Abstract: The challenging and major role of the doctor in human life is to predict as well as diagnose the disease which has got infected in the human body. This typical genomic framework on disease analysis algorithm is designed to store and drive each and every gene characteristics like shape, weight, location and normal growth culture. Whenever the disease report is feed into this data mining algorithm triggers the similarity test built upon the data mining classification rules. A gene is usually comprised of hundreds of individual nucleotides arranged in a particular order. There are almost an unlimited number of ways that the nucleotides can be ordered and sequenced to form distinct genes. The algorithm delivers the difference between ...
The knowledge of the human genome is in continuous progression: a large number of databases have bee...
Next-Generation Sequencing has become an important tool in the field of human genetics. The coding s...
Sequence analysis of the group of proteins known to be associated with hereditary diseases allows th...
With the discovery that sickle cell anaemia is the result of a structurally altered haemoglobin prot...
A major milestone in modern biology was the complete sequencing of the human genome. But it produced...
Abstract: An The purpose of the paper ―Identifying genetic mutation rare genetic disorder by analyzi...
Contains fulltext : 33210.pdf (publisher's version ) (Open Access)Disease gene ide...
Objective: We investigated the common-disease relevant information obtained from sequencing compared...
A new generation of non-Sanger-based sequencing technologies, so called “next-generation” sequencing...
The evolution of next-generation sequencing technologies has facilitated the detection of causal gen...
Less than half of patients with suspected genetic disease receive a molecular diagnosis. We have the...
Genetic make-up of an individual is responsible for expression of external characters. Genes express...
BACKGROUND: Analysis of inherited diseases and their associated phenotypes is of great importance to...
AbstractSince the genome project in 1990s, a number of studies associated with genes have been condu...
The protein-coding exome of a patient with a monogenic disease contains about 20,000 variants, only ...
The knowledge of the human genome is in continuous progression: a large number of databases have bee...
Next-Generation Sequencing has become an important tool in the field of human genetics. The coding s...
Sequence analysis of the group of proteins known to be associated with hereditary diseases allows th...
With the discovery that sickle cell anaemia is the result of a structurally altered haemoglobin prot...
A major milestone in modern biology was the complete sequencing of the human genome. But it produced...
Abstract: An The purpose of the paper ―Identifying genetic mutation rare genetic disorder by analyzi...
Contains fulltext : 33210.pdf (publisher's version ) (Open Access)Disease gene ide...
Objective: We investigated the common-disease relevant information obtained from sequencing compared...
A new generation of non-Sanger-based sequencing technologies, so called “next-generation” sequencing...
The evolution of next-generation sequencing technologies has facilitated the detection of causal gen...
Less than half of patients with suspected genetic disease receive a molecular diagnosis. We have the...
Genetic make-up of an individual is responsible for expression of external characters. Genes express...
BACKGROUND: Analysis of inherited diseases and their associated phenotypes is of great importance to...
AbstractSince the genome project in 1990s, a number of studies associated with genes have been condu...
The protein-coding exome of a patient with a monogenic disease contains about 20,000 variants, only ...
The knowledge of the human genome is in continuous progression: a large number of databases have bee...
Next-Generation Sequencing has become an important tool in the field of human genetics. The coding s...
Sequence analysis of the group of proteins known to be associated with hereditary diseases allows th...