Cancer pathway network analysis using cellular automata
Mahata, Kalyan and Sarkar, Anasua LU
(2015)
p.145-159
- Abstract
Identification of cancer pathways is the central goal in the cancer gene expression data analysis. Data mining refers to the process analyzing huge data in order to find useful pattern. Data classification is the process of identifying common properties among a set of objects and grouping them into different classes. A cellular automaton is a discrete, dynamical system with simple uniformly interconnected cells. Cellular automata are used in data mining for reasons such as all decisions are made locally depend on the state of the cell and the states of neighboring cells. A high-speed, low-cost pattern-classifier, built around a sparse network referred to as cellular automata (ca) is implemented. Lif-stimulated gene regulatory network... (More)
Identification of cancer pathways is the central goal in the cancer gene expression data analysis. Data mining refers to the process analyzing huge data in order to find useful pattern. Data classification is the process of identifying common properties among a set of objects and grouping them into different classes. A cellular automaton is a discrete, dynamical system with simple uniformly interconnected cells. Cellular automata are used in data mining for reasons such as all decisions are made locally depend on the state of the cell and the states of neighboring cells. A high-speed, low-cost pattern-classifier, built around a sparse network referred to as cellular automata (ca) is implemented. Lif-stimulated gene regulatory network involved in breast cancer has been simulated using cellular automata to obtain biomarker genes. Our model outputs the desired genes among inputs with highest priority, which are analysed for their functional involvement in relevant oncological functional enrichment analysis. This approach is a novel one to discover cancer biomarkers in cellular spaces.
(Less)
- author
- Mahata, Kalyan
and Sarkar, Anasua
LU
- publishing date
- 2015-08-03
- type
- Chapter in Book/Report/Conference proceeding
- publication status
- published
- host publication
- Improving Knowledge Discovery through the Integration of Data Mining Techniques
- pages
- 145 - 159
- publisher
- IGI Global
- external identifiers
-
- scopus:84957362118
- ISBN
- 1466685131
- 9781466685130
- 9781466685147
- DOI
- 10.4018/978-1-4666-8513-0.ch008
- language
- English
- LU publication?
- no
- id
- 94cb03e0-f284-43d3-80f2-1bc98b58ee07
- date added to LUP
- 2018-10-09 09:48:47
- date last changed
- 2024-01-15 03:20:00
@inbook{94cb03e0-f284-43d3-80f2-1bc98b58ee07,
abstract = {{<p>Identification of cancer pathways is the central goal in the cancer gene expression data analysis. Data mining refers to the process analyzing huge data in order to find useful pattern. Data classification is the process of identifying common properties among a set of objects and grouping them into different classes. A cellular automaton is a discrete, dynamical system with simple uniformly interconnected cells. Cellular automata are used in data mining for reasons such as all decisions are made locally depend on the state of the cell and the states of neighboring cells. A high-speed, low-cost pattern-classifier, built around a sparse network referred to as cellular automata (ca) is implemented. Lif-stimulated gene regulatory network involved in breast cancer has been simulated using cellular automata to obtain biomarker genes. Our model outputs the desired genes among inputs with highest priority, which are analysed for their functional involvement in relevant oncological functional enrichment analysis. This approach is a novel one to discover cancer biomarkers in cellular spaces.</p>}},
author = {{Mahata, Kalyan and Sarkar, Anasua}},
booktitle = {{Improving Knowledge Discovery through the Integration of Data Mining Techniques}},
isbn = {{1466685131}},
language = {{eng}},
month = {{08}},
pages = {{145--159}},
publisher = {{IGI Global}},
title = {{Cancer pathway network analysis using cellular automata}},
url = {{http://dx.doi.org/10.4018/978-1-4666-8513-0.ch008}},
doi = {{10.4018/978-1-4666-8513-0.ch008}},
year = {{2015}},
}