Use ANNOVAR to annotate SNPs
0
1
Entering edit mode
6.7 years ago
zhang248 ▴ 40

I am using ANNOVAR to annotate WGS SNPs with default parameters, and I get two output files, variant_function and exonic_variant_function. The variant_function file contain "downstream,exonic,intergenic,intronic,ncRNA_exonic,splicing,upstream,UTR3,UTR5" and I know the exonic_variant_function file has more detailed annotation for exonic, "synonymous,nonsynonymous,stopgain,stoploss,unknown". Then I change the parameter "-precedence", make "ncRNA" be the last one, and now the output contain "downstream,exonic,intergenic,intronic,splicing,upstream,UTR3,UTR5", the "ncRNA_exonic" are annotated to be "exonic".

My question is when I change the "-precedence", the exonic_variant_function has no change, it's the same as before. I want to know how can I make the exonic_variant_function file contain the added "exonic". Any suggestion is appreciated. Thank you very much in advance.

SNP genome • 2.2k views
ADD COMMENT

Login before adding your answer.

Traffic: 1034 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6