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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            Fitness decreased with increasing inbreeding coefficients.
6 rointestinal helminth parasites, and genomic inbreeding coefficients.
7 en individuals that produced offspring (mean inbreeding coefficient = 0.07, mean mate kinship = 0.08)
8 we have derived recurrence equations for the inbreeding coefficient and coancestries between individu
9 we have derived recurrence equations for the inbreeding coefficient and coancestry between individual
10 ue solutions to the recurrence equations for inbreeding coefficient and coancestry in this article, w
11 ity of captive-bred cohorts had an increased inbreeding coefficient and decreased genetic variability
12 d migration) is important in determining the inbreeding coefficient and effective size.
13            However, the relationship between inbreeding coefficient and heterozygosity has only rarel
14 gree, finding strong concordance between the inbreeding coefficient and heterozygosity measured at 13
15 used to investigate the relationship between inbreeding coefficient and multilocus heterozygosity.
16  success in both sexes, and between maternal inbreeding coefficient and offspring survival.
17                    Estimating the individual inbreeding coefficient and pairwise kinship is an import
18 he individual level, we estimated individual inbreeding coefficients and examined the relationship be
19 ee depth = 6 generations), we estimated both inbreeding coefficients and kinship between individuals
20 terozygosity was only weakly correlated with inbreeding coefficient, and heterozygosity was not posit
21 rates, locus-specific dropout rates, and the inbreeding coefficient; and (3) successfully correct the
22                                              Inbreeding coefficients are currently within acceptable
23 mes and across individuals, and estimates of inbreeding coefficients are subject to unexpected levels
24  the efficiency of our method for evaluating inbreeding coefficients as compared to previous methods
25  inbreeding (Wright's, partial and ancestral inbreeding coefficients) as well as purging parameters (
26  sheep population of St Kilda, using genomic inbreeding coefficients based on 37 037 single-nucleotid
27                                              Inbreeding coefficient, but not multilocus heterozygosit
28                                 In contrast, inbreeding coefficients calculated from a deep and compa
29                                              Inbreeding coefficients can be predicted from pedigrees
30                                              Inbreeding coefficient, coancestry between individuals w
31  the highest nucleotide diversity and lowest inbreeding coefficients compared to other breeds.
32 of our proposed method by applying it to the inbreeding coefficient computation.
33 Cervus elaphus) in Scotland using individual inbreeding coefficients derived from dense Single-Nucleo
34                              Analyses of the inbreeding coefficient detected highly significant relat
35 oh) was found to correlate strongly with the inbreeding coefficient estimated from pedigrees (r = 0.8
36                              We compared the inbreeding coefficient estimated using known height asso
37 rogram BORICE (Bayesian Outcrossing Rate and Inbreeding Coefficient Estimation) that effectively esti
38                                  The average inbreeding coefficient (F(ROH)) was 0.031 +/- 0.003 with
39 he population outcrossing rate (t) and adult inbreeding coefficient (F) are key parameters in mating
40  and d2) and pedigree-based estimates of the inbreeding coefficient (f) were compared to each other a
41 ta, and among inbred individuals of the same inbreeding coefficient (F), those that die early are mor
42                          The mean individual inbreeding coefficient (F=0.16) did not differ significa
43                                              Inbreeding coefficients (F(IS)) ranged from - 0.1 to 0.0
44                          Here, using genomic inbreeding coefficients (F(ROH)) for >1.4 million indivi
45 data, it is necessary to obtain estimates of inbreeding coefficients (F) for each individual before c
46 date a method for estimating an individual's inbreeding coefficient, f, using amplified fragment leng
47 als given that every individual has the same inbreeding coefficient, F.
48 icrosatellite loci were used to estimate the inbreeding coefficient Fis within each population.
49 ensitive population-level statistics such as inbreeding coefficients for the concerns around marginal
50             We observed significantly higher inbreeding coefficients for the height associated varian
51            We compare the ability of various inbreeding coefficients ([Formula: see text]) to quantif
52 t (IBDG) is predicted better by the pedigree inbreeding coefficient (FP) or by genomic (marker-based)
53  Here, we present two methods for estimating inbreeding coefficients from NGS data based on an expect
54 here were very few plants that had estimated inbreeding coefficients greater than one-half.
55 cess was reduced by 24% for individuals with inbreeding coefficients greater than twice the populatio
56 al and joint posterior distributions for the inbreeding coefficient in females and the male to female
57        However, the estimation of individual inbreeding coefficients in natural populations has been
58 sociated with low genetic diversity and high inbreeding coefficients (including increased selfing rat
59                                              Inbreeding coefficient indicated an overall 10% decrease
60 kelihood estimator and F (the simulated true inbreeding coefficient) is about 8 approximately 35% hig
61                                      Genomic inbreeding coefficients may resolve the long-standing pa
62 ses, whereas Wright thought that because his inbreeding coefficient measured both they should be rega
63                                          The inbreeding coefficient of an individual, F, is one of th
64  and the probability of such identity is the inbreeding coefficient of the individual.
65                                              Inbreeding coefficients of and relatedness (or kinship c
66 olve the use of pedigree records to estimate inbreeding coefficients or molecular markers to measure
67 , are either biased, or not able to estimate inbreeding coefficients, or produce a large proportion o
68 n treatments in using the disequilibrium and inbreeding coefficient parameterizations.
69 tion in nucleotide diversity, or increase in inbreeding coefficient, relative to history of exposure.
70 eeding date varied with female, but not male inbreeding coefficient, revealing direct, but not indire
71                                   We observe inbreeding coefficients similar to wild populations, alt
72 zygosity (ROH) and have significantly higher inbreeding coefficients than managed populations.
73 rs that derive from them such as kinship and inbreeding coefficients using a concise matrix framework
74                               The population inbreeding coefficient was calculated to be 0.19 (SE=0.0
75                        Furthermore, a higher inbreeding coefficient was correlated with higher inbree
76            Historically, computations of the inbreeding coefficient were used to prohibit inbred marr
77 f lineages was nonlinear with respect to the inbreeding coefficient, which suggested that nonadditive