23091 results for "ega"

in 22.23 milliseconds.

• ACUITI BAM files

  This dataset contains WES bam/bai files associated with 51 patients as part of the ACUITI Study

  Dataset EGAD50000001401

• Clonal IGHV rearrangements in IGH+ and IGHUND HGBCL-DH-BCL2(-BCL6)

  PCR-based VDJ profiling in IGH+ and IGHUND HGBCL-DH-BCL2(-BCL6) lymphomas

  Dataset EGAD50000001523

• WGS Sequencing of Urothelial Carcinoma from Taiwan

  Normal and Tumor paired WGS sequencing of UC Tissues

  Dataset EGAD50000001547

• RNAseq for CIAO Clinical Trial

  RNAseq (QuantSeq) from FFPE tissues for the CIAO clinical trial

  Dataset EGAD50000001676

• Dutch - BP

  The dataset encompasses 1110 Runs from the WGSPD Project 3 - Genomic Strategies to Identify High-impact Psychiatric Risk Variants Project

  Dataset EGAD50000001738

• Dutch - SCZ

  The dataset encompasses 804 Runs from the WGSPD Project 3 - Genomic Strategies to Identify High-impact Psychiatric Risk Variants Project

  Dataset EGAD50000001739

• germline pathogenic variants found in African patients of prostate cancer

  70 new blood samples added in this project

  Study EGAS50000001132

• Papua New Guinea Pangenome Project Data Access Policy

  This data policy applies to data access to the PNG15 and PNG16 sequencing data as well as derived genomic variant calls.

  Dac EGAC50000000674

• ERDERA Diagnostic Research Workstream DAC

  The ERDERA Diagnostic Research Workstream DAC decides on data access requests according to the principles defined in the ERDERA Data Sharing Framework Agreement.

  Dac EGAC50000000728

• CD4 auto-antigens

  The CD4 auto-antigen Access Committee (DAC) manages and oversees data access, ensuring compliance with ethical and regulatory guidelines while facilitating secure sharing with authorized researchers.

  Dac EGAC50000000864

• PacBio long-read scRNA-seq

  Full-length single-cell cDNA PacBio Kinnex whole-transcriptome sequencing data for adrenal sampleA and sampleB.

  Dataset EGAD50000002211

• Chun Lab DAC

  Data Access Committee (DAC) for datasets produced by the Chun Lab @ Sanford Burnham Prebys Medical Discovery Institute in La Jolla, California.

  Dac EGAC50000000011

• 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_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008281

• Aneuploidy_and_human_development

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

  Study EGAS00001005267

• Bulk_RNA_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008282

• 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 EGAS00001008283

• ICGC medulloblastoma whole genome sequencing data, ICGC release 16

  ICGC medulloblastoma whole genome sequencing data, ICGC release 16

  Study EGAS00001000744

• Whole_genome_sequencing_of_Crohn_s_disease_patients

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

  Study EGAS00001000065

• Wilms_Tumour_organoid_sequencing_WGS

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

  Study EGAS00001002692

• The_mutational_landscape_of_recurrent_Glioblastome_multiforme

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

  Study EGAS00001001764

• 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

• Placental_genomics

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

  Study EGAS00001003297

• Targeted capture ctDNA Library CRCQV42Run050-24

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

  Dataset EGAD00001010797

• Targeted capture ctDNA Library CRCQV42Run048-9

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

  Dataset EGAD00001010762

• Targeted capture ctDNA Library CRCQV42Run049-11

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

  Dataset EGAD00001010764

• Single_cell_ATAC_sequencing_of_rhabdomyosarcoma_tumour_tissue

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

  Study EGAS00001008279

• Targeted capture ctDNA Library CRCQV42Run047-19

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

  Dataset EGAD00001010731

• 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

• RNASeq files for GenomePaint paper

  RNASeq files for GenomePaint paper titled "Exploration of coding and non-coding variants in cancer using GenomePaint."

  Dataset EGAD00001006680

• 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

• WES sequencing of TRACERx NSCLC patient-derived xenograft models

  WES sequencing of TRACERx NSCLC patient-derived xenograft models

  Study EGAS00001007364

• 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

• Targeted capture ctDNA Library CRCQV42Run048-18

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

  Dataset EGAD00001010750

• 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

• Targeted capture ctDNA Library CRCQV42Run050-16

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

  Dataset EGAD00001010789

• Infant HGG WES

  Whole exome sequencing of infant high grade gliomas. BAM files of paired end reads aligned to GRCh37 with bwa

  Dataset EGAD00001005247

• Targeted capture ctDNA Library CRCQV42Run049-6

  Targeted capture ctDNA Library CRCQV42Run049-6 from patient PBC0005013, buffy coat sample

  Dataset EGAD00001010779