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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_018726

    This resource has 1+ mentions.

https://github.com/yanzhanglab/Graph2GO

Software tool as graph based representation learning method for protein function prediction. Multi modal graph based representation learning model that can integrate heterogeneous information including multiple types of interaction networks including sequence similarity network and protein-protein interaction network, and protein features including amino acid sequence, sub cellular location and protein domains, to predict protein functions on Gene Ontology.

Proper citation: Graph2GO (RRID:SCR_018726) Copy   


  • RRID:SCR_018735

    This resource has 1+ mentions.

http://www.pirx.com/iMol/index.shtml

Software molecular visualization application for Mac OS X operating system. Tool for chemists and molecular biologists used for handling small and large molecules, loading multiple molecules, moving and rotating them independently, or displaying molecular dynamics trajectory. Allows loading molecules using file formats: PDB, XYZ, MOL2, HIN, CAR, ALC, BIO.

Proper citation: iMol (RRID:SCR_018735) Copy   


  • RRID:SCR_018693

    This resource has 1+ mentions.

http://pinet-server.org

Web platform for downstream analysis and visualization of proteomics data. Server that facilitates integrated annotation, analysis and visualization of quantitative proteomics data, with emphasis on PTM networks and integration with LINCS library of chemical and genetic perturbation signatures in order to provide further mechanistic and functional insights. Primary input for server consists of set of peptides or proteins, optionally with PTM sites, and their corresponding abundance values.

Proper citation: piNET (RRID:SCR_018693) Copy   


  • RRID:SCR_018737

    This resource has 1000+ mentions.

https://cistrome.shinyapps.io/timer/

Web server for comprehensive analysis of tumor infiltrating immune cells. Web tool for systematical analysis of immune infiltrates across diverse cancer types. Allows users to input function specific parameters, with resulting figures dynamically displayed to access tumor immunological, clinical, and genomic features.

Proper citation: TIMER (RRID:SCR_018737) Copy   


  • RRID:SCR_018863

    This resource has 50+ mentions.

https://imspectordocs.readthedocs.io/en/latest/intro.html

Software tool for real time analysis and data visualization. Software system for experimental control and quantitative data analysis in microscopy and spectroscopy.Integration of data processing and acquisition allows real time analysis and visualization of experimental results.

Proper citation: Imspector (RRID:SCR_018863) Copy   


  • RRID:SCR_018901

    This resource has 10+ mentions.

https://www.repetier.com/

Open source 3D printing software which supports multi part printing and has slicers.

Proper citation: Repetier Host (RRID:SCR_018901) Copy   


  • RRID:SCR_018707

    This resource has 10+ mentions.

https://rvista.dcode.org/

Web tool for analyzing regulatory potential of noncoding sequences. rVISTA web server is interconnected with TRANSFAC database, allowing users to either search for matrices present in TRANSFAC library collection or search for user defined consensus sequences. rVISTA 2.0 web server is used for high throughput discovery of cis-regulatory elements. Can process alignments generated by zPicture and blastz alignment programs or use pre-computed pairwise alignments of several vertebrate genomes available from ECR Browser and GALA database. Evolutionary analysis of transcription factor binding sites.

Proper citation: rVista (RRID:SCR_018707) Copy   


  • RRID:SCR_018831

    This resource has 1+ mentions.

https://github.com/viromelab/tracespipe

Software tool as hybrid pipeline for reconstruction and analysis of viral and host genomes at multi-organ level. Pipeline for identification, assembly, and analysis of viral genomes, that combine DNA sequence data from multiple organs. Cooperation between compression based prediction, sequence alignment, and de-novo assembly. Provides transmission and storage of data.

Proper citation: TRACESPipe (RRID:SCR_018831) Copy   


https://github.com/TMinchington/sass

Software tool as custom analysis code combining single-cell traces and spot detection from live imaging movies and using Imaris output.

Proper citation: Simple Assignment of Spots to Surfaces (RRID:SCR_018797) Copy   


  • RRID:SCR_018711

    This resource has 1+ mentions.

http://funcoup.sbc.su.se/search/

Database of genome wide functional coupling networks. Provides tools to explore predicted networks and to retrieve detailed information about data underlying each prediction. Web service for functional coupling search.

Proper citation: FunCoup (RRID:SCR_018711) Copy   


  • RRID:SCR_018716

    This resource has 1+ mentions.

https://github.com/GGFHF/NGScloud2

Software tool for RNA-seq analysis of non model species using cloud computing. Provides user friendly front end to operate Amazon hardware resources and to control workflows of bioinformatic analysis of de novo RNA-seq, reference-based RNA-seq and functional annotation specifically oriented to plant species.

Proper citation: NGScloud2 (RRID:SCR_018716) Copy   


  • RRID:SCR_018720

    This resource has 100+ mentions.

http://www.consort-statement.org/

Standards for transparent trials reporting. Encompasses various initiatives developed by CONSORT Group to alleviate problems arising from inadequate reporting of randomized controlled trials. Main product of CONSORT is CONSORT Statement, which is evidence based, minimum set of recommendations for reporting randomized trials. CONSORT Statement is endorsed by medical journals and leading editorial organizations.

Proper citation: CONSORT (RRID:SCR_018720) Copy   


  • RRID:SCR_018685

    This resource has 100+ mentions.

https://cole-trapnell-lab.github.io/monocle3/

Software analysis toolkit for single cell RNA-seq. Used for single cell RNA-Seq experiments. Unsupervised algorithm that increases temporal resolution of transcriptome dynamics using single-cell RNA-Seq data collected at multiple time points.

Proper citation: Monocle3 (RRID:SCR_018685) Copy   


  • RRID:SCR_018967

    This resource has 50+ mentions.

http://dgenies.toulouse.inra.fr/

Open source software package developed in Python and JavaScript. Standalone and web application tool performing large genome alignments and generating interactive dot plots. Designed to compare two genomes. Used to sort query sequences along reference, zoom in plot and download several image, alignment or sequence files. Allows to display dot plots from other aligners by uploading their PAF or MAF alignment file.

Proper citation: D-GENIES (RRID:SCR_018967) Copy   


  • RRID:SCR_018724

    This resource has 1+ mentions.

https://www.mbfbioscience.com/microfileplus

Software tool as microscopy image file format converter by MBF Bioscience. Converts common microscopy image files to JPEG2000 and OME-TIFF. Used to view, analyze, and share big image data from many sources.

Proper citation: MicroFilePlus (RRID:SCR_018724) Copy   


  • RRID:SCR_018805

    This resource has 100+ mentions.

https://robetta.bakerlab.org/

Web tool as protein structure prediction service. Provides automated structure prediction and analysis tools that can be used to infer protein structural information from genomic data. Produces model for entire protein sequence in presence or absence of sequence homology to protein of known structure.

Proper citation: Robetta (RRID:SCR_018805) Copy   


  • RRID:SCR_018804

    This resource has 100+ mentions.

http://protein.ict.ac.cn/FALCON/

Web tool as high throughput protein structure prediction service. High throughput server for protein structure prediction.

Proper citation: FALCON (RRID:SCR_018804) Copy   


  • RRID:SCR_018925

    This resource has 10+ mentions.

https://support.10xgenomics.com/genome-exome/software/pipelines/latest/what-is-long-ranger

Software tool as set of analysis pipelines that processes Chromium sequencing output to align reads and call and phase SNPs, indels, and structural variants by 10x Genomics.

Proper citation: Long Ranger (RRID:SCR_018925) Copy   


  • RRID:SCR_018807

    This resource has 10+ mentions.

https://somapp.ucdmc.ucdavis.edu/pharmacology/bers/maxchelator/webmaxc/webmaxcE.htm

Web tool for computing metal ion concentrations in physiological solutions. Used for determining free metal concentration in presence of chelators or total metal given desired free concentration.

Proper citation: WEBMAXC EXTENDED (RRID:SCR_018807) Copy   


  • RRID:SCR_018775

    This resource has 1+ mentions.

http://150.146.2.1/C-IMMSIM/

Web prediction tool for molecular binding in simulation of immune system. Agent based simulator of immune response that represents pathogens, as well as lymphocytes receptors, by means of their amino acid sequences and makes use of bioinformatics methods for T and B cell epitope prediction.Calculates immune response to generic pathogenic secondary structure. Allows users to submit antigen protein sequence and specify schedule of its injection as well as host haplotype.

Proper citation: C-IMMSIM (RRID:SCR_018775) Copy   



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