There is an increasing number of next-generation sequencing based diagnostic assays are validated and enter into clinical practice in every yerar. Hundreds more are developed for pre-clinical research purposes. NGS applications being used in the clinic today include pre-implantation genetic screening (PGS) for in vitro fertilization, chromosomal aneuploidy detection, mutation analysis of patient samples, and sequence driven chemotherapeutics.
Comprehensive assays that identify single base substitutions and fusion events are commonly performed to establish a diagnosis or to help in deciding what drug treatment is best. While routine implementation of clinical NGS in oncology is still in it’s infancy, several assays are currently being performed in CLIA-certified environments: amplicon-based gene panels targeted capture based gene panels , full exome and transcriptome-seq, whole genome and RNA-seq Some patients are even being treated with drugs for off-label indications, based on NGS tests (of all chemotherapeutic prescriptions, 33-47% are off-label ). As assays are standardized and confirmed by orthogonal platforms, we expect see an increase in the number of these clinical applications.
NGS-based pre-implantation genetic screening has significantly changed prenatal testing and screening. Currently only ~ 25% of invitro-fertilization procedures are successful. This low rate of success is due to an increasing maternal age and chromosomal aneuploidy. PGS is performed to select chromosomally balanced embryos during the IVF process, ensuring only euploid embryos are implanted. This NGS based assay has been shown to improve implantation success rates and is being used in clinics today.
Non-invasive prenatal testing using cell-free fetal DNA circulating in maternal blood allows for the detection of genetic diseases and common chromosomal aneuploidies such as trisomies 13, 18, and 21. Fetal DNA, comprising about 10% of the DNA in maternal circulation becomes detectable between 5-10 weeks after conception. The method allows for an early assessment of aneuploidy without the risk of harming the fetus. Sequenom, Verinata Health, Ariosa Diagnostics and Natera each offer CAP and CLIA certified tests and are available at OB/GYN offices.
In November 2013, the FDA cleared the Illumina MiSeqDx platform as a class II device and a cystic fibrosis carrier screening assay. The assay detects 139 variants in the cystic fibrosis transmembrane conductance regulator gene (CFTR) gene.