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. 2017 May 12;12(5):e0176280. doi: 10.1371/journal.pone.0176280

Fig 8. Sanger sequencing of FGFR3, CHEK2, and MAGI1.

Fig 8

Variant calls at high frequency were invalidated by Sanger sequencing of amplified products from matched fresh-frozen DNA (upper panel) and FFPE DNA (lower panel). Arrows indicate the positions of a deletion (FGFR3), an SNV (CHEK2) and an insertion (MAGI1), and the variant sequences are shown below the reference sequences.