Tom prepared some DNA samples for illumina sequencing. The sample has been confirmed that it has high purity and is free of nuclease contamination. The adapters and indices are also added. The sample can be successfully attached to the chip but the machine cannot identify qualified clusters for further reading. What could be the reason for this problem

i can't see the full page, therefore, can't answer it

explanation:

step 1: initiation

initiation is the beginning of transcription. it occurs when the enzyme rna polymerase binds to a region of a gene called the promoter. this signals the dna to unwind so the enzyme can ‘‘read’’ the bases in one of the dna strands. the enzyme is now ready to make a strand of mrna with a complementary sequence of bases.

step 2: elongation

elongation is the addition of nucleotides to the mrna strand. rna polymerase reads the unwound dna strand and builds the mrna molecule, using complementary base pairs. there is a brief time during this process when the newly formed rna is bound to the unwound dna. during this process, an adenine (a) in the dna binds to an uracil (u) in the rna.

step 3: termination

termination is the ending of transcription, and occurs when rna polymerase crosses a stop (termination) sequence in the gene. the mrna strand is complete, and it detaches from dna.

the answer is c on e2020, bud.