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Additional file 1 of Detection of leukemia gene fusions by targeted RNA-sequencing in routine diagnostics

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posted on 2020-07-30, 06:19 authored by Marie Engvall, Nicola Cahill, Britt-Inger Jonsson, Martin Höglund, Helene Hallböök, Lucia Cavelier
Additional file 1 Figure S1 Original image of the agarose gel in Fig. 4d showing the RT-PCR result of the KMT2A-MLLT4 gene fusion. P1 and P2 = patient 1 and 2 carrying KMT2A-MLLT4 e8-e2 gene fusions, P3 = patient 3 with a KMT2A-AFF1 gene fusion (negative control), NTC = non template control. Figure S2 Original image of the ScreenTape result and expected fragment sizes from the TapeStation analysis of the breakpoint verification of the KMT2A exon 6-ARHGEF12 exon 22 fusion breakpoint using RT-PCR from Fig. 6. Sample is from a patient with a KMT2A-ARHGEF12 fusion. NC = negative control (cDNA from patient with no KMT2A-ARHGEF12 fusion). NTC = non template control. Arrows with F1-F3: forward primers. Arrows with R1-R3: reverse primers.

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Science for Life Laboratory Lion’s Cancer Research Foundation, Uppsala

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