-
Comparison of 133/144bp dominant phenotype vs 166bp dominant phenotype.
Study
EGAS00001004135
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
-
Small_molecule_inhibitors_in_melanoma___Kenski___Kong___WES
Study
EGAS00001002863
-
Transcriptional and DNA binding profiling of CEBPE in REH acute lymphoblastic leukaemia cells using shRNA RNA-Seq and ChIP-Seq
Study
EGAS00001002877
-
scRNA-seq data of human nuclei collected from the temporal cortex of 17 individuals.
Study
EGAS00001002882
-
Glioblastoma epigenome profiling identifies SOX10 as a master regulator of molecular tumour subtype
Study
EGAS00001003953
-
Deep multi-region whole-genome sequencing reveals heterogeneity and gene-by-environment interactions in treatment-naive, metastatic lung cancer
Study
EGAS00001003830
-
Bulk-tissue RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Study
EGAS00001005305
-
SG Peranakan Project: Genetic admixture in the culturally unique Peranakan Chinese population in Southeast Asia
Study
EGAS00001005379
-
Sequence Data from the phase 2 PrE0505 trial of Durvalumab with First Line Platinum-Pemetrexed for Unresectable Pleural Mesothelioma
Study
EGAS00001005426
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__head___neck
Study
EGAS00001005450
-
Comprehensive Genomic Characterization of Gene Therapy-Induced T-cell Acute Lymphoblastic Leukemia (H007)
Study
EGAS00001003870
-
Transcriptome sequencing of gingivo-buccal oral squamous cell carcinoma for integrative analysis: alterations in expression of genes attributable to methylation changes
Study
EGAS00001003893
-
Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_cytoscan)
Study
EGAS00001005584
-
Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing
Study
EGAS00001004289
-
Patient-derived tumor organoids for personalized medicine in a rare case of hepatocellular carcinoma with neuroendocrine differentiation.
Study
EGAS00001005887
-
scRNA-seq of HGSC tumor and ascites
Study
EGAS00001004829
-
Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_oncoscan)
Study
EGAS00001005586
-
Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_agilent)
Study
EGAS00001005587
-
Targeted de-methylation of the FOXP3-TSDR
Study
EGAS00001004867
-
5- FU treated organoids
Study
EGAS00001003592
-
Genomic insights into the pathogenesis of Epstein-Barr virus-associated diffuse large B-cell lymphoma by whole-genome and targeted amplicon-based sequencing
Study
EGAS00001004941
-
Genetic insights into the biological mechanisms governing human ovarian ageing
Study
EGAS00001004947
-
Control of Focal Adhesion Kinase Activation by RUNX1-regulated miRNAs in high-risk AML
Study
EGAS00001006491
-
BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Study
EGAS00001006663
-
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Study
EGAS00001004020
-
Cell-free DNA fragmentation patterns and personalized sequencing reveal circulating tumor DNA in urine and plasma of glioma patients
Study
EGAS00001004355
-
Loss of LGR4/GPR48 causes severe neonatal salt-wasting due to disrupted WNT signaling altering adrenal zonation
Study
EGAS00001006808
-
Dynamics of sequence and structural cell-free DNA landscapes in small-cell lung cancer
Study
EGAS00001006831
-
cfDNA dataset from extracelular vesicles and paired non-fractionated samples
Study
EGAS00001006848
-
Germline whole genome sequencing of patients with Li-Fraumeni syndrome
Study
EGAS00001007061
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
ATAC-Seq of CD4 T cell subsets
Study
EGAS00001007345
-
Machine Learning Signal Enrichment for Ultrasensitive Plasma Tumor Burden Monitoring
Study
EGAS00001007451
-
RRBS data (cfSort study) from noncancer tissue DNA
Dataset
EGAD00001010880
-
WES data (cfTrack study) from NSCLC patients and OC patients
Dataset
EGAD00001008454
-
RBMX functional retrocopy safeguards brain development
Study
EGAS50000001650
-
The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH
Study
EGAS00001004285
-
Bulk-tissue RNA-sequencing paired nuclear and cytoplasmic fractions of anterior prefrontal cortex, cerebellar cortex and putamen tissues from post-mortem neuropathologically-confirmed control individuals.
Study
EGAS00001006380
-
Characterization of individual foci of multicentric/multifocal breast cancer using targeted next generation sequencing
Dataset
EGAD00001000624
-
The patterns and dynamics of genomic instability in metastatic pancreatic cancer
Study
EGAS00000000064
-
Nanopore sequencing enables allelic phasing of FLG loss-of-function variants, intragenic copy number variation and methylation status in atopic dermatitis and ichthyosis vulgaris
Study
EGAS50000000166
-
The tissue origin of highly elevated cell-free DNA in patients with and without cancer
Study
EGAS00001005400
-
Characterizing the Role of the Immune Microenvironment in Multiple Myeloma Progression at a Single Cell Level
Study
phs002756
-
Integrated Epigenetic Maps of Human Embryonic, Extraembryonic and Adult Cells
Study
phs000791
-
Cell-Free, Methylated DNA in Blood Samples Reveals Tissue-Specific, Cellular Damage from Radiation Treatment
Study
phs003290
-
NIMH (National Institute of Mental Health) De Novo Mutation Identification in Taiwanese Schizophrenia Trios
Study
phs001196
-
Genetics of Disorders Affecting Tooth Structure, Number, Morphology and Eruption
Study
phs001491
-
RNA-Sequencing of B-Lymphoblastic Leukemia with Glucocorticoids and PI3K Delta Inhibition
Study
phs003085