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• PRESENTED BY GUIDED BY
• KARTHIGA R
Dr.ADLIN SHEEBA
• 312414104049
Associate Professor
Genetic disease identification and medical
diagnosis using MF, CC, BF, MicroRNA and
transcription factors
Abstract
• The Main aim of our project is to create and maintain a Genomic and Proteomic
Knowledge Base (GPKB), which integrates the most relevant sources of bio
information.
• Cross ontology is used to manipulate the Protein values from three sub ontologies
for identifying the gene attacked disease.
• Based on cellular component, molecular function and biological process values
intrinsic and extrinsic calculation would be manipulated.
• Comparing the regulations between miRNA-TF interaction, TF-gene interactions
and gene-miRNA interaction with the help of integration technique.
• Iterative Multiplicative Updating Algorithm is used to solve the optimization
module function for the above interactions.
• After that interactions compare the regulatory modules and protein value for gene
and generate Bayesian rose tree for efficiency of our result.
Existing system
• The eprocessxisting system used association rules mining algorithm to
support GO terms such as Molecular function, Cellular component,
Biological.
• It is used to find all relative genetic diseases without any accuracy.
• It is time consuming.
Proposed system
• Proposal of co-regulatory modules between Transcription Factor, gene and
MiRNA on functional level with genomic data.
• The integration technique is implemented between miRNA, Transcription
Factor (TF) and gene.
• After integration, Iterative Multiplicating update algorithm is used to check
the optimization function between the regulatory modules.
• Expression or some value from this algorithm is obtained and then
compared to protein values.
• The protein value is the one got from Biological Process (BP), Molecular
Function (MF) and Cellular Component (CC) with the help of cross
ontology technique.
• At last a bayesian rose tree structure is obtained that shows our disease
which was affected in our chromosome and also how to cure it. Also we
can identify the symptoms applicable for our gene by our proposed system.
Literature survey
SI.no Title Author Year Content
1 Ontology mining in
Molecular Biology
domain
Anuraag
Vikram Kate,
Harish
Balakrishnan
2016 Ontology mining is done, inorder to
improvise the prevailing ontology
functionally by the inclusion of
DNA and RNA components, and
also structurally by expanding the
ontology in a different perspective.
2 Using GO-WAR for
mining cross-
ontology weighted
association rules
Giuseppe
Agapito, Mario
Cannataro
2015 initially we calculate the
information content for each GO
term then, we extract weighted
association rules by using a
modified FP-Tree like algorithm
able to deal with the dimension of
classical biological datasets.
3 Improving
annotation quality
Cami de Vera. 2014 (GO-WAR), Mining Weighted
Association Rules from GO, that is
System architecture
User
Cross Ontology
MF CC BP
Collaborative Filters
DB
Multiplicative Update
Algorithm
Bayesian
rose tree
Result
Protein id
MiRNA TF Gene
Integration
Module
• Cross Ontology
• Collaborative Filtering
• Regulatory modules
• Integration Technique
• Multiplicative Update Algorithm
• Tree Representation
Module description
Cross Ontology:
• It classifies functions along three aspects: molecular function molecular
activities of gene products, cellular component where gene products are
active, biological process pathways and larger processes made up of the
activities of multiple gene products.
• Intrinsic and extrinsic diseases are identified.
• Based on cellular component, molecular function and biological process
values intrinsic and extrinsic calculation would be manipulated.
Collaborative Filtering:
• Calculates the protein value of human and normal value of
particular gene id.
• cross ontology process get the BP,CC&MF value for gene to identify
the gene that have Intrinsic or extrinsic diseases.
•Intrinsic:
If the normal protein value of human is compare to lower than that
of calculating cross ontology value (comparing BP&CC or MF&CC or
MF&BP) is said to be Intrinsic.
•Extrinsic:
If the normal protein value of human is compare to higher than
that of calculating cross ontology value (comparing BP&CC or MF&CC
or MF&BP) is said to be extrinsic.
Regulatory modules:
• Sets of genes are co-regulated to respond to different conditions.
• It identifies modules of co-regulated genes, their regulators and the
conditions under which regulation occurs, generating testable hypotheses in
the form 'regulator X regulates module Y under conditions W'.
Integration Technique:
•In this module, we use a fusion technique to integrate both gene ontology
and regulatory modules.
•This is the first time of proposing a fusion technique in gene analysis which
produces increased accuracy.
Multiplicative Update Algorithm:
• A novel approach to identify miRNAs and transcription factors co-
regulatory modules.
• An objective function is constructed by integrating the miRNA,TF,gene
expression profiles, target site information (miRNA-gene and TF-gene
regulations) as well as the protein-protein interactions.
• In order to obtain the optimal solution of the objective function, we solve
the optimization model function effectively by iterative multiplicative
updating algorithm.
• Tree Representation:
Bayesian Rose Tree gives us the structure of tree with genetic diseases, its
symptoms and how to cure the diseases.

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Genetic disease identification and medical diagnosis using MF, CC, BF, MicroRNA and transcription factors

  • 1. • PRESENTED BY GUIDED BY • KARTHIGA R Dr.ADLIN SHEEBA • 312414104049 Associate Professor Genetic disease identification and medical diagnosis using MF, CC, BF, MicroRNA and transcription factors
  • 2. Abstract • The Main aim of our project is to create and maintain a Genomic and Proteomic Knowledge Base (GPKB), which integrates the most relevant sources of bio information. • Cross ontology is used to manipulate the Protein values from three sub ontologies for identifying the gene attacked disease. • Based on cellular component, molecular function and biological process values intrinsic and extrinsic calculation would be manipulated. • Comparing the regulations between miRNA-TF interaction, TF-gene interactions and gene-miRNA interaction with the help of integration technique. • Iterative Multiplicative Updating Algorithm is used to solve the optimization module function for the above interactions. • After that interactions compare the regulatory modules and protein value for gene and generate Bayesian rose tree for efficiency of our result.
  • 3. Existing system • The eprocessxisting system used association rules mining algorithm to support GO terms such as Molecular function, Cellular component, Biological. • It is used to find all relative genetic diseases without any accuracy. • It is time consuming.
  • 4. Proposed system • Proposal of co-regulatory modules between Transcription Factor, gene and MiRNA on functional level with genomic data. • The integration technique is implemented between miRNA, Transcription Factor (TF) and gene. • After integration, Iterative Multiplicating update algorithm is used to check the optimization function between the regulatory modules. • Expression or some value from this algorithm is obtained and then compared to protein values. • The protein value is the one got from Biological Process (BP), Molecular Function (MF) and Cellular Component (CC) with the help of cross ontology technique. • At last a bayesian rose tree structure is obtained that shows our disease which was affected in our chromosome and also how to cure it. Also we can identify the symptoms applicable for our gene by our proposed system.
  • 5. Literature survey SI.no Title Author Year Content 1 Ontology mining in Molecular Biology domain Anuraag Vikram Kate, Harish Balakrishnan 2016 Ontology mining is done, inorder to improvise the prevailing ontology functionally by the inclusion of DNA and RNA components, and also structurally by expanding the ontology in a different perspective. 2 Using GO-WAR for mining cross- ontology weighted association rules Giuseppe Agapito, Mario Cannataro 2015 initially we calculate the information content for each GO term then, we extract weighted association rules by using a modified FP-Tree like algorithm able to deal with the dimension of classical biological datasets. 3 Improving annotation quality Cami de Vera. 2014 (GO-WAR), Mining Weighted Association Rules from GO, that is
  • 6. System architecture User Cross Ontology MF CC BP Collaborative Filters DB Multiplicative Update Algorithm Bayesian rose tree Result Protein id MiRNA TF Gene Integration
  • 7. Module • Cross Ontology • Collaborative Filtering • Regulatory modules • Integration Technique • Multiplicative Update Algorithm • Tree Representation
  • 8. Module description Cross Ontology: • It classifies functions along three aspects: molecular function molecular activities of gene products, cellular component where gene products are active, biological process pathways and larger processes made up of the activities of multiple gene products. • Intrinsic and extrinsic diseases are identified. • Based on cellular component, molecular function and biological process values intrinsic and extrinsic calculation would be manipulated.
  • 9. Collaborative Filtering: • Calculates the protein value of human and normal value of particular gene id. • cross ontology process get the BP,CC&MF value for gene to identify the gene that have Intrinsic or extrinsic diseases. •Intrinsic: If the normal protein value of human is compare to lower than that of calculating cross ontology value (comparing BP&CC or MF&CC or MF&BP) is said to be Intrinsic. •Extrinsic: If the normal protein value of human is compare to higher than that of calculating cross ontology value (comparing BP&CC or MF&CC or MF&BP) is said to be extrinsic.
  • 10. Regulatory modules: • Sets of genes are co-regulated to respond to different conditions. • It identifies modules of co-regulated genes, their regulators and the conditions under which regulation occurs, generating testable hypotheses in the form 'regulator X regulates module Y under conditions W'.
  • 11. Integration Technique: •In this module, we use a fusion technique to integrate both gene ontology and regulatory modules. •This is the first time of proposing a fusion technique in gene analysis which produces increased accuracy.
  • 12. Multiplicative Update Algorithm: • A novel approach to identify miRNAs and transcription factors co- regulatory modules. • An objective function is constructed by integrating the miRNA,TF,gene expression profiles, target site information (miRNA-gene and TF-gene regulations) as well as the protein-protein interactions. • In order to obtain the optimal solution of the objective function, we solve the optimization model function effectively by iterative multiplicative updating algorithm.
  • 13. • Tree Representation: Bayesian Rose Tree gives us the structure of tree with genetic diseases, its symptoms and how to cure the diseases.