Corpus 1,272 assessed · 1,173 scored · 643 reproduced ≥75 · 168 flagged ·∅ 74.1/100
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ERR2438055

ENA 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

100/100 · A

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

What this means
claude:haiku

Whole-genome short-read sequencing from NovaSeq 6000 with exceptional quality (96.7% Q30), ~30x coverage, and 313M reads; ideal for diploid genotyping and rare-variant discovery across the human genome.

Data type / assay
WGS
Organism
Homo sapiens
Instrument
Illumina NovaSeq 6000
Platform
ILLUMINA
Read type
short-read
Files available
FASTQ (raw reads), submitted files
N numbers (samples, groups)
1 runs
Metrics (value · how obtained)
checksum ok yes reported
total bases 94114838100 reported
total reads 313716127 reported
mean coverage 30.4 extrapolated
n content pct 0 measured
pct q20 bases 98 measured
pct q30 bases 96.7 measured
gc content pct 41.2 measured
mean read length 150 measured
mean base quality 36.3 measured
adapter content pct 0 measured
duplication rate pct 4.61 measured
How this grade was computed
Weighted mean of 4 scored metric(s) → 100/100

The A 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 30.4 extrapolated ×1.2 100%
pct q30 bases 96.7 measured ×1 100%
duplication rate pct 4.61 measured ×0.5 100%
adapter content pct 0 measured ×0.4 100%
QC cost 33 s compute

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