GGP Bovine 100K

SKU N°  40  |  Numéro de catalogue 

Recently upgraded to include 100,000 markers, Neogen’s GGP Bovine 100K is the backbone of many formal genetic evaluations. Key features of the GGP Bovine 100K include:

  • Smart design. SNPs specifically chosen for high minor allele frequency and uniform coverage of the genome for most beef and dairy breeds of cattle.
  • Comprehensive information. Includes significant overlap to many other bovine SNP panels for increased imputation accuracy.
  • Parentage Verification. Includes all commonly utilized USDA and ISAG parentage markers.
$43.00 chacune
Quantité minimale requise : 1
Pour cet article, la quantité commandée doit être un multiple d’une boîte. Quantité par boîte : 1

GeneSeek Genomic Profiler (GGP) Bovine 100K lassos the knowledge of industry leading scientists who have designed and processed more animal genotyping arrays than any other organization. The new generation GGP Bovine 50K leverages Neogen's leading SNP selection processes to precisely choose the best 100,000 SNPs. This delivers more accurate evaluation of genetic merit, genome wide selection, comparative genetic studies, and higher density imputation. The GGP Bovine 100K contains all the content from popular lower density commercial arrays. Additionally, it has validated and retained the most informative SNPs from the original Illumina Bovine SNP50 and Illumina Bovine HD Bead Chips. Utilize the best content from the most commonly used commercial genotyping arrays, and for a low affordable price, PLUS comprehensive parentage, disease and trait relevant SNPs.

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Spécifications
MarqueGeneSeek® Genomic Profiler™
Races prises en chargeAll breeds supported
EspèceBovin, Bœuf, Produits laitiers
Résultats des donnéesGGP Bovine 100K provides raw genotype information back to industry partners for use in a formal genetic evaluation. Parentage analysis can be performed by Neogen, if desired.
Informations sur la soumissionProducers may purchase GGP Bovine 100K through one of Neogen’s partner breed associations or their genetic evaluation provider. If interested in the product for research purposes, please contact Neogen directly.
Conditions génétiquesBVDV, Chondrodysplasie (CHO), Couleur de robe, Malformation vertébrale complexe (MVC), Duplication du développement (DD), Couleur de robe Dun (DN), À corne/sans corne (« Horned/Polled », HP), Hypotrichose (HY), Épilepsie idiopathique (IE), Alpha Mannosidose (MA), Maladie des urines à odeur de sirop d'érable (« Maple Syrup Urine Disease », MSUD), Myostatine (MYO), Hydrocéphalie neuropathique (HN), Ostéopétrose (OS), Hypoplasie Pulmonaire Anasarca (« Pulmonary Hypoplasia Anasarca », PHA), BLAD, DUMPS, Brachyspina, Caséine kappa, Leptine, Tendreté, Lait A2, CMS, Lait de poisson

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