GSM1085361[Accession] - GEO DataSets

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Items: 3

Select item 2000444401.

244K array Comparative Genomic Hybridization for the characterization of CNVs among inbred Fayoumi, inbred Leghorn, Line A broiler, and Line B broiler chicken

(Submitter supplied) Chromosomal structural variation can cause alterations in gene dosage and gene regulation between genomes. Structural variants producing a change in the number of copies of a genomic region are termed copy number variants (CNVs). CNVs have been demonstrated to have causative effects on both Mendelian and complex traits, including susceptibility to infectious diseases. We are interested in mapping CNVs to domesticated chicken breeds to help determine structural variation between genomes that influences economically important traits. more...

Organism:: Gallus gallus

Type:: Genome variation profiling by genome tiling array

Platform:: GPL11041
24 Samples

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Accession:: GSE44440

ID:: 200044440

Select item 1000110412.

Agilent-019553 Gallus gallus (chicken) Genome CGH Microarray 244K(Feature Number version)

(Submitter supplied) Gallus gallus (chicken) Genome CGH Microarray 244K Design ID: 019553 Control Grid: IS-243504-1-V1_244K_CGH_Gga_20080227 Arrays of this design have barcodes that begin with 16019553 or 2519553. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. more...