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ENU_NCI_H508_Cetuximab_SecondRound
Study
EGAS00001001745
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Circulating tumor cells Exome sequencing from breast cancer
Study
EGAS00001005228
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Genome-wide search to find the genetic elements underlying visual contour perception
Study
EGAS00001003639
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Genetic landscape of pediatric Adrenocortical Tumor
Study
EGAS00001000257
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Latency and interval therapy affect the evolution in metastatic colorectal cancer
Study
EGAS00001003646
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RNA_Seq_in_Patients_with_Primordial_Dwarfism
Study
EGAS00001000283
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multi-OMICs study of a pair of infant monozygotic twins with concordant B-cell ALL
Study
EGAS00001003651
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Indonesian methylation data
Study
EGAS00001003653
-
UK10K OBESITY TWINSUK
Study
EGAS00001000306
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Pilot study for Illumina TST170 NGS panel on cutaneous T cell lymphoma samples
Study
EGAS00001002567
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Identifying genetic consequences of Epstein-Barr Virus transformation by comparing an individual’s genomic DNA with that of its lymphoblastoid cell line.
Study
EGAS00001000323
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Native_American_Ancient_DNA_sequencing
Study
EGAS00001001802
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RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Study
EGAS00001002484
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Characterization of a human iPSC-derived endocrine pancreas model
Study
EGAS00001001803
-
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
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Large-scale viral genome analysis identifies novel clinical associations between hepatitis B virus and chronically infected patients
Study
EGAS00001003689
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Whole-exome sequencing of acute erythroid leukemia
Study
EGAS00001003696
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Renal_habitat_WXS
Study
EGAS00001003703
-
The 3D evolution of glioma cell populations
Study
EGAS00001003710
-
Whole exome sequencing of Finnish hereditary breast cancer families
Study
EGAS00001001835
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Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
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Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness
Study
EGAS00001003288
-
Chromosome Y Philogeny in Sardinia
Study
EGAS00001000532
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Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Study
EGAS00001005403
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Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838