RNA sequencing for KSHV circular RNAs
The purpose was to detect viral circular RNAs from infected cells.
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.
Deep data QC
81/100 · BStandardized, 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 sequencing platform (HTTP error), but exceptional quality metrics (95.8% Q30, 126 bp read length, 23.02% adapter content). This dataset enables human transcriptomics with long reads suited for isoform resolution. The high adapter content suggests partial adapter trimming, requiring verification of preprocessing steps before downstream analysis.
The B 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