-
HipSci HumanExome BeadChip analysis - Macular Dystrophy
Study
EGAS00001002014
-
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
-
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
-
The_Little_Princess_Knowledge_Bank_RNAseq
Study
EGAS00001005244
-
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
-
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
-
Resolving_the_Genetic_Architecture_of_Aseptic_Loosening_After_Total_Hip_Replacement
Study
EGAS00001001883
-
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
-
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
-
Paediatric IBD Mosaicism
Study
EGAS00001002489
-
UK10K NEURO ABERDEEN
Study
EGAS00001000109
-
Human Pancreatic Islet RNAseq - Lund
Study
EGAS00001004042
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
RNAseq_Pulldown_
Study
EGAS00001000230
-
Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance
Study
EGAS00001002627
-
Epigenetic Intratumor Heterogeneity and Clonal Evolution in Aggressive Prostate Cancer
Study
EGAS00001000682