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用于cDNA群体定量和定性评估的牛津纳米孔MinION测序的基准测试。

Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations.

作者信息

Oikonomopoulos Spyros, Wang Yu Chang, Djambazian Haig, Badescu Dunarel, Ragoussis Jiannis

机构信息

McGill University and Genome Quebec Innovation Centre, Department of Human Genetics, 740 Dr. Penfield Avenue, McGill University, Montréal, Québec, Canada.

Department of Bioengineering, McGill University, Montréal, Québec, Canada.

出版信息

Sci Rep. 2016 Aug 24;6:31602. doi: 10.1038/srep31602.

DOI:10.1038/srep31602
PMID:27554526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4995519/
Abstract

To assess the performance of the Oxford Nanopore Technologies MinION sequencing platform, cDNAs from the External RNA Controls Consortium (ERCC) RNA Spike-In mix were sequenced. This mix mimics mammalian mRNA species and consists of 92 polyadenylated transcripts with known concentration. cDNA libraries were generated using a template switching protocol to facilitate the direct comparison between different sequencing platforms. The MinION performance was assessed for its ability to sequence the cDNAs directly with good accuracy in terms of abundance and full length. The abundance of the ERCC cDNA molecules sequenced by MinION agreed with their expected concentration. No length or GC content bias was observed. The majority of cDNAs were sequenced as full length. Additionally, a complex cDNA population derived from a human HEK-293 cell line was sequenced on an Illumina HiSeq 2500, PacBio RS II and ONT MinION platforms. We observed that there was a good agreement in the measured cDNA abundance between PacBio RS II and ONT MinION (rpearson = 0.82, isoforms with length more than 700bp) and between Illumina HiSeq 2500 and ONT MinION (rpearson = 0.75). This indicates that the ONT MinION can sequence quantitatively both long and short full length cDNA molecules.

摘要

为评估牛津纳米孔技术公司的MinION测序平台的性能,对来自外部RNA对照联盟(ERCC)RNA加标混合物的cDNA进行了测序。该混合物模拟哺乳动物mRNA种类,由92种已知浓度的多聚腺苷酸化转录本组成。使用模板切换方案生成cDNA文库,以便于不同测序平台之间的直接比较。评估了MinION在丰度和全长方面直接对cDNA进行准确测序的能力。MinION测序的ERCC cDNA分子的丰度与其预期浓度相符。未观察到长度或GC含量偏差。大多数cDNA被测序为全长。此外,在Illumina HiSeq 2500、PacBio RS II和ONT MinION平台上对源自人HEK-293细胞系的复杂cDNA群体进行了测序。我们观察到,PacBio RS II和ONT MinION之间(rpearson = 0.82,长度超过700bp的异构体)以及Illumina HiSeq 2500和ONT MinION之间(rpearson = 0.75)在测得的cDNA丰度方面有很好的一致性。这表明ONT MinION可以对长和短的全长cDNA分子进行定量测序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/6bd0d63e05e9/srep31602-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/d2d7865251a9/srep31602-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/bbc3d5630f95/srep31602-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/27548bc6d7fd/srep31602-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/3f27464a9f33/srep31602-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/6bd0d63e05e9/srep31602-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/d2d7865251a9/srep31602-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/bbc3d5630f95/srep31602-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/27548bc6d7fd/srep31602-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/3f27464a9f33/srep31602-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1aae/4995519/6bd0d63e05e9/srep31602-f5.jpg

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