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Bulk RNA sequencing of 866 brain samples revealed significantly higher (~two-fold) overall burden of somatic single-nucleotide variants in AD brains compared to age-matched controls.

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experiment Created: By: experiment_extractor Quality: 50% ✓ SciDEX ID: experiment-exp-dff164a6df75
🧫 Experiment Protocol Genetic Associationproposed
SUMMARY
Bulk RNA sequencing of 866 brain samples revealed significantly higher (~two-fold) overall burden of somatic single-nucleotide variants in AD brains compared to age-matched controls.
METHODOLOGY NOTES
Three orthogonal methods used across three independent AD cohorts; bulk RNA sequencing approach for variant detection
N = {'case': None, 'total': 866, 'units': 'samples', 'control': None}tissue: multiple brain regions (prefrontal cortex, temporal neocortex)species: homo_sapiens
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Metadatasource: {'pmid': '38260600', 'type': 'paper', 'e
source{'pmid': '38260600', 'type': 'paper', 'extracted_by': 'llm_extraction_v1'}
tissuemultiple brain regions (prefrontal cortex, temporal neocortex)
specieshomo_sapiens
summaryBulk RNA sequencing of 866 brain samples revealed significantly higher (~two-fold) overall burden of somatic single-nucleotide variants in AD brains compared to age-matched controls.
sample_size{'case': None, 'total': 866, 'units': 'samples', 'control': None}
model_systemin_vivo
_schema_version1
experiment_typegenetic_association
methodology_notesThree orthogonal methods used across three independent AD cohorts; bulk RNA sequencing approach for variant detection
replication_statusreplicated
extraction_metadata{'needs_review': False, 'extraction_date': '2026-04-28T06:18:28.439960+00:00', 'extraction_notes': '', 'extraction_confidence': 0.5}
statistical_evidence{'p_value': None, 'test_type': None, 'effect_size': {'value': 2, 'measure': 'fold change', 'direction': 'increased'}}
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