Corpus 1,285 assessed · 1,186 scored · 647 reproduced ≥75 · 174 flagged ·∅ 73.9/100
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SRR3439490

ENA first seen 2016

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.

Reused by

1 further paper cites this accession but reuse could not be confirmed.

Deep data QC

86/100 · B

Standardized, field-standard QC computed by touching the data — every metric states how it was obtained · evidence: measured

What this means
claude:haiku

HiSeq 4000 RNA-seq from Homo sapiens (26.6M reads, 7.7 billion bases, 44.7% GC, 85.1% ≥Q30) profiles human transcriptome variation. The dataset addresses tissue-specific expression and genetic variation across samples.

Data type / assay
bulk-RNA-seq
Organism
Homo sapiens
Instrument
Illumina HiSeq 4000
Platform
ILLUMINA
Read type
short-read
Files available
FASTQ (raw reads)
N numbers (samples, groups)
1 runs
Metrics (value · how obtained)
checksum ok yes reported
total bases 7725663275 reported
total reads 26624635 reported
n content pct 0.009 measured
pct q20 bases 91.9 measured
pct q30 bases 85.1 measured
gc content pct 44.7 measured
mean read length 145.2 measured
mean base quality 33.6 measured
adapter content pct 0.21 measured
duplication rate pct 36.51 measured
How this grade was computed
Weighted mean of 4 scored metric(s) → 86/100

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.

pct q30 bases 85.1 measured ×1 76%
mean base quality 33.6 measured ×0.6 93%
adapter content pct 0.21 measured ×0.4 100%
duplication rate pct 36.51 measured ×0.4 86%
QC cost 13 s compute

measured = computed from the data · extrapolated/reported = derived or from the repository · dq-1.0