@platforma-open/milaboratories.sort-seq-analysis.block 1.0.2
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- package/block-pack/CHANGELOG.md +28 -0
- package/block-pack/block-logo.png +0 -0
- package/block-pack/description.md +27 -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 +12826 -0
- package/dist/AGENTS.d.ts.map +1 -0
- package/dist/AGENTS.js +0 -0
- package/dist/index.d.ts +12839 -0
- package/dist/index.d.ts.map +1 -0
- package/dist/index.js +12910 -0
- package/dist/index.js.map +1 -0
- package/package.json +63 -0
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# @platforma-open/milaboratories.sort-seq-analysis.block
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## 1.0.2
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### Patch Changes
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- bd2c759: Release fix
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## 1.0.1
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### Patch Changes
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- 2efd95b: Sort-Seq Analysis — first implementation.
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Scores protein variants from a sort-seq (FACS bin) experiment. Per condition the block emits the
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read-weighted mean of the gate ranks each variant sorted into (`pl7.app/facsBin/gateRankMean`) and that
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value minus the parent's (`pl7.app/facsBin/binScore`), both keyed on the profiler's variant axis and
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carrying the condition — and, on the bin score, the reference mode — as matchable domain keys.
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- **software** — the score computation as a Python package on the scientific-slim runenv, with its own
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pytest suite pinning the arithmetic clause by clause against hand-computed numbers.
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- **workflow** — resolves the inputs against the abundance anchor, exports the reads and variants tables,
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invokes the entrypoint once, and constructs one PColumn per file the manifest names.
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- **model** — the seven-argument surface with every configuration rule validated before the run, the four
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option lists, and the outputs the three views read.
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- **ui** — one settings drawer plus Results, Read distribution and Run summary.
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Integration tests against the real upstream chain are not in this change.
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## Overview
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A sort-seq experiment hands you a library of protein variants and, for each gate the sorter collected, a
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count of how many reads of each variant landed in it. Nothing in that table is a binding measurement: it is
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a spread of reads across gates, and the gates' order along the binding axis is the only thing that makes one
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variant's spread better than another's.
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This block turns that spread into a score, one per condition. For every variant it emits:
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- **Gate rank mean** — the read-weighted mean of the gate ranks the variant's reads fell in, in gate-rank
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units. Higher means the variant sorted into higher gates. Not an affinity and not calibrated.
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- **Bin score** — the gate rank mean minus the parent's. Zero means the variant behaves like the parent at
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that condition.
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A run over N conditions emits both quantities N times, once per condition. A one-condition run is an
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ordinary run: it gets both quantities, with the run's single condition on each column exactly as a
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two-condition run would carry two.
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## Downstream
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Everything downstream of this block is a comparison of these scores — a pH switch is the difference between
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a variant's bin score at two pH arms, the on-state is its raw score at the arm the campaign treats as *on*,
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and a shortlist is a ranking over one of them.
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## Status
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Under development. The specification lives in `docs/text/work/projects/sequence-repertoires/facs-bin-analysis/`.
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