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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 316 showing 6301 ~ 6320 out of 26,943 results
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  • RRID:SCR_024028

https://github.com/gpertea/gclib

Software genomic C++ library of reusable code for bioinformatics projects.Provides core collection of data structures, trying to avoid unnecessary code dependencies of other heavy libraries, while minimizing build time.

Proper citation: GCLib (RRID:SCR_024028) Copy   


  • RRID:SCR_023988

    This resource has 1+ mentions.

https://github.com/dutilh/CAT

Software pipeline for taxonomic classification of contigs and metagenome-assembled genomes. Contig Annotation Tool and Bin Annotation Tool for the taxonomic classification of long DNA sequences and metagenome assembled genomes of both known and unknown microorganisms, as generated by contemporary metagenomics studies.

Proper citation: CAT and BAT (RRID:SCR_023988) Copy   


  • RRID:SCR_024097

https://github.com/RoelofBerg/limereg

Open source commandline based application and/or software development library, that performs 2D, rigid image registration on two greyscale images and outputs either the transformation parameters or the registered image.

Proper citation: limereg (RRID:SCR_024097) Copy   


  • RRID:SCR_024131

https://neobio.sourceforge.net/

Software library of sequence alignment algorithms implemented in Java.

Proper citation: NeoBio (RRID:SCR_024131) Copy   


  • RRID:SCR_024132

http://murasaki.dna.bio.keio.ac.jp/wiki/

Software language-theory based homology detection tool across multiple large genomes.

Proper citation: Murasaki (RRID:SCR_024132) Copy   


  • RRID:SCR_024136

    This resource has 10+ mentions.

https://www.ncbi.nlm.nih.gov/books/NBK179288/

Software provides access to NCBI's suite of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from Unix terminal window. Search terms are entered as command-line arguments. Individual operations are connected with Unix pipes to construct multi-step queries. Selected records can then be retrieved in variety of formats.

Proper citation: Entrez Direct (RRID:SCR_024136) Copy   


  • RRID:SCR_024137

    This resource has 1+ mentions.

https://doua.prabi.fr/software/njplot

Software tool as tree drawing program to draw any phylogenetic tree expressed in Newick phylogenetic tree format (e.g., the format used by the PHYLIP package).Used for rooting the unrooted trees obtained from parsimony, distance or maximum likelihood tree-building methods.

Proper citation: NJplot (RRID:SCR_024137) Copy   


  • RRID:SCR_024096

https://github.com/xdf-modules/libxdf

Software cross-platform C++ library for loading multimodal, multi-rate signals stored in XDF files. Used in biosignal viewing application SigViewer and the LSL application XDFStreamer. Can also be integrated into other C++ applications.

Proper citation: Libxdf (RRID:SCR_024096) Copy   


  • RRID:SCR_023437

    This resource has 1+ mentions.

https://robokop.renci.org/

ROBOKOP system consists of web based user interface, API server, and several worker servers. Biomedical knowledge graph that integrates and semantically harmonizes important knowledge sources. Contains nodes representing entities such as genes, chemicals, and diseases, and edges representing relationships between them. Abstraction layer and user interface for knowledge graphs to support question answering. Used for reasoning over structured biomedical knowledge databases as part of NCATS translator and reasoner programs. ROBOKOP Knowledge Graph Builder constructs KG and provides extensible framework to handle graph query over and integration of federated data sources.

Proper citation: ROBOKOP (RRID:SCR_023437) Copy   


  • RRID:SCR_024127

    This resource has 1+ mentions.

https://github.com/mroosmalen/nanosv

Software package that can be used to identify structural genomic variations in long-read sequencing data, such as data produced by Oxford Nanopore Technologies� MinION, GridION or PromethION instruments, or Pacific Biosciences RSII or Sequel sequencers.

Proper citation: NanoSV (RRID:SCR_024127) Copy   


  • RRID:SCR_024007

https://github.com/WorkflowConversion/CTDConverter

Software Python scripts to convert CTD files into other formats such as Galaxy, CWL.

Proper citation: CTDConverter (RRID:SCR_024007) Copy   


  • RRID:SCR_024128

    This resource has 100+ mentions.

https://github.com/wdecoster/NanoPlot

Software package as plotting tool for long read sequencing data and alignments.

Proper citation: NanoPlot (RRID:SCR_024128) Copy   


  • RRID:SCR_024141

    This resource has 10+ mentions.

https://pypi.org/project/OBITools/

Software package for analysing NGS data in DNA metabarcoding context. Used to filter and edit sequences while taking into account taxonomic annotation to set up tailor-made analysis pipelines for broad range of DNA metabarcoding applications, including biodiversity surveys or diet analyses.

Proper citation: OBITools (RRID:SCR_024141) Copy   


  • RRID:SCR_024022

    This resource has 1+ mentions.

https://freeimage.sourceforge.io/

Open Source software library for developers who would like to support popular graphics image formats like PNG, BMP, JPEG, TIFF and others as needed by today's multimedia applications.

Proper citation: FreeImage (RRID:SCR_024022) Copy   


  • RRID:SCR_024145

    This resource has 1+ mentions.

https://www.orthanc-server.com/

Open source lightweight DICOM server for medical imaging.Vendor neutral archive to automate and optimize imaging flows. Can be extended with plugins that provide solutions for teleradiology, digital pathology, or enterprise ready databases.

Proper citation: Orthanc (RRID:SCR_024145) Copy   


  • RRID:SCR_024026

    This resource has 1+ mentions.

https://github.com/bioinfo-ut/GenomeTester4

Software toolkit for performing set operations - union, intersection and complement on k-mer lists.

Proper citation: GenomeTester4 (RRID:SCR_024026) Copy   


  • RRID:SCR_024027

    This resource has 1+ mentions.

http://gdcm.sourceforge.net/

GDCM includes file format definition and network communications protocol, both of which should be extended to provide full set of tools for researcher or small medical imaging vendor to interface with existing medical database.Implementation of DICOM standard designed to be open source so that researchers may access clinical data directly.

Proper citation: GDCM (RRID:SCR_024027) Copy   


  • RRID:SCR_023848

    This resource has 1+ mentions.

https://github.com/brainglobe/bg-atlasapi

Software lightweight python module to interact with atlases for systems neuroscience. Provides consistent way to process brain atlas data from various sources.

Proper citation: BrainGlobe Atlas API (RRID:SCR_023848) Copy   


  • RRID:SCR_023964

    This resource has 50+ mentions.

https://github.com/nextstrain/augur

Software package to track evolution from sequence and serological data. Provides collection of commands which are designed to be composable into larger processing pipelines.

Proper citation: Augur (RRID:SCR_023964) Copy   


  • RRID:SCR_024017

https://github.com/tjhladish/EpiFire/wiki

Open source C++ library and application for contact network epidemiology. Application programming interface that models the spread of infectious disease in population and generates and manipulates networks of nodes and edges.

Proper citation: EpiFire (RRID:SCR_024017) Copy   



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