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.changeset/adapt-synthetic-repertoire-profiler.md

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block/CHANGELOG.md

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## 1.0.0
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## 1.5.2
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### Patch Changes
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- Updated dependencies [f966ff5]
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- @platforma-open/milaboratories.sequence-properties.model@1.3.2
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- @platforma-open/milaboratories.sequence-properties.workflow@1.3.3
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- @platforma-open/milaboratories.sequence-properties.ui@1.4.1
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## 1.5.1
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block/package.json

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{
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"name": "@platforma-open/milaboratories.sequence-properties",
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"version": "1.5.1",
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"version": "1.5.2",
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"scripts": {
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"build": "shx rm -rf ./block-pack && block-tools pack",
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"mark-stable": "block-tools mark-stable -r 's3://milab-euce1-prod-pkgs-s3-block-registry/pub/releases/?region=eu-central-1'",

model/CHANGELOG.md

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# @platforma-open/MiLaboratories.sequence-properties.model
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## 1.3.2
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### Patch Changes
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- f966ff5: Support `synthetic-repertoire-profiler` (amplicon) variant datasets:
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- `detectMode` now recognizes the profiler's `pl7.app/variantKey` axis (axis domain `pl7.app/repertoire/extractionRunId`) as a new `"amplicon"` mode, instead of falling through to the "no recognized sequence key axis" panic.
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- Amplicon runs the same whole-sequence physicochemical computation as peptide mode (the Python engine runs it under its `peptide` path), reading the whole-variant amino-acid sequence (`pl7.app/feature: "amplicon-sequence"`).
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- Output property columns (and the AA-fraction column) are labeled with the `amplicon-sequence` feature instead of `peptide`, so they attach to the correct entity.
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- The UI's default scatter/histogram axes are amplicon-aware (charge / hydrophobicity on the `amplicon-sequence` feature).
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Per-region properties for amplicon (using the profiler's region subsequences) are out of scope here — whole-sequence descriptors only.
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## 1.3.1
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model/package.json

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"name": "@platforma-open/milaboratories.sequence-properties.model",
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"version": "1.3.1",
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"version": "1.3.2",
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"description": "Block model",
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"type": "module",
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"main": "dist/index.js",

test/CHANGELOG.md

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# @platforma-open/MiLaboratories.sequence-properties.test
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## 1.1.10
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### Patch Changes
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- Updated dependencies [f966ff5]
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- @platforma-open/milaboratories.sequence-properties.model@1.3.2
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## 1.1.9
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test/package.json

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{
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"name": "@platforma-open/milaboratories.sequence-properties.test",
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"version": "1.1.9",
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"version": "1.1.10",
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"private": true,
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"description": "Block tests",
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"keywords": [],

ui/CHANGELOG.md

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# @platforma-open/MiLaboratories.sequence-properties.ui
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## 1.4.1
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### Patch Changes
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- f966ff5: Support `synthetic-repertoire-profiler` (amplicon) variant datasets:
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- `detectMode` now recognizes the profiler's `pl7.app/variantKey` axis (axis domain `pl7.app/repertoire/extractionRunId`) as a new `"amplicon"` mode, instead of falling through to the "no recognized sequence key axis" panic.
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- Amplicon runs the same whole-sequence physicochemical computation as peptide mode (the Python engine runs it under its `peptide` path), reading the whole-variant amino-acid sequence (`pl7.app/feature: "amplicon-sequence"`).
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- Output property columns (and the AA-fraction column) are labeled with the `amplicon-sequence` feature instead of `peptide`, so they attach to the correct entity.
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- The UI's default scatter/histogram axes are amplicon-aware (charge / hydrophobicity on the `amplicon-sequence` feature).
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Per-region properties for amplicon (using the profiler's region subsequences) are out of scope here — whole-sequence descriptors only.
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- Updated dependencies [f966ff5]
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- @platforma-open/milaboratories.sequence-properties.model@1.3.2
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## 1.4.0
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### Minor Changes

ui/package.json

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{
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"name": "@platforma-open/milaboratories.sequence-properties.ui",
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"version": "1.4.0",
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"version": "1.4.1",
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"type": "module",
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"scripts": {
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"fmt": "ts-builder format",

workflow/CHANGELOG.md

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# @platforma-open/MiLaboratories.sequence-properties.workflow
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## 1.3.3
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### Patch Changes
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- f966ff5: Support `synthetic-repertoire-profiler` (amplicon) variant datasets:
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- `detectMode` now recognizes the profiler's `pl7.app/variantKey` axis (axis domain `pl7.app/repertoire/extractionRunId`) as a new `"amplicon"` mode, instead of falling through to the "no recognized sequence key axis" panic.
10+
- Amplicon runs the same whole-sequence physicochemical computation as peptide mode (the Python engine runs it under its `peptide` path), reading the whole-variant amino-acid sequence (`pl7.app/feature: "amplicon-sequence"`).
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- Output property columns (and the AA-fraction column) are labeled with the `amplicon-sequence` feature instead of `peptide`, so they attach to the correct entity.
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- The UI's default scatter/histogram axes are amplicon-aware (charge / hydrophobicity on the `amplicon-sequence` feature).
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Per-region properties for amplicon (using the profiler's region subsequences) are out of scope here — whole-sequence descriptors only.
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## 1.3.2
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### Patch Changes

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