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Updated: May 26, 2025

Improved UPLC-UV Method for the Quantification of Vitamin C in Lettuce Varieties Lactuca sativa L. and Crop Wild Relatives Lactuca spp.
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Improved UPLC-UV Method for the Quantification of Vitamin C in Lettuce Varieties Lactuca sativa L. and Crop Wild Relatives Lactuca spp.

Published on: June 30, 2020

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使用GWAS衍生标记改善了西班牙菜中维生素C含量的基因组预测

Jana Jeevan Rameneni1, A S M Faridul Islam1, Carlos A Avila2,3,4

  • 1Texas A&M AgriLife Research and Extension Center, 2415 Highway 83, Weslaco, TX, 78596, USA.

BMC genomics
|February 21, 2025
PubMed
概括

使用显著的SNP标记物的基因组预测改善了菜中维生素C (甲酸) 含量选择. 这加快了繁殖,以提高这一重要的叶绿的营养价值.

关键词:
全基因组协会研究研究基因组选择 基因组选择预测的准确性 预测的准确性在SNP中,SNP是SNP.菜和西班牙菜.

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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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