Targeted next generation sequencing as a tool for precision medicine.

Markus GulilatTyler LambWendy A TeftJian WangJacqueline S DronJohn F RobinsonRommel G TironaRobert A HegeleRichard B KimUte I Schwarz

Published in: BMC medical genomics (2019)

PGxSeq can serve as a comprehensive, rapid, and reliable approach for the detection of common and novel SNVs in pharmacogenes benefiting the emerging field of precision medicine.

Keyphrases

loop mediated isothermal amplification
sensitive detection
cancer therapy
copy number
real time pcr
label free
circulating tumor
drug delivery
dna methylation
cell free