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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
DRUT Resource Report Resource Website |
DRUT (RRID:SCR_004351) | DRUT | software resource | Software for Discovery and Reconstruction of Unannotated Transcripts in Partially Annotated Genomes from High-Throughput RNA-Seq Data. | c++, reconstruction, frequency estimation, transcript, rna-seq, annotation |
is listed by: OMICtools has parent organization: Georgia State University; Georgia; USA |
NSF IIS-0546457; NSF IIS-0916401; NSF IIS-0916948 |
PMID:23202426 | OMICS_01273 | SCR_004351 | Discovery and Reconstruction of Unannotated Transcripts | 2025-02-14 10:30:56 | 0 | ||||||
|
ACT: Artemis Comparison Tool Resource Report Resource Website 10+ mentions |
ACT: Artemis Comparison Tool (RRID:SCR_004507) | ACT | software resource | A free tool for displaying pairwise comparisons between two or more DNA sequences. It can be used to identify and analyze regions of similarity and difference between genomes and to explore conservation of synteny, in the context of the entire sequences and their annotation. It is based on the software for Artemis, the genome viewer and annotation tool. ACT runs on UNIX, GNU/Linux, Macintosh and MS Windows systems. It can read complete EMBL and GENBANK entries or sequences in FASTA or raw format. Other sequence features can be in EMBL, GENBANK or GFF format. | dna sequence, genome, synteny, pairwise comparison |
is listed by: OMICtools has parent organization: Wellcome Trust Sanger Institute; Hinxton; United Kingdom |
Wellcome Trust | PMID:15976072 | GNU General Public License | OMICS_00928, nlx_48986 | SCR_004507 | Artemis Comparison Tool | 2025-02-14 10:30:23 | 15 | |||||
|
Squeezambler Resource Report Resource Website |
Squeezambler (RRID:SCR_004385) | Squeezambler | software resource | Software to sequence and de novo assemble all distinct genomes present in a microbial sample with a sequencing cost and computational complexity proportional to the number of genome types, rather than the number of cells. |
is listed by: OMICtools has parent organization: Wayne State University; Michigan; USA |
PMID:23918251 | OMICS_01503 | SCR_004385 | 2025-02-14 10:30:15 | 0 | |||||||||
|
SNiPer-HD Resource Report Resource Website 1+ mentions |
SNiPer-HD (RRID:SCR_004383) | SNiPer-HD | software resource | Improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays. | is listed by: OMICtools | PMID:17062589 | OMICS_00735 | SCR_004383 | SNiPer-HD: Improved genotype calling accuracy | 2025-02-14 10:30:21 | 2 | ||||||||
|
Vanator Resource Report Resource Website 1+ mentions |
Vanator (RRID:SCR_004370) | Vanator | software resource | A Perl pipeline utilising a large variety of common alignment, assembly and analysis tools to assess the metagenomic profiles of Illumina deep sequencing samples. The emphasis is on the discovery of novel viruses in clinical and environmental samples. | perl, metagenomic, illumina, alignment, assembly, analysis, profile, virus, clinical, environment, next-generation sequencing, taxonomy, read |
is listed by: OMICtools has parent organization: SourceForge has parent organization: University of Glasgow; Glasgow; United Kingdom |
PMID:23296970 | OMICS_01505 | SCR_004370 | Vanator-CVR, Vanator-CVR - A metagenomics & virus discovery pipeline, Virus Alignment de Novo Assembly and Taxonomy On Reads, Vanator-CVR: A metagenomics and virus discovery pipeline | 2025-02-14 10:30:56 | 2 | |||||||
|
Basic OligoNucleotide Design Resource Report Resource Website 10+ mentions |
Basic OligoNucleotide Design (RRID:SCR_004492) | BOND | software resource | Software program to compute highly specific DNA oligonucleotides, for all the genes that admit unique probes, while running orders of magnitude faster than the existing programs. | dna, oligonucleotide, design, oligonucleotide design |
is listed by: OMICtools has parent organization: Western University; Ontario; Canada |
PMID:23444904 | OMICS_00827 | SCR_004492 | BOND: Basic OligoNucleotide Design | 2025-02-14 10:30:23 | 15 | |||||||
|
RJaCGH Resource Report Resource Website 1+ mentions |
RJaCGH (RRID:SCR_008381) | RJaCGH | software resource | Software for Bayesian analysis of CGH microarrays fitting Hidden Markov Chain models. | is listed by: OMICtools | GNU General Public License, v3 | OMICS_00731 | SCR_008381 | RJaCGH: Reversible Jump MCMC for the analysis of CGH arrays | 2025-02-14 10:31:15 | 1 | ||||||||
|
OnlineCall Resource Report Resource Website |
OnlineCall (RRID:SCR_008263) | OnlineCall | software resource | A fast basecalling scheme for Illumina''s Next Generation sequencing machines, specifically designed for GAII. | is listed by: OMICtools | OMICS_01153 | SCR_008263 | 2025-02-14 10:31:13 | 0 | ||||||||||
|
IsaCGH Resource Report Resource Website |
IsaCGH (RRID:SCR_008375) | IsaCGH | software resource | Software to analyze CNV that will now normalize arrays CGH and it will visually integrate different genome annotations. | microarray, array cgh, bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian |
OMICS_00727, biotools:isacgh | https://bio.tools/isacgh | SCR_008375 | 2025-02-14 10:31:44 | 0 | ||||||||
|
SeqPig Resource Report Resource Website 1+ mentions |
SeqPig (RRID:SCR_008548) | SeqPig | software resource | A software library for Apache Pig for the distributed analysis of large sequencing datasets on Hadoop clusters. | mapreduce/hadoop |
is listed by: OMICtools has parent organization: SourceForge |
PMID:24149054 | OMICS_01226 | SCR_008548 | 2025-02-14 10:31:26 | 2 | ||||||||
|
CAT Resource Report Resource Website 10+ mentions |
CAT (RRID:SCR_008421) | CAT | software resource | A repository of tools for analysis and annotation of CAZYmes (Carbohydrate Active enZYmes). | bio.tools |
is listed by: OMICtools is listed by: bio.tools is listed by: Debian |
OMICS_01676, biotools:CAt | https://bio.tools/CAT | SCR_008421 | 2025-02-14 10:31:44 | 13 | ||||||||
|
Ultrasome Resource Report Resource Website |
Ultrasome (RRID:SCR_008465) | Ultrasome | software resource | An efficient methodology for detecting and delineating gains and losses of chromosomal material in DNA copy-number data. |
is listed by: OMICtools has parent organization: Broad Institute |
PMID:19228802 | Acknowledgement requested, Free for academic use | OMICS_00737 | SCR_008465 | 2025-02-14 10:31:16 | 0 | ||||||||
|
OligoPicker Resource Report Resource Website 1+ mentions |
OligoPicker (RRID:SCR_008720) | OligoPicker | software resource | Software to help selecting up to five oligo probes for each of the DNA sequences you provided for microarray spotting. | is listed by: OMICtools | PMID:12724288 | GNU General Public License, Acknowledgement requested | OMICS_00830 | SCR_008720 | 2025-02-14 10:31:28 | 2 | ||||||||
|
Biodoop Resource Report Resource Website |
Biodoop (RRID:SCR_008711) | Biodoop | software resource | A suite of parallel bioinformatics applications based upon a popular open-source Java implementation of MapReduce, Hadoop. | mapreduce/hadoop | is listed by: OMICtools | OMICS_01224 | SCR_008711 | 2025-02-14 10:31:28 | 0 | |||||||||
|
DrGaP Resource Report Resource Website 10+ mentions |
DrGaP (RRID:SCR_008670) | DrGaP | software resource | Designed to identify Driver Genes and Pathways in cancer genome sequencing studies. | is listed by: OMICtools | Cancer | OMICS_00149 | SCR_008670 | 2025-02-14 10:31:47 | 10 | |||||||||
|
InVEx Resource Report Resource Website 1+ mentions |
InVEx (RRID:SCR_008734) | InVEx | software resource | A permutation-based method (written in Python) for ascertaining genes with a somatic mutation distribution showing evidence of positive selection for non-silent mutations. |
is listed by: OMICtools has parent organization: Broad Institute |
OMICS_00151 | SCR_008734 | Introns Vs Exons | 2025-02-14 10:31:47 | 4 | |||||||||
|
IsoformEx Resource Report Resource Website 1+ mentions |
IsoformEx (RRID:SCR_005235) | software resource | Software that estimates transcript expression levels and gene expression levels from mRNA-Seq data. Technically speaking, IsoformEx parses bowtie alignment files in a project directory (e.g. ~yourid/isoformex/xxx, where xxx is the project name) and generates two files: (1) xxx/xxx_transcript_1.txt: expression levels of all transcripts, (2) xxx/xxx_gene_1.txt: expression levels of all genes. |
is listed by: OMICtools has parent organization: University of Pennsylvania; Philadelphia; USA |
Free for academic use, Commercial use with permission | OMICS_01260 | SCR_005235 | IsoformEx: Isoform level gene expression estimation using non-negative least squares from mRNA-Seq data | 2025-02-14 10:31:22 | 2 | |||||||||
|
aldex Resource Report Resource Website 10+ mentions |
aldex (RRID:SCR_005110) | aldex | software resource | RNA-seq tool that uses the Dirichlet distribution and a transformation to identify genes that exhibit small within-condition and large between-condition variance. | transcriptome, meta-transcriptome |
is listed by: OMICtools is related to: ALDEx2 |
GNU General Public License, v3 | OMICS_01297 | SCR_005110 | aldex: ANOVA-like RNA-seq analysis | 2025-02-14 10:30:32 | 10 | |||||||
|
ABSOLUTE Resource Report Resource Website 100+ mentions |
ABSOLUTE (RRID:SCR_005198) | ABSOLUTE | software resource | Software to estimate purity / ploidy, and from that compute absolute copy-number and mutation multiplicities. When DNA is extracted from an admixed population of cancer and normal cells, the information on absolute copy number per cancer cell is lost in the mixing. The purpose of ABSOLUTE is to re-extract these data from the mixed DNA population. This process begins by generation of segmented copy number data, which is input to the ABSOLUTE algorithm together with pre-computed models of recurrent cancer karyotypes and, optionally, allelic fraction values for somatic point mutations. The output of ABSOLUTE then provides re-extracted information on the absolute cellular copy number of local DNA segments and, for point mutations, the number of mutated alleles. |
is listed by: OMICtools has parent organization: Broad Institute |
Cancer, Normal | PMID:22544022 | Account required | OMICS_00217 | SCR_005198 | 2025-02-14 10:30:34 | 231 | |||||||
|
qSNP Resource Report Resource Website 10+ mentions |
qSNP (RRID:SCR_005105) | qSNP | software resource | A single nucleotide variant caller optimised for identifying somatic variants in low cellularity cancer samples. |
is listed by: OMICtools has parent organization: University of Queensland; Brisbane; Australia |
Cancer | PMID:24250782 | OMICS_00089 | SCR_005105 | 2025-02-14 10:30:25 | 22 |
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