SRR10143168

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

98/100 · A

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

What this means

claude:haiku

Illumina short-read bulk RNA-seq; grade A, excellent for reuse. Outstanding base quality (Q30=95%, mean BQ=36.1) enables sensitive transcript detection; moderate duplication (35.99%) has minimal impact on quantification accuracy.

Data type / assay

bulk-RNA-seq

Organism

Bombyx mori

Instrument

Illumina HiSeq 2000

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 8715732000 reported

total reads 29052440 reported

n content pct 0 measured

pct q20 bases 98.2 measured

pct q30 bases 95 measured

gc content pct 44.3 measured

mean read length 150 measured

mean base quality 36.1 measured

adapter content pct 0.01 measured

duplication rate pct 35.99 measured

How this grade was computed

Weighted mean of 4 scored metric(s) → 98/100

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 95 measured ×1 100%

mean base quality 36.1 measured ×0.6 100%

adapter content pct 0.01 measured ×0.4 100%

duplication rate pct 35.99 measured ×0.4 87%

QC cost 43 s compute

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