22950 results for "ega"

in 23.03 milliseconds.

• FFPE Normal Panel V3 Cancer Panel

  FFPE normal panel generation for use with V3 cancer panel 0618521

  Dataset EGAD00001001122

• Cloning of the breakpoint of a novel translocation associated with T-acute lymphoblastic leukaemia

  Single case of T-ALL carrying t(4;6), a novel translocation.

  Dataset EGAD00001002193

• WXS files for Zhang PanNBL

  WXS files for Zhang PanNBL paper titled "Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations"

  Dataset EGAD00001005484

• 108 samples liver cancer and normal controls (54 pairs), whole exome sequencing

  liver cancer paired with normal controls, viral and non-viral origin

  Dataset EGAD00001006005

• RNAseq

  This dataset contains RNAseq performed on 35 human acute erythroid leukemia patient samples and Xenografts.

  Dataset EGAD00001006076

• Additional Neuroblastoma whole genome sequencing data

  Additional Neuroblastoma whole genome sequencing data

  Dataset EGAD00001006196

• Single Cell RNAseq of PBMC from renal cancer patients

  Single Cell RNAseq of PBMC from renal cancer patients

  Dataset EGAD00001006175

• GRIDSS somatic sv vcfs for EGAS00001004572

  Bulk GRIDSS somatic sv vcfs from tumour-normal analysis in EGAS00001004572

  Dataset EGAD00001006906

• Strelka somatic snv vcfs for EGAS00001004572

  Bulk Strelka somatic snv vcfs from tumour-normal analysis in EGAS00001004572

  Dataset EGAD00001006907

• Ovarian cancer EV RNA-seq

  Ovarian cancer EV RNA-seq

  Dataset EGAD00001008972

• Targeted capture ctDNA Library CRCQV34Run002-10

  Targeted capture ctDNA Library CRCQV34Run002-10 from patient PBC0002108, plasma baseline sample

  Dataset EGAD00001010327

• Targeted capture ctDNA Library CRCQV34Run002-11

  Targeted capture ctDNA Library CRCQV34Run002-11 from patient PBC0002429, plasma baseline sample

  Dataset EGAD00001010328

• Targeted capture ctDNA Library CRCQV34Run002-12

  Targeted capture ctDNA Library CRCQV34Run002-12 from patient PBC0002459, plasma baseline sample

  Dataset EGAD00001010329

• Targeted capture ctDNA Library CRCQV34Run002-13

  Targeted capture ctDNA Library CRCQV34Run002-13 from patient PBC0002595, plasma baseline sample

  Dataset EGAD00001010330

• Targeted capture ctDNA Library CRCQV34Run002-6

  Targeted capture ctDNA Library CRCQV34Run002-6 from patient PBC0001627, plasma baseline sample

  Dataset EGAD00001010339

• Targeted capture ctDNA Library CRCQV34Run007-22

  Targeted capture ctDNA Library CRCQV34Run007-22 from patient PBC0002816, buffy coat sample

  Dataset EGAD00001010359

• Targeted capture ctDNA Library CRCQV42Run016-11

  Targeted capture ctDNA Library CRCQV42Run016-11 from patient PBC0001467, plasma baseline sample

  Dataset EGAD00001010399

• Targeted capture ctDNA Library CRCQV42Run021-13

  Targeted capture ctDNA Library CRCQV42Run021-13 from patient PBC0001299, plasma baseline sample

  Dataset EGAD00001010436

• Targeted capture ctDNA Library CRCQV42Run026-4

  Targeted capture ctDNA Library CRCQV42Run026-4 from patient PBC0002872, plasma baseline sample

  Dataset EGAD00001010496

• Targeted capture ctDNA Library CRCQV42Run029-23

  Targeted capture ctDNA Library CRCQV42Run029-23 from patient PBC0004350, plasma baseline sample

  Dataset EGAD00001010516

• Targeted capture ctDNA Library CRCQV42Run033-13

  Targeted capture ctDNA Library CRCQV42Run033-13 from patient PBC0002429, buffy coat sample

  Dataset EGAD00001010552

• Targeted capture ctDNA Library CRCQV42Run033-14

  Targeted capture ctDNA Library CRCQV42Run033-14 from patient PBC0002459, buffy coat sample

  Dataset EGAD00001010553

• Targeted capture ctDNA Library CRCQV42Run034-14

  Targeted capture ctDNA Library CRCQV42Run034-14 from patient PBC0004414, buffy coat sample

  Dataset EGAD00001010568

• 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