BACKGROUND: With the completion of the Human Genome Project and recent advancements in mutation detection technologies, the volume of data available on genetic variations has risen considerably. These data are stored in online variation databases and provide important clues to the cause of diseases and potential side effects or resistance to drugs. However, the data presentation techniques employed by most of these databases make them difficult to use and understand. RESULTS: Here we present a visualisation toolkit that can be employed by online variation databases to generate graphical models of gene sequence with corresponding variations and their consequences. The VariVis software package can run on any web server capable of executing Pe...
Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insert...
The collection of genetic variants that cause inherited disease (causative mutation) has occurred fo...
The study of Copy Number Variations (CNVs) is recently emerging as a hot topic for biomedical cancer...
Abstract Background With the completion of the Human Genome Project and recent advancements in mutat...
International audienceABSTRACT: BACKGROUND: Sharing of data about variation and the associated pheno...
Background: Sharing of data about variation and the associated phenotypes is a critical need, yet va...
SUMMARY: There is an immediate need for tools to both analyse and visualize in real-time single-nucl...
The study of such a complex phenomenon as cancer, which depends on several but unexplored and unclea...
Summary: Over the past decade, there has been an exponential increase in the amount of disease-relat...
The collection of genetic variants that cause inherited disease (causative mutation) has occurred fo...
We report the development of a flexible database management system, based on a relational database f...
Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insert...
The collection of genetic variants that cause inherited disease (causative mutation) has occurred fo...
The study of Copy Number Variations (CNVs) is recently emerging as a hot topic for biomedical cancer...
Abstract Background With the completion of the Human Genome Project and recent advancements in mutat...
International audienceABSTRACT: BACKGROUND: Sharing of data about variation and the associated pheno...
Background: Sharing of data about variation and the associated phenotypes is a critical need, yet va...
SUMMARY: There is an immediate need for tools to both analyse and visualize in real-time single-nucl...
The study of such a complex phenomenon as cancer, which depends on several but unexplored and unclea...
Summary: Over the past decade, there has been an exponential increase in the amount of disease-relat...
The collection of genetic variants that cause inherited disease (causative mutation) has occurred fo...
We report the development of a flexible database management system, based on a relational database f...
Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insert...
The collection of genetic variants that cause inherited disease (causative mutation) has occurred fo...
The study of Copy Number Variations (CNVs) is recently emerging as a hot topic for biomedical cancer...