22938 results for "ega"

in 32.34 milliseconds.

• 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

• WES sequencing of TRACERx NSCLC patient-derived xenograft models

  WES sequencing of TRACERx NSCLC patient-derived xenograft models

  Study EGAS00001007364

• Reference epigenome Islet-derived_MSC06 h3k27ac ChIP-Seq data generated from KEP study

  Islet-derived_MSC06 h3k27ac ChIP-Seq paired end data

  Dataset EGAD00001007895

• Reference epigenome Islet-derived_MSC06 h3k9me3 ChIP-Seq data generated from KEP study

  Islet-derived_MSC06 h3k9me3 ChIP-Seq paired end data

  Dataset EGAD00001007900

• Targeted capture ctDNA Library CRCQV42Run021-15

  Targeted capture ctDNA Library CRCQV42Run021-15 from patient PBC0001323, plasma baseline sample

  Dataset EGAD00001010437

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

  Islet-derived_MSC06 input ChIP-Seq paired end data

  Dataset EGAD00001007901

• Reference epigenome Islet-derived_MSC06 h3k4me3 ChIP-Seq data generated from KEP study

  Islet-derived_MSC06 h3k4me3 ChIP-Seq paired end data

  Dataset EGAD00001007899

• Reference epigenome Islet-derived_MSC08 h3k27ac ChIP-Seq data generated from KEP study

  Islet-derived_MSC08 h3k27ac ChIP-Seq paired end data

  Dataset EGAD00001007902

• 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

• Targeted capture ctDNA Library CRCQV42Run048-9

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

  Dataset EGAD00001010762

• Bulk_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008278

• Targeted capture ctDNA Library CRCQV42Run049-11

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

  Dataset EGAD00001010764

• Targeted capture ctDNA Library CRCQV42Run048-18

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

  Dataset EGAD00001010750

• Targeted capture ctDNA Library CRCQV42Run050-16

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

  Dataset EGAD00001010789

• Targeted capture ctDNA Library CRCQV42Run050-22

  Targeted capture ctDNA Library CRCQV42Run050-22 from patient PBC0001486, buffy coat sample

  Dataset EGAD00001010795

• Targeted capture ctDNA Library CRCQV42Run033-10

  Targeted capture ctDNA Library CRCQV42Run033-10 from patient PBC0002255, buffy coat sample

  Dataset EGAD00001010549

• 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

• Targeted capture ctDNA Library CRCQV42Run050-24

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

  Dataset EGAD00001010797

• 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 CRCQV42Run043-18

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

  Dataset EGAD00001010647

• Targeted capture ctDNA Library CRCQV34Run011-11

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

  Dataset EGAD00001010365

• Targeted capture ctDNA Library CRCQV42Run033-6

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

  Dataset EGAD00001010562

• Targeted capture ctDNA Library CRCQV42Run033-5

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

  Dataset EGAD00001010561

• Targeted capture ctDNA Library CRCQV42Run033-22

  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 CRCQV42Run034-10

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

  Dataset EGAD00001010565

• Targeted capture ctDNA Library CRCQV42Run039-9

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

  Dataset EGAD00001010625

• Targeted capture ctDNA Library CRCQV42Run044-21

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

  Dataset EGAD00001010671

• Targeted capture ctDNA Library CRCQV42Run047-19

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

  Dataset EGAD00001010731

• Targeted capture ctDNA Library CRCQV42Run046-15

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

  Dataset EGAD00001010706

• Targeted capture ctDNA Library CRCQV42Run046-17

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

  Dataset EGAD00001010708

• 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 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 CRCQV42Run051-17

  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

• Targeted capture ctDNA Library CRCQV42Run051-16

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

  Dataset EGAD00001010810

• Targeted capture ctDNA Library CRCQV42Run051-21

  Targeted capture ctDNA Library CRCQV42Run051-21 from patient PBC0001665, buffy coat sample

  Dataset EGAD00001010814

• WGS data of multiple myeloma patients

  48 samples of individuals with rare germline variants in familial multiple myeloma, whole genome sequencing

  Dataset EGAD00001007747

• Reference epigenome Islet-derived_MSC06 h3k36me3 ChIP-Seq data generated from KEP study

  Islet-derived_MSC06 h3k36me3 ChIP-Seq paired end data

  Dataset EGAD00001007897

• Targeted capture ctDNA Library CRCQV42Run030-15

  Targeted capture ctDNA Library CRCQV42Run030-15 from patient PBC0003014, buffy coat sample

  Dataset EGAD00001010521

• Targeted capture ctDNA Library CRCQV42Run031-14

  Targeted capture ctDNA Library CRCQV42Run031-14 from patient PBC0001310, buffy coat sample

  Dataset EGAD00001010528

• Targeted capture ctDNA Library CRCQV42Run033-11

  Targeted capture ctDNA Library CRCQV42Run033-11 from patient PBC0002294, buffy coat sample

  Dataset EGAD00001010550

• Single-cell RNA-seq data of angioimmunoblastic T-cell lymphoma

  Single-cell RNA-seq data of angioimmunoblastic T-cell lymphoma

  Dataset EGAD00001011361

• Targeted capture ctDNA Library CRCQV42Run019-12

  Targeted capture ctDNA Library CRCQV42Run019-12 from patient PBC0001295, plasma baseline sample

  Dataset EGAD00001010419