Evidence map›Paper›PMID 42862224›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2027

Guidelines to Study Transcriptome Remodeling by Proteins Using Deep Sequencing (RNA-Seq).

Pamela Guerillot, Eric Eveno

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Pamela GuerillotCentre de Biophysique Moléculaire, CNRS, Orléans, France.
Eric EvenoCentre de Biophysique Moléculaire, CNRS, Orléans, France. eric.eveno@cnrs.fr.ORCID http://orcid.org/0000-0002-7282-280X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA remodeling proteins (RRPs) are key regulators of RNA metabolism, often exerting broad, pleiotropic effects on the cellular transcriptome. Deep RNA sequencing (RNA-seq) has become a standard approach for investigating these effects on a global scale, particularly for identifying patterns of differential gene expression or splicing associated with RRP activity. In this chapter, we outline best-practice guidelines for designing and executing RNA-seq experiments, integrating bench and computational steps into a rigorous workflow. Data generated through this process provide a strong foundation for deploying other advanced approaches such as CLIP-seq or SHAPE-seq to uncover RRP targets, elucidate RRP functions, or detect RNA structural changes at global scale.

Indexed as

Gene Expression ProfilingHigh-Throughput Nucleotide SequencingRNA-Binding ProteinsRNA-SeqSequence Analysis, RNATranscriptomeAnimalsComputational BiologyHumansRNASoftwareRNARNA-Binding ProteinsBioinformatics pipelineMethodological frameworkRemodeling proteinsRNA sequencingTranscriptome analysis

Identifiers

What OpenQuestion holds

Textmetadata
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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.