-
Molecular Genetics of Histiocytic Sarcoma
Study
phs001748
-
Assessment of Complex Chromosomal Changes in De-Identified Cell Lines
Study
phs004000
-
Melanoma multi site metastases
Dataset
EGAD00001005487
-
Biallelic tumor suppressor loss and DNA repair defects in de novo small cell prostate cancer
Study
EGAS00001003007
-
Possible DNA damage after paternal exposure to ionizing radiation in radar technicians
Study
EGAS00001007321
-
Patient Microbiome and Surgical Site Infection in Spine Surgery
Study
phs003358
-
Anaplastic meingioma methylation
Dataset
EGAD00010001629
-
Error-corrected sequencing of 26 driver genes
Dataset
EGAD50000000079
-
WGS in insulinomas
Dataset
EGAD50000000464
-
The clinicopathologic spectrum and genomic landscape of de-/trans-differentiated melanoma
Dataset
EGAD00001007033
-
The clinicopathologic spectrum and genomic landscape of de-/trans-differentiated melanoma
Dataset
EGAD00001007034
-
HGSOC genome-wide SNP (project ITH)
Dataset
EGAD00010002482
-
Melanoma multi site metastases
Dataset
EGAD00001005483
-
Gut metagenomic data of 2,338 Pinggu adults
Study
EGAS00001004820
-
Pancreatic adenocarcinoma QCMG 20110901
Dataset
EGAD00001000049
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
Error-corrected sequencing of 26 driver genes (additional cohort)
Dataset
EGAD50000000641
-
RNAseq dataset
Dataset
EGAD50000001243
-
Whole Exome Sequencing
Dataset
EGAD00001011117
-
Whole_genome_sequence_of__third_generation_family_member__SFHS_
Study
EGAS00001000429
-
Genetic landscape of relapsed DLBCL
Study
EGAS00001001553
-
Whole exome sequencing of 69 trios with bipolar disorder
Study
JGAS000273
-
HV31 - De novo assembly of eight immune system regions
Dataset
EGAD00001007050
-
Multi-focal genomic dissection of synchronous primary and metastatic tissue from de novo metastatic prostate cancer
Study
EGAS00001006466
-
WES of der(1;7)(q10;p10) myeloid neoplasms
Study
EGAS50000000704
-
Long-read and short-read isoform sequencing in breast cancer
Study
EGAS00001004819
-
Childhood Cancer Model Atlas
Study
EGAS00001006320
-
Sequencing data for oesophageal and related samples - OACs release 2 (RNA)
Dataset
EGAD00001003839
-
Prostate cancer datasets WES
Dataset
EGAD00001004467
-
Exome reads and RNA-seq
Dataset
EGAD00001002722
-
RNAseq
Dataset
EGAD00001006008
-
Novel genes for Intellectual Disability identified using whole genome sequence and pathway analysis
Study
EGAS00001001386
-
alopecia areata
Dataset
EGAD00001006370
-
Transcriptomic predictors of survival for palbociclib + endocrine therapy vs. capecitabine in aromatase inhibitor-resistant breast cancer from GEICAM/2013-02 PEARL
Study
EGAS00001008177
-
Directeur de Recherches
Dac
EGAC00001002511
-
Clinical and Genetic Analysis of Costa Rican Patients with Parkinson's Disease
Study
phs002495
-
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
Study
EGAS00001002333
-
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Study
EGAS00001005417
-
Sant Joan de Déu Research Institute (IRSJD)
Dac
EGAC50000000253
-
Prostate cancer datasets WGS
Dataset
EGAD00001004466
-
Exome-sequencing of human B cell lymphoma cell lines
Study
EGAS00001001463
-
Metastatic Adrenocortical Carcinoma Displays Higher Mutation Rate and Tumor Heterogeneity than Primary Tumors
Study
phs001658
-
Melanoma_multi_site_metastases
Study
EGAS00001001348
-
Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma
Dataset
EGAD00001007762
-
Abnormal foetal development exome trios
Dataset
EGAD00001001442
-
Oncogenic cooperation in a human de novo T-ALL model
Study
EGAS00001006055
-
Transcriptomic profiling of patient-derived xenografts and organoids in prostate cancer
Dataset
EGAD00001006404
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
Study
phs000482
-
The Genetic Landscape of Ocular Adnexa MALT Lymphoma Reveals Frequent Aberrations in NFAT and MEF2B Signaling Pathways
Study
EGAS00001006631
-
Searching for variants associated with endometriosis
Study
EGAS00001001741