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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 119 showing 2361 ~ 2380 out of 2,818 results
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  • RRID:SCR_008184

    This resource has 50+ mentions.

https://github.com/eturro/mmseq#mmseq-transcript-and-gene-level-expression-analysis-using-multi-mapping-rna-seq-reads

Software package that contains a collection of statistical tools for analysing RNA-seq expression data.

Proper citation: MMSEQ (RRID:SCR_008184) Copy   


  • RRID:SCR_008308

    This resource has 1+ mentions.

https://igor.sbgenomics.com/

A cloud platform for next-generation sequencing analysis.

Proper citation: Seven Bridges Genomics (RRID:SCR_008308) Copy   


  • RRID:SCR_008320

    This resource has 1+ mentions.

http://epicenter.immunbio.mpg.de/services/chromos/

Combines genetic and epigenetic data to facilitate SNP classification, prioritization and prediction of their functional effect.

Proper citation: ChroMoS (RRID:SCR_008320) Copy   


  • RRID:SCR_008527

    This resource has 50+ mentions.

http://bioinfo-out.curie.fr/projects/vamp/

Software for visualization and Analysis of CGH arrays, transcriptome and other Molecular Profiles.

Proper citation: VAMP (RRID:SCR_008527) Copy   


  • RRID:SCR_008480

    This resource has 1000+ mentions.

http://www.bioconductor.org/packages/2.6/bioc/html/DEGseq.html

R package to identify differentially expressed genes from RNA-Seq data.

Proper citation: DEGseq (RRID:SCR_008480) Copy   


  • RRID:SCR_008493

    This resource has 1000+ mentions.

http://emboss.sourceforge.net/

Software analysis package for molecular biology community. Automatically copes with data in variety of formats and allows transparent retrieval of sequence data from web. Libraries are provided with package. Provides toolkit for creating bioinformatics applications or workflows. Provides set of sequence analysis programs. Provided programs cover areas such as sequence alignment, rapid database searching with sequence patterns, protein motif identification, nucleotide sequence pattern analysis, codon usage analysis for small genomes, rapid identification of sequence patterns in large scale sequence sets, and presentation tools for publication.

Proper citation: EMBOSS (RRID:SCR_008493) Copy   


  • RRID:SCR_008505

    This resource has 1000+ mentions.

http://www.who.int/en/

The directing and coordinating authority responsible for public health within the United Nations system. The WHO Regional Office for Europe (WHO/Europe) is one of the six regional offices around the world. It serves the WHO European Region, which comprises 53 countries from the Atlantic to the Pacific oceans. WHO/Europe collaborates with a range of public health stakeholders in the Region and globally, to ensure that coordinated action is taken to develop and implement efficient health policies and to strengthen health systems. WHO/Europe is made up of public health, scientific, and technical experts.

Proper citation: World Health Organization (RRID:SCR_008505) Copy   


  • RRID:SCR_008637

    This resource has 1000+ mentions.

http://lowelab.ucsc.edu/tRNAscan-SE

Web server to search for tRNA genes in genomic sequence. If you would like to run tRNAscan-SE locally, you can get the UNIX source code (gzip''d tar file).

Proper citation: tRNAscan-SE (RRID:SCR_008637) Copy   


  • RRID:SCR_008599

https://sites.google.com/site/drivermutationidentification/

Computational tool developed to help identify cancer-associated ''driver'' mutations from ''passenger'' ones in a cancer genome.

Proper citation: DMI (RRID:SCR_008599) Copy   


  • RRID:SCR_008653

    This resource has 5000+ mentions.

Ratings or validation data are available for this resource

http://www.ingenuity.com/products/pathways_analysis.html

A web-based software application that enables users to analyze, integrate, and understand data derived from gene expression, microRNA, and SNP microarrays, metabolomics, proteomics, and RNA-Seq experiments, and small-scale experiments that generate gene and chemical lists. Users can search for targeted information on genes, proteins, chemicals, and drugs, and build interactive models of experimental systems. IPA allows exploration of molecular, chemical, gene, protein and miRNA interactions, creation of custom molecular pathways, and the ability to view and modify metabolic, signaling, and toxicological canonical pathways. In addition to the networks and pathways that can be created, IPA can provide multiple layering of additional information, such as drugs, disease genes, expression data, cellular functions and processes, or a researchers own genes or chemicals of interest.

Proper citation: Ingenuity Pathway Analysis (RRID:SCR_008653) Copy   


  • RRID:SCR_008672

http://www.tutegenomics.com/

A robust, secure, medical-grade, web application that lives in the cloud and has the ability to analyze and annotate entire human genomes in a rapid and cost-effective way.

Proper citation: Tute Genomics (RRID:SCR_008672) Copy   


  • RRID:SCR_008671

    This resource has 1+ mentions.

http://homes.esat.kuleuven.be/~bioiuser/eXtasy/

A pipeline for ranking nonsynonymous single nucleotide variants given a specific phenotype.

Proper citation: eXtasy (RRID:SCR_008671) Copy   


  • RRID:SCR_008584

    This resource has 100+ mentions.

http://bg.upf.edu/condel/home

A method to assess the outcome of nonsynonymous SNVs using a consensus deleteriousness score that combines various tools (e.g. SIFT, Polyphen2, MutationAssessor).

Proper citation: Condel (RRID:SCR_008584) Copy   


  • RRID:SCR_008760

http://cran.r-project.org/web/packages/DWD/

This software package provides the implementation of distance weighted discrimination (DWD) using an interior point method for the solution of second order cone programming problems.

Proper citation: DWD (RRID:SCR_008760) Copy   


  • RRID:SCR_008818

    This resource has 1+ mentions.

http://cbil.upenn.edu/RUM/

An alignment, junction calling, and feature quantification pipeline specifically designed for Illumina RNA-Seq data.

Proper citation: RUM (RRID:SCR_008818) Copy   


  • RRID:SCR_003353

    This resource has 1+ mentions.

https://github.com/hangelwen/miR-PREFeR

An accurate, fast, and easy-to-use plant miRNA prediction software tool using small RNA-Seq data. It utilizes expression patterns of miRNA and follows the criteria for plant microRNA annotation to accurately predict plant miRNAs from one or more small RNA-Seq data samples of the same species.

Proper citation: miR-PREFeR (RRID:SCR_003353) Copy   


  • RRID:SCR_003343

    This resource has 1000+ mentions.

http://www.pictar.org

An algorithm for the identification of microRNA targets. Details are provided (3' UTR alignments with predicted sites, links to various public databases etc) regarding: # microRNA target predictions in vertebrates (Krek et al, Nature Genetics 37:495-500 (2005)) # microRNA target predictions in seven Drosophila species (Grn et al, PLoS Comp. Biol. 1:e13 (2005)) # microRNA targets in three nematode species (Lall et al, Current Biology 16, 1-12 (2006)) # human microRNA targets that are not conserved but co-expressed (i.e. the microRNA and mRNA are expressed in the same tissue) (Chen and Rajewsky, Nat Genet 38, 1452-1456 (2006)) co-expressed targets

Proper citation: PicTar (RRID:SCR_003343) Copy   


  • RRID:SCR_003347

    This resource has 1+ mentions.

https://github.com/bgruening/galaxytools/tree/master/workflows/blockclust

Software for efficient clustering and classification of non-coding RNAs from short read RNA-seq profiles.

Proper citation: BlockClust (RRID:SCR_003347) Copy   


  • RRID:SCR_003406

    This resource has 1+ mentions.

http://www.bioconductor.org/packages/release/bioc/html/EasyqpcR.html

Software package for low-throughput real-time quantitative PCR data analysis. The package allows you to import easily qPCR data files. Thereafter, you can calculate amplification efficiencies, relative quantities and their standard errors, normalization factors based on the best reference genes choosen (using the SLqPCR package), and then the normalized relative quantities, the NRQs scaled to your control and their standard errors.

Proper citation: EasyqpcR (RRID:SCR_003406) Copy   


  • RRID:SCR_003362

    This resource has 1000+ mentions.

https://planttfdb.gao-lab.org/

Comprehensive plant transcription factor database. Interface to allow users to search the database by IDs or free texts, to make sequence similarity search against TFs of all or individual species, and to download TF sequences for local analysis.PlantTFDB 3.0: a portal for the functional and evolutionary study of plant transcription factors

Proper citation: PLANTTFDB (RRID:SCR_003362) Copy   



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