| identifier | PRJEB12504 |
|---|---|
| type | bioproject |
| sameAs |
|
| organism | |
| title | Targeted enrichment to elucidate the Holstein-Frisian haplotypes HH5 and CDH |
| description | We have used targeted enrichment NGS sequencing to elucidate the causative mutations for two important disorders in HF-cattle. HH5, which was defined as one of the recessive haplotypes derived from large scale SNP-genotyping data and was be positioned to BTA9 is found to be caused by a 138kbp deletion. Cholesterol deficiency, which ws positioned to BTA11 is caused by an insertion into the coding region of APOB, causing a premature stop codon. |
| data type | Other |
| organization |
|
| publication | |
| external link |
|