@datagrok/peptides 1.23.0 → 1.23.2

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package/package.json CHANGED
@@ -1,7 +1,7 @@
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  {
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  "name": "@datagrok/peptides",
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  "friendlyName": "Peptides",
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- "version": "1.23.0",
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+ "version": "1.23.2",
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  "author": {
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  "name": "Davit Rizhinashvili",
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  "email": "drizhinashvili@datagrok.ai"
@@ -17,7 +17,7 @@
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  "@datagrok-libraries/math": "^1.2.5",
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  "@datagrok-libraries/ml": "^6.8.2",
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  "@datagrok-libraries/statistics": "^1.2.12",
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- "@datagrok-libraries/tutorials": "^1.4.2",
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+ "@datagrok-libraries/tutorials": "^1.6.1",
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  "@datagrok-libraries/utils": "^4.4.0",
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  "datagrok-api": "^1.23.0",
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  "@webgpu/types": "^0.1.40",
@@ -4,6 +4,7 @@ import * as C from '../utils/constants';
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  import * as type from '../utils/types';
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  import {addExpandIconGen, getSeparator, setGridProps} from '../utils/misc';
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  import {renderCellSelection} from '../utils/cell-renderer';
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+ import {SeqTemps} from '@datagrok-libraries/bio/src/utils/macromolecule/seq-handler';
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  export type MutationCliffsOptions = {
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  mutationCliffs: type.MutationCliffs, mutationCliffsSelection: type.Selection, sequenceColumnName: string,
@@ -177,6 +178,7 @@ function cliffsPairsWidgetParts(table: DG.DataFrame, options: MutationCliffsOpti
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  substCol.tags[C.TAGS.SEPARATOR] = getSeparator(alignedSeqCol);
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  substCol.tags[DG.TAGS.UNITS] = alignedSeqCol.tags[DG.TAGS.UNITS];
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  substCol.tags[DG.TAGS.CELL_RENDERER] = 'MacromoleculeDifference';
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+ substCol.temp[SeqTemps.notationProvider] = alignedSeqCol.temp[SeqTemps.notationProvider];
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  let keyPress = false;
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  let lastSelectedIndex: number | null = null;
@@ -257,6 +259,10 @@ function cliffsPairsWidgetParts(table: DG.DataFrame, options: MutationCliffsOpti
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  uniqueSequencesTable.name = 'Unique sequences that form Mutation Cliffs pairs';
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  const seqIdxCol = uniqueSequencesTable.columns.addNewInt('~seqIdx');
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  const seqIdxColData = seqIdxCol.getRawData();
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+ if (uniqueSequencesTable.col(options.sequenceColumnName)) {
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+ uniqueSequencesTable.col(options.sequenceColumnName)!.temp[SeqTemps.notationProvider] =
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+ alignedSeqCol.temp[SeqTemps.notationProvider];
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+ }
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  const selectedIndexes = uniqueSequencesBitSet.getSelectedIndexes();
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  seqIdxCol.init((idx) => selectedIndexes[idx]);
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  const uniqueSequencesGrid = uniqueSequencesTable.plot.grid();
@@ -9,6 +9,7 @@ import {TooltipOptions} from '../utils/tooltips';
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  import {calculateMonomerPositionStatistics} from '../utils/algorithms';
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  import {AggregationColumns} from '../utils/statistics';
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  import {SeqPalette} from '@datagrok-libraries/bio/src/seq-palettes';
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+ import {SeqTemps} from '@datagrok-libraries/bio/src/utils/macromolecule/seq-handler';
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  export type SelectionWidgetOptions = {
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  tableSelection: DG.BitSet, gridColumns: DG.GridColumnList, positionColumns: DG.Column<string>[],
@@ -123,5 +124,12 @@ export function getSelectionWidget(table: DG.DataFrame, options: SelectionWidget
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  tooltipOptions);
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  }
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+ (table.columns.bySemTypeAll(DG.SEMTYPE.MACROMOLECULE) ?? []).forEach(
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+ (col) => {
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+ if (newTable.col(col.name))
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+ newTable.col(col.name)!.temp[SeqTemps.notationProvider] = col.temp[SeqTemps.notationProvider];
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+ },
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+ );
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+
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  return gridHost;
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  }