Answer:
C. Because an RNA-seq reaction could tell if the fragments were encoded by the genome.
Step-by-step explanation:
The combination of single-cell RNA sequencing (RNA-Seq) and bioinformatic tools to assemble and annotate sequence reads is currently the most common methodology used to obtain complete transcriptomes from individual cells. RNA-seq is a Next-Generation Sequencing (NGS) technology that enables the analysis of the entire transcriptome, thereby this method can be used to examine gene, allelic and ncRNA expression. In the last years, RNA-seq has become the gold standard technique for direct analysis of ncRNA expression profiles in biological samples and clinical research.