rewirebio.iobenchmarks
Method

Small somatic variant classifier on a 507-gene panel (GRAIL prototype)

Gene-level counts of variants expected to disrupt function and panel copy number, classified by elastic net logistic regression.

Results are recorded on linked configurations and versions of this method. Their settings and evaluations are kept separate below.

1 configuration with results

Results on linked records

This method has no results of its own in this release. One linked record has results. They are not assigned to the underlying method: each record keeps its own settings and evaluations, and its scores are on its own page.

Overview

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Consult the linked sources for architecture or protocol details. Missing evidence is not evidence of a missing capability.

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Strengths, limitations and unresolved questions

Evidence

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Evidence table

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0 evidence rows matching the loaded filters

Claims, original sources and review scope · Release 2026-10-10-cbb3da59bc08
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Sources and history

Release 2026-10-10-cbb3da59bc08 · Record review: source checked

1 source record and release historyDownload this release (gzip)
Technical metadata and extraction receipts

Stable ID: ctdnajam-20261010-method-snv

areas
dna-genomes
contexts
clinical_research
method types
supervised_machine_learning
reported name
SNV
entity level
method
source locator
STAR Methods, TS: SNV and SNV-WBC classifiers
missing metadata
version: reason: inapplicable; note: Family record; settings are on configurations
Related records

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