Abstract

There has been a spate of interest in association networks in biological and medical research, for example, genetic interaction networks. In this paper, we propose a novel method, the extended joint hub graphical lasso (EDOHA), to estimate multiple related interaction networks for high dimensional omics data across multiple distinct classes. To be specific, we construct a convex penalized log likelihood optimization problem and solve it with an alternating direction method of multipliers (ADMM) algorithm. The proposed method can also be adapted to estimate interaction networks for high dimensional compositional data such as microbial interaction networks. The performance of the proposed method in the simulated studies shows that EDOHA has remarkable advantages in recognizing class-specific hubs than the existing comparable methods. We also present three applications of real datasets. Biological interpretations of our results confirm those of previous studies and offer a more comprehensive understanding of the underlying mechanism in disease.

Highlights

  • We present the extended joint hub graphical lasso (EDOHA) algorithm for constructing multiple interaction networks from multiple classes

  • We compare the performance of EDOHA with the existing methods, such as the graphical lasso (JGL) and JRmGRN

  • Results show that EDOHA is more efficient than other methods when analyzing compositional data correlation networks which have both common and class-specific hub nodes

Read more

Summary

Introduction

With advances in high-throughput sequencing and omics technologies, biological information is being collected at an amazing rate, which stimulates researchers to discover modular. Extended graphical lasso for interaction networks for high dimensional omics data. The population-based proteomic datasets are from lung(https://cptc-xfer.uis. Georgetown.edu/publicData/Phase_III_Data/ CPTAC_LUAD_S046/CPTAC_LUAD_Proteome_ CDAP_Protein_Report.r1/CPTAC3_Lung_Adeno_ Carcinoma_Proteome.tmt10.tsv); liver(https://cptcxfer.uis.georgetown.edu/publicData/External/ S049_Liver_Cancer_Gao2019/Liver_Cancer_ Proteome_CDAP_Protein_Report.r1/Zhou_Liver_ Cancer_Proteome.tmt11.tsv); colon(https://cptcxfer.uis.georgetown.edu/publicData/Phase_II_ Data/CPTAC_Colon_Cancer_S037/CPTAC_ COprospective_PNNL_Proteome_CDAP_Protein_ Report.r1/CPTAC2_Colon_Prospective_Collection_ PNNL_Proteome.tmt10.tsv); kidney(https://cptcxfer.uis.georgetown.edu/publicData/Phase_III_ Data/CPTAC_CCRCC_S044/CPTAC_CCRCC_ Proteome_CDAP_Protein_Report.r1/CPTAC3_ Clear_Cell_Renal_Cell_Carcinoma_Proteome. The population-based proteomic datasets are from lung(https://cptc-xfer.uis. georgetown.edu/publicData/Phase_III_Data/ CPTAC_LUAD_S046/CPTAC_LUAD_Proteome_ CDAP_Protein_Report.r1/CPTAC3_Lung_Adeno_ Carcinoma_Proteome.tmt10.tsv); liver(https://cptcxfer.uis.georgetown.edu/publicData/External/ S049_Liver_Cancer_Gao2019/Liver_Cancer_ Proteome_CDAP_Protein_Report.r1/Zhou_Liver_ Cancer_Proteome.tmt11.tsv); colon(https://cptcxfer.uis.georgetown.edu/publicData/Phase_II_ Data/CPTAC_Colon_Cancer_S037/CPTAC_ COprospective_PNNL_Proteome_CDAP_Protein_ Report.r1/CPTAC2_Colon_Prospective_Collection_ PNNL_Proteome.tmt10.tsv); kidney(https://cptcxfer.uis.georgetown.edu/publicData/Phase_III_ Data/CPTAC_CCRCC_S044/CPTAC_CCRCC_ Proteome_CDAP_Protein_Report.r1/CPTAC3_ Clear_Cell_Renal_Cell_Carcinoma_Proteome. tmt10.tsv)

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call