| Accession | Title | Series type(s) | Organism(s) | Samples | GDS | Supplementary | Contact | Release date |
|---|---|---|---|---|---|---|---|---|
 Filter
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Genome variation profiling by genome tiling array
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Homo sapiens
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PAIR
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| GSE100845 |
CNV analysis of 140 Filipinos with Cleft Lip and/or Palate
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140 | J. Robert Manak | Jan 17, 2018 | ||
| GSE16400 |
The pitfalls of platform comparison: DNA copy number array technologies assessed
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179 | Christina Curtis | Dec 03, 2009 | ||
| GSE18679 |
TimEX from human embryonic stem cells, mesenchymal stem cells, and erythroid cells
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27 |
|
Eric Bouhassira | Nov 04, 2009 | |
| GSE20290 |
Towards a comprehensive structural variation map of an individual human genome for personalized medicine
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100 | Andy Pang | Feb 12, 2013 | ||
| GSE25893 |
A comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
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385 | Stephen W Scherer | Jun 30, 2011 | ||
| GSE27367 |
Prospective comparison of genome-wide aCGH platforms for the detection of CNVs in MR
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375 | Tracy Tucker | Feb 17, 2011 | ||
| GSE31257 |
Isolation and in vitro expansion of human colonic stem cells
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15 |
|
Eduard Batlle | Nov 22, 2011 | |
| GSE45495 |
PTEN loss defines a PI3K/AKT pathway-dependent germinal center subtype of diffuse large B-cell lymphoma
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55 | Michael Grau | Jul 09, 2013 | ||
| GSE46848 |
The distribution of genomic variations in human iPSCs is related to replication timing reorganization during reprogramming
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17 | Hu Li | Mar 28, 2014 | ||
| GSE53251 |
The DNA Double-Strand Break Response Is Abnormal in Myeloblasts From Patients With Therapy-Related Acute Myeloid Leukemia
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44 |
|
Matt Walter | Dec 13, 2013 | |
| GSE60259 |
DNA copy number detection from exome sequencing - Exploiting the off-targets
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10 |
|
Oscar Krijgsman | Aug 12, 2014 | |
| GSE64122 |
Detection of copy number variation in patients with Pelizaeus-Merzbacher disease (PMD)
|
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14 | Grace Hobson | Feb 09, 2015 | ||
| GSE87915 |
Individuals with excess numbers of germline de novo CNVs
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52 | Pengfei Liu | Oct 14, 2016 | ||
| GSE13172 |
Mismatch oligonucleotides in human
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3 |
|
Michael R Seringhaus | Feb 18, 2009 | |
| GSE13175 |
Mismatch oligonucleotides in human and yeast
|
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6 |
|
Michael R Seringhaus | Feb 18, 2009 | |
| GSE12731 |
Evaluation of the amplicons for detection of known CNVs using Cs22 HR-CGH
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9 |
|
Xinghua Pan | Sep 24, 2008 | |
| GSE12751 |
Evaluation of Wpa-generated amplicons for SNP typing (allele bias), locus bias, and detection of known CNVs
|
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19 |
|
Xinghua Pan | Sep 24, 2008 | |
| GSE13238 |
DNA packaging of human and murine spermatozoal chromatin
|
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16 | David Miller | Jun 09, 2009 | ||
| GSE17463 |
Somatic CNV profile of congenital ectopic thyroids
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3 | Johnny Yvan Deladoëy | Oct 27, 2010 | ||
| GSE20289 |
NimbleGen 42M data for the HuRef individual
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60 |
|
Andy Pang | Feb 12, 2013 |
