TY - GEN
T1 - Detecting aberrant signal transduction pathways from high-throughput data using GIST algorithm
AU - Gu, Jinghua
AU - Xuan, Jianhua
AU - Wang, Chen
AU - Chen, Li
AU - Wang, Tian Li
AU - Shih, Ie Ming
PY - 2012/7/25
Y1 - 2012/7/25
N2 - It is biologically important to integrate high-throughput data to identify aberrant signal transduction pathways in cancer research. The high-throughput data acquired from The Cancer Genome Atlas (TCGA) Project offer a comprehensive picture of the genomic and transcriptional changes across hundreds of tumor samples. In this paper we propose a novel method, namely Gibbs sampler to Infer Signal Transduction pathways (GIST), to detect aberrant pathways that are highly associated with biological phenotypes or clinical information. GIST endeavors to estimate the edge probability by using a Markov Chain Monte Carlo (MCMC) method (i.e., a Gibbs sampling strategy). Through the sampling process, GIST is able to infer the correct signal transduction direction because the sampled edge probabilities are jointly determined by gene expression data and network topology. We first tested the efficacy of the GIST algorithm on yeast data and successfully uncovered several biologically meaningful signaling pathways. A case study on TCGA ovarian cancer data was further designed, aiming to unravel diverse signaling pathways associated with the development of ovarian cancer. The experimental results demonstrated the feasibility of applying GIST to identify and prioritize important signaling pathways in ovarian cancer for further biological validation.
AB - It is biologically important to integrate high-throughput data to identify aberrant signal transduction pathways in cancer research. The high-throughput data acquired from The Cancer Genome Atlas (TCGA) Project offer a comprehensive picture of the genomic and transcriptional changes across hundreds of tumor samples. In this paper we propose a novel method, namely Gibbs sampler to Infer Signal Transduction pathways (GIST), to detect aberrant pathways that are highly associated with biological phenotypes or clinical information. GIST endeavors to estimate the edge probability by using a Markov Chain Monte Carlo (MCMC) method (i.e., a Gibbs sampling strategy). Through the sampling process, GIST is able to infer the correct signal transduction direction because the sampled edge probabilities are jointly determined by gene expression data and network topology. We first tested the efficacy of the GIST algorithm on yeast data and successfully uncovered several biologically meaningful signaling pathways. A case study on TCGA ovarian cancer data was further designed, aiming to unravel diverse signaling pathways associated with the development of ovarian cancer. The experimental results demonstrated the feasibility of applying GIST to identify and prioritize important signaling pathways in ovarian cancer for further biological validation.
KW - Gibbs sampling
KW - Markov chain Mote Carlo
KW - gene expression
KW - protein-protein interaction
KW - signal transduction pathway
UR - http://www.scopus.com/inward/record.url?scp=84864037011&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84864037011&partnerID=8YFLogxK
U2 - 10.1109/CIBCB.2012.6217240
DO - 10.1109/CIBCB.2012.6217240
M3 - Conference contribution
AN - SCOPUS:84864037011
SN - 9781467311892
T3 - 2012 IEEE Symposium on Computational Intelligence and Computational Biology, CIBCB 2012
SP - 267
EP - 274
BT - 2012 IEEE Symposium on Computational Intelligence and Computational Biology, CIBCB 2012
T2 - 2012 IEEE Symposium on Computational Intelligence and Computational Biology, CIBCB 2012
Y2 - 9 May 2012 through 12 May 2012
ER -