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  2. SNP array - Wikipedia

    en.wikipedia.org/wiki/SNP_array

    An SNP array is a useful tool for studying slight variations between whole genomes. The most important clinical applications of SNP arrays are for determining disease susceptibility [5] and for measuring the efficacy of drug therapies designed specifically for individuals. [6] In research, SNP arrays are most frequently used for genome-wide ...

  3. SNP genotyping - Wikipedia

    en.wikipedia.org/wiki/SNP_genotyping

    In high-density oligonucleotide SNP arrays, hundreds of thousands of probes are arrayed on a small chip, allowing for many SNPs to be interrogated simultaneously. [1] Because SNP alleles only differ in one nucleotide and because it is difficult to achieve optimal hybridization conditions for all probes on the array, the target DNA has the ...

  4. Single-nucleotide polymorphism - Wikipedia

    en.wikipedia.org/wiki/Single-nucleotide_polymorphism

    In genetics and bioinformatics, a single-nucleotide polymorphism (SNP / s n ɪ p /; plural SNPs / s n ɪ p s /) is a germline substitution of a single nucleotide at a specific position in the genome. Although certain definitions require the substitution to be present in a sufficiently large fraction of the population (e.g. 1% or more), [ 1 ...

  5. Genome-wide association study - Wikipedia

    en.wikipedia.org/wiki/Genome-wide_association_study

    The allele count of each measured SNP is evaluated—in this case with a chi-squared test—to identify variants associated with the trait in question. The numbers in this example are taken from a 2007 study of coronary artery disease (CAD) that showed that the individuals with the G-allele of SNP1 ( rs1333049 ) were overrepresented amongst CAD ...

  6. Genealogical DNA test - Wikipedia

    en.wikipedia.org/wiki/Genealogical_DNA_test

    A person's haplogroup can often be inferred from their STR results, but can be proven only with a Y-chromosome SNP test (Y-SNP test). A single-nucleotide polymorphism (SNP) is a change to a single nucleotide in a DNA sequence. Typical Y-DNA SNP tests test about 20,000 to 35,000 SNPs. [34] Getting a SNP test allows a much higher resolution than ...

  7. Copy number analysis - Wikipedia

    en.wikipedia.org/wiki/Copy_number_analysis

    Array-based methods have been accepted as the most efficient in terms of their resolution and high-throughput nature and the highest coverage (choose an array with over 2 million probes) [3] and they are also referred to as virtual karyotype. Data analysis for an array-based DNA copy number test can be very challenging though due to very high ...

  8. Suspension array technology - Wikipedia

    en.wikipedia.org/wiki/Suspension_array_technology

    Suspension array technology (or SAT) is a high throughput, large-scale, and multiplexed screening platform used in molecular biology.SAT has been widely applied to genomic and proteomic research, such as single nucleotide polymorphism (SNP) genotyping, genetic disease screening, gene expression profiling, screening drug discovery and clinical diagnosis.

  9. SNP annotation - Wikipedia

    en.wikipedia.org/wiki/SNP_annotation

    Single nucleotide polymorphism annotation (SNP annotation) is the process of predicting the effect or function of an individual SNP using SNP annotation tools. In SNP annotation the biological information is extracted, collected and displayed in a clear form amenable to query.