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Items: 3

1.

X-linked CNV burden and male infertility

(Submitter supplied) Male factor infertility affects about 7% of men in the general population and it can be related to a number of different etiologic factors, including genetic anomalies. Both sex chromosomes are enriched in genes prevalently or exclusively expressed in the testis. Nevertheless only the Y chromosome-linked Copy Number Variants (CNVs) and Y-linked genes have been demonstrated as important contributors to impaired sperm production in humans Data on the potential role of X-linked gene products in spermatogenesis derives mainly from model organisms. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platform:
GPL15560
200 Samples
Download data: PDF, TXT
Series
Accession:
GSE37948
ID:
200037948
2.

Agilent-024772 Human custom chromosome X 63K (elena)

(Submitter supplied) custom elena Arrays of this design have barcodes that begin with 16024772 or 2524772. 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. The ID column represents the Agilent Feature Extraction feature number. more...
Organism:
Homo sapiens
1 Series
200 Samples
Download data: TXT
Platform
Accession:
GPL15560
ID:
100015560
3.

DNA infertile 2

Organism:
Homo sapiens
Source name:
genomic DNA extracted from lymphocytes of an infertile patient (channel 1) genomic DNA extracted from lymphocytes of the reference normozoospermic control subject (channel 2)
Platform:
GPL15560
Series:
GSE37948
Download data: TXT
Sample
Accession:
GSM930624
ID:
300930624
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db=gds|term=GSM930624[Accession]|query=1|qty=2|blobid=MCID_6705a4c291df3b340a7df694|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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