Computational Systems Biology Methods and Protocols.7z

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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
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