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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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On page 44 showing 861 ~ 880 out of 997 results
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  • RRID:SCR_018983

    This resource has 1+ mentions.

http://had.co.nz/reshape/

Software R package for flexibly restructuring and aggregating data.

Proper citation: reshape (RRID:SCR_018983) Copy   


  • RRID:SCR_018980

    This resource has 10+ mentions.

http://annotree.uwaterloo.ca/

Web tool for visualization of genome annotations across large phylogenetic trees.Used for visualization and exploration of functionally annotated microbial tree of life. Integrates taxonomic, phylogenetic and functional annotation data from bacterial and archaeal genomes.

Proper citation: Annotree (RRID:SCR_018980) Copy   


  • RRID:SCR_019093

    This resource has 1+ mentions.

http://easybioai.com/sc2disease/

Manually curated database of single cell transcriptome for human diseases. scRNA-seq database derived from numerous human studies. Provides researchers with encyclopedia of biomarkers at level of genes, cells, and diseases.

Proper citation: SC2diseases (RRID:SCR_019093) Copy   


  • RRID:SCR_019018

    This resource has 1+ mentions.

https://github.com/auranic/ClinTrajan

Software Python package for analysis of trajectories in clinical datasets.

Proper citation: ClinTrajAn (RRID:SCR_019018) Copy   


  • RRID:SCR_019078

    This resource has 100+ mentions.

https://cftr2.org/

International initiative led by team of researchers and clinicians and supported by the US Cystic Fibrosis Foundation that seeks to provide complete, advanced and expert reviewed functional and clinical information on CFTR mutations. Provides information for patients, researchers, and general public about specific variants. For each variant or variant combination included in database, website will provide information about whether variant or variant combination is CF-causing, and information about sweat chloride, lung function, pancreatic status, and Pseudomonas infection rate in patients in CFTR2 database with this variant or variant combination.

Proper citation: CFTR2 (RRID:SCR_019078) Copy   


  • RRID:SCR_019058

    This resource has 1+ mentions.

https://github.com/ShaokunAn/D-EE

Software tool for distributed dimensionality reduction and visualization. Distributed software for visualizing intrinsic structure of large scale single cell data written in C language. Its distributed storage and distributed computation technique allows efficiently analyze large scale single cell data at cost of constant time speedup.

Proper citation: D-EE (RRID:SCR_019058) Copy   


  • RRID:SCR_019270

    This resource has 1+ mentions.

https://www.axionbiosystems.com/products/software/neural-module

Neural Module by Axion BioSystems Inc, provides simplified approach to set up, execution and analysis of neural experiments. Enables Maestro Pro and Edge to record and analyze key parameters of neural network function, including activity, synchrony, and network oscillations.

Proper citation: Neural Module (RRID:SCR_019270) Copy   


  • RRID:SCR_019157

    This resource has 10+ mentions.

http://incelldownload.gehealthcare.com/bin/download_data/SoftWoRx/7.0.0/SoftWoRx.htm

Software for acquisition, deconvolution, processing, analysis, and display of DeltaVision images. Used in DeltaVision OMX SR imaging system., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025.

Proper citation: SoftWoRx software (RRID:SCR_019157) Copy   


http://www.nitrc.org/projects/dcl_model/

Software tool as deep collaborative learning with application to study of multimodal brain development. Uses deep network to represent original data and then seeks their correlations, while also linking data representation with phenotypical information.

Proper citation: Deep Collaborative Learning (RRID:SCR_019258) Copy   


  • RRID:SCR_019193

    This resource has 50+ mentions.

https://github.com/constantAmateur/SoupX

Software R package for estimation and removal of cell free mRNA contamination in droplet based single cell RNA-seq data.

Proper citation: SoupX (RRID:SCR_019193) Copy   


  • RRID:SCR_019236

https://github.com/datatagsuite

Software suite to enable discoverability of datasets. Enables submission of metadata on datasets to DataMed. Has core set of elements, which are generic and applicable to any type of dataset, and extended set that can accommodate more specialized data types. Platform independent model developed by NIH BD2K bioCADDIE project for DataMed Data Discovery Index prototype being developed. Also available as annotated serialization in schema.org, which in turn is widely used by major search engines like Google, Microsoft, Yahoo and Yandex.

Proper citation: DatA Tag Suite (RRID:SCR_019236) Copy   


  • RRID:SCR_019162

    This resource has 10+ mentions.

http://www.bionet.nsw.gov.au/

Repository for biodiversity data products managed by Department of Planning, Industry and Environment, New South Wales, Australia. It stores species sightings, systematic surveys, threatened biodiversity records and species names.

Proper citation: NSW BioNet (RRID:SCR_019162) Copy   


  • RRID:SCR_015987

    This resource has 100+ mentions.

https://github.com/pezmaster31/bamtools/wiki

Software that provides both a C++ API and a command-line toolkit for reading, writing, and manipulating genome sequence alignment files in the BAM and SAM formats. It is used for research analysis and management of data produced by sequencing technologies.

Proper citation: Bamtools (RRID:SCR_015987) Copy   


  • RRID:SCR_015994

    This resource has 1+ mentions.

http://www.sanger.ac.uk/science/tools/seqtools

Software for sequence alignments that displays multiple match sequences aligned against a single genomic reference sequence. It can be used for manipulation, display and annotation of genomic data, to check the quality of an alignment, to find missing/misaligned sequence, and to identify splice sites and polyA sites.

Proper citation: Blixem (RRID:SCR_015994) Copy   


  • RRID:SCR_016015

https://github.com/ABCD-STUDY/auto-scoring

Visualization software that calculates derived scores for the electronic record system REDCap (Research Electronic Data Capture) to build and manage online surveys and databases. Used in the ABCD-STUDY (Adolescent Brain Cognitive Development - STUDY) report framework.

Proper citation: auto-scoring (RRID:SCR_016015) Copy   


  • RRID:SCR_016018

https://github.com/ABCD-STUDY/little-man-task

Software tool to manage data and derived results. It is used for import of derived measures into REDCap (Research Electronic Data Capture).

Proper citation: little-man-task (RRID:SCR_016018) Copy   


  • RRID:SCR_016019

https://github.com/ABCD-STUDY/redcap-completion

Software to measure item level completion in a large REDCap project. It provides a web-interface to review data and it is used in the ABCD project to assess data collection sites for the reached level of completion.

Proper citation: redcap-completion (RRID:SCR_016019) Copy   


  • RRID:SCR_016026

https://github.com/ABCD-STUDY/aux-file-upload

Software application to upload functional MR imaging runs produce auxilary data that can be collected centrally. Connects to a subject database research electronic data capture (REDCap).

Proper citation: aux-file-upload (RRID:SCR_016026) Copy   


  • RRID:SCR_016024

    This resource has 1+ mentions.

https://github.com/ABCD-STUDY/FIONA-QC-PHANTOM

Software for online quality control operations performed on Phantom MRI data. It checks the accuracy and reproducibility of data.

Proper citation: FIONA-QC-PHANTOM (RRID:SCR_016024) Copy   


https://github.com/ABCD-STUDY/nih-ipad-app-end-point

Data collection software for centrally and securely storing data from the NIH iPad application. It allows users to capture results from multiple iPads at a central location.

Proper citation: nih-ipad-app-end-point (RRID:SCR_016029) Copy   



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