23249 results for "ega"

in 30.17 milliseconds.

• Targeted nanopore sequencing of MARCHF6 repeat expansions

  This dataset includes FASTQ files from MARCHF6 alleles sequenced by targeted nanopore in 8 patients.

  Dataset EGAD50000000812

• Exonic Counts

  Read counts, per gene, aligning to exons. Alignment performed with GSNAP. 20 samples.

  Dataset EGAD50000000820

• PDiamond Korean Lung Cancer Data

  WES and RNA-seq data of PDiamond Korean lung cancer data

  Dataset EGAD50000000844

• Foundation Medicine Binary Calls

  Binary calls for all available samples in 4 Atezo trials.

  Dataset EGAD50000000709

• Whole Exome Sequencing data from Neodurvarib Clinical Trial

  Sequencing data related to the genomic profiling of advanced urotelial carcinomas, including tissues from pre and postneoadyuvancy (Olaparib and Durvalumab)

  Dac EGAC50000000471

• Picuris Pueblo Genomic Project (Modern Data)

  Data Access Committee for the present-day dataset of the project "Picuris Pueblo oral history and genomics reveal continuity in US Southwest".

  Dac EGAC50000000526

• Neurodevelopment_Nantes_hospital

  The neurodevelopmental team in the genetics unit of Nantes hospital focus on the identification on new genes causing neurodevelopmental disorders through whole-genome and transcriptomics sequencing.

  Dac EGAC50000000542

• DNABR

  Genome variation data for 2723 Brazilian individuals from the DNA do Brasil Project.

  Dataset EGAD50000001012

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

  Dataset EGAD00001010049

• WGS data from MTB-Guided Targeted Treatments paper

  WGS data from biliary tract cancer samples (Beaudry et al, 2025; n=55)

  Dataset EGAD50000001418

• DAC for DRS peripheral blood, University Medical Center Johannes Gutenberg University Mainz

  This DAC is in relation to the DRS samples of peripheral blood of healthy control

  Dac EGAC50000000667

• WGSPD Project 3 UCLA DAC

  Data Access Committee to review applications to access Whole Genome Sequencing in Psychiatric Disorders (WGSPD) Project 3 data (WGS) from Dutch cohorts.

  Dac EGAC50000000442

• University Clinic Golnik DAC

  DAC of the University Clinic Golnik, that will decide regarding the requests for data submitted on behalf of research groups of the Clinic

  Dac EGAC50000000820

• WES of bladder tumors from 24 patients

  This dataset contains 144 files fastq files sequenced with Illumina HiSeqX.

  Dataset EGAD50000001775

• WGS_TALL_t_14_16_translocation

  WGS data for patients with t(14;16) translocated T-ALL.

  Dataset EGAD50000001782

• NANOPORE_TALL_t_14_16_translocation

  Nanopore sequencing for patients with t(14;16) translocated T-ALL

  Dataset EGAD50000001785

• U12 Spliceosome Defect Data Access Committee

  This Data Access Committee controls access to data pertaining to the study of the minor spliceosome and it's role in monogenic diabetes.

  Dac EGAC50000000892

• RNAseq of fibroblasts

  RNA sequencing data of fibroblasts from 3 controls and 3 patients with RBMX variants.

  Dataset EGAD50000002371

• Dnase1l3 knockout causes aberrations in plasma DNA fragmentation

  Dnase1l3 knockout causes aberrations in plasma DNA fragmentation

  Study EGAS00001003174

• Wilm's tumor sequencing data

  This study shares DNA and RNA sequencing data from Wilm's tumor patients

  Study EGAS00001005690

• HCA_Skin_Disease_WSSS_Spatial_NCL

  Defining the spatial transcriptome and cell-cell interactions in eczema and psoriasis skin

  Study EGAS00001005278

• Brain_Disease_Wellcome_Leap_Delta_Tissue_Spatial

  Utilising Spatial Transcriptomics to investigate how the tumour microenvironment regulates glioblastoma cell states.

  Study EGAS00001005801

• Gene_Discovery_in_Age_Related_Hearing_Loss

  The aim is to find new candidate genes associated with progressive hearing loss

  Study EGAS00001000295

• Whole genome and transcriptome analysis of anaplastic thyroid carcinoma

  Whole genome and transcriptome analysis of anaplastic thyroid carcinoma

  Study EGAS00001001214

• ORCADES_15x

  15x whole genome sequencing in samples from the isolated population of Orkney

  Study EGAS00001001891

• Identifying_new_diagnostic_and_treatment_pathways_for_patients_with_unclassifiable_sarcomas

  Whole genome sequencing of tumour normal pairs of human undifferentiated sarcomas.

  Study EGAS00001001604

• MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__pancreas_LCM_

  Samples prepared by LCM - 5 cases for pilot study. Bulk DNA not available.

  Study EGAS00001003197

• SSBP1

  SSBP1 mutations cause a complex optic atrophy spectrum disorder with mitochondrial DNA depletion

  Study EGAS00001004003

• Genome-wide association study of prognosis in Crohn's disease

  Genome-wide association study of prognosis in Crohn's disease

  Study EGAS00001002147

• GIST_SSGXVIII_trial_targeted_gene_sequencing

  Targeted cancer gene sequencing of samples enrolled in the SSGXVIII trial from Finland.

  Study EGAS00001001054

• The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer

  Mapping genetic evolution of pancreatic cancer precursor lesions such as IPMNs and PanINs.

  Study EGAS00001001573

• BLUEPRINT EpiVar ChIP-seq of Monocytes & Neutrophils

  BLUEPRINT EpiVar ChIP-seq of Monocytes & Neutrophils

  Study EGAS00001000870

• Alveolar Rhabdomyosarcoma sequencing data

  This study shares DNA and RNA sequencing data from alveolar rhadbomyosarcoma patients

  Study EGAS00001005387

• Embryonal Rhabdomyosarcoma sequencing data

  This study shares DNA and RNA sequencing data from embryonal rhadbomyosarcoma patients

  Study EGAS00001005502

• Epithelioid sarcoma sequencing data

  This study shares DNA and RNA sequencing data from Epithelioid sarcoma patients

  Study EGAS00001005983

• Genomic diversity of Vietnamese

  This study assess the genomic diversity of 22 ethnolinguistic groups in Vietnam

  Study EGAS00001006011

• Placental_mosaicism

  The aim of this study is to survey somatic mutations in human placentas.

  Study EGAS00001003549

• Rhabdoid tumor sequencing data

  This study contains sequencing DNA and RNA sequencing data for rhabdoid tumors

  Study EGAS00001006351

• IACS treatment on breast cancer bone metastases

  Off-target effect of IACS on breast cancer bone metastases.

  Study EGAS00001006908

• HSP90 inhibitor resistant cell line

  Genetic analysis of K562 cell which are resistant against HSP90 inhibitors.

  Study EGAS00001006381

• Whole genome and whole exome sequencing of ATCWGS42

  This dataset contains whole genome and whole exome sequencing data of ATCWGS42

  Dataset EGAD50000002147

• Targeted capture ctDNA Library CRCQV42Run021-6

  Targeted capture ctDNA Library CRCQV42Run021-6 from patient PBC0001304, saliva sample

  Dataset EGAD00001010447

• Pulldown DNA methylation study v2

  Pilot study to set up sequencing protocols for targeted pulldown methylation profiling

  Dataset EGAD00001001242

• Targeted capture ctDNA Library CRCQV42Run051-9

  Targeted capture ctDNA Library CRCQV42Run051-9 from patient PBC0003587, plasma sample

  Dataset EGAD00001010822

• UK10K_RARE_NEUROMUSCULAR REL-2013-04-20

  UK10K_RARE_NEUROMUSCULAR REL-2013-04-20

  Dataset EGAD00001000418

• UK10K_NEURO_EDINBURGH REL-2013-04-20

  UK10K_NEURO_EDINBURGH REL-2013-04-20

  Dataset EGAD00001000438

• SF10432 Wildtype Primary GBM Female, 50

  Single Cell-RNA Seq of Wildtype Primary GBM for Female, Age 50.

  Dataset EGAD00001006019

• WES of tumor tissue of RCC patients

  Whole exome sequencing (WES) of tumor tissues from RCC patients (DIAMOND cohort)

  Dataset EGAD00001005812

• Sardinia Population SNPs frequencies

  List of SNPs, and their frequencies, extracted from a low pass whole genome sequencing of 3,514 individuals.

  Dataset EGAD00001003141

• Fecal WMS HV metadata

  Metadata for fecal WMS data from NCT02749630 healthy volunteers.

  Dataset EGAD00001008819

• Reference epigenome ADMSC08 WGBS data generated from KEP study

  ADMSC08 WGBS paired end data

  Dataset EGAD00001007139

• Reference epigenome ADMSC06 WGBS data generated from KEP study

  ADMSC06 WGBS paired end data

  Dataset EGAD00001007137

• Targeted capture ctDNA Library CRCQV42Run022-18

  Targeted capture ctDNA Library CRCQV42Run022-18 from patient PBC0002826, saliva sample

  Dataset EGAD00001010453

• Reference epigenome IPS-NPC02 h3k4me3 ChIP-Seq data generated from KEP study

  IPS-NPC02 h3k4me3 ChIP-Seq paired end data

  Dataset EGAD00001007288

• Reference epigenome IPS01_N_Fibroblast_WGBS data generated from KEP study

  A IPS01_N_Fibroblast_WGBS paired end data for iPSC(Oct4)

  Dataset EGAD00001003473

• Targeted capture ctDNA Library CRCQV42Run42-17

  Targeted capture ctDNA Library CRCQV42Run42-17 from patient PBC0001375, saliva sample

  Dataset EGAD00001010828

• RNAseq data for EGAS00001004572

  Bulk RNA-seq data of tumours in EGAS00001004572.

  Dataset EGAD00001006876

• Targeted capture ctDNA Library CRCQV42Run051-8

  Targeted capture ctDNA Library CRCQV42Run051-8 from patient PBC0002294, plasma sample

  Dataset EGAD00001010821

• Targeted capture ctDNA Library CRCQV42Run021-23

  Targeted capture ctDNA Library CRCQV42Run021-23 from patient PBC0001516, saliva sample

  Dataset EGAD00001010444

• RNA sequencing of uveal melanoma metastases.

  RNA sequencing of uveal melanoma metastases.

  Dataset EGAD00001007912

• Targeted capture ctDNA Library CRCQV42Run020-14

  Targeted capture ctDNA Library CRCQV42Run020-14 from patient PBC0001312, saliva sample

  Dataset EGAD00001010426

• Targeted capture ctDNA Library CRCQV42Run021-24

  Targeted capture ctDNA Library CRCQV42Run021-24 from patient PBC0001653, saliva sample

  Dataset EGAD00001010445

• Targeted capture ctDNA Library CRCQV42Run025-17

  Targeted capture ctDNA Library CRCQV42Run025-17 from patient PBC0003595, saliva sample

  Dataset EGAD00001010481

• Clonal evolution study of Intrahepatic cholangiocarcinoma: 69 PDPCs and 6 tissues.

  Clonal evolution study of Intrahepatic cholangiocarcinoma: 69 PDPCs and 6 tissues.

  Dataset EGAD00001003574

• Reference epigenome ADMSC05 WGBS data generated from KEP study

  ADMSC05 WGBS paired end data

  Dataset EGAD00001007136

• Reference epigenome ADMSC07 WGBS data generated from KEP study

  ADMSC07 WGBS paired end data

  Dataset EGAD00001007138

• Whole genome sequencing of adult t-cell leukemia/lymphoma

  Whole genome sequencing of single adult t-cell leukemia/lymphoma case

  Dataset EGAD00001001326

• RNA seq reads

  RNA seq reads constituting of FASTQ paired end reads from 5 FHD/FHDL patients

  Dataset EGAD00001003790

• Targeted capture ctDNA Library CRCQV42Run016-17

  Targeted capture ctDNA Library CRCQV42Run016-17 from patient PBC0001467, saliva sample

  Dataset EGAD00001010401

• HipSci - Monogenic Diabetes - RNA Sequencing - April 2015

  HipSci - Monogenic Diabetes - RNA Sequencing - April 2015

  Dataset EGAD00001001953

• HipSci - Monogenic Diabetes - RNA Sequencing - January 2016

  HipSci - Monogenic Diabetes - RNA Sequencing - January 2016

  Dataset EGAD00001001955

• TST170 Pilot RNA FASTQ

  TST170 Pilot RNA FASTQ

  Dataset EGAD00001005711

• Taste Receptor Genotypes_Centenarians and Young

  This dataset includes targeted genotyping data for six BMI-associated polymorphisms across four candidate genes in young and centenarian individuals.

  Dataset EGAD00010002829

• ChIPseq Sequencing data for epigenetic subgroups of meningioma

  Bam files for 16 meningioma tumor samples; ChIPseq performed on Illumina HiSeq 2000

  Dataset EGAD00001005021

• DATA FILES FOR BALL-PAX5

  DATA FILES FOR BALL-PAX5

  Dataset EGAD00001000654

• RCRF release 1

  Transcriptome sequencing from the Rare Cancer Research Foundation: leiomyosarcoma, large cell neuroendocrine carcinoma, clear cell carcinoma

  Dataset EGAD00001010198

• Targeted capture ctDNA Library CRCQV34Run011-23

  Targeted capture ctDNA Library CRCQV34Run011-23 from patient PBC0001328, saliva sample

  Dataset EGAD00001010374

• Targeted capture ctDNA Library CRCQV34Run011-22

  Targeted capture ctDNA Library CRCQV34Run011-22 from patient PBC0002294, saliva sample

  Dataset EGAD00001010373

• Targeted capture ctDNA Library CRCQV40Run027-13

  Targeted capture ctDNA Library CRCQV40Run027-13 from patient PBC0005116, saliva sample

  Dataset EGAD00001010389

• Targeted capture ctDNA Library CRCQV42Run016-16

  Targeted capture ctDNA Library CRCQV42Run016-16 from patient PBC0001396, saliva sample

  Dataset EGAD00001010400

• Exome sequencing

  Exome sequencing of peripheral blood from 4 individuals of a family with familial colorectal cancer type X

  Dataset EGAD00001001009

• Targeted capture ctDNA Library CRCQV42Run041-5

  Targeted capture ctDNA Library CRCQV42Run041-5 from patient PBC0001375, saliva sample

  Dataset EGAD00001010635

• Targeted capture ctDNA Library CRCQV42Run041-13

  Targeted capture ctDNA Library CRCQV42Run041-13 from patient PBC0001413, saliva sample

  Dataset EGAD00001010627

• Targeted capture ctDNA Library CRCQV42Run051-10

  Targeted capture ctDNA Library CRCQV42Run051-10 from patient PBC0001665, plasma sample

  Dataset EGAD00001010804

• Targeted capture ctDNA Library CRCQV42Run028-23

  Targeted capture ctDNA Library CRCQV42Run028-23 from patient PBC0002533, saliva sample

  Dataset EGAD00001010508

• Small variants in HAE of patients from Canary Islands (ITER)

  Small variants in HAE of several Canary Islanders sequenced with Illumina WES.

  Dataset EGAD00001009318

• UK10K_NEURO_ABERDEEN REL-2013-04-20

  UK10K_NEURO_ABERDEEN REL-2013-04-20

  Dataset EGAD00001000433

• Shallow sequencing of organoid/xenograft or human colorectal metastases

  Shallow sequencing of organoid/xenograft or human colorectal metastases

  Dataset EGAD00001009661

• KUI6280

  RNA seq data normal and hypomethylation

  Dataset EGAD00001009887

• Somatic cancer gene mutation screening

  Sequencing of colorectal tumors and normal tissue using Ion AmpliSeq Cancer Hotspot Panel V2

  Dataset EGAD00001001010

• Long-term organoid culture of a small intestinal neuroendocrine tumor

  tissue, organoid and normal bam files for whole exome samples

  Dataset EGAD00001010162

• Targeted capture ctDNA Library CRCQV42Run026-19

  Targeted capture ctDNA Library CRCQV42Run026-19 from patient PBC0002872, saliva sample

  Dataset EGAD00001010492

• DNA-seq from plasma of 14 liver transplantation patients

  DNA-seq from plasma of 14 liver transplantation patients

  Dataset EGAD00001004590

• Paired-end Hi-C analysis of the 3D spatially mapped GBM samples.

  Dataset contains 21 paired-end Hi-C samples from 9 patients.

  Dataset EGAD00001010312

• Paired-end snATAC-seq analysis of the 3D spatially mapped GBM samples.

  Dataset contains 11 paired-end snATAC-seq samples from 4 patients.

  Dataset EGAD00001010313

• DNA (exome) sequencing of uveal melanoma metastases

  DNA (exome) sequencing of uveal melanoma metastases.

  Dataset EGAD00001007911

• COVID-19 Postmortem Medulla and Olfactory Mucosa snRNA-seq

  Time-dependent characterization of CNS response in COVID-19

  Dataset EGAD00001009075

• Targeted capture ctDNA Library CRCQV34Run002-23

  Targeted capture ctDNA Library CRCQV34Run002-23 from patient PBC0002595, saliva sample

  Dataset EGAD00001010337

• OT2_Illumina_WXS_T

  Whole-exome sequencing on Illumina HiSeq2000/2500 of colorectal cancer primary tumor sample (OT2_cohort)

  Dataset EGAD00001003383

• Reference epigenome IPS04_X_Fibroblast_WGBS data generated from KEP study

  A IPS04_X_Fibroblast_WGBS paired end data for iPSC(Oct4)

  Dataset EGAD00001003476