Genomic Inbreeding 

Genomic inbreeding measures the actual level of inbreeding present within an animal’s DNA. It does this by analysing the animal’s SNP (Single Nucleotide Polymorphism) profile and identifying long regions of DNA that are homozygous, meaning the DNA inherited from the sire matches the DNA inherited from the dam. 

These matching regions, often referred to as Runs of Homozygosity (ROH), occur when both parents pass down the same segment of DNA inherited from a common ancestor. The larger the proportion of an animal’s genome that consists of these homozygous regions, the higher its genomic inbreeding percentage. 

Unlike pedigree inbreeding, which estimates inbreeding from recorded ancestry, genomic inbreeding measures the actual DNA inherited by an individual animal. As a result, it can identify variation in inbreeding between full siblings and detect inbreeding that may not be visible in pedigree records. 

The Australian Wagyu Association (AWA) maintains the most complete pedigree records available for the Wagyu breed, tracing ancestry back to the foundation animals imported from Japan during the 1990s. However, these pedigrees typically truncate 2–4 generations prior to export. It is well understood that considerable inbreeding existed within the Japanese Black population before exportation. Because this historical ancestry is not fully captured in pedigree records, genomic inbreeding provides a valuable measure of the actual inbreeding present within an animal’s DNA, regardless of whether the common ancestors are recorded in the pedigree. 

The genomic inbreeding percentage displayed on an animal profile helps breeders identify the actual level of inbreeding inherited by an animal, enabling more informed breeding decisions and improved management of genetic diversity within their herd. 

How Genomic Inbreeding is calculated 

Every animal inherits approximately 50% of its DNA from its sire and 50% from its dam. However, the specific DNA segments inherited from each parent are randomly combined during reproduction. This means that while siblings share the same parents, they do not inherit exactly the same DNA and can therefore differ in both performance and genetic composition. 

In the example below, Generation 0 represents the original parents. The coloured chromosome segments represent different portions of DNA inherited from each parent. 

In Generation 1, two full siblings are produced from the same mating. Although both animals inherit 50% of their DNA from the sire (blue shades) and 50% from the dam (purple shades), the exact DNA segments inherited differ between the siblings. This demonstrates why full siblings can vary in traits despite having the same pedigree. 

In Generation 2, these siblings are mated to unrelated animals (shown in white). Their offspring inherit 50% of their DNA from the unrelated parent and 50% from their respective parent. Because the Generation 1 siblings inherited different DNA segments, their progeny also inherit different combinations of the original Generation 0 DNA. 

When these cousins are later mated together, some chromosome segments inherited from the original Generation 0 ancestors can be passed down through both the sire and dam lines. Where identical DNA segments are inherited from both parents, regions of the genome become homozygous by descent (identical because they originated from the same ancestor). 

Genomic inbreeding is calculated by identifying these regions within the DNA. The larger the proportion of the genome that is identical by descent, the higher the animal’s genomic inbreeding percentage. 

 

Genomic Inbreeding

 

 

Understanding Genomic Inbreeding 

Genomic inbreeding and pedigree inbreeding are closely related, but they measure different things. 

Pedigree inbreeding estimates the likelihood that inbreeding has occurred based on recorded ancestry, while genomic inbreeding measures the amount of inbreeding actually present within an animal’s DNA. 

As a result, two animals with identical pedigree inbreeding percentages can have different levels of genomic inbreeding. This is because siblings inherit different combinations of DNA from their parents, resulting in variation in the amount of homozygous DNA inherited. 

As genomic inbreeding increases, a larger proportion of the animal’s genome consists of regions that are identical by descent. This reduces genetic diversity within the animal because fewer alternative gene variants are present. 

As a general rule: 

  • Higher genomic inbreeding indicates lower genetic diversity within the individual animal. 
  • Animals with similar pedigree inbreeding can have very different genomic inbreeding levels. 
  • Genomic inbreeding can detect historical inbreeding that may not be visible in pedigree records. 
  • Higher genomic inbreeding increases the likelihood that harmful recessive variants may be expressed. 

Limitations 

While genomic inbreeding provides a more accurate measure of actual inbreeding than pedigree-based calculations, there are also some limitations to consider. 

Genomic inbreeding is calculated using thousands of SNP markers spread across the genome. While this provides a highly accurate representation of inbreeding, it remains an estimate of whole-genome inbreeding rather than a direct measurement of every DNA sequence within the genome. 

The accuracy of genomic inbreeding calculations also depends on the quality of the genomic sample. Genomic inbreeding is only calculated for animals with a SNP call rate greater than 95% (0.95). Samples with lower call rates may not contain sufficient genomic information to accurately identify regions of homozygosity and therefore will not receive a genomic inbreeding value. 

Additionally, genomic inbreeding identifies regions of homozygosity but does not indicate whether the genes contained within those regions are favourable or unfavourable. Two animals may have similar genomic inbreeding percentages but differ considerably in performance, productivity and genetic merit. 

For this reason, genomic inbreeding should be considered alongside other breeding tools, including Wagyu Breeding Values (WBVs), pedigree inbreeding values and genetic diversity measures when making selection and mating decisions. 

Why Inbreeding Matters in Wagyu 

Inbreeding increases the likelihood that an animal inherits identical copies of DNA from common ancestors, reducing genetic diversity within the population. 

Animals with high levels of inbreeding may experience reduced: 

  • Developmental growth 
  • Fertility 
  • Survival  

Animals also carry recessive genetic variants that may not affect performance when only one copy is present. As inbreeding increases, there is a greater chance an animal inherits identical copies of these variants from a common ancestor, increasing the likelihood that harmful genetic defects are expressed. 

While linebreeding can be used to concentrate desirable genetics within a herd, excessive use of closely related animals can increase inbreeding levels over time. Introducing less-related or outcross animals can help maintain genetic diversity and reduce the accumulation of inbreeding. 

Therefore, managing inbreeding within the herd is vital for overall herd performance and welfare.  

Key takeaway 

Pedigree inbreeding predicts the likelihood of shared ancestry based on a family tree, whereas genomic inbreeding measures the actual DNA inherited by an animal. As a result, genomic inbreeding provides a more accurate picture of the true level of inbreeding present within an animal and can reveal differences between full siblings that are not visible from pedigree records alone. 

RELATED

Genomic inbreeding measures the actual level of inbreeding present within an animal's DNA. It does this by analysing the animal's SNP (Single Nucleotide Polymorphism) profile and identifying long regions of DNA that are homozygous, meaning the DNA inherited from the sire matches the DNA inherited from the dam.
Entry weight is the liveweight of animals recorded at induction into a feedlot production system. This weight provides an indication of the animals starting point and may influence pen allocation and feed ration to meet market specifications.
Feedlot check weights are the liveweights of animals recorded during the feedlot production period between entry and exit weights. They provide an indication of growth performance and weight gain throughout the feeding period and can assist in monitoring progress towards target market specifications.
Exit weight is the liveweight of animals recorded as they exit the feedlot for processing. This weight provides an indication of the animal's end point and growth performance during feedlot production, as well as its suitability for meeting market specifications.

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It is a condition of use of this database that you accept these terms and conditions. 

It is important that you appreciate when accessing the Australian Wagyu Association Limited (AWA) database (which may be hosted on an external website) that the information contained on the AWA database, including but not limited to pedigree, DNA information, Wagyu Breeding Values (WBVs) and Index values (together called Database Information), is based on data supplied by AWA members and/or third parties.  

Whilst sincere effort is made to ensure the Database Information is accurate and complete, to the extent permitted by law, AWA, its officers and employees, shall not be responsible for its use or interpretation, and you use the Database Information at your own risk. Please be aware of the following limitations of the Database Information.  

Regarding WBVs and Index values, it is important to appreciate, and you need to be aware that:  

  • WBVs are derived using genetic evaluation technology developed for the AWA, using information contained within the AWA database and parameters derived from it.
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  • Animals whose registration identifiers start with PED are Pedigree Recorded Animals. What this means is that the details which AWA used to register the animal were obtained from a Recognised Wagyu Registry Organisation – in other words a Wagyu breed association based outside of Australia. AWA has not independently verified the information with respect to the animal or the details recorded about the animal. You should read AWA’s by-laws which set out details regarding the definition of a Pedigree Recorded Animal.  
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Regarding prefectural content, it is important to appreciate, and you need to be aware that:  

  • Prefectural content is based on the estimation of prefectural origin from Japanese breeding records of 201 foundation sires and 168 foundation dams. As genotype-based parent verification is not used in Japan, and full Japanese registration certificates are not available for all foundation animals, exact prefectural composition for these sires and dams cannot be validated.  
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  • As genetic testing results are provided by independent DNA testing laboratories at the request of AWA members, AWA relies solely on the accuracy of the reporting of genetic testing as completed by the laboratories.  
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