Evidence map›Paper›PMID 31366910›Full record

ArticleNature communications2019

A comprehensive examination of Nanopore native RNA sequencing for characterization of complex transcriptomes.

Charlotte Soneson, Yao Yao, Anna Bratus-Neuenschwander, Andrea Patrignani, Mark D Robinson, Shobbir Hussain

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

172 citing papers in PubMed.

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112 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Charlotte SonesonInstitute of Molecular Life Sciences, University of Zurich, 8057, Zurich, Switzerland. charlotte.soneson@fmi.ch.ORCID http://orcid.org/0000-0003-3833-2169
Yao YaoInstitute of Molecular Life Sciences, University of Zurich, 8057, Zurich, Switzerland.
Anna Bratus-NeuenschwanderFunctional Genomics Centre Zurich, ETHZ/University of Zurich, 8057, Zurich, Switzerland.
Andrea PatrignaniFunctional Genomics Centre Zurich, ETHZ/University of Zurich, 8057, Zurich, Switzerland.
Mark D RobinsonInstitute of Molecular Life Sciences, University of Zurich, 8057, Zurich, Switzerland. mark.robinson@imls.uzh.ch.ORCID http://orcid.org/0000-0002-3048-5518
Shobbir HussainDepartment of Biology and Biochemistry, University of Bath, Bath, BA2 7AY, UK. S.Hussain@bath.ac.uk.

Funding

Biotechnology and Biological Sciences Research Council BB/N000749/1Biotechnology and Biological Sciences Research Council BB/R006431/1
6 · The paper itself

Abstract

A platform for highly parallel direct sequencing of native RNA strands was recently described by Oxford Nanopore Technologies, but despite initial efforts it remains crucial to further investigate the technology for quantification of complex transcriptomes. Here we undertake native RNA sequencing of polyA + RNA from two human cell lines, analysing ~5.2 million aligned native RNA reads. To enable informative comparisons, we also perform relevant ONT direct cDNA- and Illumina-sequencing. We find that while native RNA sequencing does enable some of the anticipated advantages, key unexpected aspects currently hamper its performance, most notably the quite frequent inability to obtain full-length transcripts from single reads, as well as difficulties to unambiguously infer their true transcript of origin. While characterising issues that need to be addressed when investigating more complex transcriptomes, our study highlights that with some defined improvements, native RNA sequencing could be an important addition to the mammalian transcriptomics toolbox.

Indexed as

Base SequenceCell LineDNA, ComplementaryHEK293 CellsHigh-Throughput Nucleotide SequencingHumansPoly ASequence Analysis, RNATranscriptomeDNA, ComplementaryPoly A

Identifiers

PMID31366910
PMCPMC6668388

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.