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Fig. 5 | BMC Medical Genomics

Fig. 5

From: Error-corrected sequencing strategies enable comprehensive detection of leukemic mutations relevant for diagnosis and minimal residual disease monitoring

Fig. 5

Novel RNA variants identified at time of diagnosis. a An aberrant RNA molecule in ZCCHC7 was identified in several of the B-ALL samples. b Novel cryptic gene fusion in SPTAN1-ABL1 was identified in a T-ALL subject and confirmed via Sanger sequencing. ExPASy translation of the fusion product sequence revealed the in-frame fusion of SPTAN1 (amino acids in red) and ABL1 (amino acids in black)

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BMC Medical Genomics

ISSN: 1755-8794

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