Data provider

Wellcome Trust Sanger Institute

Data provider ID Acronym URL
EGAO00000000020 WTSI

This data provider is associated with 580 studies:

Study ID Title Type
EGAS00001000109 UK10K NEURO ABERDEEN Other
EGAS00001000179 Renal Matched Pair Cell Line Exome Sequencing Cancer Genomics
EGAS00001000075 Functional characterisation of CpG islands in human and mouse tissues Epigenetics
EGAS00001000053 Investigation of the genetic basis of the rare syndrome Post-Transfusion Purpura (PTP) Other
EGAS00001000225 UK10K NEURO GURLING Other
EGAS00001000208 Cancer Genome Libraries Tests Whole Genome Sequencing
EGAS00001000088 Familial Thrombocytosis germline exome sequencing Cancer Genomics
EGAS00001000016 The GENCODE exome sequencing the complete human exome Exome Sequencing
EGAS00001000206 Cancer Exome Resequencing Cancer Genomics
EGAS00001000124 UK10K OBESITY SCOOP Exome Sequencing
EGAS00001000200 Acute Lymphoblastic Leukemia Exome sequencing 2 Cancer Genomics
EGAS00001000011 CLL cancer Sample Sequencing Cancer Genomics
EGAS00001000209 Acute Myeloid Leukemia Sequencing Cancer Genomics
EGAS00001000139 Splenic Marginal Zone Lymphoma with villous lymphocytes exome sequencing Cancer Genomics
EGAS00001000201 Acute Lymphoblastic Leukemia Exome sequencing Cancer Genomics
EGAS00001000118 UK10K NEURO FSZ Other
EGAS00001000027 TMD AMLK Exome Study Cancer Genomics
EGAS00001000037 Gastric and Esophageal tumour rearrangement screen Cancer Genomics
EGAS00001000054 Identifying causative mutations for Thrombocytopenia with Absent Radii Other
EGAS00001000025 Whole exome sequencing of Severe Insulin Resistant patients Other
EGAS00001000026 Whole Exome Sequencing for Characterization of Disease Causing Mutations in two Pakistani Families Suffering from Autosomal Recessive Ocular Disorders Other
EGAS00001000218 CML Discovery Project Cancer Genomics
EGAS00001000091 Grey Platelet Syndrome GPS Other
EGAS00000000052 A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome Whole Genome Sequencing
EGAS00001000129 UK10K RARE HYPERCHOL Exome Sequencing
EGAS00001000106 Bleeding Other
EGAS00001000009 SCLC Synthetic Genomics
EGAS00001000057 An exome sequencing pilot study of HIV elite-long term non progressors and rapid progressors Other
EGAS00001000161 Triple Negative Breast Cancer sequencing Cancer Genomics
EGAS00001000142 Exome sequencing of patients with structural brain malformations Other
EGAS00001000033 1 Fanconi Anemia transformation to AML Cancer Genomics
EGAS00001000111 UK10K NEURO ASD BIONED Other
EGAS00001000245 A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome Cancer Genomics
EGAS00001000049 Exome sequencing in patients with Calcific Aortic Valve Stenosis Other
EGAS00001000125 UK10K RARE CHD Other
EGAS00001000123 UK10K NEURO UKSCZ Exome Sequencing
EGAS00001000356 Exome sequencing of Bilateral Anophthalmia cases Pilot Study Other
EGAS00001000052 PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis. Other
EGAS00001000064 Genetics of Microcephalic Osteodysplatics Primordial Dwarfism Other
EGAS00001000305 P647 Targeted resequencing project Whole Genome Sequencing
EGAS00001000189 Dyslipidemia Other
EGAS00000000062 Complex Landscapes of Somatic Rearrangements in Human Breast Cancer Genomes Whole Genome Sequencing
EGAS00000000051 A small cell lung cancer genome reports complex tobacco exposure signatures Whole Genome Sequencing
EGAS00001000198 Myeloproliferative Disorder Sequencing Cancer Genomics
EGAS00001000176 FRCC Exome sequencing Cancer Genomics
EGAS00001000093 Unraveling the genetic basis of a collagen migration defect in patients with a combined platelet dysfunction and reduced bone density Other
EGAS00001000193 ADCC Exome Sequencing Cancer Genomics
EGAS00001000087 Burden of Disease in Sarcoma Cancer Genomics
EGAS00001000188 Chordoma Exome Sequencing Cancer Genomics
EGAS00001000160 Matched Pair Cancer Cell line Whole Genomes Cancer Genomics
EGAS00001000127 UK10K RARE COLOBOMA Other
EGAS00001000006 Renal Cancer Exome Sequencing Cancer Genomics
EGAS00001000046 Mutational Screening of Human Acute Myleloid Leukaemia Samples Other
EGAS00001000119 UK10K NEURO FSZNK Other
EGAS00001000166 Breast Cancer Matched Pair Cell Line Whole Genomes Cancer Genomics
EGAS00001000211 Breast Cancer Exome Sequencing Cancer Genomics
EGAS00001000148 Lung Cancer Whole Genomes Cancer Genomics
EGAS00001000076 Screening for abnormal CGI methylation in primary colorectal tumours Epigenetics
EGAS00001000047 Whole Exome Sequencing of Permanent Neonatal Diabetes Patients Other
EGAS00001000202 Glioma cell lines rearrangement screen Cancer Genomics
EGAS00001000066 Congenital Heart Disease in UK Families Other
EGAS00001000191 CML blast phase rearrangement screen Cancer Genomics
EGAS00001000005 Lung Rearrangement Study Cancer Genomics
EGAS00001000003 Cancer Single Cell Sequencing Other
EGAS00001000131 UK10K RARE THYROID Exome Sequencing
EGAS00001000102 ET Exome Cancer Genomics
EGAS00001000077 Human Colorectal Cancer Exome Sequencing Other
EGAS00001000028 PV Exome Study Cancer Genomics
EGAS00001000055 Analysis of genomic integrity of disease corrected human induced pluripotent stem cells by exome sequencing Other
EGAS00001000104 Hyperfibrinolysis Other
EGAS00001000041 Disorders of growth and insulin action Other
EGAS00001000038 Chondrosarcoma Exome Cancer Genomics
EGAS00001000207 Breast Cancer Exome Resequencing Cancer Genomics
EGAS00001000128 UK10K RARE FIND Other
EGAS00001000048 Paroxysmal neurological disorders Other
EGAS00001000122 UK10K NEURO MUIR Exome Sequencing
EGAS00001000103 Genomics of Colorectal Cancer Metastases Massively Parallel Sequencing of Matched Primary and Metastatic tumours to Identify a Metastatic Signature of Somatic Mutations MOSAIC Cancer Genomics
EGAS00001000205 Non Tumour Renal Cell Line Sequencing Cancer Genomics
EGAS00001000110 UK10K NEURO ASD FI Exome Sequencing
EGAS00001000163 Osteosarcoma Exome Sequencing Cancer Genomics
EGAS00001000082 ALK inhibitors in the context of ALK dependent cancer cell lines Cancer Genomics
EGAS00001000134 An evaluation of different strategies for large scale pooled sequencing study design Resequencing
EGAS00001000014 CLL Cancer Whole Genome Sequencing Cancer Genomics
EGAS00001000074 Screening for human epigenetic variation at CpG islands Epigenetics
EGAS00001000105 Platelet collagen defect Other
EGAS00001000175 PMF Exome Study Cancer Genomics
EGAS00001000081 CRLF2 sequencing project Exomes Cancer Genomics
EGAS00001000012 Various Cancer Fusion Gene Sequencing Cancer Genomics
EGAS00001000004 Multifocal Breast Project Cancer Genomics
EGAS00001000089 Myelodysplastic Syndrome Exome Sequnecing Other
EGAS00001000095 Renal Follow Up Series Cancer Genomics
EGAS00001000114 UK10K NEURO ASD SKUSE Other
EGAS00001000036 Integrative Oncogenomics of Multiple Myeloma Cancer Genomics
EGAS00001000042 HER2 positive Breast Cancer Cancer Genomics
EGAS00001000196 SCAT osteosarcoma sequencing Cancer Genomics
EGAS00001000035 Sequencing Acute Myeloid Leukaemia Synthetic Genomics
EGAS00001000107 Various Platelet Disorders Other
EGAS00001000090 UK10K COHORT ALSPAC Whole Genome Sequencing
EGAS00001000269 Identification of the underlying causal variant in a multi generational family with autosomal dominant common variable immunodeficiency Other
EGAS00001000178 Cell Line Sub Clone Rearrangement Screen Cancer Genomics
EGAS00001000031 Matched breast cancer fusion gene study Cancer Genomics
EGAS00001000120 UK10K NEURO IMGSAC Other
EGAS00001000023 Identifying autosomal recessive mutations causing neurological disorders Other
EGAS00001000140 Xenograft Sequencing Cancer Genomics
EGAS00001000030 ADCC Rearrangement Screen Cancer Genomics
EGAS00001000002 Breast Cancer Follow Up Series Cancer Genomics
EGAS00001000212 MuTHER adipose tissue small RNA expression Transcriptome Analysis
EGAS00000000029 Massive Genomic Rearrangment Acquired in a Single Catastrophic Event During Cancer Development Whole Genome Sequencing
EGAS00001000199 Myeloproliferative Disorder Sequencing Cancer Genomics
EGAS00001000080 CRLF2 sequencing project Cancer Genomics
EGAS00001000210 Breast Cancer Whole Genome Sequencing Cancer Genomics
EGAS00001000013 Osteosarcoma Sequencing Cancer Genomics
EGAS00001000061 Lethal malformation syndrome Other
EGAS00001000220 Identifying Novel Fusion Genes in Myeloma Cancer Genomics
EGAS00001000094 PREDICT Cancer Genomics
EGAS00001000159 Exome sequencing of patients with rare neurological disorders Other
EGAS00001000071 Tetralogy of Fallot Exome Trios Other
EGAS00001000177 Meningioma Exome Cancer Genomics
EGAS00001000180 Mixed Leukemia Rearrangement Screen Cancer Genomics
EGAS00001000032 Kaposi sarcoma exome Cancer Genomics
EGAS00001000024 Piloting exome resequencing in consanguineous families with homozygosity mapping intervals Other
EGAS00001000020 Genetic variation in Kuusamo Population Genomics
EGAS00001000108 UK10K COHORT TWINSUK Whole Genome Sequencing
EGAS00001000130 UK10K RARE SIR Other
EGAS00001000058 Acute Lymphoblastic Leukemia Sequencing Cancer Genomics
EGAS00001000113 UK10K NEURO ASD MGAS Other
EGAS00001000197 ER HER2 PR breast Cancer genome sequencing Cancer Genomics
EGAS00000000064 The patterns and dynamics of genomic instability in metastatic pancreatic cancer Whole Genome Sequencing
EGAS00001000170 20 Matched Pair Breast Cancer Genomes Cancer Genomics
EGAS00001000069 Determination of the molecular nature of the Vel blood group by exome sequencing Other
EGAS00001000147 Osteosarcoma Whole Genome Cancer Genomics
EGAS00001000034 MDSMPN Rearrangement Screen Cancer Genomics
EGAS00001000112 UK10K NEURO ASD GALLAGHER Exome Sequencing
EGAS00001000063 Exome sequencing in patients with cardiac arrhythmias Other
EGAS00001000040 Exome sequencing of hyperplastic polyposis patients Other
EGAS00001000155 Matched Ovarian Cancer Sequencing Cancer Genomics
EGAS00001000230 RNAseq Pulldown Other
EGAS00001000466 FFPE CPA Accreditation Study Cancer Genomics
EGAS00001000261 Transcriptome Sequencing of Cancer Cell Lines Cancer Genomics
EGAS00001000278 Osteosarcoma Targeted Sequencing Study Cancer Genomics
EGAS00001000156 Otosclerosis gene discovery Other
EGAS00001000289 Lung Plasma rearrangement screen Cancer Genomics
EGAS00001000362 Ewings Sarcoma Rearrangement Screen Cancer Genomics
EGAS00001000433 ICGC Benchmarking Exercise Whole Genome Sequencing
EGAS00001000492 Assessment of genetic and epigenetic variation in human IPS cells Other
EGAS00001000490 Sequencing component for the whole genome methylation analysis in PBMCs and cell subsets pilot study Epigenetics
EGAS00001000360 Balanced Brain Tumour Whole Genome Sequencing Cancer Genomics
EGAS00001000427 Prostate Cancer Whole Genome Validations Cancer Genomics
EGAS00001000282 Meningioma Targeted Sequencing Study Cancer Genomics
EGAS00001000426 Triple Negative Breast Cancer Whole Genome Validations Cancer Genomics
EGAS00001000359 Mutation analysis in human iPS cells Resequencing
EGAS00001000408 Targeted sequencing of genes recurrently mutated in AML Cancer Genomics
EGAS00001000243 Integrative Oncogenomics of multiple myeloma Other
EGAS00001000390 Targeted gene fusion sequencing Fus seq in mesothelioma Cancer Genomics
EGAS00001000173 Testing the feasibility of genome scale sequencing in routinely collected FFPE cancer specimens versus matched fresh frozen samples Cancer Genomics
EGAS00001000292 Molecular characterization of invasive lobular carcinoma Cancer Genomics
EGAS00001000403 BASIS Genome Validation Study Cancer Genomics
EGAS00001000295 Gene Discovery in Age Related Hearing Loss Other
EGAS00001000297 Feasibility of targeted capture sequencing in routinely collected FFPE cancer specimens Cancer Genomics
EGAS00001000291 Myelodysplastic syndrome whole genomes Cancer Genomics
EGAS00001000280 Chordoma Targeted Sequencing Study Cancer Genomics
EGAS00001000137 ENGAGE Amendment 500 genes exon sequencing Other
EGAS00001000301 Cancer Genome Project Exome Sequencing Other
EGAS00001000354 Primary Lung Cancer whole genome study Cancer Genomics
EGAS00001000216 Melanoma TIL Study Exomes Other
EGAS00001000174 Balanced Ependymoma Cancer Genomics
EGAS00001000068 ORCADES WGA Whole Genome Sequencing
EGAS00001000425 Congenital Heart Disease Pilot Other
EGAS00001000262 ICGC Prostate Cancer Whole Genome Sequencing Cancer Genomics
EGAS00001000008 Whole Genome Sequencing of hiPS cells Whole Genome Sequencing
EGAS00001000242 UK10K OBESITY GS Other
EGAS00001000157 Hearing loss in adults from South Carolina Other
EGAS00001000290 Myeloproliferative Disease Whole Genomes Cancer Genomics
EGAS00001000214 Test of PCR library method on whole genmoe samples Cancer Genomics
EGAS00001000275 AML targeted resequencing study Cancer Genomics
EGAS00001000293 Evaluation of size selection on cancer specific sequencing libraries Cancer Genomics
EGAS00001000181 Chondrosarcoma Validation Study Cancer Genomics
EGAS00001000300 Breast cancer sequential sampling study Cancer Genomics
EGAS00001000332 Helleday HRAS Project Cancer Genomics
EGAS00001000086 Dilgom Exome Other
EGAS00001000404 Myeloproliferative Neoplasms MPN Exome Validation Study Cancer Genomics
EGAS00001000059 De novo mutations in schizophrenia Other
EGAS00001000001 Exome Resequencing of Progressive Hearing Loss Resequencing
EGAS00001000405 Angiosarcoma follow up study Cancer Genomics
EGAS00001000224 Myelodysplastic Syndrome Follow Up Series Cancer Genomics
EGAS00001000406 Myeloproliferative Neoplasms MPN Targeted Gene Screen Cancer Genomics
EGAS00001000233 Pulldown cytosine deaminases Cancer Genomics
EGAS00001000244 Integrative Oncogenomics of multiple myeloma Other
EGAS00001000276 Genetic mechanisms of resistance to chemotherapy in breast cancer Other
EGAS00001000428 Neoadjuvant Breast Cancer Validations Cancer Genomics
EGAS00001000330 Osteosarcoma whole genome rearrangement screen Cancer Genomics
EGAS00001000165 Monotherapy Breast Cancer Cancer Genomics
EGAS00001000353 The genomic architecture of mesothelioma Cancer Genomics
EGAS00001000420 Breast Cancer FRT RNA seq Cancer Genomics
EGAS00001000367 Assessment of genetic and epigenetic variation in human IPS cells RNA Other
EGAS00001000285 Validation of a Haloplex platform for targeted re sequencing of the exons of 25 genes Resequencing
EGAS00001000373 Deep sequencing analysis of human iPSC specific SNVs in donor cell population Resequencing
EGAS00001000437 Deep sequencing of S7EPC genome Resequencing
EGAS00001000441 Subclonal analysis in S7RE2 and S7RE14 iPS cells Resequencing
EGAS00001000413 The Transcriptome of PLX4032 resistance Transcriptome Analysis
EGAS00001000238 Ethiopia Genome Project low coverage Whole Genome Sequencing
EGAS00001000322 De novo mutations in cell free foetal DNA cffDNA Whole Genome Sequencing
EGAS00001000250 Poikiloderma syndrome RNAseq Cancer Genomics
EGAS00001000419 Ewings Sarcoma RNA seq drug sensitivity Cancer Genomics
EGAS00001000584 Assessing the impact of low frequency coding variants on disease risk using the Exomechip Other
EGAS00001000388 Whole exome sequencing of young onset Primary Sclerosing Cholangitis Other
EGAS00001000387 Susceptibility genes for the development of SLE during treatment of IBD Other
EGAS00001000518 Angiosarcoma follow up 2 validation study Cancer Genomics
EGAS00001000410 Chordoma Sequencing Project RNAseq Cancer Genomics
EGAS00001000267 RNAseq of patients with Ewings sarcoma Cancer Genomics
EGAS00001000377 Triple Negative Breast Cancer RNA Sequencing Cancer Genomics
EGAS00001000251 Melanoma Til Study RNAseq Cancer Genomics
EGAS00001000434 Matched Pair Cell Line Tumour RNAseq Cancer Genomics
EGAS00001000283 RNA Seq in Patients with Primordial Dwarfism Transcriptome Analysis
EGAS00001000488 Sequencing probands and families with severe insulin resistance syndromes Other
EGAS00001000237 Ethiopia Genome Project high coverage Whole Genome Sequencing
EGAS00001000630 Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS Other
EGAS00001000310 RNA sequencing Other
EGAS00001000050 Investigating low frequency variants in CAD MI cases controls and pedigrees using whole exome sequencing and custom pulldowns Other
EGAS00001000551 Discovery of resistance mechanisms to the BRAF inhibitor vemurafenib in metastatic BRAF mutant melanoma Other
EGAS00001000588 Angiosarcoma whole exome Cancer Genomics
EGAS00001000252 Whole genome sequencing of Italian genetic isolates Friuli Venezia Giulia Whole Genome Sequencing
EGAS00001000458 Whole Genome sequencing of individuals from Val Borbera Italy Whole Genome Sequencing
EGAS00001000606 Pseudogene RNAseq Cancer Genomics
EGAS00001000062 The International 1q type 2 diabetes consortium Other
EGAS00001000385 Crohn s Exome Sequencing Other
EGAS00001000079 Cardiogenics re sequencing Resequencing
EGAS00001000043 Investigating low frequency variants in CAD MI cases controls and pedigrees using whole exome sequencing and custom pulldowns Other
EGAS00001000060 Whole genome sequencing in a multiplex Crohn s disease family Whole Genome Sequencing
EGAS00001000065 Whole genome sequencing of Crohn s disease patients Whole Genome Sequencing
EGAS00001000133 Genetic factors underlying premature coronary heart disease in patients with normal coronary arteries Other
EGAS00001000145 A study of the genetic basis of evation by Acute Myeloid Leukaemia of Graft vs Leukaemia effects after allogeneic bone marrow transplantation Other
EGAS00001000151 Exome sequencing Parkinson s disease patients Other
EGAS00001000171 Exome sequencing of blastic plasmacytoid dendritic cell neoplasms Other
EGAS00001000190 Paroxysmal Neurological Disorders 2 Other
EGAS00001000228 Whole exome sequencing of rare autoimmune related phenotypes Other
EGAS00001000240 Whole Exome sequencing in a large IBD pedigree Other
EGAS00001000329 Identification of low frequency variants associated with ulcerative colitis using whole genome sequencing Whole Genome Sequencing
EGAS00001000335 A study of the molecular pathogenesis of Splenic Marginal Zone and Diffuse Large B Cell Lymphoma Other
EGAS00001000384 Oulu Dyslipidemia families Other
EGAS00001000386 Paroxysmal neurological Disorders Other
EGAS00001000590 Angiosarcoma RNA sequencing Cancer Genomics
EGAS00001000631 WGS low coverage sequencing of Mossi from Burkina Faso Whole Genome Sequencing
EGAS00001000138 Radiotherapy induced sarcoma Cancer Genomics
EGAS00001000570 Targeted sequencing of genes recurrently mutated in AML part2 Cancer Genomics
EGAS00001000501 Bone Cancer Rare Types Whole Genome Cancer Genomics
EGAS00001000596 Breast Cancer Sequential Sampling Targeted Capture Cancer Genomics
EGAS00001000569 TMD AMKL targeted follow up Cancer Genomics
EGAS00001000571 POT1 splice site mutant analysis Transcriptome Analysis
EGAS00001000687 Illumina Human OmniExpress genotyping data from the Cretan Greek isolate collection HELIC MANOLIS Other
EGAS00001000187 Exome sequencing of Congenital Heart Disease families Royal Brompton Other
EGAS00001000231 Assessment of genetic and epigenetic variation in human IPS cells Whole Genome Sequencing
EGAS00001000185 Exome sequencing of Congenital Heart Disease families Leuven Other
EGAS00001000317 xome sequencing of Congenital Heart Disease families Toronto Other
EGAS00001000368 Exome sequencing of Congenital Heart Disease families from the Competence Network Berlin Other
EGAS00001000587 Epi Tax targeted sequencing Cancer Genomics
EGAS00001000615 Osteosarcoma RNAseq Cancer Genomics
EGAS00001000430 Validation of AML Mutational Screening Resequencing
EGAS00001000603 Use of Deep Sequencing to Dectect Clonal Mutations In Sun Exposed Skin Epidermis PART2 Cancer Genomics
EGAS00001000470 CMF RNA sequencing Cancer Genomics
EGAS00001000741 Assessment of epigenetic variation in human iPS cells Medip Epigenetics
EGAS00001000464 Validation of SNVs found by Exome seq in S2 SF1 SF5 and SF9 hiPSCs Resequencing
EGAS00001000264 Shwachman Diamond syndrome SDS Exome sequencing Other
EGAS00001000663 MPN mutation order followup Cancer Genomics
EGAS00001000742 Role of Epigenetic Memory in Human Induced Pluripotent Stem Cells Pilot Transcriptome Analysis
EGAS00001000409 Chordoma Sequencing Project Whole Genome Cancer Genomics
EGAS00001000655 Combination therapies for personalized cancer medicine Cancer Genomics
EGAS00001000692 FFPE CPA Accreditation Study Part 2 Cancer Genomics
EGAS00001000649 GEL WGS Comparison Cancer Genomics
EGAS00001000648 FinHer Breast Cancer Study Cancer Genomics
EGAS00001000740 DNA repair in BLM deficient hiPSCs Other
EGAS00001000651 Mutational Signatures of relapse in rectal cancer FFPE samples in the CR07 clinical trial Cancer Genomics
EGAS00001000732 TMD AMKL targeted follow up part 2 Cancer Genomics
EGAS00001000866 HipSci HumanExome BeadChip analysis-Healthy volunteers Other
EGAS00001000867 HipSci HumanHT 12v4 Expression BeadChip analysis-Healthy volunteers Other
EGAS00001000592 HipSci-Whole Exome sequencing-healthy volunteers Other
EGAS00001000865 HipSci Illumina 450K Methylation analysis Healthy volunteers Other
EGAS00001000593 HipSci-RNAseq-healthy volunteers Transcriptome Analysis
EGAS00001000902 Metastatic Breast Cancer Whole Genome Cancer Genomics
EGAS00001000612 PLCRC study Cancer Genomics
EGAS00001000613 Mosaic Colorectal Metastasis Cancer Genomics
EGAS00001000703 MDS Sequential Treatment Validation Cancer Genomics
EGAS00001000891 Multisite Primary Breast Cancer Cancer Genomics
EGAS00001000878 Genome wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity Other
EGAS00001000896 An isolated cohort of samples from the Greek island of Crete that have been genotyped on the Illumina CoreExome array. Other
EGAS00001000421 Paroxysmal Neurological Disorders rare epilepsies Other
EGAS00001000407 Characterization of individual foci of multicentric multifocal breast cancer using targeted next generation sequencing Cancer Genomics
EGAS00001000344 Exome sequencing of thyroid disease in Val Borbera Other
EGAS00001000436 Lung Multi site Targeted Sequence Capture Cancer Genomics
EGAS00001000704 Metastatic breast cancer targeted gene screen Cancer Genomics
EGAS00001000743 Myeloma Follow up Pilot Cancer Genomics
EGAS00001000751 Transposome Bisulfite Sequencing Cancer Genomics
EGAS00001000511 Autozygosity pilot Pakistani from Birmingham Cancer Genomics
EGAS00001000717 Autozygosity pilot QMUL Other
EGAS00001000567 Autozygosity pilot British Pakistani from Birmingham 2 Other
EGAS00001001001 Illumina HumanCoreExome genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study. Other
EGAS00001000968 Origins and functional consequence of somatic mitochondrial DNA mutations Other
EGAS00001000996 Illumina HumanOmniExpress genotyping data from the TEENAGE (TEENs of Attica: Genes and Environment) study. Other
EGAS00001000840 Spatial and temporal diversity in genomic instability processes define early stage lung cancer evolution. Other
EGAS00001000978 Cancer Cell Line Exome Sequencing Cancer Genomics
EGAS00001000286 APCDR AGV Project: WGS of South African Zulu Other
EGAS00001000363 APCDR AGV Project: WGS of an Ugandan population Other
EGAS00001000730 Metastatic Prostate Follow Up Cancer Genomics
EGAS00001000756 Metastatic Prostate Follow Up 2 Cancer Genomics
EGAS00001000763 Expressed fusion transcripts in rare bone tumours Cancer Genomics
EGAS00001000468 Harnessing transposons for drug resistance gene discovery in cancer Cancer Genomics
EGAS00001000772 MYD88/TLR mutations in CLL Other
EGAS00001000813 RNAseq Discovery of resistance mechanisms to the BRAF inhibitor vemurafenib in metastatic BRAF mutant melanoma Cancer Genomics
EGAS00001000812 Discovery of resistance mechanisms to the BRAF inhibitor vemurafenib in metastatic BRAF mutant melanoma Cancer Genomics
EGAS00001000333 Multiple Malignancy Familial Comparison Cancer Genomics
EGAS00001000533 Chondromyxoid fibroma Cancer Genomics
EGAS00001000589 Angiosarcoma targeted pulldown cancer gene panel Cancer Genomics
EGAS00001000260 Targeted Pulldown Validation of mutations found in whole genome sequencing Cancer Genomics
EGAS00001000990 Fetal hemoglobin in sickle cell disease patients from Tanzania Other
EGAS00001000515 Use of Deep Sequencing to Dectect Clonal Mutations In Sun Exposed Skin Epidermis Cancer Genomics
EGAS00001000462 Autozygosity pilot Born in Bradford Other
EGAS00001000523 ESGI Identification of novel genes and mechanisms leading to Primary Ciliary Dyskinesia Other
EGAS00001000728 SPECTA NGS Screening Program for Efficient Clinical Trial Access Cancer Genomics
EGAS00001000775 Deciphering Developmental Disorders (DDD) Other
EGAS00001001047 Finnish population cohort genotyping B Population Genomics
EGAS00001000860 Use of deep sequencing to detect clonal mutations in sun exposed human epidermis whole genome Cancer Genomics
EGAS00001000836 FFPE Normal Panel V3 Cancer Panel Cancer Genomics
EGAS00001000078 SFHS pedigrees Whole Genome Sequencing
EGAS00001000880 Myeloma Targeted Follow up Study Cancer Genomics
EGAS00001000935 Single Cell Sequencing of Sperm scSperm Population Genomics
EGAS00001000162 Genetic background for the major psychiatric disorders in the general Finnish population Whole Genome Sequencing
EGAS00001001132 DPY30 ChIP seq Epigenetics
EGAS00001000632 WGS low coverage sequencing of Bantu from Cameroon Whole Genome Sequencing
EGAS00001000460 Whole Genome sequencing of individuals from Carlantino Italy Whole Genome Sequencing
EGAS00001000633 WGS low coverage sequencing of Semi Bantu from Cameroon Whole Genome Sequencing
EGAS00001000636 WGS low coverage sequencing of Chagga from Tanzania Whole Genome Sequencing
EGAS00001000637 WGS low coverage sequencing of Pare from Tanzania Whole Genome Sequencing
EGAS00001000638 WGS low coverage sequencing of Wasambaa from Tanzania Whole Genome Sequencing
EGAS00001000979 Pulldown DNA methylation study v2 Cancer Genomics
EGAS00001000765 MPN TGS2 Follow up PT1 Vori other Cancer Genomics
EGAS00001000879 Prognostic factors in prostate cancer deep sequencing pilot project TAPG Cancer Genomics
EGAS00001000892 Chordoma Extension Study Cancer Genomics
EGAS00001000895 Chordoma Extension known cancer genes Cancer Genomics
EGAS00001000229 Genetic background for cardio vascular disorders in the general Finnish population Whole Genome Sequencing
EGAS00001000830 Mesothelioma Whole Genomes Cancer Genomics
EGAS00001000707 BASIS RNAseq Cancer Genomics
EGAS00001000851 Primary angiosarcoma Whole Genome Sequencing Cancer Genomics
EGAS00001000859 Anaplastic Meningioma WGS X10 Cancer Genomics
EGAS00001000837 Lung Progression versus Regression Whole Genome Sequencing Cancer Genomics
EGAS00001000814 Study to investigate the prevalence of leukaemic mutations in whole blood DNA in a cohort of blood donors Resequencing
EGAS00001000513 COLORS in IBD Whole exome sequencing of early onset IBD patients Other
EGAS00001000758 TCELL PILOT ATAC SEQ Transcriptome Analysis
EGAS00001000947 ATAC SEQ MAIN PHASE 1 Transcriptome Analysis
EGAS00001001213 Pilot experiment on functional genomics in osteoarthritis Population Genomics
EGAS00001001129 IBDCA Edinburgh Other
EGAS00001001203 Pilot experiment on functional genomics in osteoarthritis RNA Transcriptome Analysis
EGAS00001001204 G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells Whole Genome Sequencing
EGAS00001001021 Exome sequencing of EBV driven lymphoma Cancer Genomics
EGAS00001001234 Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells Other
EGAS00001000530 Whole exome sequencing of inflammatory bowel disease cases Other
EGAS00001001253 Microinjection of hIPSC derived intestinal organoids with Salmonella Typhimurium Transcriptome Analysis
EGAS00001000315 Human Evolution 3 Whole Genome Sequencing
EGAS00001000480 Egypt Genome Project low coverage whole genome sequencing Whole Genome Sequencing
EGAS00001000946 Mechanisms of patient response to Dabrafenib in Melanoma Cancer Genomics
EGAS00001001212 Pilot experiment on functional genomics in osteoarthritis Population Genomics
EGAS00001000336 Understanding population genetics and patterns of genome wide heterozygosity in a sample of the Croatian isolated populations ESGIDalmatians Other
EGAS00001000482 Egypt Genome Project high coverage whole genome sequencing Whole Genome Sequencing
EGAS00001001060 CRISPR screen M14 NCI H3122 Cancer Genomics
EGAS00001001285 Ribosome Profiling of Macrophages during Salmonella Infection Whole Genome Sequencing
EGAS00001000195 Breast Cancer Somatic Genetics Study Cancer Genomics
EGAS00001000916 Developmental Dysplasia of the Hip DDH Population Genomics
EGAS00001000747 ESGI Exome sequencing in Circulating Tumor Cells to determine therapy related markers Other
EGAS00001000958 TGS Comprehensive Molecular Characterization of Colorectal Cancer Metastases MOSAIC Cancer Genomics
EGAS00001001054 GIST SSGXVIII trial targeted gene sequencing Cancer Genomics
EGAS00001001095 NGS based viability screening using haploid cell line Cancer Genomics
EGAS00001001145 FWO project G 0687 12 X10 WGS Cancer Genomics
EGAS00001001155 Anaplastic Meningioma V3 cancer gene panel Cancer Genomics
EGAS00001000203 ChIP sequencing in Cancer Cell Lines Cancer Genomics
EGAS00001001206 Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren's Disease consortium (BSSH-GODD consortium) collection Other
EGAS00001000988 30X WGS sequencing of 100 individuals from the general Greek population Whole Genome Sequencing
EGAS00001000167 Abnormal foetal development exome trios Other
EGAS00001000857 Deep sequencing of melanoma for driver mutations Cancer Genomics
EGAS00001000872 Chugai colorectal organoid sequencing Cancer Genomics
EGAS00001000881 Colorectal organoids and tumour tissue Cancer Genomics
EGAS00001000402 Feasibility of targeted capture sequencing in FFPE cancer specimens 2 Cancer Genomics
EGAS00001000423 Validation of Exome sequencing of S7RE iPSC lines Resequencing
EGAS00001000435 Single Cell Targeted Sequence Capture Cancer Genomics
EGAS00001000429 Whole genome sequence of third generation family member SFHS Whole Genome Sequencing
EGAS00001000955 EBV AID project Cancer Genomics
EGAS00001000985 RNAseq Colorectal organoids and tumoroids Cancer Genomics
EGAS00001001114 Whole exome sequencing of additional thyroid disease cases Other
EGAS00001001218 Validation for human early embryonic substitutions Cancer Genomics
EGAS00001000067 Samples from the Greek island of Crete, MANOLIS cohort Whole Genome Sequencing
EGAS00001000602 Whole exome sequencing for HELIC Other
EGAS00001000392 Low coverage whole genome sequencing of samples from the Cretan Greek isolate collection HELIC MANOLIS Whole Genome Sequencing
EGAS00001001059 Cell lines with telomere fusion induced rearrangements Cancer Genomics
EGAS00001001301 PRDM9 loss of function follow up from Born in Bradford Autozygosity sequencing Whole Genome Sequencing
EGAS00001001158 Leeds Melanoma Cohort Cancer Genomics
EGAS00001001304 Resistance to MAPK inhibitor induces internal duplication in BRAF Other
EGAS00001001171 Mutational Analysis of Colorectal PDX models Cancer Genomics
EGAS00001000858 Integrative genome profiling in AML Cancer Genomics
EGAS00001001207 15x WGS HELIC MANOLIS Whole Genome Sequencing
EGAS00001001299 Multiple Myeloma Diagnosis to Relapse study samples Cancer Genomics
EGAS00001001256 Genetic screening of GPI anchor protein synthesis Other
EGAS00001001591 RNAseq of ribosomal footprints Cancer Genomics
EGAS00001001713 PAGE Prenatal Assessment of Genomes and Exomes Other
EGAS00001001743 ENU CCK 81 cetuximab pilot project Cancer Genomics
EGAS00001001744 ENU NCI H508 cetuximab fixed concentration project Cancer Genomics
EGAS00001001266 WTCCC3 case control study for pre eclampsia Population Genomics
EGAS00001001090 GWAS of tuberculosis in Russia Other
EGAS00001000544 Consanguineous families with CHD KAIMRC Other
EGAS00001001137 HipSci RNAseq Rare Monogenic Diabetese Other
EGAS00001001140 HipSci Whole Exome sequencing Monogenic Diabetes Other
EGAS00001001318 HipSci RNAseq Rare BBS Transcriptome Analysis
EGAS00001001613 GILD ExomeSeq PTNHL Cancer Genomics
EGAS00001001726 HipSci whole exome sequencing for embryonic stem cell control lines Other
EGAS00001001727 HipSci RNA sequencing for embryonic stem cell control lines Other
EGAS00001001597 Low depth whole genome sequencing across multiple isolated populations Whole Genome Sequencing
EGAS00001001247 Papuan Genomes: whole genome sequencing Whole Genome Sequencing
EGAS00001001728 HipSci Methylation analysis for embryonic stem cell control lines Other
EGAS00001001729 HipSci expression microarray for embryonic stem cell control lines Other
EGAS00001001730 HipSci genotyping microarray for embryonic stem cell control lines Other
EGAS00001001343 Somatic Genetics of lesions from a POT1 patient Cancer Genomics
EGAS00001001178 560 whole-genome sequenced breast cancers Other
EGAS00001001777 ENU LS 411N TripleTherapy Cancer Genomics
EGAS00001001195 ICGC Breast Cancer Project Other
EGAS00001001778 ENU HT 29 BRAF Triple Therapy Clones Cancer Genomics
EGAS00001001745 ENU NCI H508 Cetuximab SecondRound Cancer Genomics
EGAS00001001173 Reference DNA standards for GCLP pipeline Cancer Genomics
EGAS00001001837 Dense fine mapping study identifies new susceptibility loci for primary biliary cirrhosis Population Genomics
EGAS00001001802 Native American Ancient DNA sequencing Whole Genome Sequencing
EGAS00001001519 Glioblastoma CRISPR Screen Cancer Genomics
EGAS00001000478 Genetic factors underlying premature MI in Greek families without vessel disease Other
EGAS00001000522 An exome sequencing study of the HIV elite long term non progressors and rapid progressors CASCADE cohorts Other
EGAS00001000525 Analysis of somatic mutations in normal blood AML and MDS samples Other
EGAS00001000531 Exome sequence of probands in Barrett s oesophagus families Other
EGAS00001000562 Whole genome sequencing of a Grem1 mutant human tumour Whole Genome Sequencing
EGAS00001000415 Analysis of resistance to PLX4032 Other
EGAS00001000564 Lymphocyte RNA profiling Transcriptome Analysis
EGAS00001000591 Sequencing of rare human histiocytic tumour Cancer Genomics
EGAS00001000626 Haemoglobin E beta thalassaemia in a patient group from Sri Lanka Other
EGAS00001000627 Leiden melanomafamilies Whole Genome Sequencing
EGAS00001000520 Cloning of the breakpoint of a novel translocation associated with T acute lymphoblastic leukaemia Cancer Genomics
EGAS00001000619 Acquisition of additional mutations drives accelerated progression of NPM1 positive CMML to AML Resequencing
EGAS00001000620 Identification of rare variants associated with cardiovascular traits in Cilento isolates Other
EGAS00001000017 Familial Melanoma Sequencing Exome Sequencing
EGAS00001000617 Identification of drug resistance genes in melanoma Other
EGAS00001000691 miRNA expression in response to LPS stimulus in macrophages Transcriptome Analysis
EGAS00001000711 Identification of cardiovascular biomarkers through an integrative omics approach Transcriptome Analysis
EGAS00001000733 Barcelona kids with melanoma Whole Genome Sequencing
EGAS00001000768 Low Coverage Sequencing of rare human histiocytic tumour Cancer Genomics
EGAS00001000808 Whole exome sequencing CHD trios Other
EGAS00001001516 Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study Other
EGAS00001000870 BLUEPRINT EpiVar ChIP-seq of Monocytes & Neutrophils Other
EGAS00001001035 Identification of drug resistance genes in cancer cell lines by insertional mutagenesis Cancer Genomics
EGAS00001001086 Exome sequencing of short SGA children with IGF I and insulin resistance Other
EGAS00001001124 Congenital anosmia 1 Other
EGAS00001001182 Genome Diversity in Africa Project ancient samples standard libraries Population Genomics
EGAS00001001238 Targeted replication of LVOTO genes Other
EGAS00001001263 Exome Sequencing of Human myeloid malignancies Cancer Genomics
EGAS00001000545 APCDR Uganda GWAS: Genome wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component) Other
EGAS00001001289 Targeted Sequencing of Human Myeloid Malignancies Cancer Genomics
EGAS00001001294 Transcriptome human nasal epithelium Transcriptome Analysis
EGAS00001001323 Whole Genome Sequencing of JK Family Whole Genome Sequencing
EGAS00001001429 Congenital anosmia 2 Other
EGAS00001001520 BAP1 sequence of uveal melanoma cell lines Cancer Genomics
EGAS00001001537 RNA expression profiling of melanoma patient derived xenograft Transcriptome Analysis
EGAS00001001573 The genetic evolution of precursor lesions in pancreatic cancer Cancer Genomics
EGAS00001001590 TTV018 RORC IBD associated genotype effects on RORgT expression and function in ex vivo T cells Transcriptome Analysis
EGAS00001001614 Melanoma C32 ENU resistance to Combination Therapy Cancer Genomics
EGAS00001001625 PSCP bisulphite analysis in hESCs Epigenetics
EGAS00001000762 Genetics and Networks of Congenital Heart Defects Other
EGAS00001000266 Exome sequencing of patients with Ewings sarcoma Other
EGAS00001001558 APCDR Uganda GWAS: Genome wide sequence variation and susceptibility loci for cardiometabolic traits in a sub-Saharan African population (UGWAS component) Other
EGAS00001001733 Illumina HumanCoreExome 12v1 1 A chip typing in a Greek adolescent population Population Genomics
EGAS00001001272 HipSci HumanExome BeadChip analysis-Rare BBS Other
EGAS00001001273 HipSci HumanExome BeadChip analysis-Rare ND Other
EGAS00001001274 HipSci Illumina 450K Methylation analysis-Rare BBS Other
EGAS00001001275 HipSci Illumina 450K Methylation analysis - monogenic diabetes Other
EGAS00001001276 HipSci HumanHT 12v4 Expression BeadChip analysis-Rare BBS Other
EGAS00001001277 HipSci HumanHT 12v4 Expression BeadChip analysis-Rare ND Other
EGAS00001001017 Genotype data of osteoarthritis cases from the UK collected by the arcOGEN Consortium ( Other
EGAS00001001968 Metastatic Breast Cancer Validation Cancer Genomics
EGAS00001000092 Triple Negative Breast Cancer Whole Genomes Cancer Genomics
EGAS00001001180 Methylation changes in OA patients with chronic exposure to cobalt and chromium Population Genomics
EGAS00001000913 WTCCC3 Anorexia Nervosa Population Genomics
EGAS00001001967 FFPE whole genome pilot Cancer Genomics
EGAS00001001971 In Situ Transcription whole genome sequencing Cancer Genomics
EGAS00001001972 Breast Heterogeneity Validation Cancer Genomics
EGAS00001000959 APCDR AGV Project: The African Genome Variation Project (dense array genotyping data) Other
EGAS00001001232 Understanding Society GWAS Population Genomics
EGAS00001001710 The Haplotype Reference Consortium Other
EGAS00001000869 Colorectal organoids and tumoroids pulldown Cancer Genomics
EGAS00001000969 HipSci Whole Exome sequencing Bardet Biedl Syndrome Other
EGAS00001001231 Yemen and Chad Genotyping Cancer Genomics
EGAS00001000960 APCDR AGV Project: Whole genome sequencing of 3 African populations (curated data) Other
EGAS00001002082 T19 Chad xten Whole Genome Sequencing
EGAS00001002083 T19 Yemen Whole Genome Sequencing
EGAS00001002085 Lebanon HighCov seq Whole Genome Sequencing
EGAS00001002081 Sequencing melanoma germlines Other
EGAS00001002084 Lebanon LowCov seq Whole Genome Sequencing
EGAS00001002159 Assessment of de novo copy number variations in Italian patients with schizophrenia. Other
EGAS00001000924 Genotyping of additional Inflammatory Bowel Disease cases 2014 Other
EGAS00001001752 Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors Other
EGAS00001000825 Whole Exome Sequencing of INTERVAL Other
EGAS00001002236 Genetics of gene expression in human macrophage response to Salmonella Transcriptome Analysis
EGAS00001000629 WGS low coverage sequencing of Fulani from Burkina Faso Whole Genome Sequencing
EGAS00001001486 Transcriptomics of human olfactory mucosa Transcriptome Analysis
EGAS00001001538 Human Evolution 3C Population Genomics
EGAS00001001422 Precursor lesions clonal architecture and relapse in Wilms nephroblastoma Cancer Genomics
EGAS00001001604 Identifying new diagnostic and treatment pathways for patients with unclassifiable sarcomas Cancer Genomics
EGAS00001000277 Chondrosarcoma Targeted Sequencing Study Cancer Genomics
EGAS00001001115 Genetic profiling of mucosal melanoma Other
EGAS00001001697 Melanoma C32 ENU Resistance to Single Agent Therapy Cancer Genomics
EGAS00001001698 Warm Autopsy Single Cell X10 Cancer Genomics
EGAS00001001708 RNA seq of Toxoplasma gondii response in human macrophages Transcriptome Analysis
EGAS00001000815 Identification of drug resistance genes in melanoma by mRNA gene expression Transcriptome Analysis
EGAS00001000816 Identification of drug resistance genes in melanoma by small RNAs expression analysis Transcriptome Analysis
EGAS00001001780 V2 panel bait design test Cancer Genomics
EGAS00001001639 Amplicon based sequencing of drug resistant organoids Cancer Genomics
EGAS00001001687 Clonal expansion of mutated cell population in bladder urothelium Cancer Genomics
EGAS00001001797 Targeted gene screen of drug resistant organoids Cancer Genomics
EGAS00001001873 Transcriptome analysis of anaplastic meningiomas Transcriptome Analysis
EGAS00001001806 V2 Colorectal panel test Cancer Genomics
EGAS00001001565 The British Autozygosity Populations BioResource Other
EGAS00001001048 Genetic studies of pregnancy related cardiometabolic disorders in Central Asian Northern European and Colombian populations Cancer Genomics
EGAS00001001856 Low input LC ISC Cancer Genomics
EGAS00001000563 Comparison of transcriptional response of induced pluripotent stem iPS cell derived and monocyte derived macrophages to bacterial lipopolysaccharide stimulation Transcriptome Analysis
EGAS00001000172 BRAF and MEK resistant cell line clones Cancer Genomics
EGAS00001001465 HipSci - Human Induced Pluripotent Stem Cells Initiative Other
EGAS00001001149 Mapping regulatory variation in sensory neurons using IPS lines from the HIPSCI project Gene Regulation Study
EGAS00001000194 Radiotherapy induced Sarcoma exome Cancer Genomics
EGAS00001000876 Characterization of iPSC derived macrophages cardiovascular pilot Transcriptome Analysis
EGAS00001000718 Human Evolution 3B Whole Genome Sequencing
EGAS00001002483 Hip OA Functional Genomics Transcriptome Analysis
EGAS00001001899 Knee OA Functional Genomics Transcriptome Analysis
EGAS00001002505 H3K27ac and RNA-seq data of neuroblastoma PDXs and/or primary tumors Other
EGAS00001002501 Genome wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma. Other
EGAS00001001853 Australia and New Guinea haplotype phasing Population Genomics
EGAS00001002404 Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population. Other
EGAS00001001675 Amplicon based sequencing of drug resistant lung cancer cell lines Cancer Genomics
EGAS00001001883 Resolving the Genetic Architecture of Aseptic Loosening After Total Hip Replacement Population Genomics
EGAS00001002490 Mutational signatures of aflatoxin Other
EGAS00001000934 PREDICT Whole Genomes Cancer Genomics
EGAS00001002335 Drugging the catalytically inactive state of RET kinase in RET-rearranged tumors. Other
EGAS00001001653 Comprehensive genomic characterization of cholangiocarcinoma Other
EGAS00001002576 Comparative genomic analysis of colorectal cancer in different stage Other
EGAS00001000414 Methylation analysis in GM01240 GM01247 Epigenetics
EGAS00001000894 Helleday MYC Cancer Genomics
EGAS00001000929 GDAP High depth sequencing Illumina X Ten Whole Genome Sequencing
EGAS00001001974 HipSci Whole Exome sequencing Alport Other
EGAS00001001975 HipSci Whole Exome sequencing Battens Other
EGAS00001001976 HipSci Whole Exome sequencing BPD Other
EGAS00001001977 HipSci Whole Exome sequencing Congenital hyperinsulinia Other
EGAS00001001978 HipSci Whole Exome sequencing Ataxia Other
EGAS00001001979 HipSci Whole Exome sequencing HSP Other
EGAS00001001980 HipSci Whole Exome sequencing Cardiomyopathy Other
EGAS00001001982 HipSci Whole Exome sequencing Macular dystrophy Other
EGAS00001001981 HipSci Whole Exome sequencing Kabuki Other
EGAS00001001983 HipSci Whole Exome sequencing PID Other
EGAS00001001984 HipSci Whole Exome sequencing Retinitis Pigmentosa Other
EGAS00001001985 HipSci Whole Exome sequencing Usher syndrome and congenital eye defects Other
EGAS00001001986 HipSci RNASEQ Alport Transcriptome Analysis
EGAS00001001988 HipSci RNASEQ Congenital hyperinsulinia Transcriptome Analysis
EGAS00001001989 HipSci RNASEQ Kabuki Transcriptome Analysis
EGAS00001001990 HipSci RNASEQ PID Transcriptome Analysis
EGAS00001001991 HipSci RNASEQ Spastic paraplegia Transcriptome Analysis
EGAS00001001992 HipSci RNASEQ Ataxia Transcriptome Analysis
EGAS00001001993 HipSci RNASEQ BPD Transcriptome Analysis
EGAS00001001994 HipSci RNASEQ Hypertrophic Cardiomyopathy Transcriptome Analysis
EGAS00001001995 HipSci RNASEQ Macular Dystrophy Transcriptome Analysis
EGAS00001001996 HipSci RNASEQ Retinitis Pigmentosa Transcriptome Analysis
EGAS00001001997 HipSci RNASEQ Usher syndrome and congenital eye defects Other
EGAS00001002262 TSG knock out in hiPSCs Cancer Genomics
EGAS00001002059 Exome sequencing of a cohort of Rett syndromelike patients Other
EGAS00001002067 Whole exome sequencing for clarification of rare causes of axonal Charcot Marie Tooth disease Other
EGAS00001001587 Papuan Genotyping Population Genomics