W545
Building the LD Chip and an Update on the Sheep Genomes Database

Date: Monday, January 11, 2016
Time: 11:50 AM
Room: Towne - Meeting House
Rudiger Brauning , AgResearch Ltd, Invermay Agricultural Centre, Mosgiel, New Zealand
Antonello Carta , Istituto Zootecnico e Caseario per la Sardegna, Sassari, Italy
Carlos Gabriel Ciappesoni , National Institute of Agriculture Research, Rincon del Colorado, Canelones, Uruguay
Shannon Clarke , AgResearch Ltd, Invermay Agricultural Centre, Mosgiel, New Zealand
Noelle Cockett , Utah State University, Logan, UT
Christine Couldrey , LIC, Hamilton, New Zealand
Hans D. Daetwyler , Department of Economic Development, Jobs, Transport & Resources, Bundoora, Australia
Michael P. Heaton , USDA, ARS, U.S. Meat Animal Research Center (USMARC), Clay Center, NE
James Kijas , CSIRO Agriculture Flagship, St. Lucia, Australia
Denis Larkin , Aberystwyth University, London, United Kingdom
Alan McCulloch , AgResearch Ltd, Invermay Agricultural Centre, Mosgiel, New Zealand
John McEwan , AgResearch Ltd, Invermay Agricultural Centre, Mosgiel, New Zealand
Sean McWilliam , CSIRO Agriculture QBP, St. Lucia, Australia
Carole R. Moreno , INRA, Toulouse, France
Suzanne Rowe , AgResearch Ltd, Invermay Agricultural Centre, Mosgiel, New Zealand
Gary Saunders , EMBL-EBI, Cambridge, United Kingdom
Ricardo Ventura , Beef Improvement Opportunities, Guelph, ON, Canada
The LD chip is a new addition to the family of ovine SNP ships. Here we present its final design. The major driver was a low cost chip for genomic selection in industry. We designed and tested it for imputation. In addition to imputation SNPs the chip also has parentage and key functional SNPs and has backwards compatibility with earlier versions of ovine LD chips. It is the first LD chip to fully utilise version 3.1 of the genome as well as results derived from the HD ovine chip.

The SheepGenomesDB is an electronic warehouse containing sequence variants called from the expanding collection of sheep genomes being generated across our research community. Through the application of a single harmonised pipeline for read QC, mapping, variant detection and annotation, SheepGenomesDB makes available variant collections derived in a standardised manner supported by the European Variation Archive. The first analysis run has been completed, with read mapping and variant calling performed for more than 250 sheep genomes from over 50 breeds. This identified in excess of 25 million SNP. The creators view SheepGenomesDB as an essential resource for researchers interested in gene mutation discovery, imputation as it relates to genome-wide association and genomic prediction as well as investigations into genome evolution, domestication and the consequences of selection.