Difference between revisions of "Syapse"

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m (Text replace - "ChIP-Seq" to "ChIP-seq")
 
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{{Bioinformatics application
 
{{Bioinformatics application
 
|sw summary=Syapse is a platform and application suite for bringing together omics and clinical data.
 
|sw summary=Syapse is a platform and application suite for bringing together omics and clinical data.
|bio domain=DNA transcription, DNA methylation, DNA-Seq, Indel detection,  SNP detection, Structural variation, RNA-Seq, ChIP-Seq, Comparative genomics, Transcriptomics, Epigenomics, Genomics, Population genetics, Regulatory genomics, Metagenomics
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|bio domain=DNA transcription, DNA methylation, DNA-Seq, Indel detection,  SNP detection, Structural variation, RNA-Seq, ChIP-seq, Comparative genomics, Transcriptomics, Epigenomics, Genomics, Population genetics, Regulatory genomics, Metagenomics
 
|bio method=Differential expression analysis, Exome analysis, Sequence analysis, Variant classification, Visualisation, Ontology comparison,
 
|bio method=Differential expression analysis, Exome analysis, Sequence analysis, Variant classification, Visualisation, Ontology comparison,
 
|bio tech=Any, Illumina, Ion Torrent, Affymetrix, Complete Genomics, Sanger,
 
|bio tech=Any, Illumina, Ion Torrent, Affymetrix, Complete Genomics, Sanger,

Latest revision as of 10:37, 11 January 2016

Application data

Created by Syapse
Biological application domain(s) DNA transcription, DNA methylation, DNA-Seq, Indel detection, SNP detection, Structural variation, RNA-Seq, ChIP-seq, Comparative genomics, Transcriptomics, Epigenomics, Genomics, Population genetics, Regulatory genomics, Metagenomics
Principal bioinformatics method(s) Differential expression analysis, Exome analysis, Sequence analysis, Variant classification, Visualisation, Ontology comparison
Technology Any, Illumina, Ion Torrent, Affymetrix, Complete Genomics, Sanger
Created at www.Syapse.com
Maintained? Yes
Input format(s) VCF
Software features API, Cloud Computing, GUI

Summary: Syapse is a platform and application suite for bringing together omics and clinical data.

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Description

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References

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