22951 results for "ega"

in 23.23 milliseconds.

• Targeted capture ctDNA Library CRCQV42Run041-4

  Targeted capture ctDNA Library CRCQV42Run041-4 from patient PBC0001375, plasma 3 month sample

  Dataset EGAD00001010634

• 16p11.2 DA neurons

  16p11.2 CNV iPSC derived dopaminergic neuron transcriptional gene expression data.

  Dataset EGAD00001007072

• Targeted capture ctDNA Library CRCQV42Run017-20

  Targeted capture ctDNA Library CRCQV42Run017-20 from patient PBC0001051, plasma 18 month sample

  Dataset EGAD00001010412

• OT2_Solid_WXS_T

  Whole-exome sequencing on AB 5500xl Genetic Analyzer of colorectal cancer primary tumor sample (OT2_cohort)

  Dataset EGAD00001003386

• Reference epigenome SMC01 mRNA-Seq data generated from KEP study

  SMC01 mRNA-Seq paired end data

  Dataset EGAD00001007169

• Reference epigenome SMC02 mRNA-Seq data generated from KEP study

  SMC02 mRNA-Seq paired end data

  Dataset EGAD00001007170

• Reference epigenome SMC04 mRNA-Seq data generated from KEP study

  SMC04 mRNA-Seq paired end data

  Dataset EGAD00001007172

• Prostate cancer datasets WES

  WES: 48 samples (5 blood samples from 6 patient data): 22 Tumour cores and 26 normal/benign cores (HiSeq)

  Dataset EGAD00001004467

• DIPG_ICR_WGS

  Whole genome sequencing of 20 tumour and normal pairs of diffuse intrinsic pontine glioma (DIPG)

  Dataset EGAD00001000705

• Whole genome sequencing data

  Whole genome sequencing reads consisting of paired end Fastq and aligned bam files from pediatric medulloblastoma samples.

  Dataset EGAD00001004115

• Whole genome sequences of hepatocellular carcinoma (NCCRI)

  Fastq files of 213 samples of hepatocellular carcinoma (NCCRI)

  Dataset EGAD00001000446

• Carcinoid study - RNASeq dataset

  Fernandez-Cuesta et al, 2014, Nature Communication, RNA Sequencing data set

  Dataset EGAD00001000795

• HCC.GNE exome dataset

  Exome read sequences for 30 tumor-normal pairs for the study "Diverse modes of genomic alterations in Hepatocellular Carcinoma".

  Dataset EGAD00001000885

• WGS of 8 trios - affected child and both normal parents

  WGS of 8 trios - affected child and both normal parents

  Dataset EGAD00001001467

• WGS of IP-DLBCLs

  This data set includes bam files of WGS of 36 paired lymphomas in immune-privileged sites and normal controls.

  Dataset EGAD00001007753

• RNASeq files for Roussel-MBPRG

  RNASeq files for Roussel-MPBRG paper titled "Combination of ribociclib and gemcitabine for the treatment of medulloblastoma"

  Dataset EGAD00001008824

• Targeted capture ctDNA Library CRCQV42Run043-23

  Targeted capture ctDNA Library CRCQV42Run043-23 from patient PBC0002480, plasma 3 month sample

  Dataset EGAD00001010652

• Targeted capture ctDNA Library CRCQV42Run043-5

  Targeted capture ctDNA Library CRCQV42Run043-5 from patient PBC0001516, plasma 15 month sample

  Dataset EGAD00001010655

• Reference epigenome Islet-derived-iPSC04 WGBS data generated from KEP study

  Islet-derived_iPSC04 WGBS paired end data

  Dataset EGAD00001007877

• Germline variant analysis in childhood AML

  This dataset contains one vcf file with variants from whole exome sequencing of 24 paediatric AML samples at diagnosis.

  Dataset EGAD00001008783

• Targeted capture ctDNA Library CRCQV42Run043-24

  Targeted capture ctDNA Library CRCQV42Run043-24 from patient PBC0002329, plasma 3 month sample

  Dataset EGAD00001010653

• Targeted capture ctDNA Library CRCQV42Run046-6

  Targeted capture ctDNA Library CRCQV42Run046-6 from patient PBC0001666, plasma 3 month sample

  Dataset EGAD00001010718

• Follicular T cell lymphoma

  Paired-end RNA-seq of follicular T cell lymphoma for the discovery of fusion transcripts

  Dataset EGAD00001006379

• Whole genome sequencing data of 20 carcinosarcomas.

  Whole genome sequencing data of 20 carcinosarcomas.

  Dataset EGAD00001003163

• Genentech gallbladder cancer study - whole genome sequencing

  Genentech gallbladder cancer study - whole genome sequencing

  Dataset EGAD00001004855

• RNAseq BAM files

  RNAseq BAM files for Coding and non-coding mantle cell lymphoma driver mutations

  Dataset EGAD00001006268

• Targeted capture ctDNA Library CRCQV42Run017-9

  Targeted capture ctDNA Library CRCQV42Run017-9 from patient PBC0001255, plasma 18 month sample

  Dataset EGAD00001010416

• Dataset of whole-genome sequencing of primary mediastinal B-cell lymphomas.

  Bam files of whole-genome sequencing of 14 paired PMBCL samples.

  Dataset EGAD00001009078

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

  Variants called from RNA-seq data of meningioma tumors.

  Dataset EGAD00001002649

• Targeted capture ctDNA Library CRCQV34Run015-14

  Targeted capture ctDNA Library CRCQV34Run015-14 from patient PBC0002595, plasma 6 month sample

  Dataset EGAD00001010380

• Targeted capture ctDNA Library CRCQV42Run017-18

  Targeted capture ctDNA Library CRCQV42Run017-18 from patient PBC0002294, plasma 12 month sample

  Dataset EGAD00001010410

• Targeted capture ctDNA Library CRCQV42Run017-17

  Targeted capture ctDNA Library CRCQV42Run017-17 from patient PBC0002062, plasma 6 month sample

  Dataset EGAD00001010409

• Targeted capture ctDNA Library CRCQV42Run026-18

  Targeted capture ctDNA Library CRCQV42Run026-18 from patient PBC0001299, plasma baseline repeat sample

  Dataset EGAD00001010491

• Targeted capture ctDNA Library CRCQV42Run028-10

  Targeted capture ctDNA Library CRCQV42Run028-10 from patient PBC0003587, plasma baseline sample

  Dataset EGAD00001010500