CNV-seq Detection (Semiconductor Sequencing)

The detection kit, which is based on the BES 4000 platform, is used to perform
low-depth whole-genome sequencing of DNA. The sequencing results are compared
to the base sequence of the human reference genome, and CNVs in the tested
samples are discovered using bioinformatics analysis. It is often used to find
out why a woman keeps having miscarriages, find out what is wrong with an
abnormal fetus, and help with a prenatal diagnosis.

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