-
HipSci_RNASEQ_Macular_Dystrophy
Study
EGAS00001001995
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Double mutant DNMT3A AML: a unique subtype
Study
EGAS00001007966
-
HipSci HumanExome BeadChip analysis - Kabuki syndrome
Study
EGAS00001002007
-
Whole-exome sequencing of breast cancer metastasis and corresponding blood samples
Study
EGAS00001001695
-
Identification of gene mutations and fusion genes in patients with Sézary Syndrome
Study
EGAS00001001706
-
HipSci HumanExome BeadChip analysis - Macular Dystrophy
Study
EGAS00001002014
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WES analysis of a mixed cohort of pituitary tumors
Study
EGAS00001001714
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
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Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
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The_Little_Princess_Knowledge_Bank_RNAseq
Study
EGAS00001005244
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Reconstructing the dispersals and adaptive history of Bantu-speaking populations in Africa and North America
Study
EGAS00001002078
-
Epigenetic age deceleration reflects fitness improvements following a six-month endurance exercise intervention
Study
EGAS00001008221
-
RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias
Study
EGAS00001001795
-
Molecular subtypes of pancreatic neuroendocrine tumors mutated in MEN1/DAXX/ ATRX explain biological variability
Study
EGAS00001008272
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IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
-
Genetics_of_gene_expression_in_human_macrophage_response_to_Salmonella
Study
EGAS00001002236
-
Investigating genetic susceptibility to rheumatic heart disease in Oceania
Study
EGAS00001001881
-
Sequencing of pancreatic cancer primary tumors and metastases
Study
EGAS00001002186
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Resolving_the_Genetic_Architecture_of_Aseptic_Loosening_After_Total_Hip_Replacement
Study
EGAS00001001883
-
Lindsey E. Jones et al. Patient-derived cells from recurrent tumors that model the evolution of IDH-mutant glioma. Neuro-Oncology Advances, 2020. We established robust, versatile, and well-characterized Patient Derived Cells (PDC) of an IDH1-mutant astrocytoma and an IDH1-mutant oligodendroglioma that represents defined evolutionary stages of chemotherapy-induced hypermutation. The PDCs retain tumor subtype defining features over time as well as classic hallmarks of cancer, including anchorage independent growth and cell immortality. The integrated phylogenies composed of PDCs,single-cell-derived PDCs, patient-derived xenografts, and corresponding spatiotemporal tumor tissue samples also provide new insight into the clonality, evolutionary pattern, and immense mutational load of hypermutated IDH mutant gliomas.
Study
EGAS00001003992
-
The molecular landscape of colorectal cancer reveals genetic mutations.
Study
EGAS00001001893
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Study
EGAS00001005328
-
HER2_positive_Breast_Cancer_
Study
EGAS00001000042
-
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
-
Whole exome sequencing (bam files) of 55 samples of myxofibrosarcoma and 44 matched pairs
Study
EGAS00001005442
-
Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
-
PCGP Ph-like ALL
Study
EGAS00001000654
-
HipSci_RNASEQ_PID
Study
EGAS00001001990
-
whole genome sequence data of multifocal hepatocellular carcinoma
Study
EGAS00001002338
-
HipSci___Whole_Exome_sequencing___Alport
Study
EGAS00001001974
-
DERMATLAS__Hidradenoma_papilliferum_WES
Study
EGAS00001005714
-
DERMATLAS__Porocarcinoma_WES
Study
EGAS00001005720
-
RNAseq_of_healthy_mesothelial_cells_and_primary_mesothelioma_cell_lines
Study
EGAS00001005728
-
Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Study
EGAS00001005737
-
HipSci_RNASEQ_Alport
Study
EGAS00001001986
-
DERMATLAS__Poroma_RNAseq
Study
EGAS00001005759
-
SNP array data for the Milieu Intérieur cohort
Study
EGAS00001002460
-
Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
-
Combination therapies to inhibit LCK tyrosine kinase and mTOR signaling in T-cell Acute Lymphoblastic Leukemia
Study
EGAS00001005945
-
Genomic_profiling_of_B_other_Adult_ALL_WGS
Study
EGAS00001002474
-
Measuring the level of relatedness between NGS datasets
Study
EGAS00001000600
-
HipSci HumanHT 12 Expression BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002030
-
Papuan Y chromosome Diversity Panel
Study
EGAS00001006025
-
CIRdb: Array genotype data
Study
EGAS00001006050
-
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058
-
Barcelona_kids_with_melanoma
Study
EGAS00001000733
-
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform
Study
EGAS00001006103
-
Local In Time Statistics for processual research
Study
EGAS00001002520
-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076