2023
DOI: 10.1016/j.livsci.2023.105299
|View full text |Cite
|
Sign up to set email alerts
|

Mitogenome information in cattle breeding and conservation genetics: Developments and possibilities of the SNP chip

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
6
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
1
1

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(6 citation statements)
references
References 79 publications
0
6
0
Order By: Relevance
“…Our initial simulations of mDNA, indicated that we need larger N e for mDNA than for nDNA (despite an order of magnitude larger mutation rate in mDNA) to obtain a number of segregating sites in mDNA in line with the observed variation both within and across cattle populations (Dorji et al 2021; Brajkovic et al, 2023;). As expected, we noticed that the lower the diversity among the mDNA, the smaller the impact of accounting for mDNA in breeding value estimation, in line with Boettcher et al (1996).…”
Section: Discussionmentioning
confidence: 92%
See 4 more Smart Citations
“…Our initial simulations of mDNA, indicated that we need larger N e for mDNA than for nDNA (despite an order of magnitude larger mutation rate in mDNA) to obtain a number of segregating sites in mDNA in line with the observed variation both within and across cattle populations (Dorji et al 2021; Brajkovic et al, 2023;). As expected, we noticed that the lower the diversity among the mDNA, the smaller the impact of accounting for mDNA in breeding value estimation, in line with Boettcher et al (1996).…”
Section: Discussionmentioning
confidence: 92%
“…Note that n m was smaller than the number of distinct maternal founder lineages in pedigree. We calculated the mDNA genomic relationship matrix as G m = M m M m T / k , where M m = W m – P m with W m an n m × n s matrix of 0s (for ancestral allele) and 1s (for mutation) for n m distinct mDNA and n s polymorphic loci (we assume we know all these loci by sequencing mDNA within pedigrees; Brajkovic et al, 2023), P m a matrix of mutation frequencies, k = , and p l the mutation frequency at locus l . To speed up simulations, we fixed variance components to simulated values during the burn-in phase (see the next paragraphs).…”
Section: Methodsmentioning
confidence: 99%
See 3 more Smart Citations