Electronic reporting of genetic testing results is increasing, but they are often represented in diverse formats and naming conventions. Logical Observation Identifiers Names and Codes (LOINC) is a vocabulary standard that provides universal identifiers for laboratory tests and clinical observations. In genetics, LOINC provides codes to improve interoperability in the midst of reporting style transition, including codes for cytogenetic or mutation analysis tests, specific chromosomal alteration or mutation testing, and fully structured discrete genetic test reporting. LOINC terms follow the recommendations and nomenclature of other standards such as the Human Genome Organization Gene Nomenclature Committee’s terminology for gene names. In a...
Open sharing of clinical genetic data promises to both monitor and eventually improve the reproducib...
Diagnostic codes within electronic health record systems can vary widely in accuracy. It has been no...
The rapid and continuing progress in gene discovery for complex diseases is fueling interest in the ...
Many laboratories use electronic message standards to transmit results to their clients, If all labo...
(LOINC®) database provides a universal code system for reporting laboratory and other clinical obser...
To translate basic research findings into clinical practice, it is essential that information about ...
[Extract] Two recent papers have highlighted the vital importance of using standardized nomenclature...
The vocabulary currently used to describe genetic variants and their consequences reflects many year...
The vocabulary currently used to describe genetic variants and their consequences reflects many year...
Genetic testing of cancer susceptibility genes is now widely applied in clinical practice to predict...
The vocabulary currently used to describe genetic variants and their consequences reflects many year...
Genetic testing of cancer susceptibility genes is now widely applied in clinical practice to predict...
Contains fulltext : 71043.pdf (publisher's version ) (Closed access)Genetic testin...
Objective Clinicians’ ability to use and interpret genetic information depends upon how those data a...
As the rate at which whole exome and genome sequencing is used in the clinical and research settings...
Open sharing of clinical genetic data promises to both monitor and eventually improve the reproducib...
Diagnostic codes within electronic health record systems can vary widely in accuracy. It has been no...
The rapid and continuing progress in gene discovery for complex diseases is fueling interest in the ...
Many laboratories use electronic message standards to transmit results to their clients, If all labo...
(LOINC®) database provides a universal code system for reporting laboratory and other clinical obser...
To translate basic research findings into clinical practice, it is essential that information about ...
[Extract] Two recent papers have highlighted the vital importance of using standardized nomenclature...
The vocabulary currently used to describe genetic variants and their consequences reflects many year...
The vocabulary currently used to describe genetic variants and their consequences reflects many year...
Genetic testing of cancer susceptibility genes is now widely applied in clinical practice to predict...
The vocabulary currently used to describe genetic variants and their consequences reflects many year...
Genetic testing of cancer susceptibility genes is now widely applied in clinical practice to predict...
Contains fulltext : 71043.pdf (publisher's version ) (Closed access)Genetic testin...
Objective Clinicians’ ability to use and interpret genetic information depends upon how those data a...
As the rate at which whole exome and genome sequencing is used in the clinical and research settings...
Open sharing of clinical genetic data promises to both monitor and eventually improve the reproducib...
Diagnostic codes within electronic health record systems can vary widely in accuracy. It has been no...
The rapid and continuing progress in gene discovery for complex diseases is fueling interest in the ...