@platforma-open/milaboratories.sort-seq-analysis.block 1.0.2

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+ # @platforma-open/milaboratories.sort-seq-analysis.block
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+
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+ ## 1.0.2
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+
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+ ### Patch Changes
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+
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+ - bd2c759: Release fix
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+
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+ ## 1.0.1
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+
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+ ### Patch Changes
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+
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+ - 2efd95b: Sort-Seq Analysis — first implementation.
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+
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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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+
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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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+
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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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+
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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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+
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+ This block turns that spread into a score, one per condition. For every variant it emits:
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+
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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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+
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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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+
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+ ## Downstream
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+
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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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+
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+ ## Status
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+
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+ Under development. The specification lives in `docs/text/work/projects/sequence-repertoires/facs-bin-analysis/`.
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