Method and system for NGS calibration of lung cancer targeted drug and chemotherapy drug genomes by DNA and RNA double library construction
A DNA library and genome technology, applied in the field of gene sequencing, can solve the problems of low detection efficiency, inability to detect genetic variation, and high detection cost
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[0079] Such as figure 1 The method shown here provides a DNA and RNA dual library construction method for NGS calibration of the genome of lung cancer targeted drugs and chemotherapy drugs: by directly amplifying the genes of known mutation sites and then building a library, and performing NGS sequencing detection, Combined with bioinformatics analysis to determine and verify the existence of the mutant gene; specifically include the following steps:
[0080] S1: Nucleic acid extraction: extract DNA according to "FFPE Tissue Genomic DNA Extraction Standard Operating Procedure", extract RNA according to "Tissue RNA Extraction Standard Operating Procedure", and measure the concentration of DNA / RNA;
[0081] The concentration operating method of described measuring DNA / RNA is: use dsDNA / RNA HS Assay Kit ( dsDNA / RNA High Sensitivity Kit) and 3.0 Fluorometer to measure the DNA / RNA concentration, the specific operation is as follows:
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