What is happening
You arrive at a gene sequencer flagging a read as corrupted.
The codon count on the report cannot be right. The clean read is 111 bases long, and every codon takes three bases.
DNA instructionsRunning
Bases consumed
19.2bases
Bases available
111bases
DNA transcriber. Codon count at 6.4 . Bases consumed 19.2 bases, Bases available 111 bases. Currently bases consumed is short by 91.8 bases.
What has to balance