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A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers.
Study
EGAS00001002975
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Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines
Study
EGAS00001002998
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Indonesian Genome Diversity Project
Study
EGAS00001003054
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Integrative genomic profiling of hepatocellular adenomas reveals recurrent FRK activating mutations and mutational processes of malignant transformation
Study
EGAS00001000679
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Dynamics of genomic clones in breast cancer patient xenografts at single cell resolution
Study
EGAS00001000952
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1 Intratumoral genetic heterogeneity and clonal evolution following neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal tumors.
Study
EGAS00001003250
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Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
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Systems biology of Colorectal Cancer
Study
EGAS00001000854
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Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033)
Study
EGAS00001003481
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Telomerase activation by genomic rearrangements in high-risk neuroblastoma
Study
EGAS00001001308
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Evolutionary dynamics of residual disease in human glioblastoma
Study
EGAS00001003043
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Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Study
EGAS00001004733
-
Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing
Study
EGAS00001002102
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The Genetic Landscape of BCL2 Break Negative Follicular Lymphoma
Study
EGAS00001002164
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RNA seq on 19 samples of Radiation-Induced Meningiomas
Study
EGAS00001002318
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THAP11 mutations in a patient with a cblX-like phenotype implicates THAP11 in the regulation of cobalamin metabolism and early vertebrate development
Study
EGAS00001002201
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Sequencing of paediatric High Grade Gliomas and DIPG
Study
EGAS00001002314
-
Suppressors and activators of JAK-STAT signaling at diagnosis and relapse of acute lymphoblastic leukemia in Down Syndrome
Study
EGAS00001002410
-
Genomic landscape of oral cancers (Illumina RNA-Seq)
Study
EGAS00001003237
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Targeting the DNA Repair Pathway in Ewing Sarcoma
Study
EGAS00001000839
-
Exome sequencing in bipolar disorder families
Study
EGAS00001003085
-
Resolving the Full Spectrum of Human Genome Variation using Linked-Reads
Study
EGAS00001003121
-
Enhanced detection of circulating tumor DNA by fragment size analysis
Study
EGAS00001003258
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
RNA-seq as a tool for evaluating human embryo competence
Study
EGAS00001003667
-
Whole-genome Sequencing Suggests Mechanisms for 22q11.2 deletion-associated Parkinson’s disease
Study
EGAS00001002275
-
The Immune Microenvironment, Genome–Wide Copy Number Aberrations and Survival in Mesothelioma
Study
EGAS00001002323
-
Genomic landscape of oral cancers (Complete Genomics WGS)
Study
EGAS00001002393
-
Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Study
EGAS00001001244
-
Genome wide association study on coronary heart disease in patients with familial hypercholesterolemia
Study
EGAS00001000734
-
Genomic diversity of the African-descent Makranis of Pakistan
Study
EGAS00001002558
-
UK10K NEURO EDINBURGH
Study
EGAS00001000117
-
Whole exome sequencing of cell-free DNA reveals temporo-spatial heterogeneity and identifies treatment-resistant clones in neuroblastoma
Study
EGAS00001002705
-
UK10K NEURO IMGSAC
Study
EGAS00001000120
-
Targeted Gene Panel for 171 PTCLs
Study
EGAS00001002740
-
Exploiting immune cell receptor information to quantify index switching in single cell transcriptome sequencing experiment
Study
EGAS00001002911
-
Pharmacological and genomic profiling identifies NFκB-targeted treatment strategies for mantle cell lymphoma
Study
EGAS00001000622
-
Histone chaperone CHAF1A promotes proliferation and tumorigenicity in gastric cancer and impacts prognosis via context-depedent regulation of gene expression
Study
EGAS00001003064
-
Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high risk disease
Study
EGAS00001003071
-
Whole exome sequencing of small cell neuroendocrine cancer of the cervix
Study
EGAS00001003142
-
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
-
Combined MEK and BCL-2/XL inhibition is effective in high-grade serous ovarian cancer patient-derived xenograft models and BIM levels are predictive of responsiveness
Study
EGAS00001003427
-
Plasma DNA aberrations in systemic lupus erythematosus revealed by genomic and methylomic sequencing
Study
EGAS00001000962
-
A molecular cell atlas of the human lung from single cell RNA sequencing
Study
EGAS00001004344