Evidence map›Paper›PMID 40654750›Full record

ArticlebioRxiv : the preprint server for biology2025

g.nome, A Transparent Bioinformatics Pipeline that Enables Differential Expression and Alternative Splicing Analysis by Non-Computational Biologists.

Rut Bryl, Krystal C Johnson, Xiongbin Kang, Tao Wang, Kit A Fuhrman, Mark Kunitomi, Nora Kearns, David R Corey

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

8 authors.

Rut BrylUT Southwestern Medical Center, Departments of Pharmacology and Biochemistry, Dallas, TX 75390-9041.
Krystal C JohnsonUT Southwestern Medical Center, Departments of Pharmacology and Biochemistry, Dallas, TX 75390-9041.
Xiongbin KangQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, UT Southwestern Medical Center Dallas, TX 75235.
Tao WangQuantitative Biomedical Research Center, Peter O'Donnell Jr. School of Public Health, UT Southwestern Medical Center Dallas, TX 75235.
Kit A FuhrmanAlmaden Genomics, 1409 Botham Jean Blvd, Suite 1007, Dallas, TX 75215.
Mark KunitomiAlmaden Genomics, 1409 Botham Jean Blvd, Suite 1007, Dallas, TX 75215.
Nora KearnsAlmaden Genomics, 1409 Botham Jean Blvd, Suite 1007, Dallas, TX 75215.
David R CoreyUT Southwestern Medical Center, Departments of Pharmacology and Biochemistry, Dallas, TX 75390-9041.

Funding

Recognition of Cellular Targets by single and double-stranded nucleic acidsR35GM118103 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI David R Corey · 2016 to 2026
$5.7M
Defining the Boundaries of RNAi in a cellF31GM137591 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI JOHNSON, KRYSTAL COURTNEY · 2020 to 2022
$95k
NIGMS NIH HHS F31 GM137591NIGMS NIH HHS R35 GM118103
6 · The paper itself

Abstract

Reproducibility and accessibility are cardinal principles in the rapidly evolving field of bioinformatics. As the collection of biological data grows, proper use of pipelines to analyze datasets can become a bottleneck restricting efficient analysis. Biologists who collect data and test hypotheses may not have strong computational backgrounds and may not be able to fully understand the underlying strengths and weaknesses of computational approaches or fully exploit their data. Some data may be misunderstood and, perhaps more importantly, critical findings may remain unobserved. High throughput RNA sequencing (RNAseq) has advanced our understanding of transcriptomics across diverse applications. Here we introduce g.nome, a bioinformatics platform that integrates contemporary tools necessary for independent analysis. A user-friendly graphical interface simplifies running jobs and allows simplified analysis of different datasets by non-bioinformaticians. g.nome was used to analyze the consequences of localizing the critical RNAi factor argonaute (AGO) to nuclei of colorectal cancer cell line HCT116. Analysis using the pipeline facilitated the straightforward identification of splicing changes and the prioritization of these splicing changes for validation and further experimental analysis.

Identifiers

PMID40654750
PMCPMC12248123

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.