← all works
Lineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution
Why is this work in the frame?
A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.
Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Machine scores (provisional)
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Opus teacher head0.021
GPT teacher head0.290
- Teacher spread
- 0.270 · how far apart the two teachers sit on this one work
- Validation status
score_only:v0-immature-baseline· verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it
Abstract
No abstract. This is not a gap in this database — OpenAlex has none either. 23.3% of the frame is in this state, and the screen finds HALF as much metaresearch here, so the absence is a measured bias rather than a missing field.
The record
- Venue
- Nature Genetics
- Topic
- Acute Myeloid Leukemia Research
- Field
- Medicine
- Canadian institutions
- Princess Margaret Cancer CentreUniversity Health Network
- Funders
- U.S. National Library of MedicineNational Cancer InstituteNational Institute of Arthritis and Musculoskeletal and Skin DiseasesNational Human Genome Research InstituteHoward Hughes Medical Institute
- Keywords
- BiologyChromatinHaematopoiesisStem cellLineage (genetic)GeneticsHematopoietic stem cellLeukemiaComputational biologyEnhancerMyeloidEpigenomicsCancer researchGeneTranscription factorDNA methylationGene expression
- Has abstract in OpenAlex
- no