SNP Discovery via Genomic Reduction, Barcoding, and 454-Pyrosequencing in Amaranth

The grain amaranths are important pseudo-cereals native to the New World. During the last decade they have garnered increased international attention for their nutritional quality, tolerance to abiotic stress, and importance as a symbol of indigenous cultures. We report the development of a novel ge...

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Main Authors: Peter J. Maughan, Scott M. Yourstone, Eric N. Jellen, Joshua A. Udall
Format: Article
Language:English
Published: Wiley 2009-11-01
Series:The Plant Genome
Online Access:https://dl.sciencesocieties.org/publications/tpg/articles/2/3/260
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spelling doaj-7894de8f1f044961b1ae92821f333b892020-11-25T03:48:08ZengWileyThe Plant Genome1940-33722009-11-012326027010.3835/plantgenome2009.08.0022260SNP Discovery via Genomic Reduction, Barcoding, and 454-Pyrosequencing in AmaranthPeter J. MaughanScott M. YourstoneEric N. JellenJoshua A. UdallThe grain amaranths are important pseudo-cereals native to the New World. During the last decade they have garnered increased international attention for their nutritional quality, tolerance to abiotic stress, and importance as a symbol of indigenous cultures. We report the development of a novel genomic reduction protocol based on restriction-site conservation and multiplex identifiers (MID) barcodes to discover single nucleotide polymorphisms (SNPs) from a pooled amaranth library of four mapping parents. The incorporation of MID barcodes allowed for DNA sample pooling, sequence deconvolution, and the identification of SNPs for specific mapping populations without additional genotyping. Approximately 1.3 million sequence-reads with an average read length of 440 bp were collected from a single 454-pyrosequencing run. Contigs specific to each of the four mapping populations were assembled. The assembled contigs had an average read-length of 464 bp, and an average read-depth of 16X. A total of 27,658 SNPs were observed across all populations. The average base coverage at all SNPs was 20X. Thirty-four of 35 (97%) predicted SNPs were verified via resequencing and the random genomic distribution of the SNPs generated using this approach was shown in . The method does not require a priori sequence information and should be readily adaptable to other species.https://dl.sciencesocieties.org/publications/tpg/articles/2/3/260
collection DOAJ
language English
format Article
sources DOAJ
author Peter J. Maughan
Scott M. Yourstone
Eric N. Jellen
Joshua A. Udall
spellingShingle Peter J. Maughan
Scott M. Yourstone
Eric N. Jellen
Joshua A. Udall
SNP Discovery via Genomic Reduction, Barcoding, and 454-Pyrosequencing in Amaranth
The Plant Genome
author_facet Peter J. Maughan
Scott M. Yourstone
Eric N. Jellen
Joshua A. Udall
author_sort Peter J. Maughan
title SNP Discovery via Genomic Reduction, Barcoding, and 454-Pyrosequencing in Amaranth
title_short SNP Discovery via Genomic Reduction, Barcoding, and 454-Pyrosequencing in Amaranth
title_full SNP Discovery via Genomic Reduction, Barcoding, and 454-Pyrosequencing in Amaranth
title_fullStr SNP Discovery via Genomic Reduction, Barcoding, and 454-Pyrosequencing in Amaranth
title_full_unstemmed SNP Discovery via Genomic Reduction, Barcoding, and 454-Pyrosequencing in Amaranth
title_sort snp discovery via genomic reduction, barcoding, and 454-pyrosequencing in amaranth
publisher Wiley
series The Plant Genome
issn 1940-3372
publishDate 2009-11-01
description The grain amaranths are important pseudo-cereals native to the New World. During the last decade they have garnered increased international attention for their nutritional quality, tolerance to abiotic stress, and importance as a symbol of indigenous cultures. We report the development of a novel genomic reduction protocol based on restriction-site conservation and multiplex identifiers (MID) barcodes to discover single nucleotide polymorphisms (SNPs) from a pooled amaranth library of four mapping parents. The incorporation of MID barcodes allowed for DNA sample pooling, sequence deconvolution, and the identification of SNPs for specific mapping populations without additional genotyping. Approximately 1.3 million sequence-reads with an average read length of 440 bp were collected from a single 454-pyrosequencing run. Contigs specific to each of the four mapping populations were assembled. The assembled contigs had an average read-length of 464 bp, and an average read-depth of 16X. A total of 27,658 SNPs were observed across all populations. The average base coverage at all SNPs was 20X. Thirty-four of 35 (97%) predicted SNPs were verified via resequencing and the random genomic distribution of the SNPs generated using this approach was shown in . The method does not require a priori sequence information and should be readily adaptable to other species.
url https://dl.sciencesocieties.org/publications/tpg/articles/2/3/260
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