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https://github.com/jefferis/nat

Software R package for 3D visualisation and analysis of biological image data, especially tracings of single neurons.

Proper citation: NeuroAnatomy Toolbox (RRID:SCR_017248) Copy   

•   Source: SciCrunch Registry

http://www.infolanka.com/org/twin-registry/

Independent academic and research institution to establish registration for twins in Sri Lanka , to facilitate study of twins. Center for twin, sibling, family and genetic studies for South Asian Region.

Proper citation: National Twin Registry of Sri Lanka (RRID:SCR_017481) Copy   

•   Source: SciCrunch Registry

https://matr.vcu.edu/about/

Organization of twins and their families who are willing to consider taking part in twin-based, health-related research. For twins of any age, ethnicity, and zygosity (identical or fraternal), as well as higher order multiples such as triplets, quadruplets and quintuplets. Most of twins registered in MATR are from Virginia, North Carolina, and South Carolina, but twins from all over the country and all around the world are welcome to register. MATR repository containing DNA samples provided by twins and allows to study twin data collected by studies along with their DNA.

Proper citation: Mid-Atlantic Twin Registry (RRID:SCR_017484) Copy   

•   Source: SciCrunch Registry

http://www.nitrc.org/projects/vini/

Software Python tool as viewer for MRI data and numpy arrays.

Proper citation: vini: A viewer for fMRI data (RRID:SCR_017250) Copy   

•   Source: SciCrunch Registry

http://www.ariesepigenomics.org.uk/

Portal for epigenomic information on range of human tissues, including DNA methylation data on peripheral blood at multiple time points across lifecourse. Provides web interface to browse methylation variation between groups of individuals and across time.

Proper citation: Accessible Resource for Integrated Epigenomics Studies (RRID:SCR_017492) Copy   

•   Source: SciCrunch Registry

https://deepblue.mpi-inf.mpg.de/

Central data access hub for large collections of epigenomic data. It organizes data from different sources using controlled vocabularies and ontologies. Data Server for storing, organizing, searching, and retrieving genomic and epigenomic data, handling associated metadata, and to perform different types of analysis.

Proper citation: Deep Blue Epigenomic Data Server (RRID:SCR_017490) Copy   

•   Source: SciCrunch Registry

https://github.com/YosefLab/FastProject

Software Python tool for low dimensional analysis of single-cell RNA-Seq data. Software package for two dimensional visualization of single cell data. Analyzes gene expression matrix and produces output report in which two-dimensional of data can be explored.

Proper citation: FastProject (RRID:SCR_017462) Copy   

•   Source: SciCrunch Registry

https://ki.se/en/research/the-swedish-twin-registry

Registry contains information about twin pairs for which zygosity is known, both mono- and dizygotic pairs. Registry covers older, middle, and younger cohorts. There are approximately 30 projects ongoing based on data from this registry.

Proper citation: Swedish Twin Registry (RRID:SCR_017478) Copy   

•   Source: SciCrunch Registry

http://pathwaynet.princeton.edu/

Web user interface for interaction predictions of human gene networks and integrative analysis of user data types that takes advantage of data from diverse tissue and cell-lineage origins. Predicts presence of functional association and interaction type among human genes or its protein products on whole genome scale. Used to analyze experimetnal gene in context of interaction networks.

Proper citation: PathwayNet (RRID:SCR_017353) Copy   

•   Source: SciCrunch Registry

https://ccb-web.cs.uni-saarland.de/tissueatlas

Human miRNA tissue atlas. Database showing distribution of miRNA expression across human tissues.

Proper citation: TissueAtlas (RRID:SCR_017352) Copy   

•   Source: SciCrunch Registry

https://github.com/epurdom/clusterExperiment

Software open source R package for executing, evaluating and visualizing different clusterings of experimental data, including data from single cell RNA-Seq studies. Software for running and comparing different clusterings of single cell sequencing data.

Proper citation: clusterExperiment (RRID:SCR_017439) Copy   

•   Source: SciCrunch Registry

https://www.hmtphenome.uniba.it

Collection of data about variants, genes, phenotypes and diseases involved in mitochondrial functionality. Users can search for variant position, gene, phenotype or disease and retrieve all related information through integrated network of biological entities.

Proper citation: HmtPhenome (RRID:SCR_017289) Copy   

•   Source: SciCrunch Registry

https://www.mbfbioscience.com/tissue-mapper

Software for comprehensive annotation and delineation of tissue structures by MBF Bioscience. Creates 3D model from image data and annotates regions of interest from customizable ontology list. Map images acquired with brightfield, confocal, two-photon, widefield fluorescence, or light sheet microscopes.

Proper citation: Tissue Mapper (RRID:SCR_017321) Copy   

•   Source: SciCrunch Registry

http://relacs.sourceforge.net/

Software platform for closed loop data acquisition, online analysis, and stimulus generation specifically designed for, but not limited to, electrophysiological recordings.

Proper citation: Relacs (RRID:SCR_017280) Copy   

•   Source: SciCrunch Registry

https://www.mbfbioscience.com/vesselucida360

Software tool for visualization and automatic reconstruction of microvascular networks in 3D environment with built-in analysis tools by MBF Bioscience.

Proper citation: Vesselucida 360 (RRID:SCR_017320) Copy   

•   Source: SciCrunch Registry

http://www.dibsvis.com/biowheel

Software tool for interactive graphs of high dimensional data. Interactive cloud based software tool by DIBSVIS.

Proper citation: BioWheel (RRID:SCR_017441) Copy   

•   Source: SciCrunch Registry

https://github.com/ndierckx/NOVOPlasty

Software package as de novo assembler and heteroplasmy variance caller for short circular genomes. Used for de novo assembly of organelle genomes from whole genome data.

Proper citation: NOVOPlasty (RRID:SCR_017335) Copy   

•   Source: SciCrunch Registry

https://github.com/SilverLabUCL/SilverLab-Microscope-Software

Software for use with compact Acousto-Optic Lens Microscope (AOLM) developed in the Silver Lab at UCL. Written in LabVIEW. Performs multiple imaging modes and protocols including Z-stacks, multi-plane, single-plane, sub-volume, patches and points. It comes with tools for visualising data acquired with system.

Proper citation: Silver Lab Microscopy Software (RRID:SCR_017456) Copy   

•   Source: SciCrunch Registry

https://scfind.sanger.ac.uk/

Software R package as search tool for single cell RNA-seq data by gene lists. Builds index from scRNA-seq datasets which organizes information in suitable and compact manner so that datasets can be very efficiently searched for either cells or cell types in which given list of genes is expressed.

Proper citation: Scfind (RRID:SCR_017339) Copy   

•   Source: SciCrunch Registry

https://modbase.compbio.ucsf.edu/foxs/

Web server for computing theoretical scattering profile of structure and fitting of experimental profile. Computes SAXS profile of given atomistic model and fits it to experimental profile. Used for structural modeling applications with small angle X-ray scattering data.

Proper citation: FoXS (RRID:SCR_017269) Copy   

•   Source: SciCrunch Registry