23083 results for "ega"
in 23.58 milliseconds.
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REL-2017-07-1272
Dataset EGAD00010001332 -
REL-2017-07-2013
Dataset EGAD00010001360 -
Clinical and genetic analysis of a rare syndrome associated with neoteny
Dataset EGAD00001003593 -
MT alignment
Dataset EGAD00010001574 -
Methylation array
Dataset EGAD00010001720 -
USA-Immuno
Dataset EGAD00010002043 -
CML IM-Responder vs IM-Non-Responder
Dataset EGAD00001006142 -
yemcha-U-1
Dataset EGAD00010001868 -
CML IM-Responder vs IM-Non-Responder
Dataset EGAD00001006143 -
scRNA-seq of patient-derived PDAC organoids
Dataset EGAD00001006448 -
TumorSNP
Dataset EGAD00010002038 -
small_intestine
Dataset EGAD00010002201 -
Philippine Negrito Genotyping
Dataset EGAD00010002213 -
ALI transcripomics microarray data
Dataset EGAD00010002377 -
SNParray_MOCOG
Dataset EGAD00010002359 -
Dublin_TEST_GWAS
Dataset EGAD00010002093 -
Liverpool_EARTH_GWAS
Dataset EGAD00010002094 -
Genotypes_Farmers
Dataset EGAD00010002141 -
Genotypes_BaYaka
Dataset EGAD00010002139 -
Genotype_GSA
Dataset EGAD00010002165 -
ChIP_3PEAKS
Dataset EGAD00010002155 -
Pediatric Sarcoma PDX whole exome sequencing dataset
Dac EGAC50000000051 -
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer - Data Access Committee
Dac EGAC00001002905 -
ASTAR Skin Research Laboratory
Dac EGAC50000000109 -
Data for paper Mold, Weissman et al. 'Clonally heritable gene expression imparts a layer of diversity within cell types'
Dac EGAC50000000102 -
Whole genome sequencing of individuals from Latvia: the first step towards the population-specific reference of genetic variation
Study EGAS00001007406 -
OXEL WES DAC
Dac EGAC50000000163 -
INCLIVA-CC-WES DAC
Dac EGAC50000000156 -
Patient WGS for #198
Dataset EGAD50000000217 -
PDX WGS for #264
Dataset EGAD50000000033 -
PDX WES for #039 and #049
Dataset EGAD50000000034 -
DAC - organotypic co-cultures @IEO
Dac EGAC50000000238 -
HomoCulturGen
Dataset EGAD00010002663 -
Barcodes
Dataset EGAD50000000529 -
eQTL-CHiC DAC
Dac EGAC50000000445 -
DAC for Transcriptomic and genomic profiling of fragile X syndrome unmethylated full mutation carriers
Dac EGAC50000000416 -
DAC for the BCTL
Dac EGAC50000000323 -
The Sys4MS cohort: a prospective cohort of patients with Multiple Sclerosis and omics
Study EGAS00001007145 -
Distinct Phenotypes of Human Intrahepatic and Extrahepatic Bile duct Organoids and their Applications for Biliary Disease Modeling
Study EGAS00001003792 -
Two monogenic disorders masquerading as one: Severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss
Study EGAS00001004176 -
KDM4A regulates the maternal-to-zygotic transition by protecting broad H3K4me3 domains from H3K9me3 invasion in oocytes
Study EGAS00001004220 -
The transition from normal lung anatomy to minimal and established fibrosis in Idiopathic Pulmonary Fibrosis
Study EGAS00001004758 -
Targeting the Epichaperome As an Effective Precision Medicine Approach in a Novel PML-SYK Fusion Acute Myeloid Leukemia
Study EGAS00001004992 -
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Study EGAS00001004430 -
Deep MRD profiling defines outcome and unveils different modes of treatment resistance in standard and high risk myeloma
Study EGAS00001004558
