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Unknown
(17)
Genomics
(9)
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Homo sapiens
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EGA
(9)
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Illumina CytoSNP, Illumina HumanOmni2.5, ILLUMINA, Illumina 450k, Illumina HiSeq 2000
(1)
Affymetrix 6.0
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2024
(4)
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Mitochondrial polymorphisms in rat genetic models of hypertension.
Not available
S-EPMC2890981
|
biostudies-literature
Cite
Augmented rififylin is a risk factor linked to aberrant cardiomyocyte function, short-QT interval and hypertension.
Not available
S-EPMC3060303
|
biostudies-literature
Cite
De novo variants in MPP5 cause global developmental delay and behavioral changes.
Not available
S-EPMC7906781
|
biostudies-literature
Cite
Reanalysis of Clinical Exome Sequencing Data.
Not available
S-EPMC6934160
|
biostudies-literature
Cite
De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities.
Not available
S-EPMC11221546
|
biostudies-literature
Cite
Survival in BRAF V600-mutant advanced melanoma treated with vemurafenib.
Not available
S-EPMC3724515
|
biostudies-literature
Cite
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11.
Not available
S-EPMC8487929
|
biostudies-literature
Cite
Gencode_550K
Lymphoma samples using HumanOmni
EGAD00010000949
|
EGA
Cite
Gencode_15K
Lymphoma samples using CytoSNP
EGAD00010000947
|
EGA
Cite
ena-DATASET-DKFZ-HIPO-22-04-2016-18:09:52:421-12 - samples
Paired-end RNA sequencing using total RNA from 136 primary lymphoma samples. Sequencing was performed on the Illumina HiSeq2000 with 300bp insert size. The dataset contains FASTQ files.
EGAD00001002056
|
EGA
Cite
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