@platforma-open/milaboratories.clonotype-convergence 1.4.1 → 1.5.0
This diff represents the content of publicly available package versions that have been released to one of the supported registries. The information contained in this diff is provided for informational purposes only and reflects changes between package versions as they appear in their respective public registries.
- package/block-pack/description.md +10 -3
- package/block-pack/main.plj.gz +0 -0
- package/block-pack/manifest.json +1 -1
- package/block-pack/model.json +1 -1
- package/block-pack/published.json +1 -1
- package/block-pack/ui.tgz +0 -0
- package/dist/AGENTS.d.ts +106 -65
- package/dist/AGENTS.d.ts.map +1 -1
- package/dist/index.d.ts +106 -65
- package/dist/index.d.ts.map +1 -1
- package/dist/index.js +372 -371
- package/dist/index.js.map +1 -1
- package/package.json +8 -8
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# Overview
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Detects antigen-driven clonotype convergence in B-cell receptor (BCR) repertoires
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Detects antigen-driven clonotype convergence in B-cell receptor (BCR) repertoires. For each clonotype, the block counts how many other CDR3s in the same sample differ by exactly one amino acid — a per-clone neighbour density. High density signals independent B-cell lineages converging on the same CDR3 solution, a hallmark of antigen-driven selection.
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Two convergence calls are produced side by side, from that same neighbour count:
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- **fast-STAR** — always computed. A configurable threshold on the normalised neighbour frequency (Abbate et al. 2024), calibrated for human IgH by default.
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- **full-STAR** — added automatically wherever a per-clonotype generation probability is available from the **Generation Probability** block. Each clone is tested against what V(D)J recombination alone would produce for *its own* CDR3: a Poisson test of the observed neighbour count against a Pgen-derived null, with Benjamini-Hochberg control at a user-set false-discovery rate. A rare CDR3 is flagged on a few neighbours where a common one needs many. Where it runs, full-STAR is the preferred signal — fast-STAR is a fixed threshold, blind to how likely a sequence was to arise by chance.
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A clonotype seen in several samples is collapsed to one value per clonotype, ready for downstream scoring and lead selection: for each call a **score**, a **Hit / Not hit** flag, and a **reproducibility** ratio — how broadly across the dataset the clone is a hit, on a scale that compares between clones. Per-sample values are kept for QC, alongside an optional cluster filter adding a stricter "binder" call matching the paper's headline definition.
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Inputs: clonotype-level VDJ data — CDR3 amino-acid sequence, CDR3 nucleotide sequence, and per-clonotype abundance. Accepts bulk Heavy, bulk Light, or single-cell BCR data; light-chain analysis on single-cell data is an explicit opt-in. Generation Probability is optional — without it the block reports fast-STAR alone.
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**Designed for in-vivo BCR repertoires only.** In-vitro data — scFv libraries, phage / yeast display, panning-enriched repertoires — produces uninterpretable results. The algorithm runs and emits numbers, but the signal it was built to detect (germinal-center convergence under antigen-driven selection) is absent in vitro.
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Both statistics are from the Statistical Biophysics group's STAR tool. For more information, please see: [https://github.com/statbiophys/STAR](https://github.com/statbiophys/STAR) and cite the following publication if used in your research:
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> Abbate A. et al. Computational detection of antigen-specific B cell receptors following immunization. _PNAS_ 121(35):e2401058121 (2024). [https://doi.org/10.1073/pnas.2401058121](https://doi.org/10.1073/pnas.2401058121)
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package/block-pack/main.plj.gz
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Binary file
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package/block-pack/manifest.json
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{"schema":"v2","description":{"id":{"organization":"milaboratories","name":"clonotype-convergence","version":"1.
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