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/carmonalab/ProjecTILs
Software tool to project scRNA-seq data into reference single-cell atlases, enabling their direct comparison in stable, annotated system of coordinates. Predicts effects of cell perturbations and identifies gene programs that are altered in different conditions and tissues. Used for interpretation of cell states using reference single-cell maps.
Proper citation: projecTILs (RRID:SCR_026854) Copy
https://github.com/BGI-shenzhen/RectChr
Software tool for multi-level visualization of genomic statistical variables on rectangular chromosomes.
Proper citation: RectChr (RRID:SCR_026859) Copy
https://github.com/james-cole/brainageR
Software R tool for generating brain-predicted age value, using Gaussian Processes regression. Used for generating brain-predicted age value from raw T1-weighted MRI scan.
Proper citation: brainageR (RRID:SCR_026826) Copy
https://github.com/Rosemeis/pcangsd
Software framework for analyzing low-depth next-generation sequencing data in heterogeneous/structured populations using principal component analysis.
Proper citation: pcangsd (RRID:SCR_026956) Copy
https://github.com/DerrickWood/kraken2
Software tool as second version of Kraken taxonomic sequence classification system.
Proper citation: kraken2 (RRID:SCR_026838) Copy
https://github.com/BigDataBiology/SemiBin/
Software command tool for metagenomic binning with deep learning, handles both short and long reads. Used for metagenomic binning at contig level which uses deep contrastive learning.
Proper citation: SemiBin (RRID:SCR_026896) Copy
https://github.com/chklovski/CheckM2
Software tool to predict completeness and contamination of genomic bins. Used for predicting genome quality of metagenome-assembled genomes. Assessing microbial genome quality using machine learning.
Proper citation: CheckM2 (RRID:SCR_026897) Copy
https://github.com/qcxms/QCxMS
Software application as quantum chemical based program that enables users to calculate mass spectra using Born-Oppenheimer Molecular Dynamics. Quantum mechanic mass spectrometry calculation program.
Proper citation: QCxMS (RRID:SCR_026928) Copy
https://github.com/OpenTOPAS/OpenTOPAS
Software Monte Carlo tool for particle simulation. Used for simulation of medical applications of ionizing radiation with the Monte Carlo method. Allows to assemble and control library of simulation objects (geometry components, particle sources, scorers, etc.) with no need to write C++ code and without knowledge of underlying Geant4 Simulation Toolkit.
Proper citation: OpenTOPAS (RRID:SCR_026927) Copy
https://github.com/gevaertlab/DUNE
Software tool to extract low-dimensional deep features from multisequence brain MRI data using unsupervised autoencoders.
Proper citation: GevaertLab_DUNE (RRID:SCR_027208) Copy
https://opendata.cbs.nl/#/CBS/nl/dataset/85457NED
Database of Statistics Netherlands (CBS). Contains lifestyle data of Dutch population living in private households. The numbers can be broken down by various personal characteristics.
Proper citation: CBS StatLine - Lifestyle (RRID:SCR_027121) Copy
https://github.com/Danko-Lab/dREG
Software tool for detecting regulatory elements using GRO-seq and PRO-seq.
Proper citation: dREG (RRID:SCR_027012) Copy
https://github.com/steineggerlab/foldseek
Software tool for fast and sensitive comparisons of large structure sets. Used for comparisons of large protein structure sets, supporting monomer and multimer searches, as well as clustering. It runs on CPU, supports GPU acceleration for faster searches, and optionally allows ultra-fast and sensitive comparisons directly from protein sequence inputs using a language model, bypassing the need for structures.
Proper citation: Foldseek (RRID:SCR_027018) Copy
https://github.com/yichun10/BioCDQA.git
Software retrieval-augmented knowledge mining method with deep thinking LLMs for biomedical research and clinical support. Cross-document question answering dataset addressing current QA limitations, and features Progressive Retrieval-Augmented Reasoning framework that combines advanced retrieval-generation techniques with self-reflection mechanisms and deep-thinking large language models to enhance answer accuracy and contextual relevance.Used to evaluate latent knowledge retrieval and multi-hop reasoning capabilities.
Proper citation: BioCDQA (RRID:SCR_027068) Copy
https://github.com/qiankunzizairen/PanGIA
Software tool for predicting ncRNA-disease associations. Used for identifying association between ncRNAs and diseases.
Proper citation: PanGIA (RRID:SCR_027069) Copy
https://github.com/jorgemasgomez/almondcv2
Software repository provides open-source implementation of RGB imaging workflow for morphological and morphometric analysis of fruits and seeds.
Proper citation: almondcv2 (RRID:SCR_027064) Copy
https://github.com/mskcc/vcf2maf
Software tool to convert Virtual Contact File into Mutation Annotation Format, where each variant is annotated to only one of all possible gene isoforms.
Proper citation: vcf2maf (RRID:SCR_027063) Copy
Software application used for processing and editing 3D triangular meshes. Provides tools for editing, cleaning, repairing, inspecting, rendering, texturing, and converting meshes. This makes it suitable for variety of tasks related to 3D data, including preparing models for 3D printing.
Proper citation: Meshlab (RRID:SCR_027065) Copy
https://github.com/dpeerlab/Palantir/
Algorithm to align cells along differentiation trajectories. Models trajectories of differentiating cells by treating cell fate as probabilistic process and leverages entropy to measure cell plasticity along the trajectory. Generates high-resolution pseudo-time ordering of cells and, for each cell state, assigns probability of differentiating into each terminal state.
Proper citation: Palantir (RRID:SCR_027194) Copy
https://www.merative.com/real-world-evidence/real-world-data-analytics#skiptheform-marketscan
Employer-sourced medical and drugs claims database of the under-65 working population and their dependents, as well as 65+ with Medicare supplemental insurance paid by employers.
Proper citation: MarketScan by Merative (RRID:SCR_027329) 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.