Evidence map›Paper›PMID 40603900›Full record

ArticleScientific data2025

Consistently processed RNA sequencing data from 50 sources enriched for pediatric data.

Holly C Beale, Katrina Learned, Ellen T Kephart, A Geoffrey Lyle, Anouk van den Bout, Molly McCabe, Kathryn Echandia-Monroe, Mansi J Khare, Elise Y Huang, Sneha Jariwala and 11 more

Abstract readDataset
In one paragraph

Article in Scientific data, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

21 authors.

Holly C Beale *Department of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA. hcbeale@ucsc.edu.ORCID 0000-0003-4091-538X
Katrina Learned *Genomics Institute, University of California Santa Cruz, Santa Cruz, California, USA.
Ellen T Kephart *Genomics Institute, University of California Santa Cruz, Santa Cruz, California, USA.
A Geoffrey LyleDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.ORCID 0000-0002-3435-526X
Anouk van den BoutDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
Molly McCabeDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
Kathryn Echandia-MonroeDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
Mansi J KhareDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
Elise Y HuangDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
Sneha JariwalaDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
Reyna AntillaDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
Allison CheneyDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
Alex G LeeDivision of Pediatric Oncology, University of California San Francisco, San Francisco, California, USA.
Leanne C SaylesDivision of Pediatric Oncology, University of California San Francisco, San Francisco, California, USA.
Stanley G LeungDivision of Radiation Oncology, University of California San Francisco, San Francisco, California, USA.
Yvonne A VasquezDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.ORCID 0000-0001-6113-5222
Lauren SandersDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.
David HausslerGenomics Institute, University of California Santa Cruz, Santa Cruz, California, USA.ORCID 0000-0003-1533-4575
Sofie R SalamaDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA.ORCID 0000-0001-6999-7193
E Alejandro Sweet-CorderoDivision of Pediatric Oncology, University of California San Francisco, San Francisco, California, USA.
Olena M VaskeDepartment of Molecular, Cell and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, USA. olena@ucsc.edu.ORCID 0000-0002-1677-417X

Funding

Nanoparticle Tracking Analyzer (NTA) for the Center for Live Cell GenomicsRM1HG011543 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI HAUSSLER, DAVID H, SALAMA, SOFIE REDA · 2021 to 2025
$12.0M
Training Program in Molecular, Cell, and Developmental BiologyT32GM133391 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI Needhi Bhalla · 2019 to 2026
$3.0M
Development of Advanced Preclinical Models for Pediatric Solid TumorsR01CA243555 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SWEET-CORDERO, ERIC ALEJANDRO, VASKE, OLENA MOROZOVA · 2020 to 2024
$3.0M
Utilizing Multi-omics to Facilitate Cancer Biology ResearchR50CA274213 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Alex Lee · 2023 to 2026
$935k
American Association for Cancer Research (American Association for Cancer Research, Inc.) NextGen Award for Transformative Cancer ResearchNational Science Foundation (NSF) California Alliance for Minority Participation (CAMP)NCI NIH HHS R01 CA243555NCI NIH HHS R50 CA274213NHGRI NIH HHS RM1 HG011543NIGMS NIH HHS T32 GM133391St. Baldrick's Foundation (St. Baldrick's Foundation, Inc) Emily Beazley Kures for KidsU.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) 5RM1HG011543
6 · The paper itself

Abstract

Larger cohorts improve the power of tumor gene expression analysis, but the signal is muddied if datasets are processed using different methods or have inaccurate metadata. Here we present five compendia containing consistently processed gene expression data derived from 16,446 diverse RNA sequencing datasets. To create the compendia, we obtained access to RNA sequence data from repositories containing public data as well as clinical partners with access to non-published data. We then assessed the quality, quantified gene expression, harmonized clinical metadata, and released the expression values and metadata without access restrictions. These datasets have been used for diverse projects ranging from identifying similarities between tumor types to assessing how well cell lines recapitulate tumors. They have also been used for n-of-1 analysis to identify genes with unusual expression patterns in a single sample and to infer molecular diagnosis. The comparison to new data is enabled by our dockerized, freely available pipeline. The compendia have been cited in at least 20 publications.

Indexed as

NeoplasmsSequence Analysis, RNAChildHumansMetadata

Identifiers

PMID40603900
PMCPMC12222803

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.