Evidence map›Paper›PMID 32968711›Full record

ArticleNature machine intelligence2020

Gaussian Embedding for Large-scale Gene Set Analysis.

Sheng Wang, Emily R Flynn, Russ B Altman

Open access · greenAbstract read
In one paragraph

Article in Nature machine intelligence, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Graph-Based Gene Embedding.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Protein structure-based gene expression signatures.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Machine Learning for Cancer Drug Combination.Clinical pharmacology and therapeutics · 2020
    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

3 authors at 1 institution in 1 country.

Sheng WangDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Emily R FlynnBiomedical Informatics Training Program, Stanford University, Stanford, CA 94305, USA.
Russ B AltmanDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Stanford University · US

Funding

PharmGKB: pharmacogenomics discovery and implementationU24HG010615 · NHGRI · STANFORD UNIVERSITY · PI TERI Ellen KLEIN, Michelle Whirl-Carrillo · 2020 to 2026
$9.5M
Text Mining for High-fidelity Curation and Discovery of Gene-drug-phenotype RelationshipsR01LM005652 · NLM · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO · 2000 to 2018
$6.2M
Undergraduate Summer Research Experiences Support for Combining systems biology and structural biology to find new therapeuticsR01GM102365 · NIGMS · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO · 2012 to 2021
$3.0M
Biomedical Data Translator Technical Feasibility Assessment of Reasoning Tool: Stanford UniversityOT2TR002515 · NCATS · STANFORD UNIVERSITY · PI ALTMAN, RUSS BIAGIO · 2018 to 2019
$845k
Toward improved understanding of sex differences in drug response: developing gene and pathway-based informatics methods to examine sex-differential genetic effectsF31LM013053 · NLM · STANFORD UNIVERSITY · PI FLYNN, EMILY · 2019 to 2021
$92k
NCATS NIH HHS OT2 TR002515NHGRI NIH HHS U24 HG010615NIGMS NIH HHS R01 GM102365NLM NIH HHS F31 LM013053NLM NIH HHS R01 LM005652
6 · The paper itself

Abstract

Gene sets, including protein complexes and signaling pathways, have proliferated greatly, in large part as a result of high-throughput biological data. Leveraging gene sets to gain insight into biological discovery requires computational methods for converting them into a useful form for available machine learning models. Here, we study the problem of embedding gene sets as compact features that are compatible with available machine learning codes. We present Set2Gaussian, a novel network-based gene set embedding approach, which represents each gene set as a multivariate Gaussian distribution rather than a single point in the low-dimensional space, according to the proximity of these genes in a protein-protein interaction network. We demonstrate that Set2Gaussian improves gene set member identification, accurately stratifies tumors, and finds concise gene sets for gene set enrichment analysis. We further show how Set2Gaussian allows us to identify a previously unknown clinical prognostic and predictive subnetwork around NEFM in sarcoma, which we validate in independent cohorts.

Identifiers

PMID32968711
PMCPMC7505077
OpenAlexW3035387075

What OpenQuestion holds

Textmetadata
LicenceTDM
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.