23249 results for "ega"

in 55.99 milliseconds.

• SNP array karyotyping of upper urinary tract urothelial carcinoma

  Genome-wide copy number analysis of upper urinary tract urothelial carcinoma using GeneChip Human Mapping 250K Nspl

  Dataset EGAD00010002098

• Methylation_PBL_male_PSCUC

  Whole-genome DNA methylation profiling of PBL obtained from male patients with PSC-UC, or UC alone, or healthy individuals.

  Dataset EGAD00010002277

• Methylation files for Roussel-ATRT-TM

  Methylation files for Roussel-ATRT-TM paper titled "Atypical teratoid/ rhabdoid tumoroids reveal subgroup-specific drug vulnerabilities"

  Dataset EGAD00010002357

• BelCovid_2_genotype

  Cohort: Raw genotype files for BelCovid2 cohort. Genotype Chip: Illumina Global Screening Array-24 v3.0 + Multi-Disease beadchip genomic build: b37

  Dataset EGAD00010002179

• 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

• Chun Lab DAC

  Data Access Committee (DAC) for datasets produced by the Chun Lab @ Sanford Burnham Prebys Medical Discovery Institute in La Jolla, California.

  Dac EGAC50000000011

• 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_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008281

• Aneuploidy_and_human_development

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

  Study EGAS00001005267

• Bulk_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008282

• Bulk_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008278

• Single_cell_ATAC_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008283

• 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

• Wilms_Tumour_organoid_sequencing_WGS

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

  Study EGAS00001002692

• The_mutational_landscape_of_recurrent_Glioblastome_multiforme

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

  Study EGAS00001001764

• Disorders_of_growth_and_insulin_action_

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

  Study EGAS00001000041

• Paired WGS data from Wilms Tumors

  Paired whole genome sequencing tumor normal samples of pediatric Wilms tumors

  Study EGAS00001006526

• Oulu_Dyslipidemia_families

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

  Study EGAS00001000384

• Placental_genomics

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

  Study EGAS00001003297

• 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 transcriptome profiling of childhood soft tissue sarcomas

  Single cell transcriptome profiling of childhood soft tissue sarcomas

  Study EGAS00001006563

• WGS of CD138+ samples collected from MM patients

  Deep WGS performed on samples collected from MM patients

  Study EGAS00001006731

• WES sequencing of TRACERx NSCLC patient-derived xenograft models

  WES sequencing of TRACERx NSCLC patient-derived xenograft models

  Study EGAS00001007364

• 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

• Targeted capture ctDNA Library CRCQV42Run049-11

  Targeted capture ctDNA Library CRCQV42Run049-11 from patient PBC0001068, buffy coat sample

  Dataset EGAD00001010764

• Targeted capture ctDNA Library CRCQV42Run048-9

  Targeted capture ctDNA Library CRCQV42Run048-9 from patient PBC0001445, buffy coat sample

  Dataset EGAD00001010762

• Targeted capture ctDNA Library CRCQV42Run030-5

  Targeted capture ctDNA Library CRCQV42Run030-5 from patient PBC0001051, buffy coat sample

  Dataset EGAD00001010526

• Targeted capture ctDNA Library CRCQV42Run050-8

  Targeted capture ctDNA Library CRCQV42Run050-8 from patient PBC0001134, buffy coat sample

  Dataset EGAD00001010802

• Single cells of colorectal cancer organoids

  Dataset contains 854 single cell sequenced colorectal cancer organoids.

  Dataset EGAD00001005422

• Targeted capture ctDNA Library CRCQV42Run050-16

  Targeted capture ctDNA Library CRCQV42Run050-16 from patient PBC0001042, buffy coat sample

  Dataset EGAD00001010789

• 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

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

  ADMSC06 miRNA-Seq single end data

  Dataset EGAD00001007178

• Reference epigenome KNIH008 WGBS data generated from KEP study

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

  Dataset EGAD00001002756

• RNASeq files for GenomePaint paper

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

  Dataset EGAD00001006680

• Reference epigenome Islet-derived_MSC08 h3k9me3 ChIP-Seq data generated from KEP study

  Islet-derived_MSC08 h3k9me3 ChIP-Seq paired end data

  Dataset EGAD00001007907

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

  Islet-derived_MSC08 input ChIP-Seq paired end data

  Dataset EGAD00001007908

• Targeted capture ctDNA Library CRCQV42Run050-24

  Targeted capture ctDNA Library CRCQV42Run050-24 from patient PBC0002494, buffy coat sample

  Dataset EGAD00001010797

• Targeted capture ctDNA Library CRCQV40Run027-6

  Targeted capture ctDNA Library CRCQV40Run027-6 from patient PBC0001335, buffy coat sample

  Dataset EGAD00001010395

• Targeted capture ctDNA Library CRCQV42Run048-18

  Targeted capture ctDNA Library CRCQV42Run048-18 from patient PBC0003376, buffy coat sample

  Dataset EGAD00001010750

• 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

• 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

• Intellectual disability exome sequencing

  Exome sequencing of ID trios and sibpairs

  Dataset EGAD00001005442

• Targeted capture ctDNA Library CRCQV34Run011-11

  Targeted capture ctDNA Library CRCQV34Run011-11 from patient PBC0002255, plasma baseline sample

  Dataset EGAD00001010365

• 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 Spastic Paraplegia - RNA Sequencing - July 2017

  HipSci - Hereditary Spastic Paraplegia - RNA Sequencing - July 2017

  Dataset EGAD00001003537

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

  HipSci - Hereditary Cerebellar Ataxias - RNA Sequencing - July 2017

  Dataset EGAD00001003538

• Targeted capture ctDNA Library CRCQV42Run033-22

  Targeted capture ctDNA Library CRCQV42Run033-22 from patient PBC0003385, buffy coat sample

  Dataset EGAD00001010559

• Targeted capture ctDNA Library CRCQV42Run033-23

  Targeted capture ctDNA Library CRCQV42Run033-23 from patient PBC0003595, buffy coat sample

  Dataset EGAD00001010560

• Targeted capture ctDNA Library CRCQV42Run033-5

  Targeted capture ctDNA Library CRCQV42Run033-5 from patient PBC0001845, buffy coat sample

  Dataset EGAD00001010561

• Targeted capture ctDNA Library CRCQV42Run033-6

  Targeted capture ctDNA Library CRCQV42Run033-6 from patient PBC0001859, buffy coat sample

  Dataset EGAD00001010562

• Targeted capture ctDNA Library CRCQV42Run039-9

  Targeted capture ctDNA Library CRCQV42Run039-9 from patient PBC0001335, saliva, repeat sample

  Dataset EGAD00001010625

• Targeted capture ctDNA Library CRCQV42Run034-10

  Targeted capture ctDNA Library CRCQV42Run034-10 from patient PBC0004076, buffy coat sample

  Dataset EGAD00001010565

• Targeted capture ctDNA Library CRCQV42Run043-18

  Targeted capture ctDNA Library CRCQV42Run043-18 from patient PBC0002995, plasma baseline sample

  Dataset EGAD00001010647

• Targeted capture ctDNA Library CRCQV42Run044-21

  Targeted capture ctDNA Library CRCQV42Run044-21 from patient PBC0005373, plasma baseline sample

  Dataset EGAD00001010671

• Targeted capture ctDNA Library CRCQV42Run046-17

  Targeted capture ctDNA Library CRCQV42Run046-17 from patient PBC0001329, plasma baseline sample

  Dataset EGAD00001010708

• Targeted capture ctDNA Library CRCQV42Run046-15

  Targeted capture ctDNA Library CRCQV42Run046-15 from patient PBC0001183, plasma baseline sample

  Dataset EGAD00001010706

• Targeted capture ctDNA Library CRCQV42Run047-19

  Targeted capture ctDNA Library CRCQV42Run047-19 from patient PBC0002851, buffy coat sample

  Dataset EGAD00001010731

• Targeted capture ctDNA Library CRCQV42Run047-20

  Targeted capture ctDNA Library CRCQV42Run047-20 from patient PBC0004124, buffy coat sample

  Dataset EGAD00001010732

• Targeted capture ctDNA Library CRCQV42Run047-7

  Targeted capture ctDNA Library CRCQV42Run047-7 from patient PBC0001589, buffy coat sample

  Dataset EGAD00001010739

• 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

• Targeted capture ctDNA Library CRCQV42Run048-8

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

  Dataset EGAD00001010761

• Targeted capture ctDNA Library CRCQV42Run049-10

  Targeted capture ctDNA Library CRCQV42Run049-10 from patient PBC0004156, buffy coat sample

  Dataset EGAD00001010763

• Targeted capture ctDNA Library CRCQV42Run049-21

  Targeted capture ctDNA Library CRCQV42Run049-21 from patient PBC0001456, buffy coat sample

  Dataset EGAD00001010774

• Targeted capture ctDNA Library CRCQV42Run049-6

  Targeted capture ctDNA Library CRCQV42Run049-6 from patient PBC0005013, buffy coat sample

  Dataset EGAD00001010779

• Targeted capture ctDNA Library CRCQV42Run051-15

  Targeted capture ctDNA Library CRCQV42Run051-15 from patient PBC0001224, buffy coat sample

  Dataset EGAD00001010809

• Targeted capture ctDNA Library CRCQV42Run051-16

  Targeted capture ctDNA Library CRCQV42Run051-16 from patient PBC0002533, buffy coat sample

  Dataset EGAD00001010810

• Targeted capture ctDNA Library CRCQV42Run051-17

  Targeted capture ctDNA Library CRCQV42Run051-17 from patient PBC0002995, buffy coat sample

  Dataset EGAD00001010811

• Targeted capture ctDNA Library CRCQV42Run051-20

  Targeted capture ctDNA Library CRCQV42Run051-20 from patient PBC0003587, buffy coat sample

  Dataset EGAD00001010813