Searching the RRID Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Preparing word cloud

×

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.

Search

Type in a keyword to search

Filter by records added date
See new records

Options


Current Facets and Filters

  • Related Resources:debian (facet)

Facets


Recent searches

Snippet view Table view
Click the to add this resource to a Collection

2,279 Results - per page

Show More Columns | Download Top 1000 Results

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
genomicalignments
 
Resource Report
Resource Website
100+ mentions
genomicalignments (RRID:SCR_024236) software resource, software toolkit Software R package provides efficient containers for storing and manipulating short genomic alignments. This includes read counting, computing the coverage, junction detection, and working with the nucleotide content of the alignments. containers for storing and manipulating short genomic alignments, read counting, computing coverage, junction detection, working with nucleotide content of alignments. is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-bioc-genomicalignments/ SCR_024236 2026-09-19 12:56:20 147
BiocGenerics
 
Resource Report
Resource Website
10+ mentions
BiocGenerics (RRID:SCR_024226) software resource, software toolkit Software R package defines many S4 generic functions used in Bioconductor. S4 generic functions used in Bioconductor, S4 generic functions, Bioconductor, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-bioc-biocgenerics/ SCR_024226 2026-09-19 12:56:20 27
biomformat
 
Resource Report
Resource Website
biomformat (RRID:SCR_024228) software resource, software toolkit Software R package for interfacing with BIOM format. This package includes basic tools for reading biom-format files, accessing and subsetting data tables from a biom object, limited support for writing biom-object back to biom-format file. interfacing with BIOM format, reading biom-format files, accessing and subsetting data tables from biom object, writing biom-object back to biom-format file, is listed by: Debian
is related to: python-biom-format
Free, Available for download, Freely available, https://sources.debian.org/src/r-bioc-biomformat/ SCR_024228 2026-09-19 12:56:20 0
biovizBase
 
Resource Report
Resource Website
biovizBase (RRID:SCR_024229) software resource, software toolkit Software R package to provide set of utilities, color schemes and conventions for genomic data. Used for various high-level packages for biological data visualization. utilities, color schemes and conventions for genomic data, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-bioc-biovizbase/ SCR_024229 2026-09-19 12:56:20 0
go.db
 
Resource Report
Resource Website
10+ mentions
go.db (RRID:SCR_024241) software resource, software toolkit Software R package provides set of annotation maps describing entire Gene Ontology assembled using data from GO. set of annotation maps, Gene Ontology, data from GO, is listed by: Debian Free, Available for download, Freely available, OMICS_22608 https://sources.debian.org/src/r-bioc-go.db/ SCR_024241 2026-09-19 12:56:20 44
impute
 
Resource Report
Resource Website
1+ mentions
impute (RRID:SCR_024243) software resource, software toolkit Software R package for imputation for microarray data. imputation for microarray data, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-bioc-impute/ SCR_024243 2026-09-19 12:56:20 5
mergeomics
 
Resource Report
Resource Website
1+ mentions
mergeomics (RRID:SCR_024244) software resource, software toolkit Software R pacakage for multidimensional data integration to identify pathogenic perturbations to biological systems. Used for integrating multidimensional omics disease associations, functional genomics, canonical pathways and gene-gene interaction networks to generate mechanistic hypotheses. Includes Marker set enrichment analysis and Weighted Key Driver Analysis parts. integrating multidimensional omics disease associations, integrating functional genomics, integrating canonical pathways and gene-gene interaction networks, multidimensional data integration, identify pathogenic perturbations to biological systems, is listed by: Debian PMID:27814671 Free, Available for download, Freely available, OMICS_12862 https://sources.debian.org/src/r-bioc-mergeomics/ SCR_024244 2026-09-19 12:56:20 2
metagenomeseq
 
Resource Report
Resource Website
100+ mentions
metagenomeseq (RRID:SCR_024246) software resource, software toolkit Software R package to determine features that are differentially abundant between two or more groups of multiple samples. Used to address the effects of both normalization and under-sampling of microbial communities on disease association detection and testing of feature correlations. determine features that are differentially abundant, two or more groups of multiple samples, disease association detection, testing of feature correlations, is listed by: Debian OMICS_07813 https://sources.debian.org/src/r-bioc-metagenomeseq/ SCR_024246 2026-09-19 12:56:21 243
gviz
 
Resource Report
Resource Website
10+ mentions
gviz (RRID:SCR_024239) software resource, software toolkit Software R package to perform live annotation queries to Ensembl and UCSC and translates this to e.g. gene/transcript structures in viewports of the grid graphics package. genomic data analyses, perform live annotation queries, is listed by: Debian Free, Available for download, Freely available, OMICS_17191 https://sources.debian.org/src/r-bioc-gviz/ SCR_024239 2026-09-19 12:56:20 46
psychometric
 
Resource Report
Resource Website
1+ mentions
psychometric (RRID:SCR_024295) software resource, software toolkit Software R package for measurement theory, meta-analysis, reliability, item analysis, inter-rater reliability, classical utility, and correlation psychometric theory, measurement theory, meta-analysis, reliability, item analysis, inter-rater reliability, classical utility, correlation is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-cran-psychometric/ SCR_024295 Applied Psychometric Theory 2026-09-19 12:56:22 1
rniftilib
 
Resource Report
Resource Website
rniftilib (RRID:SCR_024296) software resource, software toolkit Software R package provides R-interface to the NIfTI reference implementation the niftilib C-library. R-interface, NIfTI reference implementation, niftilib C-library, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-cran-rniftilib/ SCR_024296 2026-09-19 12:56:22 0
rSNP Guide
 
Resource Report
Resource Website
1+ mentions
rSNP Guide (RRID:SCR_000087) data or information resource, database A system of databases which stores information on the influence of mutations in regulatory gene regions . This tool helps recognize protein binding sites that are being altered by mutation. It has four cross-linked sub databases that focus on specific aspects including: (1) the effect of single nucleotide mutations in regulatory gene regions and their interaction with nuclear proteins; (2) references to original publications on the subject; (3) the experimental details of these publications; and (4) the protocols of these experiments. This resource is aimed at providing information to further research on the influence of specific sequence alterations on disease susceptibility, drug resistance and healthcare. database, single nucleotide mutations, RNA, DNA, nuclear proteins, protein binding sites, drug resistance, disease susceptibility, health care, regulatory gene regions, bio.tools is listed by: bio.tools
is listed by: Debian
has parent organization: Siberian Branch of the Russian Academy of Sciences; Novosibirsk; Russia
Open Source nif-0000-03428, biotools:rsnp_guide https://bio.tools/rsnp_guide SCR_000087 rSNP Guide 2026-09-19 12:56:25 1
rook
 
Resource Report
Resource Website
rook (RRID:SCR_024298) software resource, software toolkit Web server for R with documented API to interface between R and the server. The documentation contains the Rook specification and details for building and running Rook applications. web server for R, building and running Rook applications, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-cran-rook/ SCR_024298 2026-09-19 12:56:22 0
robustrankaggreg
 
Resource Report
Resource Website
1+ mentions
robustrankaggreg (RRID:SCR_024299) RRA software resource, software toolkit Software R package for aggregating ranked lists, especially lists of genes. RRA method uses a probabilistic model for aggregation that is robust to noise and also facilitates the calculation of significance probabilities for all the elements in the final ranking. aggregating ranked lists, lists of genes aggregation, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-cran-robustrankaggreg/ SCR_024299 Robust Rank Aggregation 2026-09-19 12:56:22 4
rncl
 
Resource Report
Resource Website
rncl (RRID:SCR_024290) software resource, software toolkit Software R package provides interface to Nexus Class Library which allows parsing of NEXUS, Newick and other phylogenetic tree file formats. Provides elements of file that can be used to build phylogenetic objects such as ape's 'phylo' or phylobase's 'phylo4(d)'. interface to Nexus Class Library, parsing of NEXUS, parsing of Newick, parsing phylogenetic tree file formats, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-cran-rncl/ SCR_024290 2026-09-19 12:56:22 0
hms
 
Resource Report
Resource Website
hms (RRID:SCR_024294) software resource, software toolkit Software R package implements S3 class for storing and formatting time-of-day values, based on the 'difftime' class. storing and formatting time-of-day values, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/r-cran-hms/ SCR_024294 2026-09-19 12:56:22 0
sambamba
 
Resource Report
Resource Website
50+ mentions
sambamba (RRID:SCR_024328) software resource, software toolkit Software tools for working with SAM/BAM data working with SAM/BAM data, is listed by: Debian PMID:25697820 Free, Available for download, Freely available, OMICS_07586 https://sources.debian.org/src/sambamba/ SCR_024328 2026-09-19 12:56:23 59
seq-seq-pan
 
Resource Report
Resource Website
seq-seq-pan (RRID:SCR_024343) software resource, software toolkit Software workflow for SEQuential alignment of SEQuences to build PAN-genome data structure and whole-genome-alignment. SEQuential alignment, SEQuences, build PAN-genome data structure, is listed by: Debian PMID:29334898 Free, Available for download, Freely available, https://sources.debian.org/src/seq-seq-pan/ SCR_024343 2026-09-19 12:56:23 0
readseq
 
Resource Report
Resource Website
1+ mentions
readseq (RRID:SCR_024313) software resource, software toolkit Software package as Java based common sequence file format reader and sequence file manipulation. Java, common sequence file format reader, sequence file manipulation, is listed by: Debian Free, Available for download, Freely available, https://sources.debian.org/src/rdp-readseq/ SCR_024313 2026-09-19 12:56:23 6
rsvd
 
Resource Report
Resource Website
rsvd (RRID:SCR_024303) software resource, software toolkit Software R package used to compute near optimal low-rank singular value decomposition of massive data sets with high accuracy. Provides several randomized matrix algorithms such as randomized singular value decomposition (rsvd), randomized principal component analysis (rpca), randomized robust principal component analysis (rrpca), randomized interpolative decomposition (rid), and the randomized CUR decomposition (rcur). In addition several plot functions are provided. randomized singular value decomposition, singular value decomposition, compute optimal low-rank singular value decomposition, massive data sets, is listed by: Debian DOI:10.18637/jss.v089.i11 Free, Available for download, Freely available, https://sources.debian.org/src/r-cran-rsvd/ SCR_024303 randomized singular value decomposition 2026-09-19 12:56:22 0

Can't find your Tool?

We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.

Can't find the RRID you're searching for? X
X
  1. Neuroscience Information Framework Resources

    Welcome to the NIF Resources search. From here you can search through a compilation of resources used by NIF and see how data is organized within our community.

  2. Navigation

    You are currently on the Community Resources tab looking through categories and sources that NIF has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.

  3. Logging in and Registering

    If you have an account on NIF then you can log in from here to get additional features in NIF such as Collections, Saved Searches, and managing Resources.

  4. Searching

    Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:

    1. Use quotes around phrases you want to match exactly
    2. You can manually AND and OR terms to change how we search between words
    3. You can add "-" to terms to make sure no results return with that term in them (ex. Cerebellum -CA1)
    4. You can add "+" to terms to require they be in the data
    5. Using autocomplete specifies which branch of our semantics you with to search and can help refine your search
  5. Collections

    If you are logged into NIF you can add data records to your collections to create custom spreadsheets across multiple sources of data.

  6. Facets

    Here are the facets that you can filter the data by.

  7. Further Questions

    If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.