enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. SNP array - Wikipedia

    en.wikipedia.org/wiki/SNP_array

    A SNP array can also be used to generate a virtual karyotype using software to determine the copy number of each SNP on the array and then align the SNPs in chromosomal order. [10] SNPs can also be used to study genetic abnormalities in cancer. For example, SNP arrays can be used to study loss of heterozygosity (LOH). LOH occurs when one allele ...

  3. Exon shuffling - Wikipedia

    en.wikipedia.org/wiki/Exon_shuffling

    Exon shuffling follows certain splice frame rules. Introns can interrupt the reading frame of a gene by inserting a sequence between two consecutive codons (phase 0 introns), between the first and second nucleotide of a codon (phase 1 introns), or between the second and third nucleotide of a codon (phase 2 introns). Additionally exons can be ...

  4. Array slicing - Wikipedia

    en.wikipedia.org/wiki/Array_slicing

    Common examples of array slicing are extracting a substring from a string of characters, the "ell" in "hello", extracting a row or column from a two-dimensional array, or extracting a vector from a matrix. Depending on the programming language, an array slice can be made out of non-consecutive elements.

  5. Crossover (evolutionary algorithm) - Wikipedia

    en.wikipedia.org/wiki/Crossover_(evolutionary...

    For example, a thread cannot be cut until the corresponding hole has been drilled in a workpiece. Such problems are also called order-based permutations. In the following, two crossover operators are presented as examples, the partially mapped crossover (PMX) motivated by the TSP and the order crossover (OX1) designed for order-based permutations.

  6. Allele - Wikipedia

    en.wikipedia.org/wiki/Allele

    An allele [1], or allelomorph, is a variant of the sequence of nucleotides at a particular location, or locus, on a DNA molecule. [2]Alleles can differ at a single position through single nucleotide polymorphisms (SNP), [3] but they can also have insertions and deletions of up to several thousand base pairs.

  7. Single-nucleotide polymorphism - Wikipedia

    en.wikipedia.org/wiki/Single-nucleotide_polymorphism

    For example, a G nucleotide present at a specific location in a reference genome may be replaced by an A in a minority of individuals. The two possible nucleotide variations of this SNP – G or A – are called alleles. [5] SNPs can help explain differences in susceptibility to a wide range of diseases across a population.

  8. Today’s NYT ‘Strands’ Hints, Spangram and Answers for Friday ...

    www.aol.com/today-nyt-strands-hints-spangram...

    According to the New York Times, here's exactly how to play Strands: Find theme words to fill the board. Theme words stay highlighted in blue when found.

  9. Genome-wide association study - Wikipedia

    en.wikipedia.org/wiki/Genome-wide_association_study

    The odds ratio is the ratio of two odds, which in the context of GWA studies are the odds of case for individuals having a specific allele and the odds of case for individuals who do not have that same allele. Example: suppose that there are two alleles, T and C. The number of individuals in the case group having allele T is represented by 'A ...