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Genomicsena-DATASET-VIB-08-06-2015-13:42:05:930-599 - samples
Description not provided
EGAD00001001391 | EGA
GenomicsPLCG1 R707Q mutation is counter selected under targeted therapy in a patient with a hepatic angiosarcoma
PLCG1 R707Q mutation is counter selected under targeted therapy in a patient with a hepatic angiosarcoma
EGAS00001001281 | EGA
GenomicsVIB VRC Data Access Committee
Data Access Committee EGAC00001000042
EGAC00001000042 | EGA
TranscriptomicsExpression profiling of budding cells in colorectal cancer suggests an EMT-like phenotype and molecular subtype switching
Tumour buds undergo phenotype switching while detaching from the main tumour, as they acquire more migratory characteristics and tend to stop proliferating. Simultaneously, an EMT-like signature is observed in the tumour buds under the form of active WNT, TGF and receptor tyrosine kinase signalling....
ORGANISM(S): Homo sapiens 
2017-02-04 | E-MTAB-4065 | biostudies-arrayexpress
Genomicsena-DATASET-VIB-29-07-2013-12:55:51:690-38 - samples
DNA replication errors occurring in mismatch repair (MMR) deficient cells persist as mismatch mutations and predispose to a range of tumors. Here, we sequenced the first whole-genomes from MMR-deficient endometrial tumors.
EGAD00001000641 | EGA
GenomicsSignatures of mismatch repair deficiency in cancer genomes
DNA replication errors occurring in mismatch repair (MMR) deficient cells persist as mismatch mutations and predispose to a range of tumors. Here, we sequenced the first whole-genomes from MMR-deficient tumors and observed that mutation rates were drastically increased relative to MMR-proficient end...
EGAS00001000182 | EGA
Genomicsena-DATASET-VIB-13-03-2012-14:05:46:504-2 - samples
Tumor sample of a serious ovarian carcinoma
EGAD00001000139 | EGA
GenomicsOvarian & matched normal (Genotypes) - samples
Ovarian & matched normal (Genotypes)
EGAD00010000220 | EGA
Genomicsena-DATASET-VIB-13-03-2012-14:07:27:404-3 - samples
Blood sample of serious ovarian carcinoma patient
EGAD00001000140 | EGA
GenomicsComplete Genomics paired end sequencing; Ovarian cancer
We sequenced the genomes from a monozygotic twin discordant for schizophrenia and a tumor-normal pair of an ovarian cancer patient. Using whole-genome twin data to discriminate between correctly identified single nucleotide variants (SNVs) and errors a strategy for the accurate detection of SNVs was...
EGAS00001000158 | EGA
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