Open ShuqingL opened 5 years ago
Hi authors!
I now have 8 samples, each of which have single-cell RNA sequencing and bulk RNA sequencing. Can I prepare the VCF file by comparing the data of bulk RNASeq data with the reference genome? (eg: GATK alignment)
Hi authors!
I now have 8 samples, each of which have single-cell RNA sequencing and bulk RNA sequencing. Can I prepare the VCF file by comparing the data of bulk RNASeq data with the reference genome? (eg: GATK alignment)