Version 9 (modified by 14 years ago) (diff) | ,
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AnnotateVarianListFileViaSeattleSeqAnnotation
Annotate Files with Variants through Seattle Seq Annotation: http://gvs.gs.washington.edu/SeattleSeqAnnotation/ . The java code that wraps the forms is provided from SeattleSeq? Annotation: http://gvs.gs.washington.edu/SeattleSeqAnnotation/SubmitSeattleSeqAnnotationAutoJob.java . This method wraps the wrapper(..) and provides a python implementation. In order to run there should be a directory under the current path, named "jars" with the following jar files:
- httpunit.jar
- js-1.6R5.jar
- junit-3.8.1.jar
- nekohtml-0.9.5.jar
- xercesImpl-2.6.1.jar
Parameters
For a complete list of parameters please check the Annotation website and the example below
Example
Code highlighting:
AnnotateVarianListFileViaSeattleSeqAnnotation( inputFile=/Users/alexandroskanterakis/Data/SNP/chr1.snp.Q20.gff, outputFile=/Users/alexandroskanterakis/Tools/annotation/seattleseqannotation/output.txt, eMail=alexandros.kanterakis@gmail.com, fileFormat=GFF, geneData=CCDS2008, allelesMaq=true, allelesDBSNP=true, scorePhastCons=true, scorePhastCons=true, consScoreGERP=true, chimpAllele=true, CNV=true, geneList=true, HapMapFreqType=HapMapFreqMinor, geneList=true, hasGenotypes=true, dbSNPValidation=true, repeats=true, geneList=true, proteinSequence=true, polyPhen=true, clinicalAssociation=true )
Source Code
Pipeline Elements
This section will describe all parts of our annotation pipeline, the scripts have, and the features it will return.
script | feature | description | source |
1KGannotation.py | alleleFreq | allele freq in 1KG | 1KG |
TODO | |||
End of Pipeline
Related work
Attachments (2)
-
AnnotateIntersectionOverview.zip (760.6 KB) - added by 14 years ago.
Netbeans project for Annotation tool
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lib.zip (693.7 KB) - added by 14 years ago.
lib for AnnotateIntersectionOverview?
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