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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_023038

    This resource has 10+ mentions.

https://github.com/open2c/pairtools

Software command line framework to process sequencing data from Hi-C experiment. Used to process pair end sequence alignments.

Proper citation: pairtools (RRID:SCR_023038) Copy   


  • RRID:SCR_022999

    This resource has 1+ mentions.

https://github.com/hartwigmedical/hmftools/blob/master/purple/README.md

Software tool as purity ploidy estimator for whole genome sequenced data. Used for copy number calling and determination of sample purity.

Proper citation: PURPLE (RRID:SCR_022999) Copy   


  • RRID:SCR_022877

    This resource has 10+ mentions.

https://www.thermofisher.com/de/de/home/technical-resources/technical-reference-library/mass-spectrometry-support-center/liquid-chromatography-mass-spectrometry-software-support/freestyle-software-support/freestyle-software-support-getting-started.html

Software to visualize and qualitatively analyze mass spectrometry data. Used to display chromatograms and spectra, detect and integrate chromatographic peaks, search mass spectral libraries, simulate mass spectra, subtract background spectra, apply scan filters, annotate plots with text and graphics, create and save layouts, view the status of various instrument parameters during data acquisition, and create a 2D or 3D representation of an analysis displaying the acquired mass/wavelength scans. Part of liquid chromatography mass spectrometry system.

Proper citation: FreeStyle 1.8 SP1 (RRID:SCR_022877) Copy   


  • RRID:SCR_022998

    This resource has 10+ mentions.

https://github.com/walaj/svaba

Software tool for detecting structural variants in sequencing data using genome wide local assembly. Genome wide detection of structural variants and indels by local assembly. Used for detecting SVs from short read sequencing data using genome wide local assembly with low memory and computing requirements.

Proper citation: SvABA (RRID:SCR_022998) Copy   


http://www.brainhealthdatabank.ca

Repository of many types and sources of data including, but not limited to, assessments, imaging, wearable, and biological samples, collected from research projects at the Centre for Addiction and Mental Health. Data that individuals choose to share to advance mental health.

Proper citation: BrainHealth Databank (RRID:SCR_022996) Copy   


https://sufuorg.com/home.aspx

Organization to optimize the care of women, men, and children with lower urinary tract dysfunction and/or pelvic floor disorders through education, research and involvement in health care policy. To improve the art and science of Urology through basic and applied clinical research in urodynamics and neurourology, voiding function and dysfunction, female urology and pelvic floor dysfunction, and to disseminate and teach these concepts.

Proper citation: Society of Urodynamics, Female Pelvic Medicine and Urogenital Reconstruction (SUFU) (RRID:SCR_022874) Copy   


https://labsyspharm.org/

Research and education program in Harvard Program in Therapeutic Science at Harvard Medical School to advance science and to develop technology needed to accelerate invention of new medicines and personalization of patient care. Used to study molecular causes of disease, ways drugs exert their therapeutic and adverse effects, design and interpretation of clinical trials.

Proper citation: Laboratory of Systems Pharmacology program (RRID:SCR_022873) Copy   


  • RRID:SCR_022918

    This resource has 1+ mentions.

https://www.pinnaclet.com/sleepPRO.html

Software tool to reduce scoring time and simplify data analysis. Offers automated power analysis, semi-automated scoring methods, and advanced tabular and graphical analysis for investigating sleep data sets. Custom scoring and analysis are also available. Scoring sessions between two or more users can be compared. All EEG/EMG and video data sets recorded with Pinnacle software, as well as third party EDF files, can be imported.

Proper citation: Sirenia Sleep Pro (RRID:SCR_022918) Copy   


  • RRID:SCR_023020

    This resource has 10+ mentions.

https://www.genoscope.cns.fr/brassicanapus/

Web tool as Brassica napus genome browser.

Proper citation: CNS Genoscope (RRID:SCR_023020) Copy   


  • RRID:SCR_022965

    This resource has 500+ mentions.

https://github.com/c-zhou/yahs

Software command line tool for construction of chromosome scale scaffolds from Hi-C data. Scaffolding tool using Hi-C or Omni-C data. Used to scaffold contig level assemblies into chromosome scale scaffolded assemblies.

Proper citation: YaHS (RRID:SCR_022965) Copy   


  • RRID:SCR_022980

    This resource has 1+ mentions.

https://www.iveindhoven.com/en/article/reichert-jung-ultracut-e-ultramicrotome/

Reichert Jung Ultracut E, article number 131-960, is used to cut ultrathin and semithin sections of resin embedded samples for electron microscopy.

Proper citation: Ultracut: E ultramicrotome (RRID:SCR_022980) Copy   


  • RRID:SCR_023031

https://www.gaitor.org

Software suite to analyse gait trials collected with Experimental Dynamic Gait Arena for Rodents. Used for rodent gait analysis.

Proper citation: GAITOR Suite (RRID:SCR_023031) Copy   


https://www.bertin-technologies.com/product/sample-preparation-homogenizers/precellys24-tissue-homogenizer/

The Precellys 24 homogenizer with automatic tube locking system with the ability to process up to 24 tubes simultaneously., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: Bertin Technologies: Precellys 24 tissue homogenizer (RRID:SCR_022979) Copy   


  • RRID:SCR_022973

    This resource has 1+ mentions.

https://www.emkatech.com/product/iox2-software/

Software tool to acquire, analyze, view, and store physiological data generated during preclinical experiment. Has library of application specific analysis modules for real time signal processing.

Proper citation: IOX2 (RRID:SCR_022973) Copy   


  • RRID:SCR_023028

    This resource has 1+ mentions.

https://www.inscopix.com/nvoke

Miniature microscope system that integrates in vivo cellular resolution calcium imaging with simultaneous or sequential optogenetic manipulation to causally link neural circuit activity with behavior.

Proper citation: iNSCOPIX: nVoke System (RRID:SCR_023028) Copy   


  • RRID:SCR_022972

https://open-brain-consent.readthedocs.io/en/stable/

Platform for informing research participants and obtaining consent to share brain imaging data. Provides suggested wording/templates for MRI studies human participant consent forms (including GDPR version), reference of tools for data anonymization, etc to make prospective data sharing possible.

Proper citation: Open Brain Consent (RRID:SCR_022972) Copy   


  • RRID:SCR_022859

https://labsyspharm.github.io/jekyll-tutorial/

Website tutorial for creating Jekyll-based scientific website, including editing in GitHub, working locally with Jekyll and applying Jekyll and Markdown formatting basics, and using custom themes.

Proper citation: Jekyll Tutorial (RRID:SCR_022859) Copy   


  • RRID:SCR_023125

https://data.4tu.nl/portal

International data repository for science, engineering and design. Services include curation, sharing, long-term access and preservation of research datasets. These services are available to anyone around the world. In addition, 4TU.ResearchData also offers training and resources to researchers to support them in making research data findable, accessible, interoperable and reproducible (FAIR).

Proper citation: 4TU.ResearchData (RRID:SCR_023125) Copy   


  • RRID:SCR_023123

    This resource has 10+ mentions.

https://github.com/im3sanger/dndscv

Software R package is group of maximum likelihood dN/dS methods designed to quantify selection in cancer and somatic evolution. Contains functions to quantify dN/dS ratios for missense, nonsense and essential splice mutations, at level of individual genes, groups of genes or at whole-exome level.Used to detect cancer driver genes on datasets ranging from few samples to thousands of samples, in whole-exome/genome or targeted sequencing studies.

Proper citation: dNdScv (RRID:SCR_023123) Copy   


  • RRID:SCR_023121

    This resource has 50+ mentions.

https://github.com/AlexandrovLab/SigProfilerExtractor/

Software tool for de novo extraction of mutational signatures from data generated in matrix format. Identifies number of operative mutational signatures, their activities in each sample, and probability for each signature to cause specific mutation type in cancer sample.

Proper citation: SigProfilerExtractor (RRID:SCR_023121) Copy   



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