Evidence map›Paper›PMID 32275708›Full record

ArticlePLoS computational biology2020

Hydra: A mixture modeling framework for subtyping pediatric cancer cohorts using multimodal gene expression signatures.

Jacob Pfeil, Lauren M Sanders, Ioannis Anastopoulos, A Geoffrey Lyle, Alana S Weinstein, Yuanqing Xue, Andrew Blair, Holly C Beale, Alex Lee, Stanley G Leung and 9 more

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 64% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

19 authors at 3 institutions in 1 country.

Jacob PfeilDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0002-8773-8520
Lauren M SandersDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, California, United States of America.
Ioannis AnastopoulosDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0002-6279-0648
A Geoffrey LyleGenomics Institute, University of California, Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0002-3435-526X
Alana S WeinsteinDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0002-1563-9072
Yuanqing XueDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0003-1892-6787
Andrew BlairDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, California, United States of America.
Holly C BealeGenomics Institute, University of California, Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0003-4091-538X
Alex LeeDepartment of Pediatrics, Division of Hematology and Oncology, University of California, San Francisco, San Francisco, California, United States of America.
Stanley G LeungDepartment of Pediatrics, Division of Hematology and Oncology, University of California, San Francisco, San Francisco, California, United States of America.
Phuong T DinhDepartment of Pediatrics, Division of Hematology and Oncology, University of California, San Francisco, San Francisco, California, United States of America.ORCID 0000-0002-0273-1603
Avanthi Tayi ShahDepartment of Pediatrics, Division of Hematology and Oncology, University of California, San Francisco, San Francisco, California, United States of America.
Marcus R BreeseDepartment of Pediatrics, Division of Hematology and Oncology, University of California, San Francisco, San Francisco, California, United States of America.
W Patrick DevineDepartment of Anatomic Pathology, University of California, San Francisco, California, San Francisco, United States of America.ORCID 0000-0003-4634-8830
Isabel BjorkGenomics Institute, University of California, Santa Cruz, Santa Cruz, California, United States of America.
Sofie R SalamaDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0001-6999-7193
E Alejandro Sweet-CorderoDepartment of Pediatrics, Division of Hematology and Oncology, University of California, San Francisco, San Francisco, California, United States of America.ORCID 0000-0002-9787-9351
David HausslerDepartment of Biomolecular Engineering, University of California, Santa Cruz, Santa Cruz, California, United States of America.
Olena Morozova VaskeGenomics Institute, University of California, Santa Cruz, Santa Cruz, California, United States of America.ORCID 0000-0002-1677-417X
University of California, Santa Cruz · USUniversity of California, San Francisco · USHoward Hughes Medical Institute · US

Funding

UC Santa Cruz Training Program In Genomic SciencesT32HG008345 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI BROOKS, ANGELA NORIE, GREEN, RICHARD EDWARD · 2015 to 2020
$1.4M
Howard Hughes Medical InstituteNHGRI NIH HHS T32 HG008345
6 · The paper itself

Abstract

Precision oncology has primarily relied on coding mutations as biomarkers of response to therapies. While transcriptome analysis can provide valuable information, incorporation into workflows has been difficult. For example, the relative rather than absolute gene expression level needs to be considered, requiring differential expression analysis across samples. However, expression programs related to the cell-of-origin and tumor microenvironment effects confound the search for cancer-specific expression changes. To address these challenges, we developed an unsupervised clustering approach for discovering differential pathway expression within cancer cohorts using gene expression measurements. The hydra approach uses a Dirichlet process mixture model to automatically detect multimodally distributed genes and expression signatures without the need for matched normal tissue. We demonstrate that the hydra approach is more sensitive than widely-used gene set enrichment approaches for detecting multimodal expression signatures. Application of the hydra analysis framework to small blue round cell tumors (including rhabdomyosarcoma, synovial sarcoma, neuroblastoma, Ewing sarcoma, and osteosarcoma) identified expression signatures associated with changes in the tumor microenvironment. The hydra approach also identified an association between ATRX deletions and elevated immune marker expression in high-risk neuroblastoma. Notably, hydra analysis of all small blue round cell tumors revealed similar subtypes, characterized by changes to infiltrating immune and stromal expression signatures.

Indexed as

Biomarkers, TumorChildCluster AnalysisComputational BiologyGene Expression ProfilingGene Expression Regulation, NeoplasticHumansModels, StatisticalNeoplasmsNeuroblastomaPrecision MedicineTranscriptomeTumor MicroenvironmentBiomarkers, Tumor

Identifiers

PMID32275708
PMCPMC7176284
OpenAlexW3015974879

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.