http://www.cnr.it/ontology/cnr/individuo/prodotto/ID60725
Genome wide scan for somatic cell counts in Holstein bulls (Articolo in rivista)
- Type
- Label
- Genome wide scan for somatic cell counts in Holstein bulls (Articolo in rivista) (literal)
- Anno
- 2011-01-01T00:00:00+01:00 (literal)
- Alternative label
Minozzi G, Nicolazzi EL, Strozzi F, Stella A, Negrini R, Ajmone-Marsan P, Williams JL (2011)
Genome wide scan for somatic cell counts in Holstein bulls
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Minozzi G, Nicolazzi EL, Strozzi F, Stella A, Negrini R, Ajmone-Marsan P, Williams JL (literal)
- Pagina inizio
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#descrizioneSinteticaDelProdotto
- E stato utilizzando un pannello di 54mila marcatori genetici SNP per identificare loci con effetto sulla suscettibilità alla mastite subclinica nei bovini da latte (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- MG, SF,WJL - PTP, Lodi; AS - IBBA-CNR, Milano, NEL, AMP, NR Unicatt, Piacenza (literal)
- Titolo
- Genome wide scan for somatic cell counts in Holstein bulls (literal)
- Abstract
- Mastitis is the most costly disease for dairy production, and control of the disease is often difficult, due to its multi-factorial nature. Susceptibility to mastitis is under partial genetic control and the industry uses indirect selection for decreased concentrations of somatic cells in milk to reduce mastitis. A genome-wide scan was performed to identify genomic regions associated with deregressed estimated breeding values (EBVs) for somatic cell counts (SCC) in Holstein bulls. In total 1183 proven bulls of the Italian of Holstein population, were genotyped with the BovineSNP50 BeadChip (Illumina, San Diego, CA) and a whole genome association analysis was performed using the R package GenABEL. Two chromosomal regions showed association with SCC, a region on chromosome 14 with high significance (P < 5x10-6) and a region on chromosome 6 with moderate significance (P < 5x10-5). Two regions with effects on SCC have been identified with good statistical support. A further study of these candidate regions will be performed to verify the results and identify the causal mutations. (literal)
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