SRR10083170

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

91/100 · A

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

What this means

claude:haiku

Bulk short-read RNA-seq with exceptional basecall quality (Q30=97.4%, mean Q=39.8) and long reads (146.7 bp) supporting accurate alignment and transcript discovery. Higher technical duplication at 53.18% (scored 48/100, weight 0.4) is the primary limitation but acceptable with normalization. Excellent for isoform characterization and expression studies.

Data type / assay

bulk-RNA-seq

Organism

Bombyx mori

Instrument

HiSeq X Ten

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 6833928363 reported

total reads 23523159 reported

n content pct 0 measured

pct q20 bases 99.2 measured

pct q30 bases 97.4 measured

gc content pct 43.7 measured

mean read length 146.7 measured

mean base quality 39.8 measured

adapter content pct 0 measured

duplication rate pct 53.18 measured

How this grade was computed

Weighted mean of 4 scored metric(s) → 91/100

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 97.4 measured ×1 100%

mean base quality 39.8 measured ×0.6 100%

adapter content pct 0 measured ×0.4 100%

duplication rate pct 53.18 measured ×0.4 49%

QC cost 30 s compute

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