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Genotyping information


Genotyping is the process of determining differences in the genetic make-up (genotype) of an individual by examining the individual's DNA sequence using biological assays and comparing it to another individual's sequence or a reference sequence. It reveals the alleles an individual has inherited from their parents.[1] Traditionally genotyping is the use of DNA sequences to define biological populations by use of molecular tools. It does not usually involve defining the genes of an individual.

  1. ^ "Genotyping definition". NIH. 2011-09-21. Retrieved 2011-09-21.

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Genotyping

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technologies promise to provide whole-genome genotyping (or whole genome sequencing) in the future. Genotyping applies to a broad range of individuals, including...

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Genotype

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Genotyping refers to the method used to determine an individual's genotype. There are a variety of techniques that can be used to assess genotype. The...

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Genotype frequency

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allele frequencies and genotype frequencies. Genotype frequency in a population is the number of individuals with a given genotype divided by the total...

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Probabilistic genotyping

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Probabilistic genotyping is the use of statistical methods and mathematical algorithms in DNA Profiling. It may be used instead of manual methods in difficult...

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SNP genotyping

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SNP genotyping is the measurement of genetic variations of single nucleotide polymorphisms (SNPs) between members of a species. It is a form of genotyping...

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Genotyping by sequencing

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sequencing, genotyping by sequencing, also called GBS, is a method to discover single nucleotide polymorphisms (SNP) in order to perform genotyping studies...

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Multilocus genotype

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A multilocus genotype is the combination of alleles found at two or more loci in a single individual. For example, in a diploid species, if there are two...

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HCV genotypes

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V, Hayder Z, Hussain SS, Liao Y, Li Q (2015). "Rapid detection of HCV genotyping 1a, 1b, 2a, 3a, 3b and 6a in a single reaction using two-melting temperature...

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Noninvasive genotyping

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Noninvasive genotyping is a modern technique for obtaining DNA for genotyping that is characterized by the indirect sampling of specimen, not requiring...

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Hepatitis C virus

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et al. (2007). "New hepatitis C virus (HCV) genotyping system that allows for identification of HCV genotypes 1a, 1b, 2a, 2b, 3a, 3b, 4, 5a, and 6a". J...

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Blood type

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increasing use of blood group genotyping. In contrast to serologic tests reporting a direct blood type phenotype, genotyping allows the prediction of a phenotype...

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Blood compatibility testing

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drugs may show spurious agglutination reactions in serologic testing, so genotyping may be necessary to determine their blood type accurately.: 261  Genetic...

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Restriction site associated DNA markers

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isolating and analyzing RAD tags are referred to as RAD markers. Although genotyping by sequencing presents an approach similar to the RAD-seq method, they...

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Thrifty gene hypothesis

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and famine).[citation needed] According to the hypothesis, the 'thrifty' genotype would have been advantageous for hunter-gatherer populations, especially...

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Allele

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heterozygous genotypes), "Type B" (produced by IBIB homozygous and IBi heterozygous genotypes), "Type AB" produced by IAIB heterozygous genotype, and "Type...

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Phenotype

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from two basic factors: the expression of an organism's genetic code (its genotype) and the influence of environmental factors. Both factors may interact...

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XXYY syndrome

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XXYY syndrome is a sex chromosome anomaly in which males have 2 extra chromosomes, one X and one Y chromosome. Human cells usually contain two sex chromosomes...

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Hepatitis C

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genotype. In the United States, about 70% of cases are caused by genotype 1, 20% by genotype 2 and about 1% by each of the other genotypes. Genotype 1...

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Mendelian inheritance

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chance for their offspring to have the same genotype, and a 50% chance they would have a homozygous genotype. Since they could possible contribute two identical...

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