Evidence map›Paper›PMID 30260405›Full record

ArticleNucleic acids research2019

De novo clustering of long reads by gene from transcriptomics data.

Camille Marchet, Lolita Lecompte, Corinne Da Silva, Corinne Cruaud, Jean-Marc Aury, Jacques Nicolas, Pierre Peterlongo

Abstract read
In one paragraph

Article in Nucleic acids research, 2019. 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.

  1. Article
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  10. Review
  11. Article
  12. Article
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  14. De Novo Clustering of Long-Read Transcriptome Data Using a Greedy, Quality Value-Based Algorithm.Journal of computational biology : a journal of computational molecular cell biology · 2020
    Article
  15. Article
  16. Review
  17. Computational methods for 16S metabarcoding studies using Nanopore sequencing data.Computational and structural biotechnology journal · 2020
    Review
  18. Article
  19. Article
  20. Review
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

7 authors.

Camille MarchetUniv Rennes, Inria, CNRS, IRISA, F-35000 Rennes, France.
Lolita LecompteUniv Rennes, Inria, CNRS, IRISA, F-35000 Rennes, France.
Corinne Da SilvaCommissariat à l'Énergie Atomique (CEA), Institut de Biologie François Jacob, Genoscope, 91000 Evry, France.
Corinne CruaudCommissariat à l'Énergie Atomique (CEA), Institut de Biologie François Jacob, Genoscope, 91000 Evry, France.
Jean-Marc AuryCommissariat à l'Énergie Atomique (CEA), Institut de Biologie François Jacob, Genoscope, 91000 Evry, France.
Jacques NicolasUniv Rennes, Inria, CNRS, IRISA, F-35000 Rennes, France.
Pierre PeterlongoUniv Rennes, Inria, CNRS, IRISA, F-35000 Rennes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-read sequencing currently provides sequences of several thousand base pairs. It is therefore possible to obtain complete transcripts, offering an unprecedented vision of the cellular transcriptome. However the literature lacks tools for de novo clustering of such data, in particular for Oxford Nanopore Technologies reads, because of the inherent high error rate compared to short reads. Our goal is to process reads from whole transcriptome sequencing data accurately and without a reference genome in order to reliably group reads coming from the same gene. This de novo approach is therefore particularly suitable for non-model species, but can also serve as a useful pre-processing step to improve read mapping. Our contribution both proposes a new algorithm adapted to clustering of reads by gene and a practical and free access tool that allows to scale the complete processing of eukaryotic transcriptomes. We sequenced a mouse RNA sample using the MinION device. This dataset is used to compare our solution to other algorithms used in the context of biological clustering. We demonstrate that it is the best approach for transcriptomics long reads. When a reference is available to enable mapping, we show that it stands as an alternative method that predicts complementary clusters.

Indexed as

GenomicsAnimalsGene Expression ProfilingGenomeHigh-Throughput Nucleotide SequencingMiceRNASequence Analysis, DNATranscriptomeRNA

Identifiers

PMID30260405
PMCPMC6326815

What OpenQuestion holds

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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.