22950 results for "ega"

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• 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

• 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

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

  RNA sequencing data for the PDOX model EPD-613FH

  Dataset EGAD00001003573

• Targeted capture ctDNA Library CRCQV42Run022-7

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

  Dataset EGAD00001010458

• WES HCC-neuro

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

  Dataset EGAD00001008430

• 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

• ChIP-Seq files for PCGP ATRX study

  ChIP-Seq files for PCGP ATRX study paper titled "MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma"

  Dataset EGAD00001004429

• 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

• 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

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

  Islet-derived-MSC02 WGBS paired end data

  Dataset EGAD00001007141

• Single-cell RNA-seq cases

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

  Dataset EGAD00001008835

• 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

• WGS data from a GBM patient PT-SB3465

  WGS data from a GBM patient PT-SB3465

  Dataset EGAD00001008528

• 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

• 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

• 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

• Targeted capture ctDNA Library CRCQV42Run026-15

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

  Dataset EGAD00001010488

• PACA-CA RNASeq fastq files

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

  Dataset EGAD00001003972

• 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 OB57_D_PreA_smRNA-Seq data generated from KEP study

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

  Dataset EGAD00001003496

• 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

• 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

• PRDM13 exome sequencing set

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

  Dataset EGAD00001008420

• 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

• 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

• 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

• 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

• 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

• 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