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Copy number variation (CNV) is a phenomenon in which sections of the genome are repeated and the number of repeats in the genome varies between individuals. [1] Copy number variation is a type of structural variation : specifically, it is a type of duplication or deletion event that affects a considerable number of base pairs. [ 2 ]
Due to the CNV chromosomes of different sizes can be combined in a new cell. If this occurs around conception, the result will be a first cell of a human with a genetic variation. This can be either positive or negative. In positive cases this new human will be capable of a special skill that is assessed positively, for example, in sports or ...
Copy number analysis is the process of analyzing data produced by a test for DNA copy number variation in an organism's sample. One application of such analysis is the detection of chromosomal copy number variation that may cause or may increase risks of various critical disorders.
RCCX is a complex, multiallelic, and tandem copy number variation (CNV) human DNA locus on chromosome 6p21.3, a cluster located in the major histocompatibility complex (MHC) class III region. [1] [2] CNVs are segments of DNA that vary in copy number compared to a reference genome and play a significant role in human phenotypic variation and ...
The Chinese New Version (abbreviation:CNV; simplified Chinese: 新译本; traditional Chinese: 新譯本) is a Chinese language Bible translation that was completed in 1992 by the Worldwide Bible Society (環球聖經公會 Huanqiu Shengjing Xiehui) with the assistance of the Lockman Foundation.
In Boolean algebra, a formula is in conjunctive normal form (CNF) or clausal normal form if it is a conjunction of one or more clauses, where a clause is a disjunction of literals; otherwise put, it is a product of sums or an AND of ORs.
Through the use of DNA microarrays in conjunction with CGH techniques, the more specific form of array CGH (aCGH) has been developed, allowing for a locus-by-locus measure of CNV with increased resolution as low as 100 kilobases. [4] [5] This improved technique allows for the aetiology of known and unknown conditions to be discovered.
KoVariome is the variome of Korean ethnic groups. It was initiated in 2010 when the Genome Research Foundation in Korea was established. KoVariome has produced around 100 Korean genome diversity data on 4 April 2018 in Scientific Reports [1] and 1,094 Korean genome variation information on 27 May 2020.