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UnknownIdentifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).
Not available
S-EPMC6202811 | biostudies-literature
UnknownClinicoradiologic features distinguish tumefactive multiple sclerosis from CNS neoplasms.
Not available
S-EPMC5964866 | biostudies-literature
TranscriptomicsSingle-cell transcriptome profiling for metastatic renal cell carcinoma patient-derived cells [RNA-seq]
Clear cell renal cell carcinoma (ccRCC) initiated from the renal epithelium is the most prevalent histological type of adult kidney cancers. Dissecting intratumoral heterogeneity (ITH) of ccRCC has leveraged to extend our knowledge on how primary tumors harboring driver mutations evolve and spread t...
ORGANISM(S): Homo sapiens 
2015-09-18 | E-GEOD-73121 | biostudies-arrayexpress
UnknownWhole exome sequencing (WES) analysis of transformed small cell lung cancer (SCLC) from lung adenocarcinoma (LUAD).
Not available
S-EPMC7815376 | biostudies-literature
Genomics32c6825c-80c0-4d0f-9284-cc7c1a39e68a - samples
Whole transcriptome sequencing (RNA-seq) was performed on 39 PC specimens. Among them, 21 specimens also had WES data.
EGAD00001004365 | EGA
UnknownExome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey.
Not available
S-EPMC6079040 | biostudies-literature
Genomicsc9d38693-41de-4186-90c3-5e52d1913254 - samples
Whole-exome sequencing (WES) was performed on a total of 34 PC specimens, with 15 cases having matched gDNAs extracted from blood.
EGAD00001004364 | EGA
UnknownIdentification of a Novel Mutation in BRD4 that Causes Autosomal Dominant Syndromic Congenital Cataracts Associated with Other Neuro-Skeletal Anomalies.
Not available
S-EPMC5226720 | biostudies-literature
UnknownGenetic heterogeneity and prognostic impact of recurrent ANK2 and TP53 mutations in mantle cell lymphoma: a multi-centre cohort study.
Not available
S-EPMC7414214 | biostudies-literature
UnknownIdentification of candidate genes and pathways in retinopathy of prematurity by whole exome sequencing of preterm infants enriched in phenotypic extremes.
Not available
S-EPMC7925531 | biostudies-literature
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