Entering edit mode
7.9 years ago
manojkumarbioinfo
▴
100
Hi,
I would like to know is there any available Scripts or Tools based on Support Vector Machine (SVM) for filtering the variants from NGS data if there is any tool or code can you tell me.
Thanking you.
But VQSR is only used for identify the quality for the variants. but i want to have something different if you check the bcbio they are having a own pipeline where they use some SVM classifier for filtering the variants i need a tool like that the main thing is i dont want their full pipeline i just need the SVM for filtering the variants. https://bcbio.wordpress.com/tag/clinical/