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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.

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  • RRID:SCR_017680

    This resource has 1+ mentions.

https://github.com/ctlab/GADMA

Software tool to implement methods for automatic inferring joint demographic history of multiple populations from genetic data. Genetic algorithm for inferring demographic history of multiple populations from allele frequency spectrum data.

Proper citation: GADMA (RRID:SCR_017680) Copy   


  • RRID:SCR_018010

    This resource has 1+ mentions.

http://143.169.238.105/variantdb/index.php?page=variants

Web based interactive annotation and filtering platform that automatically annotates variants with allele frequencies, functional impact, pathogenicity predictions and pathway information. Allows filtering by all annotations, under dominant, recessive or de novo inheritance models. Flexible annotation and filtering portal for next generation sequencing data.

Proper citation: VariantDB (RRID:SCR_018010) Copy   


  • RRID:SCR_017972

    This resource has 1+ mentions.

http://omnitech-usa.com/product/Fusion-Software/510

Software for analyzing mouse behavior by Omnitech Electronics Inc.

Proper citation: Fusion software (RRID:SCR_017972) Copy   


http://www.thunderbiosci.co.kr/wp-content/uploads/2017/07/Apollo-324_brochure.pdf

Compact benchtop platform that enables rapid and full walk-away automation of next generation sequencing applications. Paired with PrepX reagents, Apollo 324 line offers complete sample-toanswer solution for NGS library prep. Apollo 324 automated protocols and PrepX reagent kits combine liquid handling and proven chemistries to produce high quality libraries for all major NGS platforms. System provides complete, walkaway solution using validated protocols and chemistries that produce consistent libraries for DNA-seq, RNA-seq, and ChIP-seq applications.

Proper citation: Wafergen: Apollo 324 NGS Library Prep (RRID:SCR_018027) Copy   


  • RRID:SCR_017970

    This resource has 10+ mentions.

https://crispy.secondarymetabolites.org

Web tool to design sgRNAs for CRISPR applications. Web tool based on CRISPy to design sgRNAs for any user-provided microbial genome. Implemented as standalone web application for Cas9 target prediction.

Proper citation: CRISPy-web (RRID:SCR_017970) Copy   


  • RRID:SCR_017976

    This resource has 1+ mentions.

https://github.com/slimsuite/pafscaff

Software as Pairwise mApping Format reference based Scaffold anchoring and super scaffolding tool. Dsigned for mapping genome assembly scaffolds to closely related chromosome level reference genome assembly.

Proper citation: PAFScaff (RRID:SCR_017976) Copy   


  • RRID:SCR_017974

    This resource has 1+ mentions.

http://bit.do/canidmeth-github

Software tool for visualisation and quantification of DNA methylation at candidate features.

Proper citation: CandiMeth (RRID:SCR_017974) Copy   


https://www.selectscience.net/products/gel-logic-212-pro/?prodID=83511#tab-2

Automated gel imaging system for imaging fluorescence or colorimetric data in sample formats such as gels (DNA/Coomassie/Silver stain) membranes, and 96 well plates. Features include autofocusing and directed autoexposure.

Proper citation: Select Science: Carestream Gel Logic 212 PRO Imaging System (RRID:SCR_018029) Copy   


  • RRID:SCR_018024

    This resource has 1+ mentions.

https://github.com/AndreMacedo88/VEnCode

Software tool to perform intersectional genetics-related operations to find VEnCodes using databases provided by FANTOM5 consortium, namely CAGE enhancer and transcription start site (TSS) databases.

Proper citation: VEnCode (RRID:SCR_018024) Copy   


  • RRID:SCR_018021

    This resource has 1+ mentions.

https://www2.bri.nrc.ca/ccb/pub/sietraj_main.php

Software tool for binding free energies from Amber-generated MD trajectories. Alternative to MM-PBSA software provided by AMBER distribution. Virtual alanine mutations are also possible. Solvated interaction energies are calculated using parameters that have been fitted to reproduce binding free energies of data set of 99 protein-ligand complexes.

Proper citation: sietraj (RRID:SCR_018021) Copy   


  • RRID:SCR_017669

    This resource has 1+ mentions.

https://www.mbfbioscience.com/wormlab

Software tool for imaging, tracking, and analyzing C. elegans and other nematodes. It has user friendly software interface with patented model specific tracking algorithm that collects data about single worm or multiple worms, even through omega bends, coiling, reversals, and entanglements. Provides quantitative analysis of locomotory behavior with user configurable metrics for crawling and swimming assays.

Proper citation: Worm Lab (RRID:SCR_017669) Copy   


  • RRID:SCR_018005

    This resource has 1+ mentions.

http://www.diploid.com/moon

Software package that autonomously diagnoses rare diseases from next generation sequencing NGS data using artificial intelligence by Diploid.

Proper citation: MOON (RRID:SCR_018005) Copy   


  • RRID:SCR_017674

    This resource has 1+ mentions.

https://www.mbfbioscience.com/help/vesselucida-explorer/Content/VesselucidaExplorer.html

Vesselucida Explorer is Vesselucida 360 companion analysis software, to perform analyses. Provides vasculature specific metrics such as segments and nodes counts, frequency of anastomoses, vessel surface and volume, and more.

Proper citation: Vesselucida Explorer (RRID:SCR_017674) Copy   


  • RRID:SCR_017677

    This resource has 100+ mentions.

http://apps.cytoscape.org/apps/cytohubba

Software tool for identifying hub objects and sub-networks from complex interactome. Predicts and explore nodes and subnetworks in given network by several topological algorithms. Provides interface to analyze topology of protein-protein interaction networks, such as human, yeast, rat, mouse, fly etc. Plugin works with Cytoscape 2.6 or above, which requires Java 1.5 or above.

Proper citation: cytoHubba (RRID:SCR_017677) Copy   


https://digitimer.com/products/human-neurophysiology/peripheral-stimulators-2/ds5-isolated-bipolar-constant-current-stimulator-clinical-product/

Stimulator allows computer control of stimulus amplitude and timing parameters. Designed to speed up and enhance human peripheral nerve diagnostics by facilitating semi-automated nerve excitability tests. It also has roles in wider aspects of clinical neurophysiology research, including psychological, vestibular system and nociceptive testing. CE marked medical device under European Medical Device Regulation.

Proper citation: Digimeter: DS5 Isolated Bipolar Current Stimulator (RRID:SCR_018001) Copy   


  • RRID:SCR_018170

    This resource has 10+ mentions.

http://paintmychromosomes.com/

Software tool as algorithm for identifying population structure using dense sequencing data. Can perform model based Bayesian clustering on large datasets, including full resequencing data.

Proper citation: fineSTRUCTURE (RRID:SCR_018170) Copy   


  • RRID:SCR_018219

    This resource has 100+ mentions.

https://servicesn.mbi.ucla.edu/SAVES/

Web server for structure validation in homology modeling. Used to validate of obtained crude models. Structure analysis and validation server.

Proper citation: SAVES (RRID:SCR_018219) Copy   


  • RRID:SCR_018217

    This resource has 100+ mentions.

https://github.com/lmcinnes/umap

Software package as dimension reduction technique that can be used for visualization similar to t-SNE, but also for general non-linear dimension reduction. Used for dimensionality reduction for visualizing single-cell data.

Proper citation: Umap (RRID:SCR_018217) Copy   


  • RRID:SCR_018178

    This resource has 1+ mentions.

https://github.com/yousra291987/ChiCMaxima

Pipeline for analyzing and identificantion of chromatin loops in CHi-C promoters data. Used to capture Hi-C visualization and interaction calling.

Proper citation: ChiCMaxima (RRID:SCR_018178) Copy   


  • RRID:SCR_018177

    This resource has 1+ mentions.

https://github.com/esctrionsit/snphub

Web Shiny-based server framework for retrieving, analyzing and visualizing large genomic variations data.

Proper citation: SnpHub (RRID:SCR_018177) Copy   



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