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http://www.amplipex.com/products/large-scale-recording/

Multiplexed biosignal amplifier used to record neural signal by Amplipex Ltd. Related to electrophysiology experiments with multichannel extracellular recordings in freely moving rodents.

Proper citation: Amplipex: KJE-1001 amplifier (RRID:SCR_018017) Copy   

•   Source: SciCrunch Registry
  

http://www.syglass.io

Software visualization tool for direct volume rendering with no segmentation required. Enables users to view, annotate and analyze 3D data in VR. Data visualization and annotation system that allows rendering of large, volumetric data in its true, three- or four-dimensional form.

Proper citation: syGlass (RRID:SCR_017961) Copy   

•   Source: SciCrunch Registry
  

http://neuronexus.com/wp-content/uploads/2018/09/nDrive_UserManual.pdf

Microdrive for chronic implantation of neural probe by NeuroNexus.

Proper citation: NeuroNexus: nDrive (RRID:SCR_018019) Copy   

•   Source: SciCrunch Registry
  

https://bioconductor.org/packages/TCGAbiolinks/

Software R Bioconductor package for integrative analysis with TCGA data.TCGAbiolinks is able to access National Cancer Institute Genomic Data Commons thorough its GDC Application Programming Interface to search, download and prepare relevant data for analysis in R.

Proper citation: TCGAbiolinks (RRID:SCR_017683) Copy   

•   Source: SciCrunch Registry
  

https://www.adobe.com/lightroom

Camera raw data processing software. Cloud-based service to edit, organize, store, and share photos across any device.

Proper citation: Adobe Photoshop Lightroom (RRID:SCR_018012) Copy   

•   Source: SciCrunch Registry
  

https://isb-cgc.appspot.com/

Web tool as flexible cloud-based platform for cancer genomics research. Platform that serves as large-scale repository and provides computational infrastructure necessary to carry out cancer genomics research at unprecedented scales. ISB-CGC is providing access to TCGA data and computation on Google Cloud Platform.

Proper citation: ISB Cancer Genomics Cloud (RRID:SCR_017681) Copy   

•   Source: SciCrunch Registry
  

https://github.com/uleroboticsgroup/SVCP4CDataset

Software tool to collect vulnerable source code from open-source repositories linked to SonarCloud. Dataset repository with tagged files with BufferOverflow features associated to source code repositories publicly available.

Proper citation: SonarCloud Vulnerable Code Prospector for C (RRID:SCR_018011) Copy   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

http://bit.do/canidmeth-github

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

Proper citation: CandiMeth (RRID:SCR_017974) Copy   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry
  

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   

•   Source: SciCrunch Registry