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://github.com/jgraving/DeepPoseKit
Software toolkit with high level API for 2D pose estimation of user defined keypoints using deep learning.Written in Python and built using Tensorflow and Keras.Method for pose estimation developed by behavioral scientists at the Max Planck Institute of Animal Behavior.
Proper citation: DeepPoseKit (RRID:SCR_021405) Copy
https://neurokit2.readthedocs.io/en/latest/
Software Python package for neurophysiological signal processing. Used to analyze physiological data.
Proper citation: Neurokit2 (RRID:SCR_021889) Copy
https://github.com/DrCoffey/DeepSqueak
Software MATLAB package for high throughput ultrasonic vocalizations detection, classification, and analysis.
Proper citation: DeepSqueak (RRID:SCR_021524) Copy
https://knowledge.brain-map.org/celltypes
Software application to examine multimodal data from thousands of cells across 3 mammalian species.
Proper citation: Cell Type Knowledge Explorer (RRID:SCR_022793) Copy
https://github.com/Vaa3D/vaa3d_tools/tree/master/hackathon/mBrainAligner
Software package provides cross modality image registration pipeline to support whole brain mapping projects. Contains three modules: (1) image preprocessing and global registration, (2) Coherent Landmark Mapping (CLM) based automatic registration, and (3) optional semi-automatic refinement.
Proper citation: mBrainAligner (RRID:SCR_022791) Copy
https://www.millisecond.com/download/
Software tool for designing and administering psychological tests and experiments on computers.
Proper citation: Inquisit LAB (RRID:SCR_022151) Copy
https://github.com/plger/scDblFinder
Software package for detection and handling of doublets/multiplets in single cell sequencing data.
Proper citation: scDblFinder (RRID:SCR_022700) Copy
https://github.com/PeterEckmann1/preprint-match
Software tool to match bioRxiv preprints with their corresponding PubMed paper.
Proper citation: PreprintMatch (RRID:SCR_022302) Copy
http://www.cgmartini.nl/index.php/downloads/tools/239-insane
Software tool for generating custom membranes for molecular simulations. Software Python script to setup Martini bilayer systems.
Proper citation: insane.py (RRID:SCR_022317) Copy
https://cran.r-project.org/web/packages/reshape2/index.html
Software R package to flexible rearrange, reshape and aggregate data. Reshape2 is reboot of reshape package.
Proper citation: reshape2 (RRID:SCR_022679) Copy
https://cran.r-project.org/web/packages/Peptides/index.html
Software R package to calculate indices and theoretical physicochemical properties of peptides and protein sequences.
Proper citation: Peptides (RRID:SCR_022675) Copy
https://www.cbcb.umd.edu/software/epiviz
Software package as interactive visualization tool for functional genomics data. Interactive visual analytics for functional genomics data.
Proper citation: Epiviz (RRID:SCR_022796) Copy
https://CRAN.R-project.org/package=ggeffects
Software R package to create tidy data frames of marginal effects for ggplot from model outputs. Used to compute marginal effects and adjusted predictions from statistical models and returns result as tidy data frames.
Proper citation: ggeffects (RRID:SCR_022496) Copy
https://CRAN.R-project.org/package=betareg
Software R package for modeling beta distributed dependent variables, e.g., rates and proportions. In addition to maximum likelihood regression (for both mean and precision of beta distributed response), bias corrected and bias reduced estimation as well as finite mixture models and recursive partitioning for beta regressions are provided.
Proper citation: Betareg (RRID:SCR_022494) Copy
https://bioconductor.org/packages/monaLisa/
Software R package to work with sequence motifs in analysis of genomics data. These include methods to annotate genomic regions or sequences with predicted motif hits and to identify motifs that drive observed changes in accessibility or expression. Functions to produce informative visualizations of obtained results are also provided.
Proper citation: monaLisa (RRID:SCR_022802) Copy
https://github.com/shooshtarilab/TMExplorer
Software package to improve studying tumour microenvironment with single cell sequencing. Developers may use this package to obtain data for validation of new algorithms and researchers interested in tumour microenvironment may use it to study specific cancers more closely. Curated collection of scRNAseq datasets sequenced from tumours.
Proper citation: TMExplorer (RRID:SCR_022768) Copy
https://spin.niddk.nih.gov/bax/software/TALOS-N/
Software package for prediction of protein backbone and sidechain torsion angles from NMR chemical shifts.
Proper citation: TALOS-N (RRID:SCR_022800) Copy
https://github.com/topepo/caret
Software R package that contains functions for training and plotting classification and regression models. Includes methods for pre-processing training data, calculating variable importance, and model visualizations.
Proper citation: Classification And Regression Training (RRID:SCR_022524) Copy
https://plexon.com/software-downloads/
Software tool used to control Plexon pattern generator for optogenetic stimulation.
Proper citation: Radiant (RRID:SCR_022645) Copy
https://CRAN.R-project.org/package=simplePHENOTYPES
Software R package that simulates pleiotropy, partial pleiotropy, and spurious pleiotropy in wide range of genetic architectures, including additive, dominance and epistatic models. Used to simulate multiple traits controlled by loci with varying degrees of pleiotropy.
Proper citation: simplePHENOTYPES (RRID:SCR_022523) 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.