Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
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.
https://cran.r-project.org/web/packages/bio3d/index.html
Softwar R package for comparative analysis of protein structures. Used to process, organize and explore protein structure, sequence and dynamics data. Used to read and write structure, sequence and dynamic trajectory data, perform sequence and structure database searches, data summaries, atom selection, alignment, superposition, rigid core identification, clustering, torsion analysis, distance matrix analysis, structure and sequence conservation analysis, normal mode analysis, principal component analysis of heterogeneous structure data, and correlation network analysis from normal mode and molecular dynamics data. Enables statistical and graphical power of R environment to work with biological sequence and structural data.
Proper citation: bio3d (RRID:SCR_024266) Copy
https://www.rostlab.org/owiki/index.php/Norsnet
Software as neural network based method that focuses on identification of unstructured loops. Trained to distinguish between very long contiguous segments with non-regular secondary structure and well-folded proteins. Trained on predicted information rather than on experimental data.
Proper citation: NORSnet (RRID:SCR_024146) Copy
Open source software framework that includes the necessary building blocks for surgical simulations, such as native device support, haptic feedback, graphics, discrete collision detection and physics simulation. Developers can refactor the physics engine, swap models, ODE solvers, or linear system solvers.
Proper citation: OpenSurgSim (RRID:SCR_024147) Copy
https://cran.r-project.org/web/packages/DoseFinding/index.html
Software R package provides functions for design and analysis of dose finding experiments. Used for multiple contrast tests, fitting non-linear dose-response models, calculating optimal designs and implementation of MCPMod methodology.
Proper citation: DoseFinding (RRID:SCR_024268) Copy
Open source software network communication interface for image guided interventions.Provides plug-and-play unified real-time communications in operating rooms for image-guided interventions, where imagers, sensors, surgical robots,and computers from different vendors work cooperatively to ensure seamless data flow among those components and enable a closed loop process of planning, control, delivery, and feedback.
Proper citation: OpenIGTLink (RRID:SCR_024148) Copy
https://cran.r-project.org/web/packages/distory/index.html
Software R package for geodesic distance between phylogenetic trees and associated functions.
Proper citation: distory (RRID:SCR_024269) Copy
https://cran.r-project.org/web/packages/alakazam/index.html
Software R package for high-throughput adaptive immune receptor repertoire sequencing analysis. In particular, immunoglobulin sequence lineage reconstruction, lineage topology analysis, diversity profiling, amino acid property analysis and gene usage.
Proper citation: alakazam (RRID:SCR_024261) Copy
https://cran.r-project.org/web/packages/ade4/index.html
Software R package for multivariate data analysis. Used for analysis of one-table, two-table, three-table and K-table.
Proper citation: ade4 (RRID:SCR_024259) Copy
https://psignifit.sourceforge.net/
Software toolbox to fit psychometric functions and to test hypotheses about psychometric data.
Proper citation: psignifit (RRID:SCR_024196) Copy
https://bioconductor.org/packages/release/bioc/html/BridgeDbR.html
Software R pacakge provides functions and load identifier mapping databases in R. Uses GitHub, Zenodo, and Figshare if you use this package to download identifier mappings files.
Proper citation: bridgedbr (RRID:SCR_024231) Copy
https://bioconductor.org/packages/CNEr/
Software R package provides large scale identification and advanced visualization of sets of conserved noncoding elements.
Proper citation: CNEr (RRID:SCR_024233) Copy
https://bioconductor.org/packages/GenomeInfoDb/
Software R package contains data and functions that define and allow translation between different chromosome sequence naming conventions, including function that attempts to place sequence names in their natural, rather than lexicographic order.
Proper citation: genomeinfodb (RRID:SCR_024235) Copy
https://bioconductor.org/packages/release/bioc/html/GenomicAlignments.html
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.
Proper citation: genomicalignments (RRID:SCR_024236) Copy
https://bioconductor.org/packages/release/bioc/html/BiocGenerics.html
Software R package defines many S4 generic functions used in Bioconductor.
Proper citation: BiocGenerics (RRID:SCR_024226) Copy
https://bioconductor.org/packages/release/bioc/html/biomformat.html
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.
Proper citation: biomformat (RRID:SCR_024228) Copy
https://bioconductor.org/packages/release/bioc/html/biovizBase.html
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.
Proper citation: biovizBase (RRID:SCR_024229) Copy
https://bioconductor.org/packages/release/data/annotation/html/GO.db.html
Software R package provides set of annotation maps describing entire Gene Ontology assembled using data from GO.
Proper citation: go.db (RRID:SCR_024241) Copy
https://bioconductor.org/packages/impute/
Software R package for imputation for microarray data.
Proper citation: impute (RRID:SCR_024243) Copy
https://bioconductor.org/packages/Mergeomics/
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.
Proper citation: mergeomics (RRID:SCR_024244) Copy
https://bioconductor.org/packages/metagenomeSeq/
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.
Proper citation: metagenomeseq (RRID:SCR_024246) Copy
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.
Welcome to the RRID Resources search. From here you can search through a compilation of resources used by RRID and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that RRID 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.
If you have an account on RRID then you can log in from here to get additional features in RRID such as Collections, Saved Searches, and managing Resources.
Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:
You can save any searches you perform for quick access to later from here.
We recognized your search term and included synonyms and inferred terms along side your term to help get the data you are looking for.
If you are logged into RRID you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the sources that were queried against in your search that you can investigate further.
Here are the categories present within RRID that you can filter your data on
Here are the subcategories present within this category that you can filter your data on
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.