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https://www.rcon-ndt.com/wp-content/uploads/Nanotom.pdf

System for scientific and industrial nanofocus computed tomography nanoCT and 3D metrology. Realizes unique spatial and contrast resolution on wide sample and application range. Used in material science, precision injection moulding, micromechanics, electronics geology and biology. Used in 3D CT applications. Allows many analysis, e.g. non-destructive visualization of slices, arbitrary sectional views, or automatic pore analysis.

Proper citation: GE: Phoenix Nanotom S (RRID:SCR_017995) Copy   

•   Source: SciCrunch Registry

https://www.thermofisher.com/order/catalog/product/4315931#/4315931

Genetic analyzer that performs fragment analysis and rapid sequencing applications. Usage per array is 100 runs with use of Applied Biosystems reagents.

Proper citation: Thermo Fisher: Applied Biosystems: 3130xl Capillary Array (RRID:SCR_018048) Copy   

•   Source: SciCrunch Registry

https://bionano.com/saphyr-systems/

Whole genome imaging instrument by Bionano Genomics for high speed, high throughput structural variant detection and analysis with exceptional sensitivity and specificity. Detects structural variations ranging from 500 bp to megabase pairs in length. For mosaic samples or heterogeneous cancer samples, detects all types of structural variants down to 5% Variant Allele Fraction. Calls repeats and complex rearrangements.

Proper citation: Marshall Scientific: Saphyr (RRID:SCR_017992) Copy   

•   Source: SciCrunch Registry

https://www.thelabworldgroup.com/ge-typhoon-9410-microarray-imager

Variable mode imager that operates in three different modes, including phosphorescence, fluorescence, and chemiluminescence. Can scan in visible range using reflected light. Scanning resolution ranges from 1000um down to 10um. Scanning software is linked to ImageQuant TL 7.0 analysis software. ImageQuant is capable of quantifying Typhoon images such as those from Northern or Western blots. Images can be saved in various formats and imported into Powerpoint slides. Instrument has three excitation lasers (532nm, 633nm, 488nm). Instrument utilizes 536SP, 670BP, 520BP emission filters for fluorescence. For DNA, RNA and protein samples you may choose from: storage phosphor auto-radiography, direct blue-excited fluorescence (457-488 nm), direct green-excited fluorescence (532 nm), direct red-excited fluorescence (633 nm), and chemiluminescence.

Proper citation: GE: Healthcare: 9410 Variable Mode Imager (RRID:SCR_018047) Copy   

•   Source: SciCrunch Registry

http://www.touptek.com/product/showproduct.php?id=103&lang=en

Software tool that controls microscope camera by Touptek Photomics. Provides functions to fully control camera and present video stream processed by Ultra FineTM color engine at high speed, which includes dedicated pipeline to process raw data into realistic scene. Compatible with ToupCam full series of digital cameras. With authorized license, ToupView software could be used with other cameras which support Twain or DirectShow interface. Used in field of medical microscopic imaging, industrial detection, machine vision, astronomical observation, etc.

Proper citation: ToupView (RRID:SCR_017998) Copy   

•   Source: SciCrunch Registry

https://www.leicabiosystems.com/histology-equipment/microtomes/products/leica-rm2265/

Automated rotary microtome that sections tissue samples. Specimen feed system with zero-backlash and maintenance-free cross roller guides and stepper motor operated coarse feed system are located in dust-proof plastic housing. Equipped with safety handwheel with handle that can be centered, as well as mechanical handwheel lock. In manual operation retraction can be adjusted. In motorized operation retraction value varies with selected sectioning speed.

Proper citation: Leica: Biosystems RM2265 Fully Automated Rotary Microtome (RRID:SCR_018041) Copy   

•   Source: SciCrunch Registry

https://www.leicabiosystems.com/histology-equipment/microtomes/leica-rm2125-rts/

Manual rotary microtome that sections tissue samples. Features include precise feed mechanism, powerBase that ensures stable operation for vibration-free sectioning, advanced knife holder and specimen clamp securely align cutting edge to block, user-selectable coarse feed wheel turn direction and retraction functions, hand wheel, in-built safety guards and rounded shape with arm rests for fatigue-free sectioning,quick-exchange specimen clamp and orientation system for object head allow rapid set up for any block, and two trim steps.

Proper citation: Leica: RM2125 RTS Manual Microtome (RRID:SCR_018040) Copy   

•   Source: SciCrunch Registry

https://www.thermofisher.com/order/catalog/product/313001R#/313001R

Genetic analyzer can run sequencing and fragment analysis applications including microsatellite analysis, AFLP, LOH, SNP validation, and SNP screening. Maintenance time is reduced by eliminating manual syringe washing and filling with automated polymer delivery. Can increase data quality for sequencing and fragment analysis applications by longer read length, and higher resolution with shorter run times. Uses 96- or 384-well plates with four capillary array.

Proper citation: Thermo Fisher: Applied Biosystems: 3130 Genetic Analyzer (RRID:SCR_018046) Copy   

•   Source: SciCrunch Registry

https://timothyspringer.org/files/tas/files/biacore3000-instrument.pdf

Biacore 3000 processing unit is an established, label-free system for detailed studies of biomolecular interactions. The system delivers comprehensive characterization of the interaction, answers questions about the rate constants, affinity, specificity, and determines the active concentration of components. The ability to recover and transfer interaction partners directly to MALDI targets for identification and further characterization makes the system highly applicable to fast identification of unknown interactants.

Proper citation: GE: Biacore 3000 Real Time Biomolecular Interaction Analyzer (RRID:SCR_018044) Copy   

•   Source: SciCrunch Registry

https://www.agilent.com/en/product/automated-electrophoresis/bioanalyzer-systems/bioanalyzer-instrument/2100-bioanalyzer-instrument-228250

Bioanalyzer system is automated electrophoresis tool that provides an analytical evaluation of various samples types in many workflows, including next generation sequencing NGS, gene expression, biopharmaceutical, and gene editing research. Digital data is provided in timely manner and delivers assessment of sizing, quantitation, integrity and purity from DNA, RNA, and proteins. Minimal sample volumes are required for accurate result, and data may be exported in many different formats.

Proper citation: Agilent: 2100 Bioanalyzer Instrument (RRID:SCR_018043) Copy   

•   Source: SciCrunch Registry

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

https://wustl.edu/

Private research university in Greater St. Louis with its main campus mostly in unincorporated St. Louis County, Missouri and Clayton, Missouri.

Proper citation: Washington University in St. Louis (RRID:SCR_017964) 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