Abstract:Background: The adoption of next-generation sequencing (NGS) may help to identify single nucleotide variants (SNVs), small insertionsedeletions (indels), and larger structural variations including chromosomal rearrangements. Many molecular alterations have protein-level associations that can be questioned using immunohistochemistry (IHC). The goal of our work was investigated molecular patterns of predictive biomarkers and new genes involved as potential therapeutic targets with an emphasis on protein IHC and … Show more
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