197 series
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Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterGenome variation profiling by SNP array Remove filterIDAT
GSE37142
SNP array for CNV calling AUTS2 project [Illumina]
  • Genome variation profiling by SNP array
1 Els Voorhoeve Jul 12, 2012
GSE111781
Tetra-Amelia with lung aplasia phenotype
  • Genome variation profiling by SNP array
1 Esra Yucel Apr 04, 2018
GSE147730
Detection of CNVs in patients with syndromic intellectual disability
1 Živilė Maldžienė Mar 31, 2020
GSE180894
The evolution of MET and NRAS gene amplification as sequential acquired resistance mechanisms in a patient with EGFR mutation positive non-small cell lung cancer
1 Robert Doebele Jul 28, 2021
GSE185549
Copy number variation analysis of desmoplastic malignant mesothelioma
1
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Rei Noguchi Oct 18, 2021
GSE68794
A large germline alteration affecting MAX and FUT8, causing familial bilateral malignant pheochromocytoma and renal oncocytoma
2 Esther Korpershoek May 13, 2015
GSE95484
Wilms Tumor in Beckwith-Wiedemann Syndrome and Loss of Methylation at Imprinting Centre 2 [HumanOmni2.5M]
2
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Jack Brzezinski Mar 01, 2017
GSE96723
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaCytoSNP850K]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 17, 2017
GSE96789
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaPsychArray]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 19, 2017
GSE96790
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanOmniExpress]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 20, 2017
GSE96791
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanOmniExpressExome]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 20, 2017
GSE96810
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanOmni2.5]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 21, 2017
GSE96816
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanCoreExome]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 21, 2017
GSE96846
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanOmni2.5Exome]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 22, 2017
GSE96893
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanOmni5Exome]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 23, 2017
GSE96895
Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans [IlluminaHumanOmni5]
  • Genome variation profiling by SNP array
2 Rajini Haraksingh Mar 23, 2017
GSE103896
Characterization of a novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient [Genotype]
  • Genome variation profiling by SNP array
2 Fares Al-Ejeh Jan 01, 2018
GSE93207
Excessive UBE3A dosage impairs fine-tuning of retinoid acid signaling in autism spectrum disorders
3 Ronggui Hu Dec 28, 2017
GSE235491
Human HFF cells large rearrangements detection after CRISPR-Cas9 nuclease (Supplentary Fig. 4)
3 Julian Boutin Jun 22, 2023
GSE21168
Gene amplification of the transcription factor DP1 and the CTNND1 in human lung cancer
4 Sandra Castillo Apr 11, 2010