TY - CHAP
T1 - Diversity arrays technology
T2 - A generic genome profiling technology on open platforms
AU - Kilian, Andrzej
AU - Wenzl, Peter
AU - Huttner, Eric
AU - Carling, Jason
AU - Xia, Ling
AU - Blois, Hélène
AU - Caig, Vanessa
AU - Heller-Uszynska, Katarzyna
AU - Jaccoud, Damian
AU - Hopper, Colleen
AU - Aschenbrenner-Kilian, Malgorzata
AU - Evers, Margaret
AU - Peng, Kaiman
AU - Cayla, Cyril
AU - Hok, Puthick
AU - Uszynski, Grzegorz
PY - 2012
Y1 - 2012
N2 - In the last 20 years, we have observed an exponential growth of the DNA sequence data and simular increase in the volume of DNA polymorphism data generated by numerous molecular marker technologies. Most of the investment, and therefore progress, concentrated on human genome and genomes of selected model species. Diversity Arrays Technology (DArT), developed over a decade ago, was among the first "democratizing" genotyping technologies, as its performance was primarily driven by the level of DNA sequence variation in the species rather than by the level of financial investment. DArT also proved more robust to genome size and ploidy-level differences among approximately 60 organisms for which DArT was developed to date compared to other high-throughput genotyping technologies. The success of DArT in a number of organisms, including a wide range of "orphan crops," can be attributed to the simplicity of underlying concepts: DArT combines genome complexity reduction methods enriching for genic regions with a highly parallel assay readout on a number of "open-access" microarray platforms. The quantitative nature of the assay enabled a number of applications in which allelic frequencies can be estimated from DArT arrays. A typical DArT assay tests for polymorphism tens of thousands of genomic loci with the final number of markers reported (hundreds to thousands) reflecting the level of DNA sequence variation in the tested loci. Detailed DArT methods, protocols, and a range of their application examples as well as DArT's evolution path are presented.
AB - In the last 20 years, we have observed an exponential growth of the DNA sequence data and simular increase in the volume of DNA polymorphism data generated by numerous molecular marker technologies. Most of the investment, and therefore progress, concentrated on human genome and genomes of selected model species. Diversity Arrays Technology (DArT), developed over a decade ago, was among the first "democratizing" genotyping technologies, as its performance was primarily driven by the level of DNA sequence variation in the species rather than by the level of financial investment. DArT also proved more robust to genome size and ploidy-level differences among approximately 60 organisms for which DArT was developed to date compared to other high-throughput genotyping technologies. The success of DArT in a number of organisms, including a wide range of "orphan crops," can be attributed to the simplicity of underlying concepts: DArT combines genome complexity reduction methods enriching for genic regions with a highly parallel assay readout on a number of "open-access" microarray platforms. The quantitative nature of the assay enabled a number of applications in which allelic frequencies can be estimated from DArT arrays. A typical DArT assay tests for polymorphism tens of thousands of genomic loci with the final number of markers reported (hundreds to thousands) reflecting the level of DNA sequence variation in the tested loci. Detailed DArT methods, protocols, and a range of their application examples as well as DArT's evolution path are presented.
KW - Complexity reduction
KW - DArT
KW - Diversity
KW - Microarrays
KW - Molecular marker
UR - http://www.scopus.com/inward/record.url?scp=84866761645&partnerID=8YFLogxK
U2 - 10.1007/978-1-61779-870-2_5
DO - 10.1007/978-1-61779-870-2_5
M3 - Chapter
C2 - 22665276
AN - SCOPUS:84866761645
SN - 9781617798696
T3 - Methods in Molecular Biology
SP - 67
EP - 89
BT - Data Production and Analysis in Population Genomics
PB - Humana Press Inc.
ER -