Identification of supervised and sparse functional genomic pathways
DOI10.1515/SAGMB-2018-0026zbMATH Open1445.92185OpenAlexW3009238540WikidataQ89935664 ScholiaQ89935664MaRDI QIDQ2195286FDOQ2195286
Authors: Fan Zhang, Jeffrey C. Miecznikowski, David L. Tritchler
Publication date: 8 September 2020
Published in: Statistical Applications in Genetics and Molecular Biology (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1515/sagmb-2018-0026
Recommendations
- Identification of consistent functional genetic modules
- A statistical framework for pathway and gene identification from integrative analysis
- Penalized differential pathway analysis of integrative oncogenomics studies
- Fast identification of biological pathways associated with a quantitative trait using group lasso with overlaps
- On the sample complexity of cancer pathways identification
Applications of statistics to biology and medical sciences; meta analysis (62P10) Genetics and epigenetics (92D10) Systems biology, networks (92C42)
Cites Work
- A penalized matrix decomposition, with applications to sparse principal components and canonical correlation analysis
- Extensions of sparse canonical correlation analysis with applications to genomic data
- Stability Selection
- Subsampling
- Title not available (Why is that?)
- Sparse canonical correlation analysis with application to genomic data integration
- Quantifying the association between gene expressions and DNA-markers by penalized canonical correlation analysis
- A sparse PLS for variable selection when integrating omics data
- Identification of consistent functional genetic modules
- Title not available (Why is that?)
Cited In (3)
Uses Software
This page was built for publication: Identification of supervised and sparse functional genomic pathways
Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q2195286)