Open rowlandm opened 2 months ago
Create examples in database already and examples where you are "loading" it into the database.
create a single cell RNASeq counts file with genes in the rows and samples on the columns
create multiple fastq files for samples that have file names that aren't changed from the sequencer eg. AGRF or AGF.
One file per sample is WES T-N. Multiple samples per file is scRNASeq.