The Frontline Support team will be slow to respond December 17-18 due to an institute-wide retreat and offline December 22- January 1, while the institute is closed. Thank you for your patience during these next few weeks. Happy Holidays!
GenomicsDBImport and Strand Bias
in the joint-calling pdf, of the workshop with the number 1809, you explain why is important to use GenomicsDB, combine all samples (g.vcf)...
If I provide to my g.vcf files the strand bias information (SB) at the HaplotypeCaller level, then the downstream tools will use the SB information to filter my variants? If yes, at which level/tool? I have to add any special option?