Method for detecting polymorphisms
AssigneeGendiag.exe, S.L.
InventorsEduardo Salas Pérez-Rasilla, Jaume Marrugat De La Iglesia, Roberto Elosua Llanos, Sergio Castillo Fernandez, Joan Salgado Gómez, Jose Maria Ordovás Munoz
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Abstract
The invention relates to a method for determining the risk of suffering a cardiovascular disease based on the presence of different polymorphisms as well as to kits for practicing the above method. The invention also relates to a method for determining the risk of suffering a cardiovascular disease by combining the absence or presence of one or more polymorphic markers in a sample from the subject with conventional risk factors for CVD as well as computer-implemented means for carrying out said method.
Claims6
A method of detecting polymorphisms in a biological sample, comprising
- (a1) assaying the biological sample isolated from a human subject for the presence of polymorphisms at position 27 within each of the nucleic acid sequences of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, and SEQ ID NO:10 by direct sequencing of nucleic acids in the sample;
- or
- (a2) assaying the biological sample isolated from a human subject for the presence of polymorphisms at position 27 within each of the nucleic acid sequences of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, and SEQ ID NO:10 by detecting hybridization or lack of hybridization of the nucleic acid sequences of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, and SEQ ID NO:10 in the biological sample with the set of nucleic acid probes;
- and
- (b) detecting polymorphisms in the biological sample at position 27 within the nucleic acid sequences of SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, and SEQ ID NO:10 based on the sequencing in (a1) or detecting hybridization or lack of hybridization in (a2);
- wherein the polymorphism at position 27 within the nucleic acid sequences of SEQ ID NOs:1, 3 and 7-10 is a C in SEQ ID NO:1, C in SEQ ID NO:3, T in SEQ ID NO:7, C in SEQ ID NO:8, C in SEQ ID NO:9, and T in SEQ ID NO:10.
Dependencies are inferred from the claim text.