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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
RNAsnp Resource Report Resource Website 10+ mentions |
RNAsnp (RRID:SCR_010837) | RNAsnp | data analysis service, analysis service resource, production service resource, service resource, software resource | Software / Web Server to predict the effect of SNPs on local RNA secondary structure based on the RNA folding algorithms implemented in the Vienna RNA package. |
is listed by: OMICtools has parent organization: University of Copenhagen; Copenhagen; Denmark |
PMID:23630321 | OMICS_00392 | SCR_010837 | RNAsnp Web Server, RNAsnp Web Server: Predicting SNP effects on local RNA secondary structure | 2026-02-14 02:02:05 | 32 | ||||||||
|
BCmicrO Resource Report Resource Website 1+ mentions |
BCmicrO (RRID:SCR_010838) | BCmicrO | software resource, web application | A Bayesian decision fusion algorithm for microRNA target prediction that combines the prediction of TargetScan, miRanda, PicTar, mirTarget, PITA, and DianamicroT. Users enter a Ref_seq ID for a query target gene and select a miRNA, which BCmicrO will use in its predictive algorithm. The prediction results can then be downloaded. | mirna, microrna, bayesian, decision fusion algorithm, computational target prediction algorithm, web application, |
is listed by: OMICtools has parent organization: University of Texas at San Antonio; Texas; USA |
Public | OMICS_00393 | SCR_010838 | 2026-02-14 02:01:50 | 7 | ||||||||
|
miRExpress Resource Report Resource Website 10+ mentions |
miRExpress (RRID:SCR_010831) | miRExpress | software resource | A stand-alone software package implemented for generating miRNA expression profiles from high-throughput sequencing of RNA without the need for sequenced genomes. |
is listed by: OMICtools has parent organization: National Chiao Tung University; Hsinchu; Taiwan |
OMICS_00379 | SCR_010831 | 2026-02-14 02:02:06 | 49 | ||||||||||
|
HugeSeq Resource Report Resource Website 10+ mentions |
HugeSeq (RRID:SCR_010803) | HugeSeq | software resource | An automated pipeline for detecting genetic variants from High-throUghput GEnome SEQuencing. | is listed by: OMICtools | OMICS_00288 | SCR_010803 | 2026-02-14 02:01:49 | 10 | ||||||||||
|
SIMPLEX Resource Report Resource Website 10+ mentions |
SIMPLEX (RRID:SCR_010807) | SIMPLEX | software resource | Cloud-enabled pipeline for the comprehensive analysis of exome sequencing data. | is listed by: OMICtools | OMICS_00294 | SCR_010807 | 2026-02-14 02:02:05 | 21 | ||||||||||
|
MoDIL Resource Report Resource Website 1+ mentions |
MoDIL (RRID:SCR_010764) | MoDIL | software resource | Software for a novel method for finding medium sized indels from high throughput sequencing datasets. | bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: University of Toronto; Ontario; Canada |
OMICS_00066, biotools:modil | https://bio.tools/modil | SCR_010764 | MoDIL: Detecting INDEL Variation with Clone-end Sequencing | 2026-02-14 02:02:05 | 4 | |||||||
|
MISA Resource Report Resource Website 500+ mentions |
MISA (RRID:SCR_010765) | MISA | software resource | Software tool that allows the identification and localization of perfect microsatellites as well as compound microsatellites which are interrupted by a certain number of bases. | bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian |
OMICS_00110, biotools:misa | https://bio.tools/misa | SCR_010765 | MISA - MIcroSAtellite identification tool | 2026-02-14 02:02:04 | 941 | |||||||
|
T-REKS Resource Report Resource Website 10+ mentions |
T-REKS (RRID:SCR_010768) | T-REKS | software resource | An algorithm for de novo detection and alignment of repeats in sequences based on K-means algorithm. | matlab | is listed by: OMICtools | PMID:19671691 | OMICS_00116 | SCR_010768 | 2026-02-14 02:02:05 | 17 | ||||||||
|
GensearchNGS Resource Report Resource Website 10+ mentions |
GensearchNGS (RRID:SCR_010802) | GensearchNGS | software resource | An integrated software solution for the analysis of DNA-Seq data from commonly used NGS equipments such as Roche/454, Illumina and Ion Torrent. | bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian |
Commercial license | OMICS_00287, biotools:gensearchngs | https://bio.tools/gensearchngs | SCR_010802 | 2026-02-14 02:02:04 | 21 | |||||||
|
AgileVariantMapper Resource Report Resource Website 1+ mentions |
AgileVariantMapper (RRID:SCR_010770) | AgileVariantMapper | software resource | Software that visualises sequence variant data from whole exome data, so that it is possible to identify autozygous regions in consanguineous individuals. | is listed by: OMICtools | PMID:23090942 | OMICS_00122 | SCR_010770 | AgileVariantMapper - Autozygosity mapping using Next generation sequence data | 2026-02-14 02:01:49 | 1 | ||||||||
|
HomSI Resource Report Resource Website 1+ mentions |
HomSI (RRID:SCR_010771) | HomSI | software resource | A software tool that identifies homozygous regions using deep sequence data. | bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools |
PMID:24307702 | Free | OMICS_00124, biotools:homsi | https://bio.tools/homsi | SCR_010771 | Homozygous Stretch Identifier from next-generation sequencing data, HomSI - Homozygous Stretch Identifier from next-generation sequencing data | 2026-02-14 02:02:03 | 4 | |||||
|
CONTRA Resource Report Resource Website 100+ mentions |
CONTRA (RRID:SCR_010814) | CONTRA | software resource | A tool for copy number variation (CNV) detection for targeted resequencing data such as those from whole-exome capture data. | bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: SourceForge |
OMICS_00331, biotools:contra | https://bio.tools/contra | SCR_010814 | 2026-02-14 02:02:06 | 283 | ||||||||
|
ExomeCNV Resource Report Resource Website 50+ mentions |
ExomeCNV (RRID:SCR_010815) | ExomeCNV | software resource | A statistical method to detect CNV and LOH using depth-of-coverage and B-allele frequencies from mapped short sequence reads in exome sequencing data. | is listed by: OMICtools | OMICS_00333 | SCR_010815 | 2026-02-14 02:02:05 | 59 | ||||||||||
|
CNAnorm Resource Report Resource Website 10+ mentions |
CNAnorm (RRID:SCR_010816) | CNAnorm | software resource | A Bioconductor package to estimate Copy Number Aberrations (CNA) in cancer samples. | is listed by: OMICtools | OMICS_00336 | SCR_010816 | 2026-02-14 02:01:50 | 15 | ||||||||||
|
breseq Resource Report Resource Website 100+ mentions |
breseq (RRID:SCR_010810) | breseq | software resource | A computational pipeline for finding mutations relative to a reference sequence in short-read DNA re-sequencing data intended for haploid microbial genomes. | windows, genomics, sequencing, bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools has parent organization: Google Code |
OMICS_00298, biotools:breseq | https://barricklab.org/twiki/bin/view/Lab/ToolsBacterialGenomeResequencing https://bio.tools/breseq |
SCR_010810 | breseq - Determine mutations in evolved microbes from next-generation sequencing data | 2026-02-14 02:02:06 | 424 | |||||||
|
MutPred Resource Report Resource Website 100+ mentions |
MutPred (RRID:SCR_010778) | MutPred | software resource, web application | Web application tool developed to classify an amino acid substitution as disease-associated or neutral in human. | bio.tools |
is used by: HmtVar is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: Indiana University; Indiana; USA |
biotools:mutpred, OMICS_00154 | https://bio.tools/mutpred | SCR_010778 | 2026-02-14 02:02:04 | 409 | ||||||||
|
MutSig Resource Report Resource Website 100+ mentions |
MutSig (RRID:SCR_010779) | MutSig | software resource | Software that analyzes lists of mutations discovered in DNA sequencing, to identify genes that were mutated more often than expected by chance given background mutation processes. | bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools has parent organization: Broad Institute |
PMID:23770567 | OMICS_00155, biotools:MutSig2CV | https://bio.tools/MutSig2CV | SCR_010779 | Mutation Significance | 2026-02-14 02:01:49 | 128 | ||||||
|
SVDetect Resource Report Resource Website 10+ mentions |
SVDetect (RRID:SCR_010812) | SVDetect | software resource | Software application for the isolation and the type prediction of intra- and inter-chromosomal rearrangements from paired-end/mate-pair sequencing data provided by the high-throughput sequencing technologies. This tool aims to identify structural variations with both clustering and sliding-window strategies, and helping in their visualization at the genome scale. It is compatible with SOLiD and Illumina (>=1.3) reads. | structural variation, sequencing, chromosomal rearrangement, high-throughput sequencing, solid, illumina, genome, insertion, deletion, inversion, duplication, translocation, command-line, perl, bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools has parent organization: SourceForge has parent organization: Curie Institute; Paris; France |
PMID:20639544 | GNU General Public License, v3 | OMICS_00324, biotools:svdetect | https://bio.tools/svdetect | SCR_010812 | SVDetect: a tool to detect genomic structural variations from paired-end and mate-pair sequencing data | 2026-02-14 02:01:50 | 23 | |||||
|
nsSNPAnalyzer Resource Report Resource Website 10+ mentions |
nsSNPAnalyzer (RRID:SCR_010780) | nsSNPAnalyzer | data processing software, data analysis service, analysis service resource, data analysis software, production service resource, service resource, software application, software resource | A tool to predict whether a nonsynonymous single nucleotide polymorphism (nsSNP) has a phenotypic effect. | bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian has parent organization: University of Tennessee Health Science Center; Tennessee; USA |
OMICS_00156, biotools:nssnpanalyzer | https://bio.tools/nssnpanalyzer | SCR_010780 | nsSNPAnalyzer: predicting disease-associated nonsynonymous single nucleotide polymorphisms | 2026-02-14 02:02:03 | 46 | |||||||
|
PhD-SNP Resource Report Resource Website 100+ mentions |
PhD-SNP (RRID:SCR_010782) | PhD-SNP | software resource | It is based a SVM-based classifier. | is listed by: OMICtools | PMID:16895930 | OMICS_00158 | SCR_010782 | Predictor of human Deleterious Single Nucleotide Polymorphisms | 2026-02-14 02:02:04 | 293 |
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