The filtering parameters are currently fixed for all sample types. It has been raised by the QC working group that single-cell and single-nucleus, and different sequencing technologies produce different distributions of reads/counts and should have different cutoffs.
Its unclear where / how to impliment this. The full metadata tables should have complete context (STUDY tables)
The filtering parameters are currently fixed for all sample types. It has been raised by the QC working group that single-cell and single-nucleus, and different sequencing technologies produce different distributions of reads/counts and should have different cutoffs.
Its unclear where / how to impliment this. The full metadata tables should have complete context (STUDY tables)