NET-Seq

scRNA-Seq

scRNA-Seq provides deeper insight to the multi-tiered complexity of different cells within the same tissue type. scRNA-Seq has now been adapted widely into other methods in the single-cell RNA sequencing field. In this method, single cells are isolated manually under a microscope and lysed. Next, mRNAs are purified and primed with a poly(T) primer for reverse transcription. Unreactive primers are removed by exonuclease I digestion. Poly(A) tails are added to the first strand cDNA at the 3' end and annealed to poly(T) primers for second-strand cDNA generation. Finally, the cDNAs are PCR-amplified, sheared, and prepared into sequencing libraries.

Pros:
  • Single-cell–resolution transcriptomic analysis
  • Able to detect unknown splice junctions
  • Various RNAPII-specific antibodies can be used to increase targeting accuracy
Cons:
  • Very low throughput
  • No molecular barcodes used
  • Can be expensive to scale up