Evidence map›Paper›PMID 31001414›Full record

ArticleF1000Research2018

Correction of gene model annotations improves isoform abundance estimates: the example of ketohexokinase (

Christophe D Chabbert, Tanja Eberhart, Ilaria Guccini, Wilhelm Krek, Werner J Kovacs

Open access · goldAbstract read
In one paragraph

Article in F1000Research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Christophe D ChabbertInstitute of Molecular Health Sciences, ETH Zurich, Zurich, 8093, Switzerland.ORCID 0000-0001-7851-4640
Tanja EberhartInstitute of Molecular Health Sciences, ETH Zurich, Zurich, 8093, Switzerland.ORCID 0000-0002-3621-5594
Ilaria GucciniInstitute of Molecular Health Sciences, ETH Zurich, Zurich, 8093, Switzerland.ORCID 0000-0002-3644-0679
Wilhelm KrekInstitute of Molecular Health Sciences, ETH Zurich, Zurich, 8093, Switzerland.
Werner J KovacsInstitute of Molecular Health Sciences, ETH Zurich, Zurich, 8093, Switzerland.ORCID 0000-0002-4440-4344
ETH Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next generation sequencing protocols such as RNA-seq have made the genome-wide characterization of the transcriptome a crucial part of many research projects in biology. Analyses of the resulting data provide key information on gene expression and in certain cases on exon or isoform usage. The emergence of transcript quantification software such as Salmon has enabled researchers to efficiently estimate isoform and gene expressions across the genome while tremendously reducing the necessary computational power. Although overall gene expression estimations were shown to be accurate, isoform expression quantifications appear to be a more challenging task. Low expression levels and uneven or insufficient coverage were reported as potential explanations for inconsistent estimates. Here, through the example of the ketohexokinase (

Indexed as

alternative splicinggene expressionKhkquantificationRNA-seqSalmontranscriptomics

Identifiers

PMID31001414
PMCPMC6464065
OpenAlexW2904572733

What OpenQuestion holds

Textmetadata
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.