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TranscriptomicsComparison of microRNA Profiling Platforms (HTS)
Global miRNA expression profiling of human malignancies is gaining popularity in both basic and clinically driven research. But to date, the majority of such analyses have used microarrays and quantitative real-time PCR. With the introduction of digital count technologies, such as next-generation s...
ORGANISM(S): Homo sapiens 
2013-10-22 | E-GEOD-51507 | biostudies-arrayexpress
UnknownStrategic treatment optimization for HCV (STOPHCV1): a randomised controlled trial of ultrashort duration therapy for chronic hepatitis C.
Not available
S-EPMC8361811 | biostudies-literature
GenomicsA Cancer Cell-Line Titration Series for Evaluating Somatic Classification
Accurate detection of somatic single nucleotide variants and small insertions and deletions from DNA sequencing experiments of tumour-normal pairs is a challenging task. Tumour samples are often contaminated with normal cells confounding the available evidence for the somatic variants. Furthermore...
EGAS00001001016 | EGA
GenomicsCell-line Mixing Experiment Verification Data - samples
Description not provided
EGAD00001001044 | EGA
GenomicsCell-line Mixing Experiment Sequencing Data - samples
Description not provided
EGAD00001001043 | EGA
GenomicsCPCG_Het_Study - samples
Aligned Sequence (bam format), Duplicates removed
EGAD00001001329 | EGA
GenomicsCPCG Het Study, Raw Fastq Sequence - samples
Raw sequence data, fastq format
EGAD00001002885 | EGA
GenomicsCPC-GENE Prostate Cancer Heterogeneity Study
Herein we describe a molecular portrait of potentially curable, Gleason 7 and intermediate risk prostate cancer based on genome-wide CNV profiles of 96 patients, and subsequent whole-genome sequencing of 28 tumours from 10 patients, using DNA quantities that are achievable in diagnostic biopsies (50...
EGAS00001000549 | EGA
UnknownEight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.
Not available
S-EPMC3258449 | biostudies-literature
GenomicsBRCA_SNV_SR - samples
single nucleotide variant calls from somatic sniper, vcf format. input for subclonal reconstruction
EGAD00001003753 | EGA
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