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Detecting and tracking circulating tumour DNA copy number profiles during first line chemotherapy in oesophagogastric adenocarcinoma
Study
EGAS00001003695
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Genomewide detection of cytosine methylation by single molecule real-time sequencing
Study
EGAS00001004642
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Foetal_phylogeny_8pcw___WGS_of_LCM_tissues
Study
EGAS00001004674
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Immunological hallmarks for clinical response to BCG in bladder cancer
Study
EGAS00001004764
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Comprehensive investigation of genome architecture of papillary thyroid cancer with whole-exon sequencing in the Chinese population.
Study
EGAS00001002402
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Spontaneous mutations in the single TTN gene represent high tumor mutation burden
Study
EGAS00001004009
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Y chromosome variability in Polish population
Study
EGAS00001004111
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Prospective high-throughput genome profiling in advanced cancers:
Study
EGAS00001004554
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Whole-genome sequencing identifies ADGRG6 enhancer mutations and FRS2 duplications as angiogenesis-related drivers in bladder cancer
Study
EGAS00001003388
-
Targeted sequencing DDR genes in cancer stem cells
Study
EGAS00001004892
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Saliva microbiota in Finnish children
Study
EGAS00001003039
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Gut metagenome/FINRISK 2002 (Salosensaari et al. Nature Comms 2021)
Study
EGAS00001005020
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The Landscape of Genetic Alterations in Hepatocellular Carcinoma, 88 matched HCC tumour/normal pairs WGS belongs to ICGC LICA-CN project
Study
EGAS00001002218
-
DNA sequencing for human normal endometrial glands
Study
EGAS00001005822
-
Molecular characterization of hepatocellular carcinoma in patients with non-alcoholic steatohepatitis
Study
EGAS00001005222
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TP53 variant detection analysis in high grade serous epithelial ovarian cancer
Study
EGAS00001004361
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Epigenetic analyses of methylation and nucleosome occupancy in cell-free DNA (cfNOMe)
Study
EGAS00001004370
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Molecular profile of IMFT for the identification of potential druggable targets and biomarkers predicting crizotinib response.
Study
EGAS00001005419
-
A GWAS meta-analysis on severe acne on a European population of 26,722 individuals
Study
EGAS00001003278
-
Whole genome sequencing of tumour and matched normal from patients with family history of breast cancer
Study
EGAS00001003305
-
RNAseq Iron-Treated iPSC-derived Microglia
Study
EGAS00001006112
-
Genomic abnormalities of TP53 define distinct risk groups of paediatric B-cell non-Hodgkin lymphoma
Study
EGAS00001005617
-
Multiomics Characterization of Low-grade Serous Ovarian Carcinoma
Study
EGAS00001004724
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Discriminating Th17.1 cell driven sarcoidosis-like inflammation from relapse after anti-BCMA CAR T cells in multiple myeloma
Study
EGAS00001006133
-
DNA and RNA sequencing data from Ovarian Carcinosarcoma patients from the Glasgow Cohort.
Study
EGAS00001006605
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Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese
Study
EGAS00001003423
-
Somatic L1 retrotranspositions in normal human cells
Study
EGAS00001006213
-
Gene regulation of human stimulated and cultured CD4+ Treg cells
Study
EGAS00001003515
-
Exome and Whole-Genome Sequencing of Central African Hunter-Gatherers and Agriculturalists
Study
EGAS00001003722
-
SPECIAL: Dissecting the melanoma ecosystem one cell at the time during immunotherapy
Study
EGAS00001006488
-
A single-cell transcriptional gradient in human cutaneous memory T cells restricts Th17/Tc17 identity
Study
EGAS00001006716
-
Population_based_analysis_of_POT1_variants_in_a_cutaneous_melanoma_case_control_cohort
Study
EGAS00001006870
-
Vitamin C boosts DNA demethylation in TET2 germline mutation carriers
Study
EGAS00001006916
-
PacBio Rare Disease Study
Study
EGAS00001008170