Abstract: An The purpose of the paper ―Identifying genetic mutation rare genetic disorder by analyzing characteristics of genotype-phenotype by implementing data mining algorithm's ‖aims at reducing the complexities involved in determining the mutation occurred in human DNA sequence. The Data mining algorithm is chosen from specific areas like association. The algorithms are grouped in such way that it can be adapt to user requirements. The visualization provided for the mined outputs are represented in graph.The available data mining tools require expert users to carry out experiments. The scope of this relies in the area of visualization of the mined data. The visualizations can be made interactive such that the outputs can be easily...
Thanks to the affordability of DNA sequencing, hundreds of thousands of individuals with rare disord...
Abstract: The challenging and major role of the doctor in human life is to predict as well as diagno...
To identify the gene underlying a human genetic disorder can be difficult and time-consuming. Typica...
Research into pathogenic mutations is vital and useful for understanding illness progression, progno...
BACKGROUND: Analysis of inherited diseases and their associated phenotypes is of great importance to...
Phenotype analysis is commonly recognized to be of great importance for gaining insight into genetic...
University of Technology, Sydney. Faculty of Engineering and Information Technology.Data mining and ...
The study of rare diseases uses next-generation sequencing (NGS) technology to detect causative muta...
Many phenotypic traits of the human body and their susceptibility to drugs and diseases may be assoc...
With the discovery that sickle cell anaemia is the result of a structurally altered haemoglobin prot...
Recent technological advances have created challenges for geneticists and a need to adapt to a wide ...
A major milestone in modern biology was the complete sequencing of the human genome. But it produced...
University of Minnesota Ph.D. dissertation. August 2012. Major: Computer Science. Advisor: Vipin Kum...
Item does not contain fulltextTo identify the gene underlying a human genetic disorder can be diffic...
Group 14 of Genetic Analysis Workshop 17 examined several issues related to analysis of complex trai...
Thanks to the affordability of DNA sequencing, hundreds of thousands of individuals with rare disord...
Abstract: The challenging and major role of the doctor in human life is to predict as well as diagno...
To identify the gene underlying a human genetic disorder can be difficult and time-consuming. Typica...
Research into pathogenic mutations is vital and useful for understanding illness progression, progno...
BACKGROUND: Analysis of inherited diseases and their associated phenotypes is of great importance to...
Phenotype analysis is commonly recognized to be of great importance for gaining insight into genetic...
University of Technology, Sydney. Faculty of Engineering and Information Technology.Data mining and ...
The study of rare diseases uses next-generation sequencing (NGS) technology to detect causative muta...
Many phenotypic traits of the human body and their susceptibility to drugs and diseases may be assoc...
With the discovery that sickle cell anaemia is the result of a structurally altered haemoglobin prot...
Recent technological advances have created challenges for geneticists and a need to adapt to a wide ...
A major milestone in modern biology was the complete sequencing of the human genome. But it produced...
University of Minnesota Ph.D. dissertation. August 2012. Major: Computer Science. Advisor: Vipin Kum...
Item does not contain fulltextTo identify the gene underlying a human genetic disorder can be diffic...
Group 14 of Genetic Analysis Workshop 17 examined several issues related to analysis of complex trai...
Thanks to the affordability of DNA sequencing, hundreds of thousands of individuals with rare disord...
Abstract: The challenging and major role of the doctor in human life is to predict as well as diagno...
To identify the gene underlying a human genetic disorder can be difficult and time-consuming. Typica...