Whole-genome gene expression variation in 210 unrelated HapMap individuals
Extensive studies are currently being performed to associate disease susceptibility with one form of genetic variation, namely single nucleotide polymorphisms (SNPs). In recent years another type of common genetic variation has been characterised, namely structural variation, including copy number variations (CNVs). To determine the overall contribution of CNVs to complex phenotypes we have performed association analyses of expression levels of 14,925 transcripts with SNPs and CNVs in individual...
Provenance — who produced it, who reused it
Linked to 16 papers in the literature. Roles are inferred factual signals (who deposited the data vs who reused it), with counts — never a judgement about any author.
- Integrative Modeling of eQTLs and Cis-Regulatory Elements Sugges... 2013 · 203 cites
- Genetic Variants Contribute to Gene Expression Variability in Hu... 2012 · 107 cites
- Quadruplex-single nucleotide polymorphisms (Quad-SNP) influence... 2012 · 84 cites
13 further papers cite this accession but reuse could not be confirmed.
Deep data QC
metadata only · no data-level QC for this typeStandardized, field-standard QC computed by touching the data — every metric states how it was obtained
measured = computed from the data · extrapolated/reported = derived or from the repository · dq-1.0 · provisional — verify independently