Evidence map›Paper›PMID 35931981›Full record

ArticleBMC bioinformatics2022

DAGBagM: learning directed acyclic graphs of mixed variables with an application to identify protein biomarkers for treatment response in ovarian cancer.

Shrabanti Chowdhury, Ru Wang, Qing Yu, Catherine J Huntoon, Larry M Karnitz, Scott H Kaufmann, Steven P Gygi, Michael J Birrer, Amanda G Paulovich, Jie Peng and 1 more

Abstract read
In one paragraph

Article in BMC bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Causal Discovery with Generalized Linear Models through Peeling Algorithms.Journal of machine learning research : JMLR · 2024
    Article
  5. 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

11 authors.

Shrabanti ChowdhuryDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Ru WangDepartment of Statistics, University of California, Davis, CA, 95616, USA.
Qing YuDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Catherine J HuntoonDivision of Oncology Research and Department of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Larry M KarnitzDivision of Oncology Research and Department of Oncology, Mayo Clinic, Rochester, MN, 55905, USA.
Scott H KaufmannDivision of Oncology Research, Mayo Clinic, Rochester, MN, 55905, USA.
Steven P GygiDepartment of Cell Biology, Harvard Medical School, Boston, MA, 02115, USA.
Michael J BirrerWinthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR, 72205, USA.
Amanda G PaulovichClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, 98109, USA.
Jie PengDepartment of Statistics, University of California, Davis, CA, 95616, USA. jiepeng@ucdavis.edu.
Pei WangDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA. pei.wang@mssm.edu.

Funding

Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
Proteogenomic Studies aimed at understanding ovarian tumor responses to agents targeting the DNA damage response and translating this knowledge into clinical benefitU01CA214114 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BIRRER, MICHAEL, PAULOVICH, AMANDA G · 2017 to 2021
$8.4M
Proteogenomic translator for cancer biomarker discovery towards precision medicineU24CA271114 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Avi Ma'ayan, Pei Wang · 2022 to 2026
$5.0M
Systems Biology based Proteogenomic Translator for Cancer Marker Discovery towards Precision MedicineU24CA210993 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SCHADT, ERIC E, WANG, PEI · 2016 to 2020
$4.6M
National Science Foundation DMS-1915894NCI NIH HHS P50 CA136393NCI NIH HHS U01 CA214114NCI NIH HHS U01 CA214114, U24 CA210993NCI NIH HHS U24 CA210993NCI NIH HHS U24 CA271114
6 · The paper itself

Abstract

backgroundApplying directed acyclic graph (DAG) models to proteogenomic data has been shown effective for detecting causal biomarkers of complex diseases. However, there remain unsolved challenges in DAG learning to jointly model binary clinical outcome variables and continuous biomarker measurements.

resultsIn this paper, we propose a new tool, DAGBagM, to learn DAGs with both continuous and binary nodes. By using appropriate models, DAGBagM allows for either continuous or binary nodes to be parent or child nodes. It employs a bootstrap aggregating strategy to reduce false positives in edge inference. At the same time, the aggregation procedure provides a flexible framework to robustly incorporate prior information on edges.

conclusionsThrough extensive simulation experiments, we demonstrate that DAGBagM has superior performance compared to alternative strategies for modeling mixed types of nodes. In addition, DAGBagM is computationally more efficient than two competing methods. When applying DAGBagM to proteogenomic datasets from ovarian cancer studies, we identify potential protein biomarkers for platinum refractory/resistant response in ovarian cancer. DAGBagM is made available as a github repository at https://github.com/jie108/dagbagM .

Indexed as

Ovarian NeoplasmsBiomarkersCausalityChildComputer SimulationConfounding Factors, EpidemiologicFemaleHumansBiomarkersBootstrap aggregationHill climbingProteomicsSensitive and resistant/refractory

Identifiers

PMID35931981
PMCPMC9354326

What OpenQuestion holds

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LicenceCC BY
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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.