ADAM Genomics Schema - Extension for Precision Medicine Research*
Bibliographic record
Abstract
High-throughput sequencing technologies have made research on precision medicine possible. Precision medicine treatments will be effective for individual patients based on their genomic, environmental, and lifestyle factors. This requires integrating this data to find one, or a combination of, single nucleotide polymorphisms (SNPs) linked to a disease or treatment [1]. In 2013, the University of California Berkeley's AmpLab created the ADAM genomic format that allows the transformation, analysis and querying of large amounts of genomics data by using a columnar file format. However, while ADAM addresses the issue of processing large genomics data; it lacks the ability to link the patients' clinical and demographical data, which is crucial in precision medicine research. This paper presents an ADAM genomic schema extension to support clinical and demographical data by automating the addition of data items to the currently available ADAM schema. This extension allows for clinical, demographical and epidemiological analysis at large scale as initially intended by the AmpLab.
Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.
How this classification was reachedexpand
Full frame machine prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.
Distilled classifier scores by category (both heads)
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.010 | 0.016 |
| Meta-epidemiology (narrow) | 0.001 | 0.001 |
| Meta-epidemiology (broad) | 0.001 | 0.002 |
| Bibliometrics | 0.002 | 0.002 |
| Science and technology studies | 0.001 | 0.001 |
| Scholarly communication | 0.004 | 0.007 |
| Open science | 0.003 | 0.005 |
| Research integrity | 0.001 | 0.003 |
| Insufficient payload (model declined to judge) | 0.018 | 0.010 |
Machine scores (provisional)
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.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".