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Items: 4

1.

Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array; Genome variation profiling by genome tiling array
6 related Platforms
375 Samples
Download data: CEL, CHP, PAIR, TXT
Series
Accession:
GSE27367
ID:
200027367
2.

Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR (Mapping250K_Nsp and Mapping250K_Sty)

(Submitter supplied) Clinical laboratories are adopting array comparative genomic hybridization (AGH) as a standard clinical test. A number of whole genome AGH systems are available, but little is known about the comparative performance in a clinical context. We prospectively studied 30 children with idiopathic MR and both unaffected parents of each child using Affymetrix 500K GeneChip SNP arrays, Agilent Human Genome 244K oligonucleotide arrays and NimbleGen 385K Whole-Genome oligonucleotide arrays. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array; SNP genotyping by SNP array
Platforms:
GPL3718 GPL3720
180 Samples
Download data: CEL, CHP
Series
Accession:
GSE27216
ID:
200027216
3.

[Mapping250K_Sty] Affymetrix Mapping 250K Sty2 SNP Array

(Submitter supplied) Affymetrix submissions are typically submitted to GEO using the GEOarchive method described at http://www.ncbi.nlm.nih.gov/projects/geo/info/geo_affy.html The GeneChip® Human Mapping 500K Array Set provides consistently high coverage across different populations. It is comprised of two arrays, each capable of genotyping on average 250,000 SNPs (approximately 262,000 for Nsp arrays and 238,000 for Sty arrays). more...
Organism:
Homo sapiens
150 Series
9570 Samples
Download data
Platform
Accession:
GPL3720
ID:
100003720
4.

8135_Child (Mapping250_Sty)

Organism:
Homo sapiens
Source name:
peripheral blood
Platform:
GPL3720
Series:
GSE27216 GSE27367
Download data: CEL, CHP
Sample
Accession:
GSM672473
ID:
300672473
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