22938 results for "ega"

in 187.96 milliseconds.

• GEN_COVID_genotype

  Cohort: Raw genotype files for GEN_COVID cohort. Genotype Chip: Illumina Global Screening Array-24 v3.0 + Multi-Disease beadchip genomic build: b37

  Dataset EGAD00010002177

• RealSeqS ovarian amplicon counts

  Dataset contains text files that describe the chromosome, position, and read count for an amplicon using the RealSeqS assay.

  Dataset EGAD50000000013

• Knoll et al Identification of drug candidates targeting monocyte reprogramming in people living with HIV CD14

  Bulk CD14 RNAseq

  Dataset EGAD50000000069

• IMvigor130 heatmap Figure 2A

  Source data for Figure.2A heatmap showing the gene expression across samples.

  Dataset EGAD50000000139

• COVID-19 whole blood bulk trasncriptomics single-center

  COVID-19 whole blood bulk trasncriptomics single-center samples (all Dexamethasone)

  Dataset EGAD50000000186

• Transcriptomics dataset from human prefrontal cortex tissue - ALS vs CTR

  Fastq files and BAM files

  Dataset EGAD50000000467

• Single nuclei RNAseq data from HGSOC primary tumour samples

  Single nuclei RNAseq data from 14 HGSOC primary tumour samples

  Dataset EGAD50000000364

• VCF dataset of Colorectal Cancer Synthetic genomes

  This dataset contains genomic variants data from VCF files of four patients synthetically generated in the EOSC4Cancer project

  Dataset EGAD50000000314

• Single-cell transcriptomics of neuroblastoma tumors

  Single-cell, single-nucleus and CITE-sequencing of neuroblastoma tumors with 10X Genomics

  Dataset EGAD50000000328

• TOPARP-B patient cell-free DNA targeted sequencing

  Targeted sequencing for TOPARP-B patients as detailed in manuscript

  Study EGAS50000000281

• Time course acetalax bisacodyl treatment

  RNA-Seq raw data of PDX treated with acetalaxor bisacodyl for 4h00 to 24h00.

  Dataset EGAD50000000875

• HIV Viremic Non-Progressors (VNPs) and HIV Progressors Data Access Committee

  Data Access Committe for the project: Analyzing exome sequencing in HIV Viremic Non-Progressors (VNPs) and HIV Progressors

  Dac EGAC50000000062

• Variant call of single Jakun Individual

  One Jakun individual was sequenced on IIllumina HiSeq 2000. Variant calling was performed through GATK

  Dataset EGAD50000001024

• A Risk Score Incorporating Low Pass Whole Genome Sequencing of Cell Free DNA from Patients Receiving CD19 CAR T-Cell Therapy for Large B-Cell Lymphoma

  Study EGAS00001006308

• Yale Policy for head and neck cancer and HPV clinical trials

  Yale Policy for human controlled access data associated with head and neck cancer and HPV clinical trials

  Dac EGAC50000000403

• LEMA WES files

  This dataset contains WES bam/bai files associated with 133 patients as part of the LEMA Study

  Dataset EGAD50000001311

• ACUITI BAM files

  This dataset contains WES bam/bai files associated with 51 patients as part of the ACUITI Study

  Dataset EGAD50000001401

• Clonal IGHV rearrangements in IGH+ and IGHUND HGBCL-DH-BCL2(-BCL6)

  PCR-based VDJ profiling in IGH+ and IGHUND HGBCL-DH-BCL2(-BCL6) lymphomas

  Dataset EGAD50000001523

• WGS Sequencing of Urothelial Carcinoma from Taiwan

  Normal and Tumor paired WGS sequencing of UC Tissues

  Dataset EGAD50000001547

• RNAseq for CIAO Clinical Trial

  RNAseq (QuantSeq) from FFPE tissues for the CIAO clinical trial

  Dataset EGAD50000001676

• Dutch - BP

  The dataset encompasses 1110 Runs from the WGSPD Project 3 - Genomic Strategies to Identify High-impact Psychiatric Risk Variants Project

  Dataset EGAD50000001738

• Dutch - SCZ

  The dataset encompasses 804 Runs from the WGSPD Project 3 - Genomic Strategies to Identify High-impact Psychiatric Risk Variants Project

  Dataset EGAD50000001739

• germline pathogenic variants found in African patients of prostate cancer

  70 new blood samples added in this project

  Study EGAS50000001132

• Papua New Guinea Pangenome Project Data Access Policy

  This data policy applies to data access to the PNG15 and PNG16 sequencing data as well as derived genomic variant calls.

  Dac EGAC50000000674

• ERDERA Diagnostic Research Workstream DAC

  The ERDERA Diagnostic Research Workstream DAC decides on data access requests according to the principles defined in the ERDERA Data Sharing Framework Agreement.

  Dac EGAC50000000728

• CD4 auto-antigens

  The CD4 auto-antigen Access Committee (DAC) manages and oversees data access, ensuring compliance with ethical and regulatory guidelines while facilitating secure sharing with authorized researchers.

  Dac EGAC50000000864

• PacBio long-read scRNA-seq

  Full-length single-cell cDNA PacBio Kinnex whole-transcriptome sequencing data for adrenal sampleA and sampleB.

  Dataset EGAD50000002211

• The_mutational_landscape_of_recurrent_Glioblastome_multiforme

  Targeted gene screen of approx 120 patients with primary GBM and recurrent samples.

  Study EGAS00001001764

• ICGC medulloblastoma whole genome sequencing data, ICGC release 16

  ICGC medulloblastoma whole genome sequencing data, ICGC release 16

  Study EGAS00001000744

• Whole_genome_sequencing_of_Crohn_s_disease_patients

  Population based sequencing of whole genomes of Crohn's disease patients.

  Study EGAS00001000065

• Disorders_of_growth_and_insulin_action_

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

  Study EGAS00001000041

• Oulu_Dyslipidemia_families

  These samples include exome sequences of family members with dyslipidemias from northern Finnish origin.

  Study EGAS00001000384

• HipSci - Primary Immune Deficiency - RNA Sequencing - July 2017

  HipSci - Primary Immune Deficiency - RNA Sequencing - July 2017

  Dataset EGAD00001003536

• Reference epigenome ADMSC08 miRNA-Seq data generated from KEP study

  ADMSC08 miRNA-Seq single end data

  Dataset EGAD00001007180

• Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas: Somatic exome variants

  Somatic variants called from whole-exome sequencing of meningioma-blood pairs

  Dataset EGAD00001002650

• Reference epigenome ADMSC04_smRNA-Seq data generated from KEP study

  A ADMSC04_smRNA-Seq single end data for adipose-derived mesenchymal stroaml cells

  Dataset EGAD00001003870

• Mediator ChIP-Seq datasets in human islets

  6 ChIP-Seq datasets of Mediator in human pancreatic islets from 6 donors

  Dataset EGAD00001005202

• Reference epigenome ADMSC06 miRNA-Seq data generated from KEP study

  ADMSC06 miRNA-Seq single end data

  Dataset EGAD00001007178

• Single cells of colorectal cancer organoids

  Dataset contains 854 single cell sequenced colorectal cancer organoids.

  Dataset EGAD00001005422

• Reference epigenome CKD27_C_Mesan_WGBS data generated from KEP study

  A CKD27_C_Mesan_WGBS paired end data for Mesangial cells(kidney)

  Dataset EGAD00001003471

• HipSci - Bardet-Biedl Syndrome - Exome Sequencing - January 2016

  HipSci - Bardet-Biedl Syndrome - Exome Sequencing - January 2016

  Dataset EGAD00001001950

• Infant HGG WES

  Whole exome sequencing of infant high grade gliomas. BAM files of paired end reads aligned to GRCh37 with bwa

  Dataset EGAD00001005247

• HipSci - Hereditary Spastic Paraplegia - RNA Sequencing - July 2017

  HipSci - Hereditary Spastic Paraplegia - RNA Sequencing - July 2017

  Dataset EGAD00001003537

• Reference epigenome CKD23_C_Mesan_WGBS data generated from KEP study

  A CKD23_C_Mesan_WGBS paired end data for Mesangial cells(kidney)

  Dataset EGAD00001003468

• Reference epigenome KNIH008 WGBS data generated from KEP study

  A KNIH008 Whole-Genome Bisulfite Sequencing(WGBS) paired end data for adipocytes

  Dataset EGAD00001002756

• HipSci - Bardet-Biedl Syndrome - RNA Sequencing - April 2015

  HipSci - Bardet-Biedl Syndrome - RNA Sequencing - April 2015

  Dataset EGAD00001001952

• Intellectual disability exome sequencing

  Exome sequencing of ID trios and sibpairs

  Dataset EGAD00001005442

• HipSci - Hereditary Cerebellar Ataxias - Exome Sequencing - July 2017

  HipSci - Hereditary Cerebellar Ataxias - Exome Sequencing - July 2017

  Dataset EGAD00001003521

• HipSci - Primary Immune Deficiency - Exome Sequencing - July 2017

  HipSci - Primary Immune Deficiency - Exome Sequencing - July 2017

  Dataset EGAD00001003526

• HipSci - Hereditary Cerebellar Ataxias - RNA Sequencing - July 2017

  HipSci - Hereditary Cerebellar Ataxias - RNA Sequencing - July 2017

  Dataset EGAD00001003538

• IfGH-10772

  Clinical and genetic information of an individual with RVOT-VT and a KCNK2 (TREK1) gene mutation obtained after whole exome sequencing.

  Dataset EGAD00001003328

• OT2_Illumina_WXS_MET

  Whole-exome sequencing on Illumina HiSeq2000/2500 of colorectal cancer metastasis sample (OT2_cohort)

  Dataset EGAD00001003379

• Promoter capture HiC on KMS11 (multiple myeloma)

  Promoter capture HiC on KMS11 (multiple myeloma)

  Dataset EGAD00001003597

• PACA-CA Whole Genome Sequence bam files

  Merged bam files for PACA-CA Whole Genome Sequencing, for DCC release 27

  Dataset EGAD00001003927

• Reference epigenome ADMSC05 miRNA-Seq data generated from KEP study

  ADMSC05 miRNA-Seq single end data

  Dataset EGAD00001007177

• Reference epigenome ADMSC07 miRNA-Seq data generated from KEP study

  ADMSC07 miRNA-Seq single end data

  Dataset EGAD00001007179

• Whole exome sequencing of matched tumor-normal brain metastases

  Whole exome sequencing of matched tumor (brain metastasis) -normal (blood) from 6 patients.

  Dataset EGAD00001006453

• HipSci - Bardet-Biedl Syndrome - RNA Sequencing - January 2016

  HipSci - Bardet-Biedl Syndrome - RNA Sequencing - January 2016

  Dataset EGAD00001001954

• Khoe-San whole genome sequencing

  25 high coverage complete genome sequences of southern African Khoe-San individuals. Bam file format.

  Dataset EGAD00001006183

• Reference epigenome Pancreas-Islet06 WGBS data generated from KEP study

  Pancreas-Islet06 WGBS paired end data

  Dataset EGAD00001007884

• Genentech gallbladder cancer study - RNA-seq

  Genentech gallbladder cancer study - RNA-seq

  Dataset EGAD00001004854

• Cohesin ChIP-Seq datasets in human islets

  3 ChIP-Seq datasets of Cohesin in human pancreatic islets from 3 donors

  Dataset EGAD00001005203

• RNASeq files for GenomePaint paper

  RNASeq files for GenomePaint paper titled "Exploration of coding and non-coding variants in cancer using GenomePaint."

  Dataset EGAD00001006680

• UK10K_OBESITY_TWINSUK REL-2013-04-20

  UK10K_OBESITY_TWINSUK REL-2013-04-20

  Dataset EGAD00001000429

• HipSci - Hereditary Spastic Paraplegia - Exome Sequencing - July 2017

  HipSci - Hereditary Spastic Paraplegia - Exome Sequencing - July 2017

  Dataset EGAD00001003522

• RNA-Seq dataset

  10 RNA-Seq bam files including 4 cases with fusion and 6 controls without fusion.

  Dataset EGAD00001004360

• THE MEDICAL RESEARCH COUNCIL – BRAIN BANK (MRC-BB) CONSORTIUM EXOME DATASET

  1461 Neuropathological and clinically characterised cases from the MRC Brain Bank

  Dataset EGAD00001001925

• Reference epigenome ADMSC02 mRNA-Seq data generated from KEP study

  ADMSC02 mRNA-Seq paired end data

  Dataset EGAD00001007151

• Illumina_WXS_T

  Whole-exome sequencing on Illumina HiSeq2000/2500 of colorectal cancer primary tumor sample

  Dataset EGAD00001002099

• HipSci - Bardet-Biedl Syndrome - Exome Sequencing - April 2015

  HipSci - Bardet-Biedl Syndrome - Exome Sequencing - April 2015

  Dataset EGAD00001001422

• Patient 16CH

  One file of patient 16 with WGS done on Illumina HiSeq X-Ten. For research purpose and authorised user only.

  Dataset EGAD00001003440

• DATA FILES FOR SJOS-WGS-2ndBatch

  DATA FILES FOR SJOS-WGS-2ndBatch

  Dataset EGAD00001001053

• Nyamasati study

  Illumina whole genome sequencing to high depth (x50) of four Tanzanian individuals. Genomic DNA derived from peripheral whole blood.

  Dataset EGAD00001004370

• Whole exome sequencing CHD trios

  Whole exome sequencing of families with Congenital Heart Defects (182 trios). Collaboration with David Brook, University of Nottingham.

  Dataset EGAD00001002200

• RNAseq

  This dataset contains RNAseq performed on 35 human acute erythroid leukemia patient samples and Xenografts.

  Dataset EGAD00001006076

• WGS fastq for EGAS00001004572

  Bulk WGS fastq files for germline and tumours in EGAS00001004572.

  Dataset EGAD00001006902

• WGS data for MMML for Study EGAS00001002198

  Whole genome sequencing data for MMML (healthy cell_line)

  Dataset EGAD00001003283

• RNA-Seq and WXS from 6 glioblastoma patients

  RNA-Seq and WXS from 6 glioblastoma patients

  Dataset EGAD00001003293

• GRIDSS somatic sv vcfs for EGAS00001004572

  Bulk GRIDSS somatic sv vcfs from tumour-normal analysis in EGAS00001004572

  Dataset EGAD00001006906

• OT2_Illumina_WGS_T

  Whole-genome sequencing on Illumina HiSeq2000/2500 of colorectal cancer primary tumor sample (OT2_cohort)

  Dataset EGAD00001003375

• PACA-CA RNASeq bam files

  Bam files for PACA-CA RNA Seq analysis, for DCC release 27

  Dataset EGAD00001003945

• PACA-CA Whole Genome Sequence bam files

  Merged bam files for PACA-CA Whole Genome Sequencing, for DCC release 27

  Dataset EGAD00001003948

• Spatial genomic heterogeneity in multiple myeloma

  Paired end Whole Exome Sequencing of fine-needle aspirates from 51 Mutliple Myeloma patients.

  Dataset EGAD00001003988

• SPTCL exome data

  Whole exome sequencing data of 17 SPTCL cases, including 7 matched-normal samples.

  Dataset EGAD00001004310

• Whole_Genome_sequencing_of_rhabdomyosarcoma_tumour_tissue

  The aim of this study is to investigate the genomic landscape of human cancer.

  Study EGAS00001008280

• Single_cell_ATAC_sequencing_of_rhabdomyosarcoma_tumour_tissue

  The aim of this study is to investigate the genomic landscape of human cancer.

  Study EGAS00001008283

• Single_cell_ATAC_sequencing_of_rhabdomyosarcoma_tumour_tissue

  The aim of this study is to investigate the genomic landscape of human cancer.

  Study EGAS00001008279

• Single_cell_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

  The aim of this study is to investigate the genomic landscape of human cancer.

  Study EGAS00001008281

• Targeted capture ctDNA Library CRCQV42Run047-8

  Targeted capture ctDNA Library CRCQV42Run047-8 from patient PBC0001304, buffy coat sample

  Dataset EGAD00001010740

• Targeted capture ctDNA Library CRCQV42Run048-10

  Targeted capture ctDNA Library CRCQV42Run048-10 from patient PBC0001488, buffy coat sample

  Dataset EGAD00001010742

• Bulk_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

  The aim of this study is to investigate the genomic landscape of human cancer.

  Study EGAS00001008282

• Wilms_Tumour_organoid_sequencing_WGS

  This study investigates the genomic and transcriptomic characteristics of Wilm's tumour organoids

  Study EGAS00001002692

• Targeted capture ctDNA Library CRCQV42Run048-15

  Targeted capture ctDNA Library CRCQV42Run048-15 from patient PBC0001818, buffy coat sample

  Dataset EGAD00001010747

• Targeted capture ctDNA Library CRCQV42Run048-8

  Targeted capture ctDNA Library CRCQV42Run048-8 from patient PBC0001376, buffy coat sample

  Dataset EGAD00001010761

• Reference epigenome Islet-derived_MSC06 h3k27me3 ChIP-Seq data generated from KEP study

  Islet-derived_MSC06 h3k27me3 ChIP-Seq paired end data

  Dataset EGAD00001007896

• Paired WGS data from Wilms Tumors

  Paired whole genome sequencing tumor normal samples of pediatric Wilms tumors

  Study EGAS00001006526

• Reference epigenome Islet-derived_MSC08 h3k4me3 ChIP-Seq data generated from KEP study

  Islet-derived_MSC08 h3k4me3 ChIP-Seq paired end data

  Dataset EGAD00001007906

• Placental_genomics

  The aim of this study is to define the mutational landscape of placentas.

  Study EGAS00001003297

• Reference epigenome Islet-derived_MSC08 h3k27me3 ChIP-Seq data generated from KEP study

  Islet-derived_MSC08 h3k27me3 ChIP-Seq paired end data

  Dataset EGAD00001007903

• Aneuploidy_and_human_development

  We will investigate the transcriptomic consequences of copy number changes in human development.

  Study EGAS00001005267