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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.
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
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
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.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
Web application for quantitative KInetic MOdels of biological SYStems. Platform includes public data repository of relevant published measurements, including metabolite concentrations, flux data, and enzyme measurements and tools in order to build ODE-based kinetic model. Designed to search, exchange and disseminate experimental data and associated kinetic models for systems modeling community.
Proper citation: Kinetic Models of Biological Systems (KiMoSys) (RRID:SCR_017423) 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://sites.google.com/site/tdtdecodingtoolbox/
Software Matlab toolbox for multivariate analysis of functional and structural MRI data. Software package for multivariate analyses of functional imaging data.
Proper citation: The Decoding Toolbox (RRID:SCR_017424) Copy
https://github.com/Sethupathy-Lab/miRquant
Software tool for accurate annotation and quantification of microRNAs and their isomiRs from small RNA-sequencing data. Provides information on quality of sequencing data, genome mapping statistics, abundance of other types of small RNAs such as tDRs and yDRs, prevalence of post transcriptional modifications.
Proper citation: miRquant (RRID:SCR_017261) Copy
https://icsd.products.fiz-karlsruhe.de/
Database for completely identified inorganic crystal structures. Collection of known inorganic crystal structures published since 1913, including their atomic coordinates. Includes only data which have passed thorough quality checks. Tool for materials research.
Proper citation: Inorganic Crystal Structure Database (ICSD) (RRID:SCR_017429) 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
Open source software package for circuit level interpretation of human EEG/MEG data. Software tool for interpreting cellular and network origin of human MEG/EEG data. Simulates electrical activity of neocortical cells and circuits that generate primary electrical currents underlying EEG/MEG recordings. Designed for researchers and clinicians, without computational neural modeling experience, to develop and test hypothesis on circuit origin of their data.
Proper citation: Human Neocortical Neurosolver (RRID:SCR_017437) 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
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
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
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