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https://labsn.github.io/expyfun/index.html

Auditory and visual stimulus delivery library for psychoacoustics in Python.

Proper citation: Expyfun (RRID:SCR_019285) Copy   

•   Source: SciCrunch Registry

https://CRAN.R-project.org/package=gbs2ploidy

Software R package as functions for inference of ploidy from Genotyping By Sequencing data, including function to infer allelic ratios and allelic proportions in Bayesian framework.

Proper citation: gbs2ploidy (RRID:SCR_019290) Copy   

•   Source: SciCrunch Registry

https://qiwei.shinyapps.io/PredictCOVID19/

Web app to help assess both short- and long-term forecasts of COVID-19 across the United States at multiple levels. Done by implementing one time-series model (ARIMA), one compartmental models (basic SIR), and six classical growth models, which all yield satisfactory prediction results in the past and current pandemics at early stage.

Proper citation: BayesEpiModels Web App (RRID:SCR_019292) Copy   

•   Source: SciCrunch Registry

https://github.com/pavanvidem/chira

Software tool suite to analyze RNA-RNA interactome experimental data such as CLASH, CLEAR-CLIP, PARIS, SPLASH, etc.

Proper citation: ChiRA (RRID:SCR_019219) Copy   

•   Source: SciCrunch Registry

http://www.conplot.org/

Web application for visualisation of information derived from residue contact predictions in combination with other sources of information, such as secondary structure predictions, transmembrane helical topology, sequence conservation.Provides interactive interface for researchers in field of protein bioinformatics that are interested in analysing data on given protein.

Proper citation: ConPlot (RRID:SCR_019216) Copy   

•   Source: SciCrunch Registry

https://github.com/bgcarlisle/TRNscreener

Software tool as R script to provide function that takes two arguments: path to folder of plain text files named by their DOI, and output filename. For each file in folder, it searches for trial identifiers based on regex matching and writes CSV that contains all trial registration numbers and in case of ClinicalTrials.gov entries, whether they correspond to registry entry on ClinicalTrials.gov.

Proper citation: Trial Registration Number screener (RRID:SCR_019211) Copy   

•   Source: SciCrunch Registry

https://www.agilent.com/en/product/liquid-chromatography/hplc-systems/application-specific-hplc-systems/1290-infinity-ii-online-spe-system

Online SPE System automates solid phase extraction to enrich analytes, remove matrix components or lower detection limits.

Proper citation: Agilent: 1290 Infinity II Online SPE System (RRID:SCR_019380) Copy   

•   Source: SciCrunch Registry

https://www.agilent.com/en/products/atomic-absorption/atomic-absorption-systems/240z-aa

Atomic Absorption System is used for detection limits and analyzes difficult matrices.

Proper citation: Agilent: 240Z AA Atomic Absorption System (RRID:SCR_019385) Copy   

•   Source: SciCrunch Registry

https://www.agilent.com/en/product/liquid-chromatography/hplc-systems/preparative-hplc-systems/1290-infinity-ii-preparative-lc-msd-system

Preparative LC/MSD System enables high throughput purification and delivers high quality compounds.

Proper citation: Agilent: 1290 Infinity II Preparative LC/MSD System (RRID:SCR_019381) Copy   

•   Source: SciCrunch Registry

https://github.com/ABCD-STUDY/DEAP

Web service for data exploration and analysis of the ABCD Study - the largest long-term study of brain development and child health in the United States.

Proper citation: DEAP - Data Exploration and Analysis Portal (RRID:SCR_016158) Copy   

•   Source: SciCrunch Registry

https://github.com/brain-life/encode

Software that implements a framework to encode structural brain connectomes into multidimensional arrays (tensors). Encoding Connectomes provides an agile framework for computing over connectome edges and nodes.

Proper citation: Linear Fascicle Evaluation (RRID:SCR_016153) Copy   

•   Source: SciCrunch Registry

https://github.com/CAMI-challenge/AMBER

Software toolkit for the comparative assessment of genome reconstructions from metagenome benchmark datasets. It provides performance metrics, results rankings, and comparative visualizations for assessing multiple programs or parameter effects.

Proper citation: AMBER (RRID:SCR_016151) Copy   

•   Source: SciCrunch Registry

https://nemoarchive.org/

Data repository specifically focused on storage and dissemination of omic data generated from BRAIN Initiative and related brain research projects. Data repository and archive for BCDC and BICCN project, among others. NeMO data include genomic regions associated with brain abnormalities and disease, transcription factor binding sites and other regulatory elements, transcription activity, levels of cytosine modification, histone modification profiles and chromatin accessibility.

Proper citation: NeMOarchive (RRID:SCR_016152) Copy   

•   Source: SciCrunch Registry

https://hirnetwork.org/consortium/ctar

Consortium that is an independent research initiative of the Human Research Information Network (HIRN). It is investigating methods to increase or maintain functional beta cell mass in T1D through targeted manipulation of islet plasticity or engineered protection of beta cells from immune-mediated destruction.

Proper citation: HIRN Consortium on Targeting and Regeneration (RRID:SCR_016201) Copy   

•   Source: SciCrunch Registry

http://hyphy.org/

Open source software package for comparative sequence analysis using stochastic evolutionary models. Used for analysis of genetic sequence data in particular the inference of natural selection using techniques in phylogenetics, molecular evolution, and machine learning.

Proper citation: HyPhy (RRID:SCR_016162) Copy   

•   Source: SciCrunch Registry

http://abacus.gene.ucl.ac.uk/software/indelible/

Software that generates nucleotide, amino acid and codon sequence data by simulating insertions and deletions (indels) as well as substitutions. It is used for biological sequence simulation of multi-partitioned nucleotide, amino-acid, or codon data sets through the processes of insertion, deletion, and substitution in continuous time.

Proper citation: Indelible (RRID:SCR_016163) Copy   

•   Source: SciCrunch Registry

https://github.com/sdparekh/zUMIs

Software pipeline to process RNA-seq data with UMIs. The input to this pipeline is paired-end fastq files, where one read contains the cDNA sequence and the other read contains UMI and Cell Barcode information.

Proper citation: zUMIs (RRID:SCR_016139) Copy   

•   Source: SciCrunch Registry

https://www.microsoft.com/en-gb/

Software application with data analysis tools and spreadsheet templates to track and visualize data. It is used to manage and process data.

Proper citation: Microsoft Excel (RRID:SCR_016137) Copy   

•   Source: SciCrunch Registry

http://fastml.tau.ac.il/

Web application for the reconstruction of ancestral sequences. It computes maximum likelihood ancestral sequence reconstruction based on the phylogenetic relations between homologous sequences.

Proper citation: Fastml (RRID:SCR_016092) Copy   

•   Source: SciCrunch Registry

https://sanger-pathogens.github.io/gubbins/

Software application as an algorithm that iteratively identifies loci containing elevated densities of base substitutions while concurrently constructing a phylogeny based on the putative point mutations outside of these regions. It is used for phylogenetic analysis of genome sequences and generating highly accurate reconstructions under realistic models of short-term bacterial evolution., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: Gubbins (RRID:SCR_016131) Copy   

•   Source: SciCrunch Registry