22938 results for "ega"

in 19.83 milliseconds.

• dataset_CML_chipseq_pairend_bam

  BMI1 ChIP-seq on human K562

  Dataset EGAD00001002062

• Exome reads

  Exome sequencing for 2 infertile brothers

  Dataset EGAD00001003193

• PPCG UK BAMs

  Pan Prostate Cancer Group UK BAM files

  Dataset EGAD00001006742

• dataset_CML_WGS_pairend_fastq

  dataset CML WGS pairend fastq

  Dataset EGAD00001002057

• dataset_CML_chipseq_pairend_fastq

  BMI1 ChIP-seq on human K562

  Dataset EGAD00001002061

• RNA sequencing reads

  Paired-end, ribosome depleted, total RNA Sequencing

  Dataset EGAD00001004327

• APL nanopore sequencing

  Nanopore sequencing for an APL patient

  Study EGAS00001005618

• Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line WXS

  Study EGAS00001006800

• Characterization of a novel MEF2D-BCL9 fusion positive acute lymphoblastic leukemia cell line RNA-Seq

  Study EGAS00001006802

• CyclomicsSeq_IMCISION_Flongle

  Contains IMCISION samples sequenced on Flongle flowcells

  Dataset EGAD00001010148

• Real_time_ssRNAseq_flow_pilot

  Real time ssRNAseq flow pilot

  Study EGAS00001006304

• Epigenomic profile of diverse cancer

  Epigenomic profile of diverse cancer.

  Study EGAS00001004352

• Paediatric Tumour Profiling

  Paediatric Tumour Profiling

  Study EGAS00001003437

• HCA_Heart_Adult_Wellcome_DNA

  Human Cell Atlas - WGS Adult Heart

  Study EGAS00001006359

• Genome sequencing in monozygotic twins discordant for Mayer-Rokitansky-Küster-Hauser syndrome

  Study EGAS00001006371

• Finnish - THL Finrisk

  Includes: Finnish -THL Finrisk

  Dataset EGAD00001008580

• ssCNV

  single cell DNA sequencing

  Dataset EGAD00001008997

• SF10328

  Unknown

  Dataset EGAD00001008303

• Lifelines-CH: processed somatic variant calls

  Processed somatic variant calls

  Dataset EGAD00001010144

• Revision Experiments UMI

  Revision Experiments UMI

  Dataset EGAD00001010310

• CyclomicsSeq_Healthy_Flongle

  Contains Healthy samples sequenced on Flongle flowcells

  Dataset EGAD00001010150

• Sample sheet

  Linking anonymized sample IDs and anonymized patient IDs.

  Dataset EGAD00001011166

• Möebius

  Exome sequencing in 3 Möbius patients

  Dataset EGAD00001001385

• Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia

  Abstract in preparation

  Study EGAS00001001315

• Integration of intra-sample contextual error modeling for improved detection of somatic mutations

  Study EGAS00001003806

• Genetic landscape of pediatric ETV6-RUNX1 acute lymphoblastic leukemia

  Abstract in preparation

  Study EGAS00001001314

• Genetic landscape of pediatric high hyperdiploid acute lymphoblastic leukemia

  Abstract in preparation

  Study EGAS00001001316

• Cologne University Hospital, Institute of Human Genetics, Pathomechanisms of Rare Kidney Diseases Research Group DAC

  Dac EGAC00001003295

• IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" Italian Cancer Center Data Access Committee

  Dac EGAC00001003223

• IRCCS Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori" Italian Cancer Center Data Access Committee

  Dac EGAC00001003227

• St. Jude Children’s Research Hospital – Washington University Pediatric Cancer Genome Project Steering Committee

  Dac EGAC00001000045

• Sequencing component for the whole genome methylation analysis in PBMCs and cell subset pilot study DAC

  Dac EGAC00001000096

• DEEP (Deutsches Epigenom Programm) DAC

  Dac EGAC00001000179

• Department of Pathology and Tumor Biology, Kyoto University Data Access Committee

  Dac EGAC00001000352

• The EMC-NICHE DAC considers appeals for hematopoietic/niche-related data sets.

  Dac EGAC00001000537

• Data access policy for PDTX Breast Cancer data from Bruna et al (2016), Cell.

  Dac EGAC00001000540

• CIR-RIMLS committee on data access to Immunological mechanisms for celiac disease database

  Dac EGAC00001000557

• MSKCC Medical Donation Program Data Access Committee

  Dac EGAC00001000588

• Data access committee for the pseudomyxoma peritonei exome sequencing vcf-files

  Dac EGAC00001000649

• DAC for "A Functional Network of Gastric-Cancer-Associated Splicing Events Controlled by Dysregulated Splicing Factors"

  Dac EGAC00001000675

• DAC for Hungarian human exome team (Department of Medical Biology, University of Szeged, Hungary)

  Dac EGAC00001000838

• Data access committee handling data access requests for biomarker data from the clinical trial IMvigor210.

  Dac EGAC00001000945

• Mutated H3 Histones Drive Human Pre-Leukemic Hematopoietic Stem Cell Expansion And Promote Leukemic Aggressiveness.

  Dac EGAC00001001054

• DAC for study: "Circulating tumour DNA abundance and potential utility in de novo metastatic prostate cancer"

  Dac EGAC00001001099

• Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases

  Dac EGAC00001001138

• Control iPSC lines with clinically annotated genetic variants for versatile multi-lineage differentiation Committee (part II)

  Dac EGAC00001001332

• Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays

  Dac EGAC00001001387

• The University of Hong Kong Colon Cancer Organoids Genomics Study Data Access Committee

  Dac EGAC00001001405

• Cologne University Hospital, Institute of Human Genetics, Pathomechanisms of Rare Kidney Diseases Research Group DAC

  Dac EGAC00001001549

• Data Access Committee - cfDNA fragmentation and personalized sequencing reveal ctDNA in urine and plasma of glioma patients

  Dac EGAC00001001593