2020
DOI: 10.3389/fpls.2020.592730
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MaizeMine: A Data Mining Warehouse for the Maize Genetics and Genomics Database

Abstract: MaizeMine is the data mining resource of the Maize Genetics and Genome Database (MaizeGDB; http://maizemine.maizegdb.org). It enables researchers to create and export customized annotation datasets that can be merged with their own research data for use in downstream analyses. MaizeMine uses the InterMine data warehousing system to integrate genomic sequences and gene annotations from the Zea mays B73 RefGen_v3 and B73 RefGen_v4 genome assemblies, Gene Ontology annotations, single nucleotide polymorphisms, pro… Show more

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Cited by 21 publications
(15 citation statements)
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“…Model convergence was assessed using trace plots of the posterior means of the parameters. For each selected SNP associated with hyperspectral patterns, genes within an interval of 50 kilobase pair (kbp) upstream and downstream of the SNP were explored using the MaizeMine V1.3 server (Shamimuzzaman et al, 2020). One challenge was the many Manhattan plots that potentially needed to be generated owing to the three manually measured phenotypes, 150 hyperspectral wavelengths, and 131 hyperspectral indices.…”
Section: Methodsmentioning
confidence: 99%
“…Model convergence was assessed using trace plots of the posterior means of the parameters. For each selected SNP associated with hyperspectral patterns, genes within an interval of 50 kilobase pair (kbp) upstream and downstream of the SNP were explored using the MaizeMine V1.3 server (Shamimuzzaman et al, 2020). One challenge was the many Manhattan plots that potentially needed to be generated owing to the three manually measured phenotypes, 150 hyperspectral wavelengths, and 131 hyperspectral indices.…”
Section: Methodsmentioning
confidence: 99%
“…Maize B73 RefGen_v4 was the data mining resource of the Maize Genetics and Genome Database (MaizeGDB). 1 We compared these clean data to the reference genome, Maize B73 RefGen_v4 ( Shamimuzzaman et al, 2020 ), using the Burrows-Wheeler Aligner (BWA) software ( Jia et al, 2013 ), and SAMtools software ( Zhou et al, 2015 ) was used to remove duplicates (command: rmdup). Then, we used a Bayesian model to detect polymorphic sites in the population, and filtered and screened high-quality SNPs using a minor allele frequency (MAF) > 0.05 and call rate >80%.…”
Section: Methodsmentioning
confidence: 99%
“…Among these, qTeller is a comparative RNA-seq expression platform that helps to compare expression between two genes visually. Maizemine is a data mining respiratory for the MaizeGDB [ 102 ]. It enables researchers to create and export customized annotated datasets that can be combined with their research data for use in downstream analyses.…”
Section: Functional Genomic Approaches To Identify Stress-responsive ...mentioning
confidence: 99%