-
Application of Hi-C sequencing to detect structural variants in B-cell acute lymphoblastic leukemia
Study
EGAS00001005605
-
Pediatric B-cell precursor acute lymphoblastic leukemia samples with very early relapse
Study
EGAS00001005615
-
Mutational_signatures_and_clonal_dynamics_in_normal_human_tissues
Study
EGAS00001002471
-
Description and determinants of the faecal resistome and microbiome of farmers and slaughterhouse workers: a metagenome-wide cross-sectional study.
Study
EGAS00001003944
-
Transcriptome_analysis_of_LCM_samples_
Study
EGAS00001003862
-
H3Africa - An integrated approach to the identification of genetic determinants of susceptibility to trypanosomiasis
Study
EGAS00001002602
-
The Southern African Human Genome Programme
Study
EGAS00001002639
-
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
-
Real-time response profiling through serial plasma analyses during FOLFOX treatment in patients with colorectal cancer
Study
EGAS00001004213
-
The molecular basis of T-PLL is an actionable perturbation of TCL1/ATM- and epigenetically instructed damage responses
Study
EGAS00001002744
-
Mitochondrial DNA mutations contribute to autism and also to the characteristics of mitochondrial disorders present in patients with autism spectrum disorders
Study
EGAS00001002750
-
Gut metagenome associations with extensive digital health data in a volunteer-based EstMB cohort
Study
EGAS00001005900
-
Gene expression in brain (Schizophrenia) study
Study
EGAS00001004199
-
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Study
EGAS00001001632
-
Sequencing of an organoid biobank for childhood soft tissue sarcoma.
Study
EGAS00001005912
-
Germline SDHB-inactivating mutation in gastric spindle cell sarcoma (HIPO-021)
Study
EGAS00001004277
-
Solve-RD Solving the Unsolved Rare Dieseases
Study
EGAS00001003851
-
Paired healthy & tumor organoid Biobank _B16PON
Study
EGAS00001005937
-
Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
-
Colorectal adenomas, carcinomas and adjacent normal NKI-AvL TGO series NGS-ProToCol
Study
EGAS00001002854
-
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_TGS
Study
EGAS00001003863
-
Deep intronic homozygous variation in PSMC3 causes a syndromic neurosensory disorder combining deafness and cataract
Study
EGAS00001003942
-
Genomic DNA of tumor tissues, adjacent normal tissues, and peripheral blood were extracted using QIAamp DNA mini Kit (QIAGEN, cat. #51306)
Study
EGAS00001003242
-
2015_AML_ETO
Study
EGAS00001002897
-
Glioblastoma epigenome profiling identifies SOX10 as a master regulator of molecular tumour subtype
Study
EGAS00001003953
-
Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer
Study
EGAS00001003791
-
2015_AML_ETO_WGS_additional
Study
EGAS00001002898
-
eccDNA in maternal plasma
Study
EGAS00001003827
-
Matching of actionable mutations with therapies in cancer patients: comparison of three commercial decision support platforms
Study
EGAS00001004383
-
Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer
Study
EGAS00001005981
-
To determine the genomic profile of Triple Negative Breast Cancer patient-derived xenografts (PDX cohort)
Study
EGAS00001005995
-
H3Africa - Collaborative African Genomics Network
Study
EGAS00001002656
-
Osteosarcoma mate-pair and RNA-sequencing
Study
EGAS00001003842
-
Clonal fitness inferred from timeseries modeling of single cell cancer genomes
Study
EGAS00001004448
-
Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Study
EGAS00001004459
-
Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma
Study
EGAS00001002936
-
Collection of Genotypic and Ethnographic Information from Individuals of South African Ethnic Groups
Study
EGAS00001004472
-
Papuan Y chromosome Diversity Panel
Study
EGAS00001006025
-
IYDP Indonesian Y chromosome Diversity Project
Study
EGAS00001006028
-
Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses
Study
EGAS00001002967
-
The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
-
Increased mutation accumulation during fetal development in Down syndrome
Study
EGAS00001003982
-
Identification of the mutational consequences of precancerous liver disease (including alcohol abuse) on the genomes of human adult stem cells.
Study
EGAS00001002983
-
Reconstruction of complex rearrangement patterns causing the initiation of clear cell renal cell carcinoma.
Study
EGAS00001004015
-
Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
-
Whole_Genome_Sequencing_of_Human_Organoid_Lines
Study
EGAS00001003538
-
Genomic and transcriptomic landscape of aggressive thyroid cancer
Study
EGAS00001003540
-
The Spatial Heterogeneity in Multiple Myeloma - from the Subclonal Architecture to the Immune Microenvironment (partly hipo_K08K)
Study
EGAS00001006090
-
Ovarian cancer organoid biobank
Study
EGAS00001003073
-
A Dose Escalation Study of Efmarodocokin Alfa (UTTR1147A) in Healthy Volunteers and Patients with Ulcerative Colitis
Study
EGAS00001006172