-
Whole exome sequencing of 103 pairs BLCA-CN
Study
EGAS00001000677
-
BLUEPRINT EpiVar Whole Genome Sequencing
Study
EGAS00001000689
-
FFPE_normals_v2_gbm_wtsi_panel
Study
EGAS00001002124
-
BLUEPRINT EpiVar ChIP-seq for naive CD4+ T-cells
Study
EGAS00001000753
-
Exome_sequencing_Parkinson_s_disease_patients
Study
EGAS00001000151
-
Enrichment of homologous recombination repair alteration in prostate cancer brain metastases
Study
EGAS00001005091
-
RNA-sequencing of HCC patients undergoing sorafenib treatment
Study
EGAS00001005662
-
Brain_Disease_Wellcome_Leap_Delta_Tissue_RNA
Study
EGAS00001005800
-
COVID_19_Challenge_2_WOOE_RNA_Managed_Access
Study
EGAS00001007636
-
Effects of nucleases on cell-free extrachromosomal circular DNA
Study
EGAS00001005873
-
Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas)
Study
phs001967
-
Method to Assess Lung Water Accumulation During Exercise
Study
phs003346
-
Evaluation of Nuclear DNA from Rootless Hairs for Forensic Purposes
Study
phs002979
-
Genome Sequencing of Circulating Tumor Cells for Minimally Invasive Molecular Characterization of Multiple Myeloma Pathology
Study
phs003084
-
Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE)
Study
phs001252
-
Human Pilocytic Astrocytoma Single Cell RNA Sequencing
Study
phs001854
-
Whole Exome and Targeted Sequencing in Tourette Syndrome Multiplex Families
Study
phs000415
-
Somatic Mutations in Single Human Neurons from Patients with Congenital Neurodegenerative Diseases
Study
phs003005
-
Systems Analysis of Single-Cell Heterogeneity Underlying Glioma Drug Resistance
Study
phs003501
-
Genetic Underpinnings of Ethnic Disparities in Bone Toxicities Between Hispanic and Non-Hispanic Children Treated for Acute Lymphoblastic Leukemia
Study
phs002317
-
Mapping Disease Pathways for Biliary Atresia
Study
phs003458
-
The Somatic Mutational Landscape of Thyroid Cancer in Patients with Germline PTEN Mutations
Study
phs003640
-
HudsonAlpha Long Read Sequencing Data of Individuals with Rare Suspected Genetic Conditions
Study
phs003537
-
Programs, Origins, and Immunomodulatory Functions of Myeloid Cells in Gliomas
Study
phs003756
-
Genomic Landscape of Colorectal Cancer in a Multi-Ancestry Cohort
Study
phs003464