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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://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
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
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
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
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
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
https://www.ibm.com/us-en/marketplace/marketscan-research-databases
Software suite of proprietary databases that contain one of longest running and largest collection of privately and publicly insured, de identified patient data in USA. Family of data sets that fully integrate many types of data for healthcare research.
Proper citation: IBM® MarketScan® Research Databases (RRID:SCR_017212) Copy
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
https://www.beckman.fr/flow-cytometry/instruments/cytoflex/software
Software program that controls instrument operation, data collection and analysis. Software for CytoFLEX Platform by Beckman Coulter.
Proper citation: CytExpert Software (RRID:SCR_017217) Copy
https://github.com/EpistasisLab/pennai
Open source software tool to leverage supervised machine learning techniques to analyze data. Can assist with tasks such as choosing appropriate models for data. Data science assistant for generating results from large and complex data problems.
Proper citation: PennAI (RRID:SCR_017215) Copy
https://www.cmrr.umn.edu/downloads/mrspa
Software package to post process MR spectroscopy data. Magnetic Resonance signal processing and analysis software. Runs under Matlab.
Proper citation: MRspa (RRID:SCR_017292) Copy
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
https://bioconductor.org/packages/release/bioc/html/Glimma.html
Software package for interactive graphics for gene expression analysis. Generates interactive visualisations for analysis of RNA-sequencing data.
Proper citation: Glimma (RRID:SCR_017389) Copy
https://github.com/JosephCrispell/homoplasyFinder/wiki
Software tool to identify and annotate homoplasies on phylogeny and sequence alignment. Used to automatically identify any homoplasies present in simulated and real phylogenetic data. Java application that can be used as standalone tool or within statistical programming environment R.
Proper citation: HomoplasyFinder (RRID:SCR_017300) Copy
https://github.com/ISUgenomics/SequelQC
Software tool that calculates key statistics and generates publication quality plots for raw PacBio Sequel data. Open source software for analyzing PacBio Sequel raw sequence data.
Proper citation: SequelQC (RRID:SCR_017279) Copy
Software tool for data analysis and scientific visualization by IONDEV SRL.
Proper citation: QtiPlot (RRID:SCR_017311) Copy
Software JAVA based application for basic analysis of Small Angle X-ray Scattering datasets.
Proper citation: SCÅTTER (RRID:SCR_017271) Copy
https://4dgenome.research.chop.edu/
Repository for chromatin interaction data. Records can be queried by genomic regions, gene names, organism, and detection technology. Database is continuously updated by curators. Contributions from scientific community.
Proper citation: 4D Genome (RRID:SCR_017489) Copy
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
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
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