Abstract Background The detection and interpretation of CNVs are of clinical importance in genetic testing. Several databases and web services are already being used by clinical geneticists to interpret the medical relevance of identified CNVs in patients. However, geneticists or physicians would like to obtain the original literature context for more detailed information, especially for rare CNVs that were not included in databases. Results The resulting CNVdigest database includes 440,485 sentences for CNV-disease relationship. A total number of 1582 CNVs and 2425 diseases are involved. Sentences describing CNV-disease correlations are indexed in CNVdigest, with CNV mentions and disease mentions annotated. Conclusions In this paper, we us...
Autoimmune diseases (ADs) arise from an abnormal immune response of the body against substances and ...
The increasing amount of scientific information available to researchers in the form of biomedical l...
Publisher's PDFThe number of published articles describing associations between mutations and diseas...
peer reviewedText mining is a flexible technology that can be applied to numerous different tasks in...
BackgroundIn recent years a large volume of clinical genomics data has become available due to rapid...
International audienceCopy number variants (CNVs) account for a major proportion of human genetic po...
Abstract Background In recent years a large volume of clinical genomics data has become available du...
We have gone through various papers describing the mutations in between them and associated disease ...
The biomedical literature constitutes a rich source of evidence tosupport the discovery of biomarker...
The number of published articles describing associations between mutations and diseases is increasin...
<div><p>The number of published articles describing associations between mutations and diseases is i...
Abstract Background Understanding the genetic networks and their role in chronic diseases (e.g., can...
This article introduces the Variome Annotation Schema, a schema that aims to capture the core concep...
Copy number variants (CNVs) are a class of structural variants containing deletions and duplications...
Autoimmune diseases (ADs) arise from an abnormal immune response of the body against substances and ...
The increasing amount of scientific information available to researchers in the form of biomedical l...
Publisher's PDFThe number of published articles describing associations between mutations and diseas...
peer reviewedText mining is a flexible technology that can be applied to numerous different tasks in...
BackgroundIn recent years a large volume of clinical genomics data has become available due to rapid...
International audienceCopy number variants (CNVs) account for a major proportion of human genetic po...
Abstract Background In recent years a large volume of clinical genomics data has become available du...
We have gone through various papers describing the mutations in between them and associated disease ...
The biomedical literature constitutes a rich source of evidence tosupport the discovery of biomarker...
The number of published articles describing associations between mutations and diseases is increasin...
<div><p>The number of published articles describing associations between mutations and diseases is i...
Abstract Background Understanding the genetic networks and their role in chronic diseases (e.g., can...
This article introduces the Variome Annotation Schema, a schema that aims to capture the core concep...
Copy number variants (CNVs) are a class of structural variants containing deletions and duplications...
Autoimmune diseases (ADs) arise from an abnormal immune response of the body against substances and ...
The increasing amount of scientific information available to researchers in the form of biomedical l...
Publisher's PDFThe number of published articles describing associations between mutations and diseas...