alignment, which affects the accuracy of quantitative analysis. The
sequencing depth determines the number of detected genes, but it
cannot yield additional information over a threshold. One previous
study showed that the threshold of sequencing depth could be one
million reads [4], but this was not supported by a recent study. In
that study, Lin Liu et al. analyzed a colon cancer scRNA-seq dataset
(SRA: SRP113436), and the results showed that the one-million-
read depth was not enough to acquire all the possible transcripts.
The one-million-read depth had been determined as the threshold
due to not considering all kinds of noncoding RNAs (ncRNAs).
For example, all the previous studies did not consider two novel
long ncRNAs (lncRNAs) discovered in human mitochondrial DNA
[5]. Longer (e.g., 125 or 150 bp) and PE reads improve the
alignment quality and the accuracy of quantitative analysis. How-
ever, most of the existing scRNA-seq datasets contain shorter (e.g.,
50 bp) or SE reads. In addition, the existing scRNA-seq datasets are
Table 1
Overview of scRNA-seq protocols [4]
Method CEL-seq2/C1 Drop-seq
MARS-
seq SCRB-seq Smart-seq/C1
Smart-
seq2
Single-cell
isolation
Automated in
the C1
system
Droplets FACS FACS Automated in
the C1
system
FACS
ERCC
Spike-ins
Yes No Yes Yes Yes Yes
UMI 6 bp 8 bp 8 bp 10 bp No No
Full-length
coverage
No No No No Yes Yes
First strand
synthesis
oligo-dT oligo-dT oligo-dT oligo-dT oligo-dT oligo-dT
Second strand
synthesis
RNAseH/
DNA Pol
Template
switching
RNAseH/
DNA Pol
Template
switching
Template
switching
Template
switching
Amplification IVT PCR IVT PCR PCR PCR
Imaging of cells
possible
Yes NoNoNoYes No
Protocol usable
for bulk
Yes No Yes Yes Yes Yes
Sequencing Paired-end Paired-end Paired-
end
Paired-end Single-end Single-end
Library cost/
cell
~9.5€ ~0.1€ ~1.3€ ~2€ ~25€ ~3/30a
aIn-house produced Tn5/commercial Tn5
Data Analysis in Single-Cell Transcriptome Sequencing 313