Hi everyone,
I have a basic question around the terminology of 'CNV calling'. Is CNV calling the same as CNV identification per se? If so, what is a CNV call data set?
Thank-you!
I have several whole-exome sequencing (WES) samples sequenced by pair-end (PE) and single-end (SE): 2 patient samples and 5 normal population samples, which were prepared …
CNV calling and detection/identification of CNVs is the same. What do you mean by CNV call data set? can you put it in a context?