-
Identification of causal mutation in two patients with Sotos Syndrome Features
Study
EGAS00001000993
-
The_British_Autozygosity_Populations_BioResource
Study
EGAS00001001565
-
2017_AML_WGS
Study
EGAS00001002388
-
IHEC DEEP Release August 2016
Study
EGAS00001001937
-
Hypothalamic transcriptome in Prader-Willi syndrome
Study
EGAS00001002901
-
Whole exome sequencing in familial Multiple Sclerosis
Study
EGAS00001004204
-
Oncogenic gene fusions in primary colon cancers
Study
EGAS00001002197
-
HipSci-RNAseq-healthy volunteers
Study
EGAS00001000593
-
Breast_Cancer_Sequential_Sampling_Targeted_Capture
Study
EGAS00001000596
-
Targeted_Sequencing_of_Human_Myeloid_Malignancies
Study
EGAS00001001289
-
Mutation_burden_in_sun_exposed_eyelid__MSSE_
Study
EGAS00001002512
-
Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics Study
Study
EGAS00001002527
-
The_Transcriptome_of_PLX4032_resistance
Study
EGAS00001000413
-
Bleeding
Study
EGAS00001000106
-
2014_AML_WES_51 samples
Study
EGAS00001002819
-
The_life_history_of_colorectal_cancer_metastases_study_WGS_X10
Study
EGAS00001000864
-
Angiopredict: predicting response for bevacizumab treatment
Study
EGAS00001002724
-
Whole-genome and transcriptome sequencing of tumor-stage mycosis fungoides
Study
EGAS00001002860
-
Meningioma_Exome
Study
EGAS00001000177
-
Paroxysmal_Neurological_Disorders_2
Study
EGAS00001000190
-
Somatic_mutation_and_clonal_evolution_in_the_human_testes
Study
EGAS00001003021
-
Whole genome sequencing of Japanese HCCs
Study
EGAS00001000671
-
Partially methylated domains across multiple cell types
Study
EGAS00001003157
-
X10_sequencing_of_Oesophageal_Adenocarcinoma_Organoids
Study
EGAS00001003264
-
Paroxysmal_neurological_Disorders
Study
EGAS00001000386
-
Validation_of_AML_Mutational_Screening
Study
EGAS00001000430
-
Whole Exome Sequencing of cohorts of Mutant Braf mouse model melanoma DNA and germline DNA.
Study
EGAS00001000729
-
Lymphocyte_LCM_WGS
Study
EGAS00001003384
-
Single cell RNA sequencing of CD19 CAR T-cell infusion products
Study
EGAS00001004576
-
Paroxysmal neurological disorders
Study
EGAS00001000048
-
Somatic_mutation_and_clonal_evolution_in_the_human_bladder_WES_NOVASEQ
Study
EGAS00001003456
-
The genomic landscape of primary cutaneous anaplastic large cell lymphoma (pcALCL)
Study
EGAS00001004429
-
Various_Platelet_Disorders
Study
EGAS00001000107
-
Integrative Analysis of Pediatric Acute Leukemia Identifies Acute Myeloid/T-Lymphoblastic Leukemia Subtype that Spans a T Lineage and Myeloid Continuum with Distinct Prognoses
Study
EGAS00001004701
-
Targeted_sequencing_of_candidate_genes_in_calcific_aortic_valve_stenosis
Study
EGAS00001000308
-
Whole-exome sequencing of acute erythroid leukemia
Study
EGAS00001003696
-
Dense_fine_mapping_study_identifies_new_susceptibility_loci_for_primary_biliary_cirrhosis
Study
EGAS00001001837
-
Orphan_Tumour_Study_NB
Study
EGAS00001003445
-
Molecular profiles and urinary biomarkers of upper tract urothelial carcinomas associated with aristolochic acid exposure
Study
EGAS00001005363
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001003488
-
Gut metagenomic data of 2,338 Pinggu adults
Study
EGAS00001004820
-
Comparison of fresh and slow-frozen cancer samples for different applications
Study
EGAS00001005891
-
A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi
Study
EGAS00001002075
-
Single-cell RNA-seq data from metastatic ovarian cancer for quality control study
Study
EGAS00001005066
-
Exome sequencing of pseudomyxoma peritonei
Study
EGAS00001002418