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Human karyomapping beadarray

Manufactured by Illumina
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The Human Karyomapping beadarray is a laboratory equipment product designed for genetic analysis. It provides a platform for visualizing and analyzing chromosomal structures and arrangements. The core function of this product is to enable karyotyping, a technique used to examine the number and appearance of chromosomes in a sample. The beadarray technology facilitates this process by capturing and processing relevant genetic data.

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Lab products found in correlation

Bluefuse multi v4, by Illumina (2 mentions) 24sure, by Illumina (2 mentions) Humancytosnp 12, by Illumina (2 mentions)

Spelling variants of this product

BeadArray (33 citations) Karyomapping (2 citations)

2 protocols using human karyomapping beadarray

1

Single-cell DNA analysis protocols

Check if the same lab product or an alternative is used in the 5 most similar protocols
For array CGH analysis, 4 μl aliquots of Sureplex single cell amplified DNA Products (PB1, PB2, oocyte or blastomere) were processed on microarray slides (24Sure; Illumina, USA). The data was imported and analysed using dedicated software (BlueFuse Multi v 4.0; Illumina, USA).
For SNP genotyping, 400 ng of genomic DNA or 8 μl of WGA products from the single cell and embryo samples (PB1, PB2, oocyte, single blastomere or whole embryo) were processed on a SNP genotyping beadarray (Human CytoSNP-12 or Human Karyomapping beadarray; Illumina, San Diego, CA, USA) for ~300K SNPs, using a shortened protocol and the genotype data analysed using a dedicated software programme for karyomapping (BlueFuse Multi v 4.0; Illumina, San Diego, CA, USA) or exported as a text file for analysis in Micrsoft Excel12 .
Ottolini C.S., Newnham L., Capalbo A., Natesan S.A., Joshi H.A., Cimadomo D., Griffin D.K., Sage K., Summers M.C., Thornhill A.R., Housworth E., Herbert A.D., Rienzi L., Ubaldi F.M., Handyside A.H, & Hoffmann E.R. (2015). “Genome-wide recombination and chromosome segregation in human oocytes and embryos reveal selection for maternal recombination rates”. Nature genetics, 47(7), 727-735.
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2

Single-cell DNA analysis protocols

Check if the same lab product or an alternative is used in the 5 most similar protocols
For array CGH analysis, 4 μl aliquots of Sureplex single cell amplified DNA Products (PB1, PB2, oocyte or blastomere) were processed on microarray slides (24Sure; Illumina, USA). The data was imported and analysed using dedicated software (BlueFuse Multi v 4.0; Illumina, USA).
For SNP genotyping, 400 ng of genomic DNA or 8 μl of WGA products from the single cell and embryo samples (PB1, PB2, oocyte, single blastomere or whole embryo) were processed on a SNP genotyping beadarray (Human CytoSNP-12 or Human Karyomapping beadarray; Illumina, San Diego, CA, USA) for ~300K SNPs, using a shortened protocol and the genotype data analysed using a dedicated software programme for karyomapping (BlueFuse Multi v 4.0; Illumina, San Diego, CA, USA) or exported as a text file for analysis in Micrsoft Excel12 .
Ottolini C.S., Newnham L., Capalbo A., Natesan S.A., Joshi H.A., Cimadomo D., Griffin D.K., Sage K., Summers M.C., Thornhill A.R., Housworth E., Herbert A.D., Rienzi L., Ubaldi F.M., Handyside A.H, & Hoffmann E.R. (2015). “Genome-wide recombination and chromosome segregation in human oocytes and embryos reveal selection for maternal recombination rates”. Nature genetics, 47(7), 727-735.
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