23249 results for "ega"

in 31.91 milliseconds.

• BCG prime DNA methylation data

  This dataset contains the DNA methylation data of 384 samples from individuals with one or more comorbidities

  Dataset EGAD00010002767

• Ovarian subtypes tumor methylation data

  This dataset contains ovarian endometriod and ovarian, stomach, pancreatic and colorectal mucinous tumor tissue samples

  Dataset EGAD00010002773

• Exome sequencing for identifying point mutations driving M haemophilum susceptibility

  To understand non tuberculous Mycobacterial susceptibility

  Study EGAS50000001076

• cfDNA shallow Whole-Genome sequencing - healthy donors

  sWGS of the blood samples from 14 (fourteen) healthy donors

  Dataset EGAD50000001860

• SiMSen‑Seq

  High resolution amplicon-bases sequencing o screen for PIK3CA hot spot mutations

  Dataset EGAD50000001668

• DNAme of pancreatic neuroendocrine tumors mutated in MEN1/DAXX/ ATRX

  primary pancreatic neuroendocrine tumors mutated in Menin, DAXX or ATRX

  Dataset EGAD00010002784

• CFTR Gene Variant Detection in Moroccan Individuals via Nanopore Long-Read Sequencing

  This is data from LRS of CFTR gene on CF Moroccan patients

  Dac EGAC50000000815

• endogene.bio

  The Endogene Bio Data Access Committee oversees and manages access to controlled genomic and clinical datasets deposited by the Endogene Bio research team.

  Dac EGAC50000000786

• FFPE_Normal_Panel_V3_Cancer_Panel

  FFPE normal panel generation for use with V3 cancer panel 0618521

  Study EGAS00001000836

• Breast_Heterogeneity_Validation

  Validation of subs and indels called in breast whole genome studies

  Study EGAS00001001972

• Otosclerosis_gene_discovery_

  DNA from patients with otosclerosis will be subjected to exome sequencing

  Study EGAS00001000156

• Whole Exome Sequencing of Permanent Neonatal Diabetes Patients

  Whole Exome Sequencing of Permanent Neonatal Diabetes Patients

  Study EGAS00001000047

• Plasma DNA motif analysis

  Plasma DNA motif analysis

  Study EGAS00001003409

• Cloning_of_the_breakpoint_of_a_novel_translocation_associated_with_T_acute_lymphoblastic_leukaemia

  Single case of T-ALL carrying t(4;6), a novel translocation.

  Study EGAS00001000520

• SHH medulloblastoma samples

  Sequencing data of human SHH medulloblastoma samples

  Study EGAS00001000607

• UROMOL 2020 - RNA-seq data for validation

  Total RNAseq data from 47 patients with NMIBC.

  Study EGAS00001005050

• Nasal brushes analysis

  scRNA-seq samples from healthy and asthma donors part 1.

  Study EGAS00001006657

• Whole exome sequencing of soft tissue sarcoma

  We characterized genomic alterations of soft tissue sarcoma.

  Study EGAS50000001673

• PTA_thyroid__RNA_

  Exploring the somatic mutations in single cells derived from the thyroid

  Study EGAS00001007946

• PTA__thyroid_

  Investigation into thyroid pathologies utilising single cell/nuclei genome sequencing.

  Study EGAS00001007833

• ICR MOPOPGEN UK exome control series

  BAM files of individuals from the 1958BC aligned to hg17

  Dataset EGAD00001004396

• IRF5 HL RNASeq dataset

  bam files associated with the study EGAS00001001205

  Dataset EGAD00001001417

• Pipeline study - RNAseq dataset

  Fernandez-Cuesta et al., RNAseq data Pipline

  Dataset EGAD00001000746

• Landscape of AL mutations

  Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis

  Dataset EGAD00001001861

• HipSci - Embryonic Stem Cells - Exome Sequencing - April 2016

  HipSci - Embryonic Stem Cells - Exome Sequencing - April 2016

  Dataset EGAD00001001999

• Illumina_WXS_CONT

  Whole-exome sequencing on Illumina HiSeq2000/2500 of normal colon control tissue

  Dataset EGAD00001002094

• Target sequencing of myxofibrosarcoma

  Target sequencing (fastq files) of 99 pairs (198 samples) of myxofibrosarcoma

  Dataset EGAD00001004101

• WGS of Asian lung cancers

  VCF files of somatic variants from tumor-normal pairs of Asian lung cancer patients

  Dataset EGAD00001001240

• ORIENT study

  scRNAseq dataset containing 5 healthy donors and 4 asthmatic donors.

  Dataset EGAD00001009687

• Bulk RNAseq

  Bulk RNAseq from 183 premalignant gastric biopsies

  Dataset EGAD00001010131

• Oxford Nanopore sequencing for APL

  Raw fast5 file of Oxford Nanopore sequencing for an APL patient sample

  Dataset EGAD00001008151

• MDS 5q- exome reads

  Cancer exome reads consisting of FASTQ paired end reads from bone marrow samples

  Dataset EGAD00001001058

• Reference epigenome OB56_N_PreA_WGBS data generated from KEP study

  A OB56_N_PreA_WGBS paired end data for Preadipocytes(fat)

  Dataset EGAD00001003479

• Microsatellite unstable colorectal cancers

  Mapped data for 10 Colon MSI cancer samples

  Dataset EGAD00001004500

• MDS Sequential Treatment Validation

  Validations of variants identified by exome sequencing in sequential samples derived after treatment cycle with AZA.

  Dataset EGAD00001000949

• LLNEXT Pilot MGS sequencing

  This dataset contains sequencing data from fecal microbiome from LLNEXT project

  Dataset EGAD00001011293

• Solid_WXS_BL

  Whole-exome sequencing on AB 5500xl Genetic Analyzer of Blood EDTA

  Dataset EGAD00001002104

• Metadata file

  "Master" file of patient clinical characteristics and outcomes, samples, and the results of certain analyses, including immunohistochemistry.

  Dataset EGAD00001008792

• Disorders of growth and insulin action

  Illumina paired-end sequencing of whole- exome pulldown DNA from Severe Insulin Resistant patients.

  Dataset EGAD00001000381

• WXS files for MATCH paper

  WXS files for paper titled "Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)"

  Dataset EGAD00001015484

• DREAM SMC-HET - WGS mapped reads

  ICGC-TCGA DREAM Somatic Mutation Calling - Tumour Heterogeneity Challenge - WGS mapped reads

  Dataset EGAD00001003971

• OT2_Illumina_WGS_BL

  Whole-genome sequencing on Illumina HiSeq2000/2500 of Blood EDTA (OT2_cohort)

  Dataset EGAD00001003370

• AI_NF1glioma_WES

  The dataset includes 59 tumor samples from 56 NF1-glioma patients profiled by Whole Exome Sequencing.

  Dataset EGAD00001004375

• RRBS melanoma biopsies

  RRBS data for melanoma biopsies at baseline and after treatment

  Dataset EGAD00001009060

• Tracing the origins of relapse in AML to stem cells

  Aligned whole genome sequence from AML relapse project

  Dataset EGAD00001003234

• snv calls for subclonal reconstruction

  single nucleotide variant calls from somatic sniper, vcf format. input for subclonal reconstruction

  Dataset EGAD00001003753

• RNA sequencing of myxofibrosarcoma

  RNA sequencing (fastq files) of 29 samples of myxofibrosarcoma

  Dataset EGAD00001004102

• Exome sequencing Parkinson's disease patients

  In this project we will sequence the exomes of 250 patients with Parkinson's disease

  Dataset EGAD00001000405

• Seminoma exome sequencing

  Exome sequencing data for 8 pairs of seminomas and matched normal

  Dataset EGAD00001001002

• RNASeq files for Stewart-MATCH

  RNASeq files for paper titled "Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)"

  Dataset EGAD00001015475

• Targeted gene screen of drug resistant organoids

  Sequencing of drug resistant organoids

  Dataset EGAD00001003252

• Multisample2 Amplicon

  Amplicon data of tumor samples generated for validation of WES findings and further sub clonal mapping

  Dataset EGAD00001004020

• KRAS Mutations in Multiple Myeloma

  Fastq files for 80 Multiple Myeloma Patients and 12 cell-lines

  Dataset EGAD00001005743

• Whole exome sequencing of myxofibrosarcoma

  Whole exome sequencing (fastq files) of 41 pairs (82 samples) of myxofibrosarcoma

  Dataset EGAD00001004095

• DATA FILES FOR SJLGG

  DATA FILES FOR SJLGG

  Dataset EGAD00001000695

• Familial CEBPA-mutated AML whole exome sequencing dataset

  Whole exome sequencing data for AML and matched normal samples

  Dataset EGAD00001000996

• LGG Epilepsy Cohort WGS

  LGG Epilepsy Cohort WGS

  Dataset EGAD00001001664

• LGG Epilepsy Cohort WXS

  LGG Epilepsy Cohort WXS

  Dataset EGAD00001001665

• Osteosarcoma exome sequencing dataset

  Whole exome sequencing data of primary, secondary and tertiary tumor from a patient.

  Dataset EGAD00001002145

• Characterization of HCV-specific CD4 T cells during DAA-Therapy

  To be added...

  Dataset EGAD00001005432

• Melanoma multi site metastases

  These are caveman, pindel, battenberg and brass calls for index patients' metastatic melanoma genomes within this study.

  Dataset EGAD00001005483

• Proteome data

  Proteome data of neuroblastoma patients

  Dataset EGAD00001006737

• IMpower133 subtype assignments

  This dataset contains subtype assignments for 271 tumor samples profiled by RNA-seq.

  Dataset EGAD00001006926

• RPPA analysis + clinical data

  RPPA analysis from FAIRLANE Trial of Neoadjuvant Ipatasertib Plus Paclitaxel for Triple-Negative Breast Cancer.

  Dataset EGAD00001008507

• Global Anaplastic Thyroid Cancer Initiative

  Raw whole genome sequence data(fastq) for the GATCI project

  Dataset EGAD00001003236

• Data upcycling, powered by EGA

  In 2012 a collaborative effort headed by the teams of Carlos Caldas in Cambridge, UK and Samuel Aparicio, Canada, produced a pivotal study aimed at defining the mutational landscape of breast cancer. They gathered a collection of over 2000 breast cancer samples (METABRIC) associated with long-term clinical follow-up. They delineated an array of inherited and somatically acquired genetic variants and associated them to gene expression. This led to the identification of putative cancer-driving events and improved stratification of breast cancer patients. The study elicited huge attention and was tackled as herculean effort by fellow researchers. Cristina Curtis and her colleagues deposited the data in the EGA archive (EGAS00000000083). What they probably could not foresee is that their data would be reused more than 100 times, becoming one of the most downloaded datasets at EGA. In 2015, Frederik S. Varn and colleagues accessed the above-mentioned data from the New Hampshire, USA, to correlate it to transcriptional programs of hematopoietic cells infiltrated in breast tumours and found that those can influence patients' prognosis. Their findings, published in Nature Communications, improved the understanding of the interplay between immune system and cancer. Again, in 2017 the dataset was downloaded by an Italian/Polish collaboration and used to corroborate their mechanistic study that demonstrate how a long non-coding RNA (lncRNA) is aberrantly localized into the chromatin, where it modulates oncogenic isoforms expression, thus contributing to breast cancer. To date, the METABRIC dataset has been reused to contribute to 147 publications. Its impact on breast cancer research is incalculable, and it even spread beyond that, with recent contributions to the understanding of pan-cancer mechanisms and features. Some of the publications are translating into improvements in diagnosis and treatment of different types of breast cancer. This is just an example of how data upcycling can amplify the potential of any dataset, well past the scope of its creation, the imagination of its owners and any geographical border. At EGA, we are proud to empower such fruitful worldwide cycles of knowledge, providing a platform that enables safe sharing of sensitive genetic data.

  Blog data-upcycling-powered-by-ega

• Data Access Committee for the DNA sequencing data included in the study "A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomes”

  Dac EGAC00001003111

• African Partnership for Chronic Disease Research (APCDR) DAC

  Dac EGAC00001000237

• Data Access Committee of DKFZ-Epigenomics

  Dac EGAC00001000279

• DAC for the Study EGAS00001006374: Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies. snRNAseq of 79 (61 CM patients + 18 controls).

  Dac EGAC00001002804

• EGAD00000000010

  WTCCC1 project Ankylosing Spondylitis (AS) samples

  Dataset EGAD00000000010

• EGAD00000000013

  WTCCC1 project Breast cancer (BC) samples

  Dataset EGAD00000000013

• EGAD00000000049

  RNA-SEQ data from oestrogen-receptor-alpha-positive metastatic lobular breast cancer sample

  Dataset EGAD00000000049

• EGAD00010000636

  WTCCC2 Visceral Leishmaniasis samples from Brazil using Illumina 670k

  Dataset EGAD00010000636

• EGAD00010000638

  WTCCC2 Visceral Leishmaniasis samples from Indial using Illumina 670k

  Dataset EGAD00010000638

• EGAD00010000640

  WTCCC2 Visceral Leishmaniasis samples from Sudanl using Illumina 670k

  Dataset EGAD00010000640

• EGAD00010000674

  ELSA genome-wide genotypes, excluding estimated related individuals. There are 3 files: .fam, .bim, .bed

  Dataset EGAD00010000674

• EGAD00010000676

  ELSA genome-wide genotypes, including estimated related individuals. There are 3 files: .fam, .bim, .bed

  Dataset EGAD00010000676

• EGAD00010000294

  1958BC control samples only (Hap300)

  Dataset EGAD00010000294

• EGAD00010000236

  WTCCC2 samples from Coronary Artery Disease Cohort

  Dataset EGAD00010000236

• EGAD00010000286

  All cases and controls (Hap550)

  Dataset EGAD00010000286

• EGAD00010000290

  NBS control samples only (Hap550)

  Dataset EGAD00010000290

• EGAD00010000298

  All cases and controls (Hap300)

  Dataset EGAD00010000298

• EGAD00010000450

  Genome Wide Genotype Data

  Dataset EGAD00010000450

• EGAD00010000486

  ccRCC case samples using expression array

  Dataset EGAD00010000486

• EGAD00010000496

  Genome-wide SNP genotyping of African rainforest hunter-gatherers and neighbouring agriculturalists

  Dataset EGAD00010000496

• "SNV detection from formalin fixed paraffin embedded (FFPE) samples"

  "SNV detection from formalin fixed paraffin embedded (FFPE) samples"

  Dataset EGAD00001000033

• "Usage of small amounts of DNA for Illumina sequencing"

  "Usage of small amounts of DNA for Illumina sequencing"

  Dataset EGAD00001000034

• Cell Line Sub Clone Rearrangement Screen

  Cell Line Sub Clone Rearrangement Screen

  Dataset EGAD00001000064

• Non Tumour Renal Cell Line Sequencing

  Non Tumour Renal Cell Line Sequencing

  Dataset EGAD00001000091

• Identifying Novel Fusion Genes in Myeloma

  Identifying Novel Fusion Genes in Myeloma

  Dataset EGAD00001000112

• AML targeted resequencing study

  AML targeted resequencing study

  Dataset EGAD00001000253

• Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments

  Dataset EGAD00001001602

• 450K_DKFZ_CLL_NB

  CLL and normal B cell samples using 450K

  Dataset EGAD00010000871

• ICGC_450k

  Medulloblastoma methylation profiling

  Dataset EGAD00010001323

• Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends

  Dataset EGAD00001003778

• HPAH Genotyping data

  Genotyping data for 32 individuals from a family affected by HPAH

  Dataset EGAD00010001633

• WTCCC2 Pre-eclampsia

  Genotype data from the Affymetrix 6.0 platform for 4,375 Colombian pre-eclampsia cases and controls

  Dataset EGAD00010001647

• Complete sequencing dataset of study EGAS00001002795

  Dataset EGAD00001004572

• APCDR AGV Fula

  APCDR AGV Project: Array data from 74 Fula

  Dataset EGAD00010001054