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GoldenGate Software Inc miscanthus goldengate array
Genotype calling using the <t>Miscanthus</t> GoldenGate™ array . The graphs in panels A-F plot normalized theta (ratio of signal intensities assayed for A and B SNP alleles) against normalized R (signal intensity) for each individual represented as a colored square. Panels A, C, and E illustrate markers that cluster as predicted for a biallelic SNP, which segregate as AA (red), AB (yellow), or BB (blue). Panels B, D, and F illustrate markers that cluster as predicted for a SNP distinguishing alleles for one of two duplicated and unlinked loci, where theta is skewed by the relative dosage of A and B SNPs. In all panels, clusters are defined as sharing alleles with either the Grosse Fontaine (green circles) or Undine (pink circles) parents, individuals that fall outside the cluster are marked as
Miscanthus Goldengate Array, supplied by GoldenGate Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/goldengate+array/pmc03355032-151-7-8?v=GoldenGate+Software+Inc
Average 90 stars, based on 1 article reviews
miscanthus goldengate array - by Bioz Stars, 2026-08
90/100 stars

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1) Product Images from "A framework genetic map for Miscanthus sinensis from RNAseq-based markers shows recent tetraploidy"

Article Title: A framework genetic map for Miscanthus sinensis from RNAseq-based markers shows recent tetraploidy

Journal: BMC Genomics

doi: 10.1186/1471-2164-13-142

Genotype calling using the Miscanthus GoldenGate™ array . The graphs in panels A-F plot normalized theta (ratio of signal intensities assayed for A and B SNP alleles) against normalized R (signal intensity) for each individual represented as a colored square. Panels A, C, and E illustrate markers that cluster as predicted for a biallelic SNP, which segregate as AA (red), AB (yellow), or BB (blue). Panels B, D, and F illustrate markers that cluster as predicted for a SNP distinguishing alleles for one of two duplicated and unlinked loci, where theta is skewed by the relative dosage of A and B SNPs. In all panels, clusters are defined as sharing alleles with either the Grosse Fontaine (green circles) or Undine (pink circles) parents, individuals that fall outside the cluster are marked as
Figure Legend Snippet: Genotype calling using the Miscanthus GoldenGate™ array . The graphs in panels A-F plot normalized theta (ratio of signal intensities assayed for A and B SNP alleles) against normalized R (signal intensity) for each individual represented as a colored square. Panels A, C, and E illustrate markers that cluster as predicted for a biallelic SNP, which segregate as AA (red), AB (yellow), or BB (blue). Panels B, D, and F illustrate markers that cluster as predicted for a SNP distinguishing alleles for one of two duplicated and unlinked loci, where theta is skewed by the relative dosage of A and B SNPs. In all panels, clusters are defined as sharing alleles with either the Grosse Fontaine (green circles) or Undine (pink circles) parents, individuals that fall outside the cluster are marked as "no calls" (NC, grey), and the doubled haploid genotype is indicated by the black arrow. Panel G reports the relative fraction of genotyped segregating SNPs within each clustering type among the Grosse Fontaine and Undine parents, the population of their F1 progeny, as well as the two doubled haploids and their respective parents. Single cluster markers (fixed differences between paralogs) behave similarly in diploids and doubled haploids. In contrast, while diploid accessions show extensive heterozygosity at segregating loci (two- and three-cluster markers), doubled haploids show no heterozygosity.

Techniques Used:

Tetraploidy of Miscanthus relative to sorghum, with extensive colinearity and a single chromosome fusion . Panel A . Horizontal axis shows genetic map position of markers on the 19 Miscanthus linkage groups, in centiMorgans; vertical axis shows physical map position of markers aligned to the 10 sorghum chromosomes in megabases. Each dot corresponds to a single marker. Markers that could not be uniquely mapped to sorghum are shown along the horizontal axis as black dots. Duplication and colinearity of nearly all chromosomes is evident (markers in magenta). A copy of sorghum chromosome 7 (markers in sky blue) has been inserted into a copy of sorghum chromosome 4 (markers in green) to produce Miscanthus linkage group 7. Markers on Miscanthus linkage group 13, which are also syntenic with sorghum chromosome 7, are shown in a darker blue. Panel B . Circos plot showing centromeric insertion of sorghum chromosome 7 into sorghum chromosome 4 to form Miscanthus linkage group 7 (approximate boundaries indicated by arrows). Each line represents an orthologous relationship between a mapped Miscanthus marker and its unique counterpart on the Sorghum bicolor genome. Both Miscanthus linkage groups 7 and 8 have a region corresponding to sorghum chromosome 4, which is inverted with respect to the other markers (dark green arrow and lines). As also shown, Miscanthus linkage group 8 is an intact copy of sorghum chromosome 4, and Miscanthus linkage group 13 is an intact copy of sorghum chromosome 7.
Figure Legend Snippet: Tetraploidy of Miscanthus relative to sorghum, with extensive colinearity and a single chromosome fusion . Panel A . Horizontal axis shows genetic map position of markers on the 19 Miscanthus linkage groups, in centiMorgans; vertical axis shows physical map position of markers aligned to the 10 sorghum chromosomes in megabases. Each dot corresponds to a single marker. Markers that could not be uniquely mapped to sorghum are shown along the horizontal axis as black dots. Duplication and colinearity of nearly all chromosomes is evident (markers in magenta). A copy of sorghum chromosome 7 (markers in sky blue) has been inserted into a copy of sorghum chromosome 4 (markers in green) to produce Miscanthus linkage group 7. Markers on Miscanthus linkage group 13, which are also syntenic with sorghum chromosome 7, are shown in a darker blue. Panel B . Circos plot showing centromeric insertion of sorghum chromosome 7 into sorghum chromosome 4 to form Miscanthus linkage group 7 (approximate boundaries indicated by arrows). Each line represents an orthologous relationship between a mapped Miscanthus marker and its unique counterpart on the Sorghum bicolor genome. Both Miscanthus linkage groups 7 and 8 have a region corresponding to sorghum chromosome 4, which is inverted with respect to the other markers (dark green arrow and lines). As also shown, Miscanthus linkage group 8 is an intact copy of sorghum chromosome 4, and Miscanthus linkage group 13 is an intact copy of sorghum chromosome 7.

Techniques Used: Marker



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