New Zealand Next Generation Sequencing Conference - Innovative ...
New Zealand Next Generation Sequencing Conference - Innovative ...
New Zealand Next Generation Sequencing Conference - Innovative ...
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!<br />
GBS method described by Elshire et al., 2011 (PLoS<br />
ONE 6:e19379), however, through the addition of<br />
specific nucleotides within and following the<br />
restriction enzyme cut site to the PCR primer we are<br />
able to reduce the complexity of the genome in a<br />
controlled manner. Varying the number of samples<br />
and the ‘size’ of the reduced genome per lane on an<br />
Illumina HiSeq2000 allows for differing magnitudes<br />
of SNPs to be genotyped and interrogated. The<br />
method for reducing the complexity of the genome,<br />
sequencing and bioinformatics pipeline for GBS in<br />
sheep will be presented.<br />
Using <strong>Next</strong> <strong>Generation</strong> <strong>Sequencing</strong> techniques to identify Single Nucleotide<br />
Polymorphisms in Chinook Salmon<br />
Hayley Baird<br />
AgResearch, Invermay<br />
Biography<br />
Hayley Baird graduated from Otago University with<br />
a BSc(Hons) in microbiology. She is now a<br />
research associate for AgResearch Animal<br />
Genomics at Invermay. The majority of her time<br />
over the last few years has involved working with<br />
the Illumina iSCAN in particular the sheep 50 and<br />
5k chips, however the area of her research<br />
thatsheI’ll be talking about is the Aquaculture<br />
industry and the process of creating a SNP chip for<br />
Chinook salmon.<br />
Abstract<br />
Understanding and improving feed conversion<br />
efficiency (FCE) in farmed <strong>New</strong> <strong>Zealand</strong> Chinook<br />
salmon is a high priority for the industry. A<br />
research programme has been established with<br />
two main goals: 1) tank-based performance and<br />
genetic evaluation of 160 families focussing on<br />
growth, feed intake, body fat and FCE and 2) the<br />
development of a new panel of single nucleotide<br />
polymorphism (SNP) markers that will be used to<br />
search for markers linked to QTL. Since there is no<br />
salmon genome assembly available we had to<br />
come up with a strategy that did not require a<br />
reference genome. We utilised three different nextgeneration<br />
sequencing platforms (454, SOLiD and<br />
Illumina HiSeq) to take us straight to SNPs. After<br />
stringent filtering we arrived at 95,000 SNPs.<br />
Comparative genomics indicated that these SNPs<br />
were evenly distributed across the salmon genome.<br />
An Illumina 6K SNP chip has been developed and<br />
4 large families genotyped for mapping and<br />
eventual QTL analysis.<br />
Session 6<br />
Tailoring high-throughput sequencing approaches to next-generation plant virology in<br />
south-west Australia<br />
Steve Wylie<br />
Murdoch University, Australia<br />
Biography<br />
Steve Wylie attended Otago University in the<br />
1980s and completed an honours degree in the<br />
botany department before moving to Western<br />
Australia to study plant viruses of pasture legumes<br />
for his PhD. The chance discovery of viruses in<br />
Abstract<br />
Given the great age of the Australian continent,<br />
high endemism amongst its plant flora, and the<br />
varied ecosystems present, we hypothesised that<br />
its indigenous viral flora would be much richer than<br />
that currently described. Many exotic plants and<br />
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