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Single cell RNAseq of lung adenocarcinoma
Study
EGAS00001005021
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Deconvolution of bulk RNA-Seq using single cell RNA-Seq
Study
EGAS00001006723
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Germline whole genome sequencing of patients with Li-Fraumeni syndrome
Study
EGAS00001007061
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cfDNAme allows early prediction of PE
Study
EGAS00001007071
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Digital tEchnology For Lung Cancer Treatment
Study
EGAS00001007219
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GOSH_Childhood_Leukemia_Behjati_WellcomeCore_RNA
Study
EGAS00001007616
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Exome_sequencing_of_UK_Birth_Cohorts___Born_in_Bradford
Study
EGAS00001006978
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Exome_sequencing_of_UK_Birth_Cohorts___Millennium_Cohort_Study
Study
EGAS00001007789
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Genetic landscape of pediatric Low Grade Gliomas & Glioneuronal tumors
Study
EGAS00001000255
-
Comprehensive analysis of the (epi)genome of pediatric atypical teratoid/rhabdoid tumours (AT/RTs)
Study
EGAS00001001297
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Oncogenic cooperation between the TCF7-SPI1 fusion and NRAS(G12D) requires β-catenin activity to drive T-cell acute lymphoblastic leukemia.
Study
EGAS00001005097
-
Mult-omics Palbociclib Resistance Study in HR+/HER2– Metastatic Breast Cancer
Study
EGAS00001005736
-
Genome-wide cell-free DNA termini in patients with cancer
Study
EGAS00001005738
-
Accumulation of copy number alterations and clinical progression across advanced prostate cancer
Study
EGAS00001006251
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Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Study
EGAS00001007099
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PanCuRx Translational Research Initiative
Study
EGAS00001002543
-
COVID-19 whole blood transcriptomic analysis
Study
EGAS00001005332
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Liquid biopsy-based minimal residual disease monitoring for early risk stratification and decision-making in advanced non-small cell lung cancer
Study
EGAS50000001554
-
Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML
Study
EGAS00001004684
-
DECONVOLUTION OF HEMATOPOIETIC STEM/PROGENITOR CELL SIGNALING IN HUMAN AML
Study
EGAS00001007330
-
Prostate cancer ancestral genomic disparity
Study
EGAS00001006425
-
HIV-phyloTSI: Subtype-independent estimation of time since HIV-1 infection for cross-sectional measures of population incidence using deep sequence data
Study
EGAS50000000895
-
Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
-
Cerebrospinal fluid cfDNA sequencing for classification of central nervous system glioma
Study
EGAS50000000060
-
Nanopore sequencing of blood, saliva, buccal mucosa samples of patients with inherited retinal disorders
Study
EGAS50000000440