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depending on your command line, if you use this 1000g file, then you need #76
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Iam getting only the intergenic region in my annovar ouptput file. Im newly using annovar tool. Please help |
If your input variants are intergenic variants, then output will be
intergenic as well.
You probably want to use ANNOVAR to annotate mutations first, making sure
that the correct genome coordinate is used, before using intervar.
…On Wed, Dec 29, 2021 at 8:53 AM Nanditha-shetty ***@***.***> wrote:
Iam getting only the intergenic region in my annovar ouptput file.
What is the reason for this?
I need to identify the missense variants. Is that any modification needed
in the commands for this issue
Im newly using annovar tool. Please help
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I have used the below commands. perl annotate_variation.pl -buildver hg38 -downdb -webfrom annovar refGene humandb/ perl annotate_variation.pl -buildver hg38 -downdb genomicSuperDups humandb/ perl annotate_variation.pl -buildver hg38 -downdb -webfrom annovar dbnsfp42a humandb/ perl annotate_variation.pl -buildver hg38 -downdb -webfrom annovar esp6500siv2_all humandb/ perl annotate_variation.pl -buildver hg38 -downdb -webfrom annovar avsnp150 humandb/ perl annotate_variation.pl -buildver hg38 -downdb -webfrom annovar 1000g2015aug_all humandb/ perl table_annovar.pl new.avinput humandb/ -buildver hg38 -out myanno -remove -protocol refGene,cytoBand,dbnsfp30a,genomicSuperDups,esp6500siv2_all,1000g2015aug_all -operation g,r,f,r,f,f -nastring . -csvout -polish -xreffile example/gene_fullxref.txt |
depending on your command line, if you use this 1000g file, then you need
to install ANNOVAR and then download this file from ANNOVAR.
On Fri, Dec 24, 2021 at 1:23 AM Nanditha-shetty @.***>
wrote:
Originally posted by @kaichop in #75 (comment)
The text was updated successfully, but these errors were encountered: