GGP Bovine 100K

SKU No.  40  |  Número de catálogo 

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 cada uno
Cantidad mínima necesaria: 1
É necessário fazer o pedido do item em múltiplos de uma caixa. Quantidade por caixa: 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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Especificaciones
MarcaGeneSeek® Genomic Profiler™
Razas admitidasAll breeds supported
EspeciesBovinos, Carne de res, Lácteos
Resultados de datosGGP 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.
Información de envíoProducers 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.
Enfermedades genéticasBVDV, Condrodisplasia (CHO), Color de capa, Malformación vertebral compleja (MVC), Polimelia, Color de capa Dun (DN), Encornado/descornado (HP), Hipotricosis (HY), Epilepsia idiopática (EI), Manosidosis alfa (MA), Enfermedad de la orina con olor a jarabe de arce (MSUD), Mioestatina (MYO), Hidrocefalía neuropática (NH), Osteopetrosis (OS), Hipoplasia pulmonar anasarca (HPA), BLAD, VERTEDEROS, Brachyspina, Kappa caseína, Leptina, Sensibilidad, Leche A2, CMS, Leche de pescado

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Capacitación

Our customers’ success is our shared success. Our customer service teams are ready to assist you and your team on our solutions, so you can rest easy knowing sampling procedures are performed properly and yield accurate results.