SRR12808979

SRA first seen 2021

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

93/100 · A

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

What this means

claude:haiku

Melitaea cinxia bulk RNA-seq (Grade A). High-quality data with excellent base composition (93.9% Q30+, mean Q34.4) and near-absent adapter contamination (0.16%). Moderate duplication (49%) falls within expected range and does not compromise reuse for standard transcriptomic analysis.

Data type / assay

bulk-RNA-seq

Organism

Melitaea cinxia

Instrument

NextSeq 500

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 850091616 reported

total reads 5592708 reported

n content pct 0.01 measured

pct q20 bases 95.7 measured

pct q30 bases 93.9 measured

gc content pct 42.2 measured

mean read length 86 measured

mean base quality 34.4 measured

adapter content pct 0.16 measured

duplication rate pct 49 measured

How this grade was computed

Weighted mean of 4 scored metric(s) → 93/100

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.

pct q30 bases 93.9 measured ×1 100%

mean base quality 34.4 measured ×0.6 100%

adapter content pct 0.16 measured ×0.4 100%

duplication rate pct 49 measured ×0.4 58%

QC cost 31 s compute

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