The invention provides a phosphorylated probe capture amplification method. The method comprises the following steps: hybridizing a phosphorylated probe to
genome DNA to form a
hybridization probe, extending and connecting the
hybridization probe to form a
closed loop by using a bridging primer to form a
closed loop PCR product, and carrying out PCR amplification on the obtained PCR product to obtain an amplified product which is an enriched target area. According to the application,
phosphorylation is carried out by taking the probe as a skeleton, a sequence on an Illumina Tru Seq joint and a bridged complementary sequence are added, by adopting a mode of increasing primer bridging, products after probe amplification are connected end to end to form cyclization, and by adopting a mode of increasing EXO1 / EXO3
enzyme digestion, the formation of a
dimer is reduced, so that the detection sensitivity is improved, and the detection sensitivity is improved. According to the invention, small-volume hybridization and small-volume amplification
modes are adopted, so that the molecular
collision probability is increased. The method has ultrahigh specificity and accuracy, each
target site is independently amplified, the PCR preference is avoided, the coverage uniformity is superior to that of multiple PCR and
hybrid capture, the operation is simple and convenient, the period is short, and the experimental process only needs several hours.