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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 96 showing 1901 ~ 1920 out of 2,279 results
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  • RRID:SCR_019103

    This resource has 10+ mentions.

https://www.bioconductor.org/packages/release/bioc/html/ensembldb.html

Software R package to create and use Ensembl based annotation resources.

Proper citation: ensembldb (RRID:SCR_019103) Copy   


  • RRID:SCR_018820

    This resource has 1+ mentions.

https://gitlab.com/biomerieux-data-science/clustlasso

Software R package to build predictive signatures of microbial phenotypes. Software package implementing cluster lasso approach.

Proper citation: clustLasso (RRID:SCR_018820) Copy   


  • RRID:SCR_018541

    This resource has 10+ mentions.

http://www.pyrosetta.org/

Interactive Python based interface to Rosetta molecular modeling suite. Stand alone Python based implementation of Rosetta molecular modeling package that allows users to write custom structure prediction and design algorithms using major Rosetta sampling and scoring functions.

Proper citation: PyRosetta (RRID:SCR_018541) Copy   


  • RRID:SCR_018507

    This resource has 100+ mentions.

https://qgis.org/en/site/

Open source cross platform desktop geographic information system application that supports viewing, editing, and analysis of geospatial data. Functions as geographic information system software, allowing users to analyze and edit spatial information, in addition to composing and exporting graphical maps.

Proper citation: QGIS (RRID:SCR_018507) Copy   


  • RRID:SCR_018915

    This resource has 100+ mentions.

https://github.com/big-data-lab-team/spot

Open source software tool for file based localization of numerical perturbations in data analysis pipelines. Identifies components in pipeline, at resolution level of system process, that produce different results in different execution conditions.

Proper citation: Spot (RRID:SCR_018915) Copy   


https://cran.r-project.org/web/packages/GALLO/vignettes/GALLO.html

Software R package developed for accurate annotation of genes and quantitative trait loci located in regions identified in common genomic analyses performed in livestock, such as Genome Wide Association Studies and transcriptomics using RNA-Sequencing. Allows graphical visualization of gene and QTL annotation results, data comparison among different grouping factors like methods, breeds, tissues, statistical models, studies and QTL enrichment in different livestock species including cattle, pigs, sheep, and chickens.

Proper citation: Genomic Annotation in Livestock for positional candidate LOci (RRID:SCR_019212) Copy   


  • RRID:SCR_018881

    This resource has 1+ mentions.

https://github.com/SMI/SmiServices

Software suite of tools for cataloguing and anonymising DICOM files, as used for Scottish Medical Imaging project. Software suite of microservices for loading, anonymising, linking and extracting large volumnes of dicom medical images to support medical research. Platform allows dicom tags extracted from clinical images to be loaded into MongoDB and relational database tables for purposes of generating anonymous linked research extracts including image anonymisation.

Proper citation: SMI Services (RRID:SCR_018881) Copy   


  • RRID:SCR_021744

    This resource has 10+ mentions.

https://cran.r-project.org/package=psych

Software R package for multivariate analysis and scale construction using factor analysis, principal component analysis, cluster analysis and reliability analysis.Procedures for Psychological, Psychometric, and Personality Research. Used for personality, psychometric theory and experimental psychology.

Proper citation: psych (RRID:SCR_021744) Copy   


  • RRID:SCR_021087

    This resource has 10+ mentions.

https://github.com/AdmiralenOla/Scoary

Software tool that scores components of pan genome for associations to observed phenotypic traits while accounting for population stratification, with minimal assumptions about evolutionary processes.Designed to take gene presence absence.csv file from Roary as well as traits file created by user and calculate associations between all genes in accessory genome and traits. It reports list of genes sorted by strength of association per trait.

Proper citation: Scoary (RRID:SCR_021087) Copy   


  • RRID:SCR_023977

http://bioinformatics.org/biococoa/

Open source framework for bioinformatics written in Objective-C. Provides Cocoa and GNUstep programmers with full suite of APIs for handling and manipulating biological sequences.

Proper citation: BioCocoa (RRID:SCR_023977) Copy   


  • RRID:SCR_023973

http://biblatex-biber.sourceforge.net/

Software bibliography processing backend for LaTeX biblatex package. Supports unsurpassed feature set for automated conformance to complex bibliography style requirements such as labelling, sorting and name handling. BibTeX replacement for users of BibLaTeX.

Proper citation: Biber (RRID:SCR_023973) Copy   


  • RRID:SCR_023965

http://johnhommer.com/academic/code/aghermann

Sotware tool designed to run Process S simulations on Slow Wave Activity profiles from human EEG recordings.Produces set of sleep homeostat parameters which can be used to describe and differentiate individual sleepers, such as short vs long sleepers, early vs late, etc.Sleep research experiment manager, with facility for reading, displaying, and manual and semi-automatic scoring EEG recordings in edf format; conventional PSD and EEG Microcontinuity profiles; artifact detection; Independent Component Analysis; basic sleep analysis NREM-REM cycle detection.

Proper citation: Aghermann (RRID:SCR_023965) Copy   


  • RRID:SCR_024056

https://metacpan.org/dist/Bio-ASN1-EntrezGene

Software regular expression based Perl Parser for NCBI Entrez Gene genome databases. Parses ASN.1-formatted Entrez Gene record and returns data structure that contains all data items from gene record.

Proper citation: Bio-ASN1-EntrezGene (RRID:SCR_024056) Copy   


  • RRID:SCR_024057

https://metacpan.org/dist/AcePerl

Software provides an interface to the ACEDB object-oriented database. Both read and write access is provided, and ACE objects are returned as similarly-structured Perl objects. Multiple databases can be opened simultaneously.

Proper citation: AcePerl (RRID:SCR_024057) Copy   


  • RRID:SCR_024335

    This resource has 10+ mentions.

https://odelaneau.github.io/shapeit4/

Software tool for estimation of haplotypes aka phasing for SNP array and high coverage sequencing data. The version 4 is refactored and improved version of SHAPEIT algorithm with multiple key additional features.

Proper citation: shapeit4 (RRID:SCR_024335) Copy   


  • RRID:SCR_023995

    This resource has 100+ mentions.

https://card.mcmaster.ca/

Comprehensive antibiotic resistance database. Bioinformatic database of resistance genes, their products and associated phenotypes.

Proper citation: CARD (RRID:SCR_023995) Copy   


  • RRID:SCR_024326

    This resource has 1+ mentions.

https://www.cs.cmu.edu/~ckingsf/software/sailfish/

Software tool that implements novel, alignment free algorithm for estimation of isoform abundances directly from set of reference sequences and RNA-seq reads.

Proper citation: sailfish (RRID:SCR_024326) Copy   


  • RRID:SCR_024206

    This resource has 1+ mentions.

https://github.com/fenderglass/Ragout/

Software tool for chromosome level scaffolding using multiple references. Given initial assembly fragments and one or multiple related references it produces chromosome scale assembly.

Proper citation: ragout (RRID:SCR_024206) Copy   


  • RRID:SCR_024066

    This resource has 1+ mentions.

https://metacpan.org/dist/Bio-SamTools

Software Perl interface to SamTools library for DNA sequencing.

Proper citation: Bio-SamTools (RRID:SCR_024066) Copy   


  • RRID:SCR_024341

    This resource has 1+ mentions.

https://github.com/ncbi/SKESA

Software de-novo sequence read assembler for microbial genomes.Designed to create breaks at repeat regions in the genome. This leads to excellent sequence quality without significantly compromising contiguity.SKESA contigs could be connected into GFA graph using GFA connector.

Proper citation: skesa (RRID:SCR_024341) Copy   



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