I get regular requests from collaborators to look if we have seen germline variants in a specific gene within our AFHCS or GA cohorts. I've created a 'Gene Search' analysis to have a quick look in our dataset: https://variantgrid.com/analysis/2466/
I always run into the issue that the rare variants are called in a somatic dataset (like the genomics collaboration one), as artefacts in 1 or 2 of the reads.
Would it be possible to exclude certain (somatic) projects/.vcfs in a gene search analysis?
Hi guys,
I get regular requests from collaborators to look if we have seen germline variants in a specific gene within our AFHCS or GA cohorts. I've created a 'Gene Search' analysis to have a quick look in our dataset: https://variantgrid.com/analysis/2466/
I always run into the issue that the rare variants are called in a somatic dataset (like the genomics collaboration one), as artefacts in 1 or 2 of the reads.
Would it be possible to exclude certain (somatic) projects/.vcfs in a gene search analysis?
Thanks! Peer