Support multiple applications: reproduction, genetics and cancer      

Reproduction and eugenics: preimplantation genetic diagnosis / screening (PGD / PGs)

Detection content: chromosome number abnormality, large deletion / duplication, single gene genetic disease of embryo

Detection significance: select normal embryo for transplantation, improve pregnancy rate, and achieve eugenics and eugenics.

One time detectable sample: 12-36 embryos

Detection of genetic diseases: gene screening for carriers of single gene genetic diseases

Detection content: detection of gene mutation of common single gene genetic diseases

Detection significance: to confirm the status of carriers of genetic diseases and provide guidance for eugenics and eugenics.

One time detectable samples: 3-24

Tumor: trusight ® tumor 15 solid tumor mutation detection

Detection content: 15 common genes in 7 solid tumors were detected

Detection significance: tumor risk and susceptibility assessment, guidance of drug use.

One time detectable samples

Miniseq highlights

Material benefits: the instrument and operation have price advantages, which are very suitable for your budget.

Simple: fully automatic button operation, process optimization to simple, no need to watch.

Accuracy: the principle of cluster generation and SBS sequencing of Illumina patent is accurate.

Extensive: widely support all kinds of DNA and RNA sequencing applications, easy project conversion.