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Inferring expressed genes by whole-genome sequencing of plasma DNA
Study
EGAS00001001754
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Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
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Lenalidomide Resistance in del(5q) Myelodysplastic Syndrome Follows Loss of RUNX1/TP53-mediated Megakaryocytic Differentiation
Study
EGAS00001004113
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Chordoma_Sequencing_Project_Whole_Genome
Study
EGAS00001000409
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APCDR Uganda GWAS: Genome-wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UG2G component)
Study
EGAS00001000545
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cfRRBS on cfDNA from pediatric cancer
Study
EGAS00001004194
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Tracking the origins and drivers of subclonal metastatic expansion in prostate cancer
Study
EGAS00001000942
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Frequent alterations in cytoskeleton remodeling genes in primary and metastatic Chinese lung adenocarcinomas
Study
EGAS00001000982
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Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Study
EGAS00001002182
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miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Study
EGAS00001002184
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Whole-Genome Sequencing of a Healthy Aging Cohort.
Study
EGAS00001002306
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White blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer
Study
EGAS00001004114
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Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
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Molecular Subtype-specific Biomarkers Improves Colorectal Cancer Prognostication
Study
EGAS00001002376
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Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Study
EGAS00001001427
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Transcriptional mechanisms of resistance to anti-PD-1 therapy
Study
EGAS00001002195
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Genomic data from analysis of the human placenta, part of the Pregnancy Outcome Prediction study (POPs)
Study
EGAS00001002205
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Searching for variants associated with endometriosis
Study
EGAS00001001741
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Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility
Study
EGAS00001001789
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DONSON encodes a novel replication fork protection factor mutated in microcephalic dwarfism.
Study
EGAS00001002224