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Claim

In a massively parallel reporter assay of human neural progenitor cells, researchers tested 9,092 cortical-structure-associated variants and reported regulatory potential for 918 variants from 150 loci, representing 76% of loci studied; more than half showed allelic effects.

Type QUANTITATIVE · truth-evaluable: yes · status at snapshot: ACTIVE · created seq 14811 · qualifiers {"population":"Human neural progenitor cells in an episomal massively parallel reporter assay; the result does not by itself establish endogenous chromatin effects or causal effects on cortical structure."}

37 words; atomic claims are usually under 25a conjunction joins clauses that may be separately evaluablea comma-separated series may list several propositions

Referenced 79 times: checked 2, looked up by assistants 0, viewed 51, shared 26. A count of attention, not evidence.

Topics

Neuroscience · 1efd24fe Biology · 1efd24fe

Assessment

Supported

Score: 0.9781 under ledger-default@0.3.0 at snapshot 27745

2 of 4 review checks done · 1 counted · 1 by the author only

2 independent evidence lineages · review checks 1 of 4 · stability HIGH

Main unresolved issue: 3 counted evidence items have no independence review; repeats of one origin may be counted as several coverage:3cd47199-67c2-8cf6-8c96-571091933119

Not yet independently audited.Evidence reviewed so far supports this claim, but only 1 of 4 review checks has been done.Every quoted passage was confirmed on the page when Galedra fetched it.

Why?

Strongest counted support: The abstract reports the tested variant count, regulatory-potential count, locus coverage, allelic effects, and Wnt-dependent enhancer finding. weight 2.000000 evidence

Suppressed as dependent: The excerpt directly reports the tested variants, regulatory-potential variants, locus coverage, and allelic-effect proportion.

Review gaps: qualifiers reviewed, opposing search done, independence reviewed

What would most change this: One independent, direct measurement that contradicts this claim would move it from Supported to Supported.

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Checked as part of

Statements this claim was broken out of. The claim is scored on its own; a statement's reading only counts its claims.

Evidence for

Evidence against

None.

Qualifications

None.

Suppressed as dependent

EvidenceGroupKept instead
decc2ed49c99c08f

Inferences

Concluded from

None.

Used as a premise in

None.

An inference is interpretation, not evidence: it never changes the assessment of its conclusion. Each premise is a claim with its own evidence.

Threads

None. Threads are for disagreements about how a determination was made — a statement whose figures are not in the passage it rests on, two sources that may share an origin. Something about the world belongs in the evidence above.

Claim edges

None. Edges are stored and displayed; v0.1 does not propagate probability across them.

Review checklist

Review checks: 1 of 4

2 checks by this claim's own author, alongside the independent review above. 1 QUALIFIER CHECK · 1 EVIDENCE VERIFICATION. A check by the person who recorded a claim does not raise its review coverage.

CheckDoneBy
qualifiers reviewedno
opposing search doneno
independence reviewedno
primary source reviewedyes9c99c08f, 9215f203, 8c709ed0

Summary

Supported. The main support is: The abstract reports the tested variant count, regulatory-potential count, locus coverage, allelic effects, and Wnt-dependent enhancer finding. 75097b26

1 further item repeats the same origin and is not independent evidence. decc2ed4

Review checks: 1 of 4. coverage:3cd47199-67c2-8cf6-8c96-571091933119

Generated by stub-v0.1; every sentence cites graph ids.

Contribution history

seqeventdetail
14811APPENDED
14812ACCEPTAUTOMATIC_AFTER_VALIDATION
14823LINK_EVIDENCEby 1efd24fe (accepted)
14827TASK_RESULTby 1efd24fe (accepted)
16834LINK_EVIDENCEby 1efd24fe (accepted)