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Thread | Thread Starter | Forum | Replies | Last Post |
intersect VCF files | adrian | Bioinformatics | 8 | 02-20-2014 12:36 PM |
1000 Genomes VCF Files | ashkot | Bioinformatics | 8 | 02-25-2013 02:12 PM |
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merging VCF files | kjaja | Bioinformatics | 2 | 12-20-2011 06:50 AM |
failed annotating the example vcf file in the installation folder of VCFtools | jianfeng.mao | Bioinformatics | 0 | 01-06-2011 05:23 AM |
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#1 |
Member
Location: United States Join Date: Jun 2011
Posts: 36
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Can anybody tell me how to annotate vcf files for hg19 aligned file? I tried GATK, vcftools and vcfCodingSnps.
GATK - I couldn't find their refGene file in their ftp server ftp://gatk-ftp:PH5UH7Pa@ftp.broadinstitute.org vcftools: I am having a hard time running it - it gives me "tabix" error vcfCodingSnps: I was not able to compile on my mac - OS X 10.6, 64 bit It will be great if anybody can give me a complied code for this architecture. Thanks. |
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#2 |
Member
Location: Sweden Join Date: Jan 2011
Posts: 12
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Maybe, try this one:
ftp://gatk-ftp:PH5UH7Pa@ftp.broadinstitute.org/refGene/ |
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#3 |
Senior Member
Location: Graz, Austria Join Date: Feb 2010
Posts: 219
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try annovar:
http://www.openbioinformatics.org/annovar/ |
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#4 | |
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Location: United States Join Date: Jun 2011
Posts: 36
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#5 | |
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Location: United States Join Date: Jun 2011
Posts: 36
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#6 | |
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Location: United States Join Date: Jun 2011
Posts: 36
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#7 |
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Location: Bonn Join Date: Feb 2010
Posts: 30
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You might also want to try www.gene-talk.de . It is an wiki-like expert platform for filtering and annotating sequence variants. The automatic annotation is based on annovar. For the interpreation of unkown variants other expert users might assist you,...
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#8 |
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Location: Taiwan Join Date: Feb 2011
Posts: 19
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Alternatively, direct upload your vcf to MegaQuery of VarioWatch (http://genepipe.ncgm.sinica.edu.tw/v...n.do?mega=true) should receive your results online in real time.
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