Additional file 1: of Targeted next generation sequencing as a tool for precision medicine
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Table S1. Genomic coordinates of PGxSeq capture probe design. Table S2. Known promoter and intronic SNVs targeted in PGxSeq panel. Table S3. Polymerase chain reaction conditions and primers used for Sanger sequencing of rare NGS variants. Table S4. TaqMan assay ID for the validated clinically relevant SNVs. Table S5. Concordance of rare variation in select genes by Sanger sequencing. Table S6. Characterization of unique variants identified by PGxSeq in 235 Caucasian subjects. (XLSX 298 kb)
创建时间：
2019-06-03
