@platforma-open/platforma-open.titeseq-analysis 2.2.0 → 2.3.0
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- package/block-pack/CHANGELOG.md +3 -0
- package/block-pack/block-logo.png +0 -0
- package/block-pack/description.md +7 -0
- package/block-pack/main.plj.gz +0 -0
- package/block-pack/manifest.json +1 -0
- package/block-pack/model.json +1 -0
- package/block-pack/organization-logo.png +0 -0
- package/block-pack/published.json +8 -0
- package/block-pack/ui.tgz +0 -0
- package/dist/AGENTS.d.ts +9090 -0
- package/dist/AGENTS.d.ts.map +1 -0
- package/dist/AGENTS.js +0 -0
- package/dist/index.d.ts +9101 -0
- package/dist/index.d.ts.map +1 -0
- package/dist/index.js +14087 -0
- package/dist/index.js.map +1 -0
- package/dist/rolldown-runtime-DC62tzP2.js +33 -0
- package/package.json +27 -11
- package/index.d.ts +0 -9
- package/index.js +0 -15
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# Overview
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Estimates apparent binding affinity (Kd,app) per antibody variant from Tite-Seq data. For each clonotype at each antigen concentration, the block computes a signal (mean-bin from per-bin FACS read counts, or clonotype frequency in no-bin mode), fits a Hill equation to the titration curve, and classifies each clonotype as Good, Partial, or Failed.
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The block runs downstream of MiXCR Clonotyping, which supplies per-sample, per-clonotype abundance, and upstream of Antibody/TCR Lead Selection, which consumes Kd,app and affinity class as In Vitro preset inputs. An optional 0 M no-antigen control fixes the Hill baseline and improves fit reliability for weak binders.
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Kd,app is apparent affinity, not thermodynamic Kd. Values support within-experiment ranking only and are not comparable across experiments, display formats (scFv vs Fab), or biophysical assays (SPR, BLI). Integer bin labels introduce a systematic compression of the mean-bin scale, following the convention in the Tite-Seq literature (Starr et al. 2020; Adams et al. 2016).
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