What do you usually use for QC using DNBseq?
I am used to analyse Illumina data and I recently got data from DNBseq... I have run FastQC but I am wondering if it is a good choice for this type of data... since this tool has been created for Illumina (or at least, it is what I have seen till now).
Does anybody use another tool for quality control for DNBseq data?
Any feedback will be really appreciated.
Thanks in advance
Regards
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If this is complete genomics data then there should be nothing special about it. FastQC should still be fine.
Sorry I forgot to mention that I was working with RNA-seq data. Would it be still fine?
(Cause complete genomics data =whole genome sequencing, right?) **Thanks very much for your reply!!!
Type of data should not matter. AFAIK DNBSeq data is still sanger encoded.