Temporal analysis of erythropoiesis
CD34+ cells were subjected to ex vivo erythropoiesis according to the protocol described in Palii et al. (doi: 10.3791/2813. J Vis Exp. 53, 2011). Samples were harvested at different time points and analyzed by RNAseq.
Provenance — who produced it, who reused it
Linked to 1 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.
- Absolute Quantification of Transcription Factors Reveals Princip... 2020 · 116 cites
Deep data QC
100/100 · AStandardized, field-standard QC computed by touching the data — every metric states how it was obtained · evidence: measured
Bulk RNA-seq of Homo sapiens with unavailable instrument metadata (HTTP error), but exceptional quality (96.2% Q30, 50 bp read length, 0.004% N content). This dataset enables human transcriptomics with short-read high-throughput sequencing. The minimal contamination and consistent quality enable reliable differential expression analysis across samples.
The A grade is a transparent weighted average. Each metric below scored from 0–100% against the published bulk-RNA-seq thresholds, weighted by its importance; nothing is hidden or subjective.
measured = computed from the data · extrapolated/reported = derived or from the repository · dq-1.0