The massive amount of data generated from genome sequencing brings tons of newly identified mutations, whose pathogenic/non-pathogenic effects need to be evaluated. This has given rise to several mutation predictor tools that, in general, do not consider the specificities of the various protein groups. We aimed to develop a predictor tool dedicated to membrane proteins, under the premise that their specific structural features and environment would give different responses to mutations compared to globular proteins. For this purpose, we created TMSNP, a database that currently contains information from 2624 pathogenic and 196 705 non-pathogenic reported mutations located in the transmembrane region of membrane proteins. By computing various...
Understanding the pathogenicity of missense mutation (MM) is essential for shed light on genetic dis...
MOTIVATION: Human single nucleotide polymorphisms (SNPs) are the most frequent type of genetic varia...
ABSTRACT: Single nucleotide polymorphisms (SNPs) are the most common form of genetic variation in hu...
The massive amount of data generated from genome sequencing brings tons of newly identified mutation...
Significant efforts have been invested into understanding and predicting the molecular consequences ...
Being able to assess the phenotypic effects of mutations is a much required capability in precision ...
Motivation: Single Nucleotide Polymorphisms (SNPs) are the most frequent type of genetic variation i...
Next-generation sequencing methods have not only allowed an understanding of genome sequence variati...
Curs 2015-2016In recent years many SNPs have been identified, some of these linked to certain diseas...
Background The automated retrieval and integration of information about protein point mutations in c...
Here, we report a webserver for the improved SDM, used for predicting the effects of mutations on pr...
Feature-based multiple models improve classification of mutation-induced stability changes Lukas Fol...
Over the past two decades, several computational methods have been proposed to predict how missense ...
MOTIVATION: Mutations play fundamental roles in evolution by introducing diversity into genomes. Mis...
Variant interpretation remains a central challenge for precision medicine. Missense variants are par...
Understanding the pathogenicity of missense mutation (MM) is essential for shed light on genetic dis...
MOTIVATION: Human single nucleotide polymorphisms (SNPs) are the most frequent type of genetic varia...
ABSTRACT: Single nucleotide polymorphisms (SNPs) are the most common form of genetic variation in hu...
The massive amount of data generated from genome sequencing brings tons of newly identified mutation...
Significant efforts have been invested into understanding and predicting the molecular consequences ...
Being able to assess the phenotypic effects of mutations is a much required capability in precision ...
Motivation: Single Nucleotide Polymorphisms (SNPs) are the most frequent type of genetic variation i...
Next-generation sequencing methods have not only allowed an understanding of genome sequence variati...
Curs 2015-2016In recent years many SNPs have been identified, some of these linked to certain diseas...
Background The automated retrieval and integration of information about protein point mutations in c...
Here, we report a webserver for the improved SDM, used for predicting the effects of mutations on pr...
Feature-based multiple models improve classification of mutation-induced stability changes Lukas Fol...
Over the past two decades, several computational methods have been proposed to predict how missense ...
MOTIVATION: Mutations play fundamental roles in evolution by introducing diversity into genomes. Mis...
Variant interpretation remains a central challenge for precision medicine. Missense variants are par...
Understanding the pathogenicity of missense mutation (MM) is essential for shed light on genetic dis...
MOTIVATION: Human single nucleotide polymorphisms (SNPs) are the most frequent type of genetic varia...
ABSTRACT: Single nucleotide polymorphisms (SNPs) are the most common form of genetic variation in hu...