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
18bases
Bases available
111bases
Bases consumed is short by 93 bases
DNA transcriber. Codon count at 6 codons. Bases consumed 18 bases, Bases available 111 bases. Currently bases consumed is short by 93 bases.
What has to balance