Entering edit mode
2.9 years ago
vpsev3
▴
20
Hello,
I would like to know if a 30X human genome sequencing with a "high-throughput MGI DNBSEQ-T7" machine presents good quality?
Approximately, how many false calls will there be in my genome?
Thank you.
What you are looking to do? If you are looking for calling SNP's then that should be adequate.
I intend to compare it with all the sequences in the ClinVar database referenced as pathogenic, and look for indel / duplications in my genome