QuantitativeTraitLocus (QTL) is a statistical method used to restrict genomic regions contributing to specific phenotypes. To further localize genes in such regions a web tool called “Candidate Gene Capture” (CGC) was developed by Andersson et al. (2005). The CGC tool was based on the textual description of genes defined in the human phenotype database OMIM. Even though the CGC tool works well, the tool was limited by a number of inconsistencies in the underlying database structure, static web pages and some gene descriptions without properly defined function in the OMIM database. Hence, in this work the CGC tool was improved by redesigning its database structure, adding dynamic web pages and improving the prediction of unknown gene functio...
In the post genome era, a major goal of biology is the identification of specific roles for individu...
Background: Modern high throughput experimental techniques such as DNA microarrays often result in l...
High-throughput gene expression data can predict gene function through the “guilt by association” pr...
QuantitativeTraitLocus (QTL) is a statistical method used to restrict genomic regions contributing t...
Many human diseases, such as rheumatoid arthritis and type 2 diabetes mellitus, have a very complex ...
Aim. To evaluate the functional annotation of genes associated with rheumatoid arthritis with differ...
Contains fulltext : 33210.pdf (publisher's version ) (Open Access)Disease gene ide...
To identify the gene underlying a human genetic disorder can be difficult and time-consuming. Typica...
To identify the gene underlying a human genetic disorder can be difficult and time-consuming. Typica...
International audienceAnnotQTL is a web tool designed to aggregate functional annotations from diffe...
Background The common disease rare variant hypothesis states that disease etiology is caused collect...
The identification of genes responsible for human disease enables an understanding of disease mechan...
International audienceBACKGROUND: Identifying the genotypes underlying human disease phenotypes is a...
Functional annotation of genetic variants including single nucleotide polymorphisms (SNPs) and copy ...
In the post genome era, a major goal of biology is the identification of specific roles for individu...
Background: Modern high throughput experimental techniques such as DNA microarrays often result in l...
High-throughput gene expression data can predict gene function through the “guilt by association” pr...
QuantitativeTraitLocus (QTL) is a statistical method used to restrict genomic regions contributing t...
Many human diseases, such as rheumatoid arthritis and type 2 diabetes mellitus, have a very complex ...
Aim. To evaluate the functional annotation of genes associated with rheumatoid arthritis with differ...
Contains fulltext : 33210.pdf (publisher's version ) (Open Access)Disease gene ide...
To identify the gene underlying a human genetic disorder can be difficult and time-consuming. Typica...
To identify the gene underlying a human genetic disorder can be difficult and time-consuming. Typica...
International audienceAnnotQTL is a web tool designed to aggregate functional annotations from diffe...
Background The common disease rare variant hypothesis states that disease etiology is caused collect...
The identification of genes responsible for human disease enables an understanding of disease mechan...
International audienceBACKGROUND: Identifying the genotypes underlying human disease phenotypes is a...
Functional annotation of genetic variants including single nucleotide polymorphisms (SNPs) and copy ...
In the post genome era, a major goal of biology is the identification of specific roles for individu...
Background: Modern high throughput experimental techniques such as DNA microarrays often result in l...
High-throughput gene expression data can predict gene function through the “guilt by association” pr...