Corpus 1,277 assessed · 1,178 scored · 644 reproduced ≥75 · 170 flagged ·∅ 74/100
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SRP144106

ENA first seen 2018

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

29/100 · F

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

What this means
claude:haiku

Whole-genome sequencing from Homo sapiens on NextSeq 500 with ~10 million reads, 0.5× estimated coverage, and notably poor quality (46.7% Q20, 33.5% Q30), representing failed or ultra-low coverage data unsuitable for analysis.

Data type / assay
WGS
Organism
Homo sapiens
Instrument
NextSeq 500
Platform
ILLUMINA
Read type
short-read
Files available
FASTQ (raw reads)
N numbers (samples, groups)
3 runs
Metrics (value · how obtained)
checksum ok yes reported
total bases 1421585760 reported
total reads 10155898 reported
mean coverage 0.5 extrapolated
n content pct 30.762 measured
pct q20 bases 46.7 measured
pct q30 bases 33.5 measured
gc content pct 29.6 measured
mean read length 70 measured
mean base quality 17.7 measured
adapter content pct 0.51 measured
duplication rate pct 8.55 measured
How this grade was computed
Weighted mean of 4 scored metric(s) → 29/100

The F grade is a transparent weighted average. Each metric below scored from 0–100% against the published WGS thresholds, weighted by its importance; nothing is hidden or subjective.

mean coverage 0.5 extrapolated ×1.2 0%
pct q30 bases 33.5 measured ×1 0%
duplication rate pct 8.55 measured ×0.5 98%
adapter content pct 0.51 measured ×0.4 100%
QC cost 1 s compute

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