Evidence map›Paper›PMID 29334379›Full record

ArticleNature methods2018

Highly parallel direct RNA sequencing on an array of nanopores.

Daniel R Garalde, Elizabeth A Snell, Daniel Jachimowicz, Botond Sipos, Joseph H Lloyd, Mark Bruce, Nadia Pantic, Tigist Admassu, Phillip James, Anthony Warland and 16 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature methods, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 651 papers.

0numbers the graph read from it
0cells of the map it votes in
651citing papers in PubMed
57.6field-weighted citation impact, top 1% of its field
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

651 citing papers in PubMed, 1,107 citations in OpenAlex.

  1. Nanopore Sequencing for Chikungunya Virus: Principles and Application.Methods in molecular biology (Clifton, N.J.) · 2027
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  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 1 institution in 1 country.

Daniel R GaraldeOxford Nanopore Technologies Ltd., Oxford, UK.
Elizabeth A SnellOxford Nanopore Technologies Ltd., Oxford, UK.
Daniel JachimowiczOxford Nanopore Technologies Ltd., Oxford, UK.
Botond SiposOxford Nanopore Technologies Ltd., Oxford, UK.
Joseph H LloydOxford Nanopore Technologies Ltd., Oxford, UK.
Mark BruceOxford Nanopore Technologies Ltd., Oxford, UK.
Nadia PanticOxford Nanopore Technologies Ltd., Oxford, UK.
Tigist AdmassuOxford Nanopore Technologies Ltd., Oxford, UK.
Phillip JamesOxford Nanopore Technologies Ltd., Oxford, UK.
Anthony WarlandOxford Nanopore Technologies Ltd., Oxford, UK.
Michael JordanOxford Nanopore Technologies Ltd., Oxford, UK.
Jonah CicconeOxford Nanopore Technologies Ltd., Oxford, UK.
Sabrina SerraOxford Nanopore Technologies Ltd., Oxford, UK.
Jemma KeenanOxford Nanopore Technologies Ltd., Oxford, UK.
Samuel MartinOxford Nanopore Technologies Ltd., Oxford, UK.
Luke McNeillOxford Nanopore Technologies Ltd., Oxford, UK.
E Jayne WallaceOxford Nanopore Technologies Ltd., Oxford, UK.
Lakmal JayasingheOxford Nanopore Technologies Ltd., Oxford, UK.
Chris WrightOxford Nanopore Technologies Ltd., Oxford, UK.
Javier BlascoOxford Nanopore Technologies Ltd., Oxford, UK.
Stephen YoungOxford Nanopore Technologies Ltd., Oxford, UK.
Denise BrocklebankOxford Nanopore Technologies Ltd., Oxford, UK.
Sissel JuulOxford Nanopore Technologies Inc., New York, New York, USA.
James ClarkeOxford Nanopore Technologies Ltd., Oxford, UK.
Andrew J HeronOxford Nanopore Technologies Ltd., Oxford, UK.
Daniel J TurnerOxford Nanopore Technologies Ltd., Oxford, UK.ORCID 0000-0002-9716-3169
Oxford Nanopore Technologies (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequencing the RNA in a biological sample can unlock a wealth of information, including the identity of bacteria and viruses, the nuances of alternative splicing or the transcriptional state of organisms. However, current methods have limitations due to short read lengths and reverse transcription or amplification biases. Here we demonstrate nanopore direct RNA-seq, a highly parallel, real-time, single-molecule method that circumvents reverse transcription or amplification steps. This method yields full-length, strand-specific RNA sequences and enables the direct detection of nucleotide analogs in RNA.

Indexed as

NanoporesHigh-Throughput Nucleotide SequencingRNA, FungalSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSequence Analysis, RNARNA, FungalSaccharomyces cerevisiae Proteins

Identifiers

PMID29334379
OpenAlexW2950063384

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.