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Items: 8

1.

Trisomy detection by PCR and comparative genomic hybridization

(Submitter supplied) PCR based detection of trisomy 18 and trisomy 21 compared against results obtained by CGH microarrrays in Preimplantation Genetic Screening
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL17760
21 Samples
Download data: TXT, XLS
Series
Accession:
GSE97903
ID:
200097903
2.

Detection of Y chromosome

(Submitter supplied) PCR based detection of Y-chromosome compared against results obtained by CGH microarrrays in Preimplantation Genetic Screening
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL17760
21 Samples
Download data: TXT
Series
Accession:
GSE97386
ID:
200097386
3.

Genomic instability in human embryonic stem cells is associated to culture density and medium acidification.

(Submitter supplied) Human embryonic stem cells (hESC) show great promise for clinical and research applications, but genomic instability hampers the development of their full potential. Here we demonstrate that increased culture density causes medium acidification due to lactic acid accumulation. hESC are able to cope with this, but acquire increased DNA damage associated to DNA replication stress. Also, single-cell genomics analysis reveals a strong correlation of the occurrence of de novo CNVs and culture density after only five days of culture. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL17760
59 Samples
Download data: TXT
Series
Accession:
GSE58281
ID:
200058281
4.

Characterization and quantification of proteins secreted by single human embryos prior to implantation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array; Genome variation profiling by array
Platforms:
GPL10558 GPL17760
20 Samples
Download data: TXT
Series
Accession:
GSE72685
ID:
200072685
5.

Karyotype assessment of whole human blastocysts by aCGH

(Submitter supplied) The use of in vitro fertilization (IVF) has revolutionized the treatment of infertility and is now responsible for 1-5% of all births in industrialized countries. During IVF, it is typical for patients to generate multiple embryos. However, only a small proportion of them possess the genetic and metabolic requirements needed in order to produce a healthy pregnancy. The identification of the embryo with the greatest developmental capacity represents a major challenge for fertility clinics. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by array
Platform:
GPL17760
14 Samples
Download data: TXT
Series
Accession:
GSE72684
ID:
200072684
6.

Chromosomal meiotic segregation, embryonic developmental kinetics and DNA (hydroxy)methylation analysis reassure the safety of human oocyte vitrification in a high security closed system

(Submitter supplied) Oocyte vitrification has been introduced into clinical settings without pre-clinical safety testing. In this study, we analyzed the safety of human oocyte
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL17760
48 Samples
Download data: TXT
Series
Accession:
GSE63866
ID:
200063866
7.

Chromosome constitution in embryos generated after in vitro maturation in a culture system supplemented with cAMP modulators

(Submitter supplied) Ten volunteers underwent 13 research IVM cycles. Immature oocytes were retrieved after mild ovarian stimulation with gonadotropins but no hCG ovulation trigger, in vitro matured and fertilized using ICSI. Oocyte maturation rate in vitro was 47% (94/199), the mean fertilization rate was 71% (67/94) and 37% (25/67) of mature oocytes developed into a morphologically good quality embryo on day 3 after ICSI, after which the blastomeres were analysed by single-cell aCGH. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL17760
123 Samples
Download data: TXT
Series
Accession:
GSE56799
ID:
200056799
8.

Non-clonal mosaicism in human somatic and embryonic stem cells revealed by single-cell array-based copy-number variation analysis

(Submitter supplied) Although it is known that cultured human cells acquire copy number variations over time, little is known about the mutation frequency in individual cells. Here we describe that human somatic and embryonic stem cell cultures show significant fractions of cells carrying unique chromosomal abnormalities, forming a non-clonal genetic mosaic. We studied 85 human single cells by array-based comparative genomic hybridisation and found that 14-31% of hESC and 8-26% of somatic cells are chromosomally abnormal. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL17760
106 Samples
Download data: TXT
Series
Accession:
GSE51126
ID:
200051126
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