Sentence examples for inheritance identification from inspiring English sources

In contrast to recessive conditions with biallelic inheritance, identification of dominant (monoallelic) mutations for Mendelian disorders is more difficult, because of the abundance of benign heterozygous variants that act as massive background noise (typically, in a 400 1 excess ratio).

Forensic genetics is the branch of genetics that, through DNA analysis and comparison, helps to resolve legal problems such as paternity tests, establishing identity in criminal cases where biological evidence is found at crime scenes, inheritance matters, identification of victims of mass disasters, and identification of missing persons from human remains [ 1, 2].

His subject, here — no less than in such films as "The Secret of the Grain" and "Games of Love and Chance" — is the conflict between cultural inheritance and group identification.

Mitochondrial DNA (mtDNA) markers are ideal for the validation of maternal inheritance and the identification of brood-stock in aquaculture breeding programs.

There is an inheritance mechanism regarding the identification of data elements within documents, i.e., the identified data elements are inherited from the previous documents within the document chain; however, the responsibility of identification belongs to the actual system role (human or business process) only in the case of the newest data elements.

All of the available studies respectively focus on seizure semiology, prevalence, mode of inheritance and gene mutation identification; and have been conducted mainly in Denmark [ 23, 37, 41], the United States [ 35, 36, 38– 40] and Finland [ 34].

In addition, it is important to provide genetic counselling to patients and their families to help them understand the medical, psychological and familial implications of this disease; educate them about management, inheritance, prevention, testing and identification of reliable sources of information and products; and support adherence to a lifelong GFD regimen [ 46].

Both the SW and SL of the segregating populations showed normal or near-normal distributions, suggesting a quantitative inheritance pattern suitable for QTL identification.

By allowing dynamic filtering of variants based on variables such as individual clinical features, diseases, genes, assigned ACMG-type pathogenicity category, allele frequency, genotype, and inheritance pattern, VIKING assists in identification of a differential diagnosis.

Apart from the manifold practical assets of these approaches, reviewed thoroughly elsewhere [ 4, 41, 42], the greatest conceptional advantage of DNA-taxonomy over morphological methods lies in the direct inheritance of the characters used for identification.

The biparental inheritance of nuclear markers facilitates the identification of possible hybridization and polyploidization events, and when used in concert with plastid markers the directionally of hybridization can be inferred [ 9, 10, 14– 14].