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Description

This amplicon was generated in a standard PCR reaction using N2 genomic DNA with the forward primer oPF388 (5 - ttgtccaataaacctttgtcc - 3) and reverse primer oPF389 (5 -tccatataaccctgtaactcc - 3) and sequenced verified using standard Sanger sequencing after PCR purification

[DOI] [PMC free article] [PubMed] [Google Scholar] 180.Daks A, Mamontova V, Fedorova O, Petukhov A, Shuvalov O, Parfenyev S

To eliminate potential tissue site biases, we limited our analyses to the subset of patients with liver metastases biopsies (Supplementary Table S3 and Supplementary Fig