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Wyszukujesz frazę "gene frequency" wg kryterium: Temat


Wyświetlanie 1-5 z 5
Tytuł:
Analysis of single gene multitrait effects in livestock by the use of Gibbs sampling
Autorzy:
Dobek, A
Molinski, K.
Szydlowski, M.
Szwaczkowski, T.
Powiązania:
https://bibliotekanauki.pl/articles/2042024.pdf
Data publikacji:
2000
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
gene
gene frequency
major gene
livestock
Gibbs sampling
Źródło:
Journal of Applied Genetics; 2000, 41, 4; 275-283
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The em Algorithm and Its Implementation for the Estimation of Frequencies of snp-Haplotypes
Autorzy:
Polańska, J.
Powiązania:
https://bibliotekanauki.pl/articles/908153.pdf
Data publikacji:
2003
Wydawca:
Uniwersytet Zielonogórski. Oficyna Wydawnicza
Tematy:
genetyka
informatyka
algorithms
haplotypes
likelihood functions
gene frequency
Opis:
A haplotype analysis is becoming increasingly important in studying complex genetic diseases. Various algorithms and specialized computer software have been developed to statistically estimate haplotype frequencies from marker phenotypes in unrelated individuals. However, currently there are very few empirical reports on the performance of the methods for the recovery of haplotype frequencies. One of the most widely used methods of haplotype reconstruction is the Maximum Likelihood method, employing the Expectation-Maximization (EM) algorithm. The aim of this study is to explore the variability of the EM estimates of the haplotype frequency for real data. We analyzed haplotypes at the BLM, WRN, RECQL and ATM genes with 8-14 biallelic markers per gene in 300 individuals. We also re-analyzed the data presented by Mano et al. (2002). We studied the convergence speed, the shape of the loglikelihood hypersurface, and the existence of local maxima, as well as their relations with heterozygosity, the linkage disequilibrium and departures from the Hardy-Weinberg equilibrium. Our study contributes to determining practical values for algorithm sensitivities.
Źródło:
International Journal of Applied Mathematics and Computer Science; 2003, 13, 3; 419-429
1641-876X
2083-8492
Pojawia się w:
International Journal of Applied Mathematics and Computer Science
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Report on the incidence of hereditary disorders (BLAD, DUMPS) in the Polish population of Holstein-Friesian cattle
Występowanie chorób genetycznych (BLAD, DUMPS) w polskiej populacji bydła rasy holsztynsko-fryzyjskiej
Autorzy:
Gozdek, M.
Kolenda, M.
Kamola, D.
Sitkowska, B.
Powiązania:
https://bibliotekanauki.pl/articles/2621939.pdf
Data publikacji:
2020
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
cattle
Polish Holstein-Friesian breed
heredity
bovine leucocyte adhesion deficiency
uridine monophosphate synthase
gene frequency
Źródło:
Acta Scientiarum Polonorum. Zootechnica; 2020, 19, 3; 15-21
1644-0714
Pojawia się w:
Acta Scientiarum Polonorum. Zootechnica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Bovine kappa-casein [CASK] gene - molecular nature and application in dairy cattle breeding
Autorzy:
Kaminski, S
Powiązania:
https://bibliotekanauki.pl/articles/2047276.pdf
Data publikacji:
1996
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
bovine kappa-casein
quantitative trait locus
polymorphism
gene frequency
milk protein content
genotype
cattle breeding
dairy cattle
Opis:
The bovine kappa-casein (CASK) gene is considered a potential marker for quantitative trait loci (QTL) in dairy cattle. A large amount of research has been performed to explore the nature and variation of the CASK gene and its possible applications in cattle breeding. The purpose of this review is to sum up the knowledge of all known aspects of the CASK gene: molecular structure and function, polymorphism and allele freqeuncy, methods of genotyping and possibilities of the use of CASK polymorphism in dairy cattle breeding.
Źródło:
Journal of Applied Genetics; 1996, 37, 2; 179-196
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Somaclonal variation in winter wheat [Triticum aestivum L.]: frequency, occurrence and inheritance
Autorzy:
Cheng, X Y
Gao, M.W.
Liang, Z.Q.
Liu, G.Z.
Powiązania:
https://bibliotekanauki.pl/articles/2044461.pdf
Data publikacji:
1998
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Tematy:
inheritance
tissue culture
Triticum aestivum
occurrence
in vitro
winter wheat
gene mutation
plant breeding
callus induction
frequency
somaclonal variation
wheat
embryo
Opis:
Plants were regenerated from immature embryo cultures of 35 winter wheat genotypes. General responses of regenerated plants were investigated and a total of 7142 R₂ spike lines from 1593 R₁ plants were assessed in the field for somaclonal variants in 1985/86, 1986/87 and 1987/88. Selected variants were studied for their possible genetic inheritance. From regenerated plantlets, 81% survived and 63% produced fertile plants. Forms with reduced plant height, length of spike and other morphological abnormalities were found in this progeny. Populations of R₁ plants were highly variable due mainly to the physiological disturbances resulting from the in vitro process. Overall somaclonal variation frequencies were 14.2% per plant basis and 5.3% per R₂ spike basis. The variants were similar in the three different R₂ generations with predominant variants being negative in plant height, maturity, awns, spike type and plant type. Both uniform R₂ variant families and spike lines were found in addition to the segregating variants which constituted the majority. On average, in a variant family or line, 18% and 14% of their component lines and plants were variants, respectively. Inheritability was demonstrated for the uniform variant families and spike lines as well as segregated variants. Of those 134 selections, about 70% were classified as inheritable. Both recessive and dominant gene mutations at one, two or three loci were evident in some variants as suggested by the segregating data.
Źródło:
Journal of Applied Genetics; 1998, 39, 1; 59-72
1234-1983
Pojawia się w:
Journal of Applied Genetics
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-5 z 5

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