22951 results for "ega"

in 20.83 milliseconds.

• Targeted capture ctDNA Library CRCQV42Run039-6

  Targeted capture ctDNA Library CRCQV42Run039-6 from patient PBC0002853, plasma baseline sample

  Dataset EGAD00001010622

• Targeted capture ctDNA Library CRCQV42Run039-8

  Targeted capture ctDNA Library CRCQV42Run039-8 from patient PBC0003334, plasma baseline sample

  Dataset EGAD00001010624

• Targeted capture ctDNA Library CRCQV42Run047-6

  Targeted capture ctDNA Library CRCQV42Run047-6 from patient PBC0001255, buffy coat sample

  Dataset EGAD00001010738

• Targeted capture ctDNA Library CRCQV42Run048-24

  Targeted capture ctDNA Library CRCQV42Run048-24 from patient PBC0005531, buffy coat sample

  Dataset EGAD00001010756

• Targeted capture ctDNA Library CRCQV42Run049-22

  Targeted capture ctDNA Library CRCQV42Run049-22 from patient PBC0002481, buffy coat sample

  Dataset EGAD00001010775

• Targeted capture ctDNA Library CRCQV42Run049-23

  Targeted capture ctDNA Library CRCQV42Run049-23 from patient PBC0001409, buffy coat sample

  Dataset EGAD00001010776

• Targeted capture ctDNA Library CRCQV42Run049-4

  Targeted capture ctDNA Library CRCQV42Run049-4 from patient PBC0004537, buffy coat sample

  Dataset EGAD00001010777

• Targeted capture ctDNA Library CRCQV42Run050-19

  Targeted capture ctDNA Library CRCQV42Run050-19 from patient PBC0001527, buffy coat sample

  Dataset EGAD00001010792

• Targeted capture ctDNA Library CRCQV42Run051-19

  Targeted capture ctDNA Library CRCQV42Run051-19 from patient PBC0002294, buffy coat sample

  Dataset EGAD00001010812

• SNF_RNAseq_CD138n_20f

  TPM matrices of counts from RNA sequencing (RNAseq) from baseline CD138(–) BM fractions.

  Dataset EGAD00001011142

• RNA-Seq files for SJOS study

  RNA-Seq files for SJOS study

  Dataset EGAD00001003154

• Whole_genome_sequencing_of_Crohn_s_disease_patients

  Population based sequencing of whole genomes of Crohn's disease patients.

  Study EGAS00001000065

• The_mutational_landscape_of_recurrent_Glioblastome_multiforme

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

  Study EGAS00001001764

• ICGC medulloblastoma whole genome sequencing data, ICGC release 16

  ICGC medulloblastoma whole genome sequencing data, ICGC release 16

  Study EGAS00001000744

• Wilms_Tumour_organoid_sequencing_WGS

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

  Study EGAS00001002692

• 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

• Single_cell_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008281

• Bulk_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008282

• Single_cell_ATAC_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008283

• Placental_genomics

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

  Study EGAS00001003297

• Aneuploidy_and_human_development

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

  Study EGAS00001005267

• 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

• 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 EGAS00001008279

• Whole_Genome_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008280

• WES sequencing of TRACERx NSCLC patient-derived xenograft models

  WES sequencing of TRACERx NSCLC patient-derived xenograft models

  Study EGAS00001007364

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

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

  Dataset EGAD00001011361

• Single-cell multiomics reveals the interplay of clonal evolution and cellular plasticity in hepatoblastoma

  spatial transcriptomics

  Dataset EGAD00001015262

• Bulk RNA-seq osteosarcoma

  We profiled 23 patient osteosarcoma tumor samples by bulk RNA-seq. The raw fastqs are provided.

  Dataset EGAD00001011371

• STAG1 and STAG2-ChIP-seq in RAD21-mutant adult acute myeloid leukemia

  STAG1 and STAG2-ChIP-seq in RAD21-mutant adult acute myeloid leukemia

  Dataset EGAD00001015361

• GenomeEUtwin Data Access Committee

  Access to data generated by the GenomeEUtwin is available by emailing application to the data access committee and will be granted to qualified investigators for appropriate use.

  Dac EGAC00000000007