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Select your SNPs (SYSNPs): a web tool for automatic and massive selection of SNPs
Belén Lorente-Galdos1, Ignacio Medina, Carlos Morcillo-Suarez
1Institut de Biologia Evolutiva (UPF-CSIC), Barcelona Biomedical Research Park (PRBB), Spain. belen.lorente@upf.edu
SYSNPs simplifies the selection and annotation of Single Nucleotide Polymorphisms (SNPs) for genetic association studies. This tool efficiently identifies informative SNPs and their functional annotations, reducing research time significantly.
Area of Science:
- Genomics
- Bioinformatics
- Statistical Genetics
Background:
- Association studies are crucial for uncovering the genetic underpinnings of complex traits.
- Selecting informative Single Nucleotide Polymorphisms (SNPs) and annotating association results are key, yet complex, steps in these studies.
- Current methods require extensive manual data aggregation from multiple sources, considering factors like functional properties, technology, and population-specific haplotype frequencies.
Purpose of the Study:
- To develop an efficient computational tool, SYSNPs, for optimizing SNP selection and functional annotation in genetic research.
- To streamline the process of identifying informative SNP sets covering specified genes or genomic regions.
- To facilitate comprehensive functional annotation of SNPs associated with markers.
Main Methods:
- SYSNPs utilizes advanced algorithms to simultaneously evaluate multiple criteria for SNP selection, including functional properties, technological data, and population haplotype frequencies.
- The system enables the selection of SNP sets that effectively cover user-defined genes or genomic regions.
- It provides complementary functionality for detailed functional annotation of SNPs related to any given marker SNP.
Main Results:
- SYSNPs significantly reduces the time required for SNP selection from days to minutes.
- The tool enables efficient and simultaneous consideration of diverse criteria for optimal SNP set generation.
- Comprehensive functional annotation of associated SNPs is readily available through the platform.
Conclusions:
- SYSNPs offers a powerful and efficient solution for SNP selection and annotation in genetic association studies.
- The tool democratizes complex genomic analyses by simplifying data integration and reducing manual effort.
- This approach accelerates the discovery of the genomic basis of complex traits.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Genome-wide Association Studies-GWAS
GWAS does not require the identification of the target gene involved in...

