ライフサイエンスコーパス: inbreeding coefficient

1 bjectively link rate of allele loss with the inbreeding coefficient.

2 the relationship between allele loss and the inbreeding coefficient.

3 proximately equal to (1 - F), where F is the inbreeding coefficient.

4 nd to correlate strongly with pedigree-based inbreeding coefficients.

5 we have derived recurrence equations for the inbreeding coefficient and coancestries between individu

6 we have derived recurrence equations for the inbreeding coefficient and coancestry between individual

7 ue solutions to the recurrence equations for inbreeding coefficient and coancestry in this article, w

8 d migration) is important in determining the inbreeding coefficient and effective size.

9 However, the relationship between inbreeding coefficient and heterozygosity has only rarel

10 gree, finding strong concordance between the inbreeding coefficient and heterozygosity measured at 13

11 used to investigate the relationship between inbreeding coefficient and multilocus heterozygosity.

12 success in both sexes, and between maternal inbreeding coefficient and offspring survival.

13 he individual level, we estimated individual inbreeding coefficients and examined the relationship be

14 terozygosity was only weakly correlated with inbreeding coefficient, and heterozygosity was not posit

15 rates, locus-specific dropout rates, and the inbreeding coefficient; and (3) successfully correct the

16 mes and across individuals, and estimates of inbreeding coefficients are subject to unexpected levels

17 the efficiency of our method for evaluating inbreeding coefficients as compared to previous methods

18 sheep population of St Kilda, using genomic inbreeding coefficients based on 37 037 single-nucleotid

19 Inbreeding coefficient, but not multilocus heterozygosit

20 In contrast, inbreeding coefficients calculated from a deep and compa

21 Inbreeding coefficient, coancestry between individuals w

22 of our proposed method by applying it to the inbreeding coefficient computation.

23 Cervus elaphus) in Scotland using individual inbreeding coefficients derived from dense Single-Nucleo

24 Analyses of the inbreeding coefficient detected highly significant relat

25 oh) was found to correlate strongly with the inbreeding coefficient estimated from pedigrees (r = 0.8

26 We compared the inbreeding coefficient estimated using known height asso

27 rogram BORICE (Bayesian Outcrossing Rate and Inbreeding Coefficient Estimation) that effectively esti

28 he population outcrossing rate (t) and adult inbreeding coefficient (F) are key parameters in mating

29 and d2) and pedigree-based estimates of the inbreeding coefficient (f) were compared to each other a

30 ta, and among inbred individuals of the same inbreeding coefficient (F), those that die early are mor

31 The mean individual inbreeding coefficient (F=0.16) did not differ significa

32 data, it is necessary to obtain estimates of inbreeding coefficients (F) for each individual before c

33 date a method for estimating an individual's inbreeding coefficient, f, using amplified fragment leng

34 als given that every individual has the same inbreeding coefficient, F.

35 icrosatellite loci were used to estimate the inbreeding coefficient Fis within each population.

36 We observed significantly higher inbreeding coefficients for the height associated varian

37 t (IBDG) is predicted better by the pedigree inbreeding coefficient (FP) or by genomic (marker-based)

38 Here, we present two methods for estimating inbreeding coefficients from NGS data based on an expect

39 here were very few plants that had estimated inbreeding coefficients greater than one-half.

40 al and joint posterior distributions for the inbreeding coefficient in females and the male to female

41 However, the estimation of individual inbreeding coefficients in natural populations has been

42 Inbreeding coefficient indicated an overall 10% decrease

43 kelihood estimator and F (the simulated true inbreeding coefficient) is about 8 approximately 35% hig

44 Genomic inbreeding coefficients may resolve the long-standing pa

45 ses, whereas Wright thought that because his inbreeding coefficient measured both they should be rega

46 The inbreeding coefficient of an individual, F, is one of th

47 olve the use of pedigree records to estimate inbreeding coefficients or molecular markers to measure

48 n treatments in using the disequilibrium and inbreeding coefficient parameterizations.

49 tion in nucleotide diversity, or increase in inbreeding coefficient, relative to history of exposure.

50 eeding date varied with female, but not male inbreeding coefficient, revealing direct, but not indire

51 The population inbreeding coefficient was calculated to be 0.19 (SE=0.0

52 f lineages was nonlinear with respect to the inbreeding coefficient, which suggested that nonadditive