Jamorham
Nightscout용 xDrip+ 버전
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1분 만에 확인하기README 전체를 불러오는 중입니다. 아래는 저장된 발췌입니다.
One blood draw. Three computed cfDNA signals. Every claim traceable.
Traceback turns Oxford Nanopore reads into fragment-length, methylation
cell-origin, and chromosome-dosage evidence, then uses a bounded AI reviewer
to check whether the written interpretation is actually supported.
Research prototype only. It does not diagnose cancer or replace a validated
clinical assay.README 전문 보기 ↗One blood draw. Three computed cfDNA signals. Every claim traceable.
The public evidence demo turns Oxford Nanopore reads into fragment-length, methylation cell-origin, and chromosome-dosage evidence, then uses a bounded AI reviewer to check whether the written interpretation is supported.
Open the live demo · View the repository · Demo walkthrough · Algorithms
Research prototype only. It does not diagnose cancer or replace a validated clinical assay.
| Workflow | Use it for | Record and qualification |
|---|---|---|
| Signed local runner | A BAM-to-record journey for fragment length; optional cell-origin and ichorCNA copy-number analyses are described in the operator guide. | Development-signed, local, unqualified records. |
| Traceback Lab | Exploratory measurements on stored ONT or supported prealigned Illumina BAMs, with local sample and cohort views. | Unsigned results with execution provenance; research use only. |
| Public evidence demo | Inspect three fixed aggregate readouts and a recorded or live bounded AI evidence review. | A demonstration, not a new analysis of your BAM. |
Lab includes read quality and depth checks; fragment, methylation, end-pattern,
and microbial measurements; exploratory copy-number and cohort comparisons;
and input-scoped prenatal or transplant calculations where an operator supplies
matching controls. Each method has its own platform, depth, asset, and tool
requirements. Run traceback lab algorithms for the registered catalog and
see the plain-language algorithm explainer
for what each method may teach you and the Lab algorithm guide
for requirements and limits.
The third readout is deliberately narrow: it is not ichorCNA, does not estimate tumor fraction, and cannot resolve focal or subclonal events.
The diagram below describes the public evidence demo, not the Lab run path.
flowchart LR
A[MinION modBAM] --> B[Fragment-length summary]
A --> C[CpG methylation extraction]
A --> J[Whole-chromosome dosage screen]
C --> D[Loyfer UXM classification]
D --> E[NNLS cell-mixture estimate]
B --> F[Registered evidence]
E --> F
J --> F
G[Source passages] --> F
F --> H[Bounded AI review]
H --> I[Cited assessment + limitations]
Requires Python 3.11 and uv.
uv sync
uv run pytest
uv run streamlit run app.py
To take your own Nanopore BAMs through the signed CLI (align, reference
register, preflight, run, catalog import, serve), start with the short
scientist quick guide. The full reference is
Real local BAM (unqualified)
in the operator guide. It needs samtools (brew install samtools) to index
the inputs. These local records are unqualified and not for clinical use.
For the separate, unsigned multi-algorithm workflow, follow the
Lab guide.
The checked-in public demo bundles contain aggregate measurements and provenance only. They do not contain BAMs, read IDs, local paths, source documents, or credentials.
TRACEBACK_DEMO_REPLAY=1 to replay validated assessments
without AWS credentials. The UI labels the result as a fixture and does not
claim a live provider call.For live review, configure the standard AWS credential chain and optionally:
| Variable | Default |
|---|---|
BEDROCK_MODEL_ID | openai.gpt-5.5 |
BEDROCK_REGION | us-east-2 |
BEDROCK_MAX_TOKENS | 1024 |
Private inputs belong under ignored data/local/ paths:
MM, ML, and MN tags, or a normalized
modkit extract calls TSVTRACEBACK_FRAGMENT_HASH_SALT='local-private-value' \
uv run python scripts/regenerate_cell_origin.py \
--extract-tsv data/local/cell-origin/calls.normalized.tsv
The validated result is written to data/local/cell-origin/result.json and
takes precedence over the public aggregate bundle.
Regenerate the experimental chromosome-dosage result:
uv run python -m scripts.regenerate_copy_number \
--bam data/local/cell-origin/full.hg38.sorted.bam
Never commit .env files, credentials, sequence files, BAMs, read IDs, source
reports, local paths, or patient/sample identifiers. Tests are fully offline.
Only bounded excerpts and aggregate check results may enter model prompts.