCR_010834) software resource A software tool developed to process and analyze small RNA-seq data with respect to a reference genome, and output a comprehensive and informative annotation of all discovered small RNA genes. ShortStack discovers small RNA ''clusters'' de novo, based on user-set thresholds, and annotates clusters with respect to small RNA size, orientation, and repetitiveness. ShortStack also discovers and annotates MIRNA genes, and other Hairpin-associated small RNA genes. In addition, ShortStack includes a robust method to detect genes producing small RNAs in a phased manner. It outputs a descriptive table of all results, useful genome browser tracks, a table describing the results of the hairpin / MIRNA analysis for each cluster, and detailed text-based alignments of all MIRNAs and hairpin-associated clusters. It can also be run in ''count'' mode, to quantify a set of input loci with genomic coordinates determined a priori by the user. ShortStack is a perl program. Besides perl, ShortStack also requires samtools and the RNALfold and RNAeval programs from the Vienna RNA Package to execute. When used to control the alignment of small RNA data to a reference genome, ShortStack also requires bowtie and bowtie-build. Finally, for optimal results, ShortStack uses a file of inverted repeats produced by the EMBOSS application einverted. is listed by: OMICtools
has parent organization: Pennsylvania State University
PMID:24139974
PMID:23610128
Acknowledgement requested OMICS_00384 http://axtell-lab-psu.weebly.com/shortstack.html SCR_010834 ShortStack : Comprehensive annotation and quantification of small RNA genes 2026-08-08 11:59:37 235
reseqtools
 
Resource Report
Resource Website
10+ mentions
reseqtools (RRID:SCR_010806) reseqtools software resource A Toolkit for analyzing next-generation DNA Re-Sequencing data. java, unix/linux is listed by: OMICtools
has parent organization: Google Code
GNU General Public License, v2 OMICS_00293 SCR_010806 2026-08-08 11:59:24 18
TREAT
 
Resource Report
Resource Website
10+ mentions
TREAT (RRID:SCR_010808) TREAT software resource THIS RESOURCE IS NO LONGER IN SERVICE. Documented on May 18,2023. Targeted RE-sequencing Annotation Tool that offers a comprehensive, open framework, end-to-end solution for analyzing and interpreting targeted re-sequencing data., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. is listed by: OMICtools THIS RESOURCE IS NO LONGER IN SERVICE OMICS_00295 SCR_010808 2026-08-08 11:59:36 49
GAMES
 
Resource Report
Resource Website
100+ mentions
GAMES (RRID:SCR_010762) GAMES software resource Software that identifies and annotates mutations in next-generation sequencing projects. is listed by: OMICtools OMICS_00060 SCR_010762 2026-08-08 11:59:35 119

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