Evidence map›Paper›PMID 25705056›Full record

ArticleJournal of the Royal Statistical Society. Series C, Applied statistics2014

Bayesian hierarchical structured variable selection methods with application to MIP studies in breast cancer.

Lin Zhang, Veerabhadran Baladandayuthapani, Bani K Mallick, Ganiraju C Manyam, Patricia A Thompson, Melissa L Bondy, Kim-Anh Do

Abstract read
In one paragraph

Article in Journal of the Royal Statistical Society. Series C, Applied statistics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Multivariate Bayesian variable selection for multi-trait genetic fine mapping.Journal of the Royal Statistical Society. Series C, Applied statistics · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Bayesian Joint Spike-and-Slab Graphical Lasso.Proceedings of machine learning research · 2019
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Bayesian hierarchical modelling for inferring genetic interactions in yeast.Journal of the Royal Statistical Society. Series C, Applied statistics · 2016
    Article
  18. Article
  19. 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

7 authors.

Lin ZhangDepartment of Statistics, Texas A&M University, College Station, Texas, U.S.A.
Veerabhadran BaladandayuthapaniDepartment of Biostatistics, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, U.S.A.
Bani K MallickDepartment of Statistics, Texas A&M University, College Station, Texas, U.S.A.
Ganiraju C ManyamDepartment of Bioinformatics and Computational Biology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, U.S.A.
Patricia A ThompsonArizona Cancer Center, University of Arizona, Tucson, U.S.A.
Melissa L BondyBaylor University, Houston, Texas, U.S.A.
Kim-Anh DoDepartment of Biostatistics, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, U.S.A.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Integrative methods for high-dimensional genomics dataR01CA160736 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BALADANDAYUTHAPANI, VEERABHADRAN · 2011 to 2014
$1.4M
NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA160736
6 · The paper itself

Abstract

The analysis of alterations that may occur in nature when segments of chromosomes are copied (known as copy number alterations) has been a focus of research to identify genetic markers of cancer. One high-throughput technique recently adopted is the use of molecular inversion probes (MIPs) to measure probe copy number changes. The resulting data consist of high-dimensional copy number profiles that can be used to ascertain probe-specific copy number alterations in correlative studies with patient outcomes to guide risk stratification and future treatment. We propose a novel Bayesian variable selection method, the hierarchical structured variable selection (HSVS) method, which accounts for the natural gene and probe-within-gene architecture to identify important genes and probes associated with clinically relevant outcomes. We propose the HSVS model for grouped variable selection, where simultaneous selection of both groups and within-group variables is of interest. The HSVS model utilizes a discrete mixture prior distribution for group selection and group-specific Bayesian lasso hierarchies for variable selection within groups. We provide methods for accounting for serial correlations within groups that incorporate Bayesian fused lasso methods for within-group selection. Through simulations we establish that our method results in lower model errors than other methods when a natural grouping structure exists. We apply our method to an MIP study of breast cancer and show that it identifies genes and probes that are significantly associated with clinically relevant subtypes of breast cancer.

Indexed as

copy number alterationhierarchical variable selectionlassoMCMCMIP data

Identifiers

PMID25705056
PMCPMC4334391

What OpenQuestion holds

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Registered trials

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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.