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| To facilitate clinical and translational research, we are developing caBench-to-Bedside (caB2B). caB2B will be used to query caGrid data services and will analyze this data using caGrid analytical services. In the first year, the scope of caB2B is confined to the query, analysis and visualization of microarray expression data. |
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caB2B: caB2B is a tool that allows research scientist to obtain the microarray data from caArray and associate it to the biospecimen information from caTissue.
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caTISSUE Core: A biospecimen inventory informatics system.
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| caTissue Core is a web-based biospecimen inventory and tracking tool that may be used by biospecimen resource facilities, regardless of the nature of biospecimen transactions that occur or the type of biospecimens involved in the transaction. In the next version of caTissue, it will support integration with associated free-text surgical pathology reports (SPR) and discrete clinical and pathology annotations |
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CIU: A tool to upload microarray experiments into our database.

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| CRS is developed to facilitate compatibility reviews by the Vocabularies and Common Data Elements (VCDE) and Architecture (ARCH) workspaces. Currently we are developing version 2.0 that will contain tools for compatibility self-checks by developers and reports that determine the true CDE reuse. |
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CRS: A tool to facilitate caBIGTM Architecture and Vocabularies and Common Data Elements compatibility reviews.
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| Function Express or FE- To analyze microarray expression data, FE allows end users to filter, normalize, cluster, and classify gene expression data. Available algorithms include Significance Analysis of Microarrays (SAM), k-means, hierarchical, and SOM clustering, GenePattern (Consensus Clustering, Comparative Marker Selection, and Weighted Voting), and R modules (SVM and PCA). FE will also allow end users to view gene networks created using co-expression, transcription factor binding site, pathway, interaction, and literature-based data |
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FE Client:Function Express provides data mining and rich visualization capabilities to view and analyze microarray data in the context of multiple publicly available gene annotation databases. details
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| Examine gene expression in the context of functional annotations such as biological processes or molecular functions from Gene Ontology, across different microarray experiments of one or more species. Filter genes on the basis of annotations or expression data. Cluster probesets /samples using different supervised / unsupervised clustering techniques.Export /import data to/from another analysis applications |
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FE Server: An automated microarray annotation system.
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GeneConnect: A caBIGTM compliant genomic identifier mapping service.
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LIMS: A management system to track proteomics experiments.
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| Mascot Viewer or MaV- To analyze proteomics data, MaV allows users to view a 'clickable' gel and to click on relevant spots to view consolidated (i.e. multiple mass spectrometry [MS] runs on one or more machines) MS and MS/MS results. |
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Mascot Search: An analytical tool to view
protein database search results.
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Mutation Viewer: A clinical resequencing pipeline.
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| Mutation Viewer or MuV- To analyze re-sequencing data. We are refining the MuV pipeline to allow users to design primers in high throughput using a web interface, to analyze sequence traces for mixed peaks and indels using multiple analytical tools, and to visualize mutation information in the context of genomic annotation (e.g. exon-intron boundaries, protein domains, and known SNPs). |
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Promoter Analysis Pipeline: A comprehensive workbench to identify transcription factor binding sites in mammalian genomes.
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| The Promoter Analysis Pipeline (PAP) is a web-based workbench for identifying transcription factor binding sites in a set of coexpressed genes in mammals. PAP is based on a statistical model which predicts the transcriptional factors and their regulatory targets in the genome using overrepresentation of binding profiles in promoter sequences. |
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Webtools: Web-based tools to download annotated microarray data, assign chip privileges, and browse gene annotation and expression information.
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