22938 results for "ega"

in 37.04 milliseconds.

• UK10K_RARE_THYROID REL-2013-04-20

  UK10K_RARE_THYROID REL-2013-04-20

  Dataset EGAD00001000420

• Whole genome sequence of condrosarcoma

  Fastq files of 10 samples of condrosarcoma

  Dataset EGAD00001000873

• scWGS PDX

  Single cell WGS (low pass) for PT1-derived PDX samples

  Dataset EGAD00001006137

• Reference epigenome Islet-derived-iPSC01 WGBS data generated from KEP study

  Islet-derived-iPSC01 WGBS paired end data

  Dataset EGAD00001007144

• Reference epigenome Islet-derived-iPSC02 WGBS data generated from KEP study

  Islet-derived-iPSC02 WGBS paired end data

  Dataset EGAD00001007145

• Reference epigenome Fat-adipocyte03 mRNA-Seq data generated from KEP study

  Fat-adipocyte03 mRNA-Seq paired end data

  Dataset EGAD00001007157

• Reference epigenome Fat-adipocyte05 mRNA-Seq data generated from KEP study

  Fat-adipocyte05 mRNA-Seq paired end data

  Dataset EGAD00001007159

• Reference epigenome Islet-derived-MSC04 WGBS data generated from KEP study

  Islet-derived-MSC04 WGBS paired end data

  Dataset EGAD00001007143

• Swedish schizophrenia control individuals

  Genomic DNA from Swedish control individuals was pooled. Then the genomic sequence of brain expressed miRNA genes was determined in the pools.

  Dataset EGAD00001001850

• Reference epigenome IPS03_N_ENeuron_WGBS data generated from KEP study

  A IPS03_N_ENeuron_WGBS paired end data for Early neuron cells(Tuj1)

  Dataset EGAD00001003475

• Reference epigenome IPS02_N_NPC_WGBS data generated from KEP study

  A IPS02_N_NPC_WGBS paired end data for Neural progenitor cells(Nestin)

  Dataset EGAD00001003474

• Reference epigenome OB57_D_PreA_mRNA-Seq data generated from KEP study

  A OB57_D_PreA_mRNA-Seq paired end data for Preadipocyte(fat)

  Dataset EGAD00001003487

• HipSci - Bardet-Biedl Syndrome - RNA Sequencing - July 2017

  HipSci - Bardet-Biedl Syndrome - RNA Sequencing - July 2017

  Dataset EGAD00001003531

• Reference epigenome CKD25_C_Podo_smRNA-Seq data generated from KEP study

  A CKD25_C_Podo_smRNA-Seq single end data for Podocytes(CD90(-) Podocalyxin(+), kidney)

  Dataset EGAD00001003499

• A98269B

  Whole genome sequencing for single cells for library A98269B 1609 cells; filetype=bam

  Dataset EGAD00001006947

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

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

  Dataset EGAD00001003181

• A96217B

  Whole genome sequencing for single cells for library A96217B 1616 cells; filetype=bam

  Dataset EGAD00001006945

• Illumina HiSeq 2000

  Three files of patients 20, 23 and 25 with WGS done on Illumina HiSeq 2000. For research purpose and authorised user only.

  Dataset EGAD00001003438

• Reference epigenome Islet-derived-MSC01 WGBS data generated from KEP study

  Islet-derived-MSC01 WGBS paired end data

  Dataset EGAD00001007140

• Reference epigenome CKD25_C_Podo_mRNA-Seq data generated from KEP study

  A CKD25_C_Podo_mRNA-Seq paired end data for Podocytes(CD90(-) Podocalyxin(+), kidney)

  Dataset EGAD00001003483

• HipSci - Bardet-Biedl Syndrome - Exome Sequencing - July 2017

  HipSci - Bardet-Biedl Syndrome - Exome Sequencing - July 2017

  Dataset EGAD00001003515

• RNA sequencing data to study "A biobank of patient-derived pediatric braintumor models"

  RNA sequencing data for the PDOX model EPD-613FH

  Dataset EGAD00001003573

• He et al. WGS data

  This dataset are the bam files of WGS data from the paper by He et al.

  Dataset EGAD00001007133

• Liquid Biopsy by NGS show differences in CRC stage

  Exome sequencing from cfDNA blood samples. 30 sets of 2x76 Illumina reads in Fastq format.

  Dataset EGAD00001004307

• Pancreatic organoid - case samples

  This dataset contains 31 pancreatic organoid samples used in the 'organoid data of pancreatic cancers ' study

  Dataset EGAD00001004528

• Reference epigenome SMC05 h3k9me3 ChIP-Seq data generated from KEP study

  SMC05 h3k9me3 ChIP-Seq paired end data

  Dataset EGAD00001007336

• HIPO blastemal Wilms (nephroblastoma) RNA sequencing samples

  HIPO blastemal Wilms (nephroblastoma) characterisation of tumor driving gene expression events

  Dataset EGAD00001000993

• Targeted deep sequencing of somatic mutations

  We used targeted deep sequencing to accurately establish the allele frequencies of the mutations identified by exome sequencing

  Dataset EGAD00001000763

• Reference epigenome Islet-derived-MSC02 WGBS data generated from KEP study

  Islet-derived-MSC02 WGBS paired end data

  Dataset EGAD00001007141

• SFHS pedigrees

  Deep (>25x mean coverage) whole genome sequencing on 5-10 families drawn from the Scottish Family Health Study with four or more children.

  Dataset EGAD00001001214

• sWGS of non-cancer controls

  Paired end shallow whole genome sequencing (sWGS) data of cell-free DNA from plasma from self-reporting healthy individuals (MonRec Cohort)

  Dataset EGAD00001005805

• WGBS data for Glioblastoma (EGAS00001003953, H016)

  Whole Genome Bisulfite data for human glioblastoma patients, EGAS00001003953. 68 human samples

  Dataset EGAD00001006546

• McGill EMC Release 4 in tissue "Brodmann (1909) area 44"

  McGill EMC Release 4 in tissue "Brodmann (1909) area 44"

  Dataset EGAD00001001285

• scRNA primaries

  Single cell RNA-seq for primary samples

  Dataset EGAD00001006135

• HipSci - Healthy Normals - Exome Sequencing - April 2015

  HipSci - Healthy Normals - Exome Sequencing - April 2015

  Dataset EGAD00001001437

• Reference epigenome Pancreas-Islet07 mRNA-Seq data generated from KEP study

  Pancreas-Islet07 mRNA-Seq paired end data

  Dataset EGAD00001007167

• Reference epigenome CKD24_C_Podo_mRNA-Seq data generated from KEP study

  A CKD24_C_Podo_mRNA-Seq paired end data for Podocytes(CD90(-) Podocalyxin(+), kidney)

  Dataset EGAD00001003482

• Genentech gastric tumor sequencing

  Exome-seq, RNA-Seq, SNP array profiling of gastric tumor samples.

  Dataset EGAD00001000815

• PACA-CA RNASeq fastq files

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

  Dataset EGAD00001003972

• Reference epigenome OB57_D_PreA_smRNA-Seq data generated from KEP study

  A OB57_D_PreA_smRNA-Seq single end data for Preadipocyte(fat)

  Dataset EGAD00001003496

• STREP GENE Study Genome-wide Genotyping by Illumina Array

  Genotyping of 43 cases of invasive GAS infection by Illumina HumanCore-24 array and Illumina Global Screening Array.

  Dataset EGAD00001004558

• Reference epigenome Pancreas-Islet06 mRNA-Seq data generated from KEP study

  Pancreas-Islet06 mRNA-Seq paired end data

  Dataset EGAD00001007166

• Reference epigenome SMC01 h3k4me3 ChIP-Seq data generated from KEP study

  SMC01 h3k4me3 ChIP-Seq paired end data

  Dataset EGAD00001007311

• RBWES

  Retinoblastoma is a rare childhood cancer of the retina. We studied retinoblastoma by Whole-Exome-Sequencing.

  Dataset EGAD00001007591

• McGill EMC Release 4 in tissue "Brodmann (1909) area 11"

  McGill EMC Release 4 in tissue "Brodmann (1909) area 11"

  Dataset EGAD00001001284

• RNA-Seq Pair End

  RNA analysis of two patients 11 and 15 with WGS done on Illumina HiSeq2000. For research purpose and authorised user only.

  Dataset EGAD00001003429

• Belgian epilepsy control individuals

  Genomic DNA from Belgian control individuals was pooled. Then the genomic sequence of brain expressed miRNA genes was determined in the pools.

  Dataset EGAD00001001852

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

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

  Dataset EGAD00001003161

• Reference epigenome CKD24_C_Podo_smRNA-Seq data generated from KEP study

  A CKD24_C_Podo_smRNA-Seq single end data for Podocytes(CD90(-) Podocalyxin(+), kidney)

  Dataset EGAD00001003498

• raw fastq file from 10x genomics sequencing

  RNA samples of bone marrow and cord blood were sequenced by 10x genomics platform.

  Dataset EGAD00001004200

• Cancer-associated genome-wide hypomethylation and copy number aberrations

  Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing

  Dataset EGAD00001001093

• Osteosarcoma RNAseq

  We propose to definitively characterise the somatic genetics of Osteosarcoma cancer through generation of comprehensive catalogues of somatic mutations by high coverage genome and transcriptome sequencing.

  Dataset EGAD00001000826

• V2 Colorectal panel test

  Targeted gene screen of cell line tumour samples for testing the new V2 Colorectal gene panel.

  Dataset EGAD00001003253

• ATAC-seq for placental and buffycoat cells.

  We performed ATAC-seq experiments using 2 placental samples and 2 buffycoat samples.

  Dataset EGAD00001004291

• ChIP-Seq files for RMS.

  ChIP-Seq files accompanying the paper titled "Identification of Therapeutic Targets in Rhabdomyosarcoma Through Integrated Genomic, Epigenomic, and Proteomic Analyses".

  Dataset EGAD00001004312

• Amplicon sequencing data from organoids of colorectal cancer patients.

  The dataset includes 13 bam files. Each bam file is a different colorectal cancer patient organoid.

  Dataset EGAD00001004313

• Multiple_myeloma_precursor_genomics

  Whole genome sequencing of up to 45 multiple myeloma precursor samples and matched normals pairs.

  Study EGAS00001006312

• Juvenile Idiopathic Arthritis exome sequencing in a consanguineous family

  Identify the causative gene defect in three affected patients with JIA.

  Study EGAS00001003510

• WES HCC-neuro

  WES data of a HCC with neuroendocrine differentiation (HCC-NED), normal and organoid from a 74-year-old man.

  Dataset EGAD00001008430

• Bolleboom-Gao peri-tumoral snRNA-seq glioblastoma dataset 2022/A

  Bolleboom-Gao peri-tumoral snRNA-seq glioblastoma dataset 2022/A

  Study EGAS00001006935

• Clear cell sarcoma sequencing data

  This study shares DNA and RNA sequencing data from Clear cell sarcoma patients

  Study EGAS00001006072

• Mutational_signatures_and_clonal_dynamics_in_normal_human_tissues

  Somatic mutations (burdens and signatures) and clonal dynamics in normal human tissues

  Study EGAS00001002471

• SCC tumor sequencing

  In this study we have sequenced the tumor of 28 Squamous Cell Carcinoma patients.

  Study EGAS00001003988

• ADAPTeR Study: WES data from ccRCC patients

  ADAPTeR study RNAseq from multi-region samples taken pre and post nivolumab.

  Study EGAS00001005638

• OAC RNASeq

  Please see our related publication, 'Molecular profiling to predict immunochemotherapy outcomes in esophageal adenocarcinoma'

  Study EGAS00001006468

• Whole Genome Sequence and RNASeq Samples for Lung Cancer

  Short Read Whole Genome Sequence and RNASeq Samples for Lung Cancer

  Study EGAS00001007832

• Targeted capture ctDNA Library CRCQV42Run024-16

  Targeted capture ctDNA Library CRCQV42Run024-16 from patient PBC0003641, TNBC FFPE sample

  Dataset EGAD00001010468

• Targeted capture ctDNA Library CRCQV42Run029-5

  Targeted capture ctDNA Library CRCQV42Run029-5 from patient PBC0002533, TNBC FFPE sample

  Dataset EGAD00001010518

• Dataset for B-ALL scRNA-seq

  10x Genomics 5' library scRNA-seq data for 85 B-ALL patients with different subtypes

  Dataset EGAD00001011327

• EV WGS

  WGS

  Dataset EGAD00001008973

• WGS data from a GBM patient PT-MS8478

  WGS data from a GBM patient PT-MS8478

  Dataset EGAD00001008524

• Fecal 16S HV metadata

  Metadata for fecal 16S-V4 rRNA gene sequence data from NCT02749630 healthy volunteers.

  Dataset EGAD00001008821

• Cord blood sequencing data

  SmMIP libraries using cord blood DNA were generated in replicates and were sequenced on the NovaSeq SP platform (Illumina)

  Dataset EGAD00001007789

• Targeted capture ctDNA Library CRCQV42Run025-8

  Targeted capture ctDNA Library CRCQV42Run025-8 from patient PBC0003385, TNBC FFPE sample

  Dataset EGAD00001010486

• Targeted capture ctDNA Library CRCQV42Run026-17

  Targeted capture ctDNA Library CRCQV42Run026-17 from patient PBC0003643, TNBC FFPE sample

  Dataset EGAD00001010490

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

  Islet-derived_MSC06 mRNA-Seq paired end data

  Dataset EGAD00001007878

• CTCF-ChIP-Seq of cohesin-mutated and wildtype adult AMLs

  ChIP-Seq targeting CTCF in cohesin-mutated (STAG2 or RAD21 mutations) and wildtype adult AMLs (CTRL-AMLs).

  Dataset EGAD00001011200

• Targeted capture ctDNA Library CRCQV42Run022-7

  Targeted capture ctDNA Library CRCQV42Run022-7 from patient PBC0002744, TNBC FFPE sample

  Dataset EGAD00001010458

• UCL Lung PCA - Whole exome multiregion sequencing data from human preinvasive airway biopsies

  UCL Lung PCA - Whole exome multiregion sequencing data from human preinvasive airway biopsies

  Dataset EGAD00001015539

• Single-cell RNA-seq cases

  Single-cell RNA-seq cases (Tumor and adjacent tissue)

  Dataset EGAD00001008835

• WGS data from a GBM patient PT-SB3465

  WGS data from a GBM patient PT-SB3465

  Dataset EGAD00001008528

• Targeted capture ctDNA Library CRCQV42Run026-14

  Targeted capture ctDNA Library CRCQV42Run026-14 from patient PBC0003587, TNBC FFPE sample

  Dataset EGAD00001010487

• Targeted capture ctDNA Library CRCQV42Run029-11

  Targeted capture ctDNA Library CRCQV42Run029-11 from patient PBC0001353, TNBC FFPE sample

  Dataset EGAD00001010511

• Finnish - THL Health2000 Dataset

  The dataset encompasses 208 Runs from the WGSPD Project 3 - Genomic Strategies to Identify High-impact Psychiatric Risk Variants Project

  Dataset EGAD00001008684

• Targeted capture ctDNA Library CRCQV42Run026-15

  Targeted capture ctDNA Library CRCQV42Run026-15 from patient PBC0002872, TNBC FFPE sample

  Dataset EGAD00001010488

• CP-NET Cram files

  WGS Cram files from the Childhood Cerebral Palsy Integrated Neuroscience Discovery Network "CP-NET" - Clinical Database Platforms - Phase 3 project.

  Dataset EGAD00001010014

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

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

  Dataset EGAD00001015697

• PRDM13 exome sequencing set

  Exome sequencing study on 4 individuals from a pedigree with CHH and cerebellar hypoplasia.

  Dataset EGAD00001008420

• Treatment arm information and sample sheet

  Table of treatment arm information for the 418 RNAseq evaluable population.

  Dataset EGAD00001009502

• CPC-GENE H3K27ac ChIP-seq

  CPC-GENE H3K27ac ChIP-seq data comprises 48 tumour samples and 6 benign samples sequenced with single end Illumina HiSeq 2000.

  Dataset EGAD00001010296

• Targeted capture ctDNA Library CRCQV42Run024-11

  Targeted capture ctDNA Library CRCQV42Run024-11 from patient PBC0001306, TNBC FFPE sample

  Dataset EGAD00001010465

• Targeted capture ctDNA Library CRCQV42Run025-6

  Targeted capture ctDNA Library CRCQV42Run025-6 from patient PBC0003014, TNBC FFPE sample

  Dataset EGAD00001010484

• H3Africa SIREN Phenotype

  Phenotype data for 3421 Samples from Nigeria and Ghana, sequenced with the Illumina NestSeq 500.

  Dataset EGAD00001011075

• Res1_PC9_exp2_MC_01.04.22

  8 cell pellet samples for genomic DNA extraction. CRISPR PCR1 and PCR2 indexing - Please use standard Kosuke primers.

  Dataset EGAD00001012233

• Res1_PC9_exp1_MC_29.03.22

  8 cell pellet samples for genomic DNA extraction. CRISPR PCR1 and PCR2 indexing - Please use standard Kosuke primers.

  Dataset EGAD00001012232

• KiCS cancer panel academic only data

  This data set contains KiCS cancer panel data for academic and for-profit use.

  Dataset EGAD00001009733

• Targeted capture ctDNA Library CRCQV42Run025-10

  Targeted capture ctDNA Library CRCQV42Run025-10 from patient PBC0001335, TNBC FFPE sample

  Dataset EGAD00001010476

• Optimizing single-cell transcriptomic discrimination of atopic dermatitis versus psoriasis vulgaris

  Optimizing single-cell transcriptomic discrimination of atopic dermatitis versus psoriasis vulgaris

  Dataset EGAD00001011104

• RNA sequencing of ALAL patients

  Transcriptomic data generated by RNA sequencing of 30 adults with acute leukemia of ambiguous lineage (ALAL)

  Dataset EGAD00001015547

• Pilocytic Astrocytoma ICGC PedBrain whole genome sequencing

  Pilocytic Astrocytoma ICGC PedBrain whole genome sequencing

  Dataset EGAD00001000616

• SeqControl

  SeqControl

  Dataset EGAD00001001115

• HipSci - Healthy Normals - Exome Sequencing - January 2016

  HipSci - Healthy Normals - Exome Sequencing - January 2016

  Dataset EGAD00001001932

• NSCCG CRC WES

  1006 Familial early onset gemrline CRC patients sequenced by the Molecular and Population Genetics group of the Institute of Cancer Research

  Dataset EGAD00001002204

• BAP1 sequence of uveal melanoma and mesothelioma samples

  Detection of BAP1 mutations in DNA from uveal melanoma and mesothelioma samples.

  Dataset EGAD00001002229

• Cryptic translocations in double hit signature DLBCL genomes

  18 DLBCL genomes

  Dataset EGAD00001006087

• WES of pcALCL

  Whole-exome sequencing of matched frozen tumor biopsies/granulocytes from patients with primary cutaneous anaplastic large cell lymphoma. 7 paired tumor/germline samples. BGISEQ-500.

  Dataset EGAD00001006177

• EORTC RP1335 SPECTA Lung cancer data - Oncomine

  EORTC RP1335 SPECTA Lung cancer data - Oncomine dataset

  Dataset EGAD00001006594

• WGS of Glioblastoma stem cells (Sachamitr et al)

  WGS of 17 GSC populations derived from patient tumours

  Dataset EGAD00001006848

• Reference epigenome Islet-derived-MSC03 WGBS data generated from KEP study

  Islet-derived-MSC03 WGBS paired end data

  Dataset EGAD00001007142

• Whole Exome Sequencing Fastq PE Files

  Anal SCC cell line and parent tumour comparative whole exome sequencing

  Dataset EGAD00001007001

• Reference epigenome ADMSC05 h3k27me3 ChIP-Seq data generated from KEP study

  ADMSC05 h3k27me3 ChIP-Seq paired end data

  Dataset EGAD00001007375

• SFHS pedigrees_X10

  Deep (>25x mean coverage) whole genome sequencing on 5-10 families drawn from the Scottish Family Health Study with four or more children.

  Dataset EGAD00001003211

• Gabriel Consortium Data Access Committee

  Dac EGAC00000000014

• McGill ECDAC

  Dac EGAC00001000250

• The EMC-HEMA-AML data access committee controlling the access to AML sequencing data generated in the Hematology department of Erasmus MC

  Dac EGAC00001002230

• EGAD00000000057

  WTCCC project samples from the Parkinson's disase cohort

  Dataset EGAD00000000057

• EGAD00010000777

  HipSci - Bardet-Biedl Syndrome - Genotyping Array - November 2014

  Dataset EGAD00010000777

• EGAD00010000779

  HipSci - Monogenic Diabetes - Genotyping Array - November 2014

  Dataset EGAD00010000779

• EGAD00010000268

  Metabric breast cancer samples (Expression raw data)

  Dataset EGAD00010000268

• EGAD00010000522

  Samples from the Greek island of Crete, MANOLIS cohort

  Dataset EGAD00010000522

• Mutational landscapes of primary triple negative breast cancers - RNA seq

  Mutational landscapes of primary triple negative breast cancers - RNA seq

  Dataset EGAD00001000132