Comparative analysis of sequencing technologies for single-cell transcriptomics

Abstract Single-cell RNA-seq technologies require library preparation prior to sequencing. Here, we present the first report to compare the cheaper BGISEQ-500 platform to the Illumina HiSeq platform for scRNA-seq. We generate a resource of 468 single cells and 1297 matched single cDNA samples, perfo...

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Main Authors: Kedar Nath Natarajan, Zhichao Miao, Miaomiao Jiang, Xiaoyun Huang, Hongpo Zhou, Jiarui Xie, Chunqing Wang, Shishang Qin, Zhikun Zhao, Liang Wu, Naibo Yang, Bo Li, Yong Hou, Shiping Liu, Sarah A. Teichmann
Format: Article
Language:English
Published: BMC 2019-04-01
Series:Genome Biology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13059-019-1676-5
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spelling doaj-66b4691e7a7a49749d396ac0be8abd992020-11-25T02:10:47ZengBMCGenome Biology1474-760X2019-04-012011810.1186/s13059-019-1676-5Comparative analysis of sequencing technologies for single-cell transcriptomicsKedar Nath Natarajan0Zhichao Miao1Miaomiao Jiang2Xiaoyun Huang3Hongpo Zhou4Jiarui Xie5Chunqing Wang6Shishang Qin7Zhikun Zhao8Liang Wu9Naibo Yang10Bo Li11Yong Hou12Shiping Liu13Sarah A. Teichmann14Wellcome Sanger InstituteWellcome Sanger InstituteBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenBGI-ShenzhenWellcome Sanger InstituteAbstract Single-cell RNA-seq technologies require library preparation prior to sequencing. Here, we present the first report to compare the cheaper BGISEQ-500 platform to the Illumina HiSeq platform for scRNA-seq. We generate a resource of 468 single cells and 1297 matched single cDNA samples, performing SMARTer and Smart-seq2 protocols on two cell lines with RNA spike-ins. We sequence these libraries on both platforms using single- and paired-end reads. The platforms have comparable sensitivity and accuracy in terms of quantification of gene expression, and low technical variability. Our study provides a standardized scRNA-seq resource to benchmark new scRNA-seq library preparation protocols and sequencing platforms.http://link.springer.com/article/10.1186/s13059-019-1676-5Single-cell RNA sequencingSequencing platformsBenchmarking scRNA-seqIllumina sequencingBGISEQ-500
collection DOAJ
language English
format Article
sources DOAJ
author Kedar Nath Natarajan
Zhichao Miao
Miaomiao Jiang
Xiaoyun Huang
Hongpo Zhou
Jiarui Xie
Chunqing Wang
Shishang Qin
Zhikun Zhao
Liang Wu
Naibo Yang
Bo Li
Yong Hou
Shiping Liu
Sarah A. Teichmann
spellingShingle Kedar Nath Natarajan
Zhichao Miao
Miaomiao Jiang
Xiaoyun Huang
Hongpo Zhou
Jiarui Xie
Chunqing Wang
Shishang Qin
Zhikun Zhao
Liang Wu
Naibo Yang
Bo Li
Yong Hou
Shiping Liu
Sarah A. Teichmann
Comparative analysis of sequencing technologies for single-cell transcriptomics
Genome Biology
Single-cell RNA sequencing
Sequencing platforms
Benchmarking scRNA-seq
Illumina sequencing
BGISEQ-500
author_facet Kedar Nath Natarajan
Zhichao Miao
Miaomiao Jiang
Xiaoyun Huang
Hongpo Zhou
Jiarui Xie
Chunqing Wang
Shishang Qin
Zhikun Zhao
Liang Wu
Naibo Yang
Bo Li
Yong Hou
Shiping Liu
Sarah A. Teichmann
author_sort Kedar Nath Natarajan
title Comparative analysis of sequencing technologies for single-cell transcriptomics
title_short Comparative analysis of sequencing technologies for single-cell transcriptomics
title_full Comparative analysis of sequencing technologies for single-cell transcriptomics
title_fullStr Comparative analysis of sequencing technologies for single-cell transcriptomics
title_full_unstemmed Comparative analysis of sequencing technologies for single-cell transcriptomics
title_sort comparative analysis of sequencing technologies for single-cell transcriptomics
publisher BMC
series Genome Biology
issn 1474-760X
publishDate 2019-04-01
description Abstract Single-cell RNA-seq technologies require library preparation prior to sequencing. Here, we present the first report to compare the cheaper BGISEQ-500 platform to the Illumina HiSeq platform for scRNA-seq. We generate a resource of 468 single cells and 1297 matched single cDNA samples, performing SMARTer and Smart-seq2 protocols on two cell lines with RNA spike-ins. We sequence these libraries on both platforms using single- and paired-end reads. The platforms have comparable sensitivity and accuracy in terms of quantification of gene expression, and low technical variability. Our study provides a standardized scRNA-seq resource to benchmark new scRNA-seq library preparation protocols and sequencing platforms.
topic Single-cell RNA sequencing
Sequencing platforms
Benchmarking scRNA-seq
Illumina sequencing
BGISEQ-500
url http://link.springer.com/article/10.1186/s13059-019-1676-5
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