You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
thank you for your tool!
I used it according your manual so I have a txt file with mappability score for my reference genome (150,2)
Could I use the produced scores to filter my variants?
My data are whole exome sequencing I used bwa aligner and then I followed the instructions of GATK tool in order to produce a vcf file
I am little bit confused how I can use the mappability score to filter my variants
Any help would welcome!
Thanks a lot,
Maria
The text was updated successfully, but these errors were encountered:
Hallo,
thank you for your tool!
I used it according your manual so I have a txt file with mappability score for my reference genome (150,2)
Could I use the produced scores to filter my variants?
My data are whole exome sequencing I used bwa aligner and then I followed the instructions of GATK tool in order to produce a vcf file
I am little bit confused how I can use the mappability score to filter my variants
Any help would welcome!
Thanks a lot,
Maria
The text was updated successfully, but these errors were encountered: