Evidence map›Paper›PMID 36961337›Full record

ArticleBioinformatics (Oxford, England)2023

nf-core/isoseq: simple gene and isoform annotation with PacBio Iso-Seq long-read sequencing.

Sébastien Guizard, Katarzyna Miedzinska, Jacqueline Smith, Jonathan Smith, Richard I Kuo, Megan Davey, Alan Archibald, Mick Watson

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

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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

8 authors.

Sébastien GuizardThe Roslin Institute and R(D)SVS, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.ORCID 0000-0001-5116-4150
Katarzyna MiedzinskaThe Roslin Institute and R(D)SVS, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.
Jacqueline SmithThe Roslin Institute and R(D)SVS, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.
Jonathan SmithThe Roslin Institute and R(D)SVS, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.
Richard I KuoWobble Genomics, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.
Megan DaveyThe Roslin Institute and R(D)SVS, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.
Alan ArchibaldThe Roslin Institute and R(D)SVS, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.
Mick WatsonThe Roslin Institute and R(D)SVS, University of Edinburgh, Edinburgh EH25 9RG, United Kingdom.ORCID 0000-0003-4211-0358

Funding

Biotechnology and Biological Sciences Research Council BBS/E/D/10002070
6 · The paper itself

Abstract

motivationIso-Seq RNA long-read sequencing enables the identification of full-length transcripts and isoforms, removing the need for complex analysis such as transcriptome assembly. However, the raw sequencing data need to be processed in a series of steps before annotation is complete. Here, we present nf-core/isoseq, a pipeline for automatic read processing and genome annotation. Following nf-core guidelines, the pipeline has few dependencies and can be run on any of platforms. AVAILABILITY AND IMPLEMENTATION: The pipeline is freely available online on the nf-core website (https://nf-co.re/isoseq) and on GitHub (https://github.com/nf-core/isoseq) under MIT License (DOI: 10.5281/zenodo.7116979).

Indexed as

Alternative SplicingGenomeMolecular Sequence AnnotationProtein IsoformsSequence Analysis, RNATranscriptomeProtein Isoforms

Identifiers

PMID36961337
PMCPMC10199315

What OpenQuestion holds

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LicenceCC BY
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.