-
Stromal-induced epithelial-mesenchymal transition induces drug resistance in acute lymphoblastic leukemia
Study
EGAS00001006120
-
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102
-
The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer
Study
EGAS00001001305
-
Enhanced detection of circulating tumor DNA by fragment size analysis
Study
EGAS00001003258
-
Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
-
Transcriptional_profiling_of_tauopathies_in_human_IPS_derived_neurons
Study
EGAS00001000382
-
Altered oligodendrocyte heterogeneity in Multiple sclerosis revealed by single nuclei RNA sequencing
Study
EGAS00001003412
-
Persistence of circulating tumor DNA in breast cancer patients during neoadjuvant treatment is a significant predictor of poor tumor response
Study
EGAS00001005798
-
Profiling the unique protective properties of intracranial arterial endothelial cells
Study
EGAS00001004479
-
BCR Signaling in human BM PC
Study
EGAS00001004948
-
Whole genome sequencing of tumor samples from advanced pre-treated NSCLC patients recruited in a phase I/II single-arm trial utilising CVA21, an oncolytic coxsackie virus, in combination with pembrolizumab.
Study
EGAS00001008258
-
Single-cell decoding of drug induced transcriptomic reprogramming in triple negative breast cancers
Study
EGAS00001007242
-
SLCO1B1 Variants and Methotrexate Clearance
Study
phs000426
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Victorian Collaborative AuTism Study (CATS): Family and Community Study of the Genetics of Autism Spectrum Disorder
Study
phs002044
-
ILyAD (Indolent Lymphoma And vitamin D)
Study
phs003503
-
Single Cell and Spatial Transcriptomic Profiling of Haemophilus ducreyi Infection
Study
phs003754
-
Study on the Genetics of Alcoholism (COGA): Smoke Screen and Exome Sequencing
Study
phs001208
-
Whole-genome and transcriptome versus panel sequencing in precision oncology: A translational-clinical comparison
Study
EGAS50000000431
-
Singel-cell RNA sequencing and CUT&RUN sequencing of human RUNX2-deficient osteoblasts
Study
JGAS000663
-
Biallelic tumor suppressor loss and DNA repair defects in de novo small cell prostate cancer
Study
EGAS00001003007
-
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia
Study
EGAS00001004440
-
Transcriptional profiling of ovarian tumours and cell lines
Study
EGAS00001004814
-
Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis
Study
EGAS00001005220
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Multimodal Developmental Neurogenetics of Females
Study
phs002043
-
Male Infertility: Genetics of Spermatogenic Failure
Study
phs001023
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Genomics of Autism Spectrum Disorder (GASD)
Study
phs002509
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Homozygosity Mapping Consortium for Autism (HMCA)
Study
phs001894
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Simons Searchlight
Study
phs002512
-
QUANTitative Chest Computed Tomography UnMasking Emphysema Progression in Alpha-1 Antitrypsin Deficiency
Study
phs000698
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Center of Excellence (ACE II)
Study
phs002042
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Study of Autism Genetics Exploration (SAGE)
Study
phs001740
-
The Library of Integrated Network-Based Cellular Signatures (LINCS) - NeuroLINCS
Study
phs001231
-
Center for Common Disease Genomics (CCDG)-Neuropsychiatric: A Study of the Genetic Causes of Complex Pediatric Disorders (CAG)
Study
phs002004
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Autism Genetic Resource Exchange
Study
phs001766
-
Whole genome and transcriptome sequencing of lung cancer patients and cell lines at Genentech
Study
phs000299
-
Small Intestine Neuroendocrine Tumors (Carcinoid Tumors)
Study
phs000579
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: The Autism Simplex Collection (TASC)
Study
phs001741
-
A Phase I Study with a Personalized Neoantigen Cancer Vaccine in Melanoma
Study
phs001451
-
Trisomy 21 Dosage Compensation Map (T21DoCoMap)
Study
phs002397
-
Prostate Cancer Upgrading Reference Set
Study
phs003670
-
Gut metagenome associations with extensive digital health data in a volunteer-based EstMB cohort second timepoint data
Study
EGAS50000001181
-
Characterization of HCV-specific CD4 T cells during DAA-Therapy
Study
EGAS00001003950
-
Negligible impact on missing heritability of autoimmune-locus rare coding-region variants
Study
EGAS00001000476
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)
Study
EGAS00001008011
-
Whole genome study of Hurthle cell thyroid carcinoma
Study
EGAS00001000940
-
GCAT | Genomes for life: cohort study of the genomes of Catalonia
Study
EGAS00001003018
-
The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
-
Prostate cancer ancestral genomic disparity
Study
EGAS00001006425
-
Whole-genome sequencing of normal Singaporean volunteers
Study
EGAS00001004007