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Efficient Integration of Target Patient Data With Dna Sequences and Structure Information Towards Medical Diagnosis
Efficient Integration of Target Patient Data With Dna Sequences and Structure Information Towards Medical Diagnosis
Efficient Integration of Target Patient Data With Dna Sequences and Structure Information Towards Medical Diagnosis
Volume 11, Issue 4, April 2020, pp. 569-579, Article ID: IJARET_11_04_055
Available online at https://iaeme.com/Home/issue/IJARET?Volume=11&Issue=4
ISSN Print: 0976-6480 and ISSN Online: 0976-6499
DOI: https://doi.org/10.34218/IJARET.12.4.2021.055
Victor S.P
Associate Professor, Department of Computer Science,
Manonmaniam Sundaranar University, Tirunelveli, Tamil Nadu, India
ABSTRACT
Nowadays the disease occurrence for the people mostly depends on the inheritance
nature of the clans. The diabetes is an example to refer it with the parent to child transfer
in most of the possible cases. The disease diagnosis is a tedious process if every
parameter of the patient is unknown, The DNA (Deoxyribonucleic Acid) sequencing and
structure helps in one way or another to study the patterns and perform the proper
guidelines to control the spread of the disease and also to cure it in an efficient way if
the next stage of its progress is known to the medical field. The process of integrating
the exact DNA sequence and structure combinations for medical analysis is a difficult
one which requires the complex DNA data collection from different medical resources
with proper comparisons along with the verifications and validations to implement. This
paper proposed the optimal integration of DNA sequence and structure information
with evaluation techniques using data mining strategies by analyzing the disease
condition for individual patient condition. In future this paper will be extended with
machine learning analysis of implementation through genetic algorithm to attain an
automated DNA analysis system.
Key words: DNA, Sequence, Structure, Diagnosis, Integration.
Cite this Article: Edward Daniel Christopher .B and Victor S.P, Efficient Integration
of Target Patient data with DNA Sequences and Structure Information towards Medical
Diagnosis, International Journal of Advanced Research in Engineering and
Technology, 11(4), 2020, pp. 569-579.
https://iaeme.com/Home/issue/IJARET?Volume=11&Issue=4
1. INTRODUCTION
1.1. DNA
DNA is a polymer composed of two polynucleotide chains that coil around each other to form
a double helix carrying genetic instructions for the development, functioning, growth, and
reproduction of all known organisms and many viruses [1]. DNA and ribonucleic acid (RNA)
are nucleic acids. Alongside proteins, lipids and complex carbohydrates (polysaccharides),
nucleic acids are one of the four major types of macromolecules that are essential for all known
forms of life [2, 4].
2. PROPOSED METHODOLOGY
The proposed methodology focuses on implementing the efficient Data Integration of DNA
Sequences and Structure Information’s towards Medical Diagnosis. The DNA data collection,
integration methodology for the pattern matching for the individual patient data analysis in
order to perform the medical data analysis in an efficient way. The following figure-1 shows
the proposed methodology structure,
2.1. Efficient data integration of DNA information towards medical diagnosis and
analysis
Figure 2 Proposed DNA data analysis for the patient disease diagnosis and analysis.
3. IMPLEMENTATION
3.1. Patient Data
The patient data contains the following information’s,
Patient History
It includes the fields as in table 1,
Patient Pretest
It contains the fields as in table 2,
DNA data
The following figure (a) represents the Helix DNA structure, (b) Bond DNA structure, (c)
Groove DNA Structure and (d) DNA sequence sample.
Sub Sequence
Generate multiple sub sequences for enabling the pattern matching procedures. The java code
is as follows,
// Java Program to print the
// 'n' lobes of DNA pattern
import java.io.*;
class GFG {
// Function to print upper half
// of the DNA or the upper lobe
static void printUpperHalf(String str)
{
char first, second;
int pos = 0;
first = str.charAt(pos);
second = str.charAt(pos+1);
pos += 2;
int x = i % 6;
}
}
Match
Check with the patient reference DNA sub sequence match with the existing internal or external
DNA extractions. The java code is as follows,
import java.util.*;
System.out.println(score);
System.out.println("Score = " + score.score());
}
if (dna1.charAt(i) == dna2.charAt(i)) {
score += 2;
} else {
score -= 1;
}
}
return score;
}
The following fig-4 shows the performance of proposed medicinal diagnosis system.
5. CONCLUSION
The integration of patient data with their clinical history along with the DNA analysis makes
the medical diagnosis system into a huge success. The process of analyzing the DNA structures
such as helix, bond, and Groove provides the essential information’s with its reared parts and
hidden data for future processing. The DNA sequence holds the entire pattern of patient medical
status which will be compared with the reference DNA sequence of stored patterns by dividing
it into several subsequences plays the vital role in the health issue variant identifications. The
Final analysis focuses on the target patients current status with the determination of future
impacts intimates the guidelines for the further medicinal paths and suggestions. This paper
produced the success rate of 67% more than that of the existing medical analysis without DNA
analysis. In future this research will be implemented with the support of genetic algorithm and
machine learning for the further developments in optimal medical diagnosis system.
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