22948 results for "ega"

in 24.67 milliseconds.

• DNA-seq from plasma of 14 liver transplantation patients

  DNA-seq from plasma of 14 liver transplantation patients

  Dataset EGAD00001004590

• DNA (exome) sequencing of uveal melanoma metastases

  DNA (exome) sequencing of uveal melanoma metastases.

  Dataset EGAD00001007911

• 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

• WGBS files for PCGP NBL_MYCN_ATRX

  WGBS files for PCGP NBL_MYCN_ATRX paper titled "MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma"

  Dataset EGAD00001004559

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

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

  Dataset EGAD00001001326

• Low input LC (ISC)

  R&D project to develop low input library construction methods.

  Dataset EGAD00001003254

• Dataset for "Genomic landscape of oral cancers" (Illumina RNA)

  Dataset for "Genomic landscape of oral cancers" (Illumina RNA)

  Dataset EGAD00001004366

• WGS data for MMML for Study EGAS00001002198

  Whole genome sequencing data for MMML (28 tumor/control pairs)

  Dataset EGAD00001003207

• EGYPT_HIGH_COVERAGE_vcf

  Integrated callset of high coverage Egyptian genomes from the Pagani et al. 2015 AJHG paper (doi: http://dx.doi.org/10.1016/j.ajhg.2015.04.019)

  Dataset EGAD00001003295

• RNA seq reads

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

  Dataset EGAD00001003790

• Embryonal Rhabdomyosarcoma sequencing data

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

  Study EGAS00001005502

• HSP90 inhibitor resistant cell line

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

  Study EGAS00001006381

• Dnase1l3 knockout causes aberrations in plasma DNA fragmentation

  Dnase1l3 knockout causes aberrations in plasma DNA fragmentation

  Study EGAS00001003174

• 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

• Wilm's tumor sequencing data

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

  Study EGAS00001005690

• 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

• Targeted capture ctDNA Library CRCQV42Run021-6

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

  Dataset EGAD00001010447

• Alveolar Rhabdomyosarcoma sequencing data

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

  Study EGAS00001005387

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

  Time-dependent characterization of CNS response in COVID-19

  Dataset EGAD00001009075

• 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

• Targeted capture ctDNA Library CRCQV42Run051-9

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

  Dataset EGAD00001010822

• Targeted capture ctDNA Library CRCQV40Run027-13

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

  Dataset EGAD00001010389

• Paired-end RNA-seq analysis of GBM, additional patient.

  Dataset contains one paired-end RNA-seq sample.

  Dataset EGAD00001011990

• Fecal WMS HV metadata

  Metadata for fecal WMS data from NCT02749630 healthy volunteers.

  Dataset EGAD00001008819

• Targeted capture ctDNA Library CRCQV42Run022-18

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

  Dataset EGAD00001010453

• Targeted capture ctDNA Library CRCQV42Run42-17

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

  Dataset EGAD00001010828

• Targeted capture ctDNA Library CRCQV42Run051-8

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

  Dataset EGAD00001010821

• RNA sequencing of uveal melanoma metastases.

  RNA sequencing of uveal melanoma metastases.

  Dataset EGAD00001007912

• Targeted capture ctDNA Library CRCQV42Run016-17

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

  Dataset EGAD00001010401

• 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 CRCQV34Run011-22

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

  Dataset EGAD00001010373

• Targeted capture ctDNA Library CRCQV34Run011-23

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

  Dataset EGAD00001010374

• Targeted capture ctDNA Library CRCQV42Run016-16

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

  Dataset EGAD00001010400

• Targeted capture ctDNA Library CRCQV42Run041-13

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

  Dataset EGAD00001010627

• Targeted capture ctDNA Library CRCQV42Run041-5

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

  Dataset EGAD00001010635

• Targeted capture ctDNA Library CRCQV42Run051-10

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

  Dataset EGAD00001010804

• Targeted capture ctDNA Library CRCQV42Run020-14

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

  Dataset EGAD00001010426

• 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

• 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

• 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