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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 5 showing 81 ~ 100 out of 2,818 results
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  • RRID:SCR_010760

http://odin.mdacc.tmc.edu/~wwang7/FamSeqIndex.html

A computational tool for calculating probability of variants in family-based sequencing data.

Proper citation: FamSeq (RRID:SCR_010760) Copy   


  • RRID:SCR_010969

    This resource has 500+ mentions.

http://www.moleculardevices.com/Products/Software/GenePix-Pro.html

Industry standard microarray image analysis software because of its unique combination of imaging and analysis tools, visualizations, automation capabilities, performance and intuitive workflows.

Proper citation: GenePix Pro (RRID:SCR_010969) Copy   


  • RRID:SCR_010961

    This resource has 10+ mentions.

http://berry.engin.umich.edu/oligoarray2_1/

A free software that computes gene specific oligonucleotides for genome-scale oligonucleotide microarray construction.

Proper citation: OligoArray (RRID:SCR_010961) Copy   


  • RRID:SCR_010963

    This resource has 10+ mentions.

http://www.complex.iastate.edu/download/Picky/

A software tool for selecting optimal oligonucleotides (oligos) that allows the rapid and efficient determination of gene-specific oligos based on given gene sets, and can be used for large, complex genomes such as human, mouse, or maize.

Proper citation: Picky (RRID:SCR_010963) Copy   


  • RRID:SCR_010967

    This resource has 1+ mentions.

http://pbil.univ-lyon1.fr/roso/help.php

A software to design optimized oligonucleotide probes (size over 25 nucleotides) for microarrays.

Proper citation: ROSO (RRID:SCR_010967) Copy   


  • RRID:SCR_010858

    This resource has 10+ mentions.

http://www.cbrc.kaust.edu.sa/hmcan/

A Hidden Markov Model based software tool that is developed to detect histone modification in cancer ChIP-seq data.

Proper citation: HMCan (RRID:SCR_010858) Copy   


  • RRID:SCR_010852

    This resource has 100+ mentions.

http://www.cos.uni-heidelberg.de/index.php/n.ha

Software for detecting Co-Occurrence and Spatial Arrangement of Transcription Factor Binding Motifs in Genome-Wide Datasets.

Proper citation: COPS (RRID:SCR_010852) Copy   


  • RRID:SCR_010973

    This resource has 1000+ mentions.

http://www.illumina.com/software/genomestudio_software.ilmn

Visualize and analyze data generated by all of Illumina''s platforms.

Proper citation: GenomeStudio (RRID:SCR_010973) Copy   


  • RRID:SCR_010974

    This resource has 1000+ mentions.

http://www.bu.edu/jlab/wp-assets/ComBat/Abstract.html

Adjusting batch effects in microarray expression data using Empirical Bayes methods.

Proper citation: ComBat (RRID:SCR_010974) Copy   


  • RRID:SCR_010976

    This resource has 10+ mentions.

http://www.bioinformatics.polimi.it/MicroGen/

Software application package for a Minimum Information About Microarray Experiments (MIAME) compliant web-based information system for managing all the information completely characterizing spotted microarray experiments and the produced data.

Proper citation: MicroGen (RRID:SCR_010976) Copy   


  • RRID:SCR_010856

http://woldlab.caltech.edu/wiki/RNASeq#Dual-use_E-RANGE

A Python package for doing RNA-seq and ChIP-seq (hence the dual-use).

Proper citation: E-RANGE (RRID:SCR_010856) Copy   


  • RRID:SCR_010857

    This resource has 100+ mentions.

http://sourceforge.net/apps/mediawiki/vancouvershortr/index.php?title=FindPeaks

Software application that can be used for converting Eland, Maq (.map), BED or other files into WIG files and identifying areas of enrichment (ChIP-Seq analysis).

Proper citation: FindPeaks (RRID:SCR_010857) Copy   


  • RRID:SCR_010947

    This resource has 500+ mentions.

http://furlonglab.embl.de/methods/tools/coco

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on February 22, 2021.A computational tool that allows the user to search, visualise and store different data associated with gene expression.

Proper citation: CoCo (RRID:SCR_010947) Copy   


  • RRID:SCR_010945

    This resource has 10+ mentions.

http://www-ps.informatik.uni-tuebingen.de/mayday/wp/

Software providing a workbench for visualization, analysis and storage of microarray data. It features a graphical user interface and supports the development and integration of existing and new analysis methods. Besides the infrastructural core functionality, Mayday offers a variety of plug-ins, such as various interactive viewers, a connection to the R statistical environment, a connection to SQL-based databases, and different clustering methods, including phylogenetic methods. In addition, so-called meta information objects are provided for annotation of the microarray data allowing integration of data from different sources. This meta information can be used to enhance visualizations, such as in the enhanced heatmap visualization. Written in the Java programming language, Mayday is extremely portable and runs on all platforms supporting the Java runtime environment 1.6.

Proper citation: Mayday (RRID:SCR_010945) Copy   


  • RRID:SCR_010959

    This resource has 1+ mentions.

http://cran.r-project.org/web/packages/RPPanalyzer/index.html

A statistical tool developed to read reverse-phase protein array data, to perform the basic data analysis and to visualize the resulting biological information.

Proper citation: RPPanalyzer (RRID:SCR_010959) Copy   


  • RRID:SCR_010953

http://www.webcitation.org/query.php?url=http://psychiatry.igm.jhmi.edu/kaminsky/software.htm&refdoi=10.1186/1471-2105-14-76

A Perl based tool for the identification of differentially enriched regions in tiling microarray data.

Proper citation: BioTile (RRID:SCR_010953) Copy   


  • RRID:SCR_010955

    This resource has 1+ mentions.

http://www.rforge.net/IMA/

A software package designed to automate the pipeline for analyzing site-level and region-level methylation changes in epigenetic studies utilizing the 450K DNA methylation microarray.

Proper citation: IMA (RRID:SCR_010955) Copy   


  • RRID:SCR_010924

http://www.cs.ubc.ca/~sshah/acgh/

A software for detection of DNA copy number alterations (CNAs) from array comparative genomic hybridization (aCGH) data.

Proper citation: CNA-HMMer (RRID:SCR_010924) Copy   


  • RRID:SCR_010887

    This resource has 1+ mentions.

http://bioinformatics.bioengr.uic.edu/TFBSGroup/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 11, 2023. A Software program for Predicting Transcription Factor Binding Sites.

Proper citation: TFBSGroup (RRID:SCR_010887) Copy   


  • RRID:SCR_010920

    This resource has 1+ mentions.

http://www.softgenetics.com/CGHExplorer.html

An easy-to-use software tool for analyzing two color copy number alteration arrays from multiple platforms, including Agilent Technologies, Illumina, AffyMetrix, NimbleGen and others.

Proper citation: CGH Explorer (RRID:SCR_010920) Copy   



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