3855 results for "*geneti*"
in 36.27 milliseconds.
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Malignant mesothelioma EWAS on European prospective study
Study EGAS00001006432 -
Mechanisms of active DNA demethylation in human monocytes
Study EGAS00001004784 -
Methylation-based deconvolution of cell-free DNA
Study EGAS00001007493 -
Expression profiles and genetic makeup of metastases of a cancer of unknown primary.
Study EGAS00001004059 -
ATAC-Seq and CTCF ChIP-Seq on the OCIAML-2 cell line
Study EGAS00001004741 -
Bulk ATAC-Seq on sorted cord blood hematopoietic populations
Study EGAS00001004742 -
AGECAN - Interespecies conservation of brain specific DNA methylation in aging and cancer
Study EGAS00001004851 -
TULIPs decorate the three-dimensional genome of PFA ependymoma
Study EGAS00001005476 -
Nasal DNA methylation at three CpG sites predicts childhood allergic disease
Study EGAS00001005189 -
Single Cell ATAC-Seq on human cord-blood derived HSPC.
Study EGAS00001004740 -
Hi-C on the OCIAML-2 Cell Line
Study EGAS00001004743 -
Low-C on Human CB-derived LT-HSC and ST-HSC
Study EGAS00001004744 -
Whole Exome Sequencing of Spanish Patients diagnosed with rare ophtalmogenetic disorders: Macular Dystrophy, Retinitis Pigmentosa and Leber's congenital amaurosis.
Study EGAS00001004084 -
Association of DNA-methylation profiles with immune responses in breast cancer patients
Study EGAS00001004211 -
Genetics and transcriptomics of human acute erythroid leukemia
Study EGAS00001004203 -
Genetic characterization of a Unique Neuroendocrine Transdifferentiation Prostate Circulating Tumor Cell - Derived eXplant (CDX) Model
Study EGAS00001004272 -
Epigenome-wide association study of asthma remission in whole blood and nasal epithelium
Study EGAS00001004766 -
Enhancer-gene rewiring in the pathogenesis of Quebec Platelet Disorder
Study EGAS00001004315 -
Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma.
Study EGAS00001004320 -
Genotype data from 'Evidence of the interplay of genetics and culture in Ethiopia'
Study EGAS00001005171 -
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Study EGAS00001004430 -
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma
Study EGAS00001004288 -
Profiling Genome-Wide DNA Methylation Patterns in Human Aortic and Mitral Valves
Study EGAS00001004559 -
The Genetic Basis of Preeclampsia in an Andean Population Adapted to High Altitude
Study EGAS00001004625 -
Sensitive and reproducible cell-free methylome quantification with synthetic spike-in controls
Study EGAS00001005069
