@datagrok/bio 2.4.15 → 2.4.16

package/package.json

@@ -5,7 +5,7 @@
     "name": "Leonid Stolbov",
     "email": "lstolbov@datagrok.ai"
   },
-  "version": "2.4.15",
+  "version": "2.4.16",
   "description": "Bioinformatics support (import/export of sequences, conversion, visualization, analysis). [See more](https://github.com/datagrok-ai/public/blob/master/packages/Bio/README.md) for details.",
   "repository": {
     "type": "git",
@@ -14,7 +14,7 @@
   },
   "dependencies": {
     "@biowasm/aioli": "^3.1.0",
-    "@datagrok-libraries/bio": "^5.28.4",
+    "@datagrok-libraries/bio": "^5.29.0",
     "@datagrok-libraries/chem-meta": "^1.0.1",
     "@datagrok-libraries/ml": "^6.3.16",
     "@datagrok-libraries/tutorials": "^1.2.1",

package/scripts/sequence_generator.py

@@ -0,0 +1,289 @@
+#!/usr/bin/env python3
+# name: Sequence generator
+# description: Create the model peptides/DNA sequences with peptides data
+# language: python
+# tags: template, demo
+# input: int clusters = 1 [Number of superclusters]
+# input: int num_sequences = 500 [Number of sequences in each supercluster]
+# input: int motif_length = 12 [Average length of motif]
+# input: int max_variants_position = 3 [Maximum number of different letters in conservative position in motif]
+# input: int random_length = 3 [Average length of random sequence parts before and after motif]
+# input: int dispersion = 2 [Variation of total sequence length]
+# input: string alphabet_key = 'PT' [Sequence alphabet: PT/DNA/RNA/custom. Custom alphabet is a list of values separated by comma]
+# input: bool disable_cliffs = False [Disable generation of cliffs]
+# input: double cliff_probability = 0.01 [Probability to make activity cliff of a sequence]
+# input: double cliff_strength = 4.0 [Strength of cliff]
+# output: dataframe sequences
+
+import random
+import argparse
+import sys
+
+from typing import List, Tuple, Dict, Iterator, Any
+
+alphabet_type = List[str]
+
+letter_choice_type = List[str]
+motif_template_type = List[letter_choice_type]
+
+sequence_record_type = Tuple[int, str, float, bool]
+sequence_record_cluster_type = Tuple[int, str, str, float, bool]
+
+alphabets: Dict[str, str] = {
+    "PT": "A,C,D,E,F,G,H,I,K,L,M,N,P,Q,R,S,T,V,W,Y",
+    "DNA": "A,T,G,C",
+    "RNA": "A,U,G,C",
+}
+
+
+def mean_range(mean: int, disp: int) -> int:
+    return random.randint(max(mean - disp, 0), mean + disp)
+
+
+def generate_motif_template(
+    motif_length: int,
+    alphabet: alphabet_type,
+    max_variants_cluster: int,
+    prob_any: float = 0.2,
+) -> motif_template_type:
+    motif_template = []
+    for position in range(motif_length):
+        # Selecting letters for position i
+        if (0 < position < motif_length - 1) and (random.random() <= prob_any):
+            letters = ["?"]  # this stands for any symbol
+        else:
+            n_variants = random.randrange(max_variants_cluster) + 1
+            letters = [random.choice(alphabet) for i in range(n_variants)]
+        motif_template.append(letters)
+    return motif_template
+
+
+def generate_motif(template: motif_template_type, alphabet: alphabet_type) -> str:
+    template_with_any = [(letters if not "?" in letters else alphabet) for letters in template]
+    return "".join([random.choice(letters) for letters in template_with_any])
+
+
+def motif_notation(motif_template: motif_template_type) -> str:
+    def motif_notation_code(letter_choice: letter_choice_type) -> str:
+        if len(letter_choice) == 1:
+            return letter_choice[0]
+        else:
+            return f"[{''.join(letter_choice)}]"
+
+    return "".join([motif_notation_code(letter_choice) for letter_choice in motif_template])
+
+
+def generate_random(n: int, alphabet: alphabet_type) -> str:
+    return "".join([random.choice(alphabet) for i in range(n)])
+
+
+def make_cliff(motif_template: motif_template_type, alphabet: alphabet_type, motif: str) -> str:
+    # Mutate conservative letter in motif
+    pos = random.randrange(len(motif_template))
+    while "?" in motif_template[pos]:
+        pos = (pos + 1) % len(motif_template)  # always will find letters since ends of motif can't be any symbol
+    outlier_letters = list(set(alphabet) - set(motif_template[pos]))
+    return motif[:pos] + random.choice(outlier_letters) + motif[pos + 1 :]
+
+
+def generate_cluster(
+    n_sequences: int,
+    motif_length: int,
+    prefix_length: int,
+    suffix_length: int,
+    max_variants_position: int,
+    make_cliffs: bool,
+    alphabet: alphabet_type,
+    cliff_probability: float,
+    cliff_strength: float,
+) -> Iterator[sequence_record_type]:
+    motif_template = generate_motif_template(motif_length, alphabet, max_variants_position)
+
+    activity_average = random.random() * 10
+    activity_dispersion = random.random()
+    sys.stderr.write(f"Motif template: {motif_notation(motif_template)}\n")
+
+    for n_seq in range(n_sequences):
+        activity = random.gauss(activity_average, activity_dispersion)
+
+        motif = generate_motif(motif_template, alphabet)
+        prefix = generate_random(prefix_length, alphabet)
+        suffix = generate_random(suffix_length, alphabet)
+        seq = prefix + motif + suffix
+
+        is_cliff = make_cliffs and (random.random() <= cliff_probability)
+        sequence_record: sequence_record_type = (n_seq, seq, activity, is_cliff)
+        yield sequence_record
+
+        if is_cliff:
+            # Making activity cliff
+            cliff_motif = make_cliff(motif_template, alphabet, motif)
+            cliff_seq = prefix + cliff_motif + suffix
+            # Recalculating activity
+            cliff_disp = activity_dispersion * cliff_strength * (0.5 + random.random())
+            activity = activity_average - cliff_disp
+            cliff_activity = activity_average + cliff_disp
+
+            # sys.stderr.write(f"Cliff for sequence #{line_number:4}, cluster {n_cluster} \n")
+            # sys.stderr.write(f"{activity_average}\t{motif}\t{activity}\n")
+            # sys.stderr.write(f"{activity_average}\t{cliff_motif}\t{cliff_activity}\n")
+            n_seq += 1
+            sequence_record = (n_seq, cliff_seq, cliff_activity, is_cliff)
+            yield sequence_record
+
+
+def generate_sequences(
+    n_clusters: int,
+    n_sequences: int,
+    average_motif_length: int,
+    max_variants_position: int,
+    average_random_length: int,
+    dispersion: int,
+    alphabet: alphabet_type,
+    make_cliffs: bool,
+    cliff_probability: float,
+    cliff_strength: float,
+) -> Tuple[List[str], List[sequence_record_cluster_type]]:
+    headers: List[str] = ["cluster", "sequence_id", "sequence", "activity", "is_cliff"]
+    sequences: List[sequence_record_cluster_type] = []
+
+    for n_cluster in range(n_clusters):
+        motif_length = mean_range(average_motif_length, dispersion)
+
+        # sys.stderr.write(f"Cluster {n_cluster:2} motif template: {motif_notation(motif_template)}\n")
+        total_length = mean_range(average_random_length * 2, args.dispersion) + motif_length
+        prefix_length = mean_range(average_random_length, args.dispersion // 2)
+        suffix_length = total_length - motif_length - prefix_length
+        sys.stderr.write(f"Generating sequences for cluster {n_cluster}\n")
+        for n_seq, seq, activity, is_cliff in generate_cluster(
+            n_sequences,
+            motif_length,
+            prefix_length,
+            suffix_length,
+            max_variants_position,
+            make_cliffs,
+            alphabet,
+            cliff_probability,
+            cliff_strength,
+        ):
+            sequences.append((n_cluster, f"c{n_cluster}_s{n_seq}", seq, activity, is_cliff))
+    return headers, sequences
+
+
+def parse_command_line_args() -> Any:
+    parser = argparse.ArgumentParser(
+        prog="MotifSequencesGenerator",
+        description="The program generates set of sequences containing sequence motifs "
+        "for SAR fucntionality testing",
+        epilog="Utility support: Gennadii Zakharov",
+    )
+
+    parser.add_argument("-c", "--clusters", type=int, default=1, help="Number of superclusters")
+    parser.add_argument(
+        "-s",
+        "--sequences",
+        type=int,
+        default=500,
+        help="Number of sequences in each supercluster",
+    )
+    parser.add_argument("-m,", "--motif-length", type=int, default=12, help="Average length of motif")
+
+    parser.add_argument(
+        "-r,",
+        "--random-length",
+        type=int,
+        default=3,
+        help="Average length of random sequence parts before and after motif",
+    )
+    parser.add_argument(
+        "-d,",
+        "--dispersion",
+        type=int,
+        default=2,
+        help="Variation of total sequence length",
+    )
+
+    available_alphabets = ",".join(list(alphabets.keys()) + ["custom"])
+    parser.add_argument(
+        "--alphabet",
+        type=str,
+        default=list(alphabets.keys())[0],
+        help=f"Sequence alphabet: {available_alphabets}. Custom alphabet is a list of values separated " f"by comma",
+    )
+    parser.add_argument(
+        "--max-variants-position",
+        type=int,
+        default=3,
+        help="Maximum number of different letters in conservative position in motif",
+    )
+    parser.add_argument(
+        "--cliff-probability",
+        type=float,
+        default=0.01,
+        help="Probability to make activity cliff of a sequence",
+    )
+    parser.add_argument(
+        "--cliff-strength",
+        type=float,
+        default=4.0,
+        help="Strength of cliff",
+    )
+    parser.add_argument(
+        "--disable-cliffs",
+        type=bool,
+        default=False,
+        help="Disable generation of cliffs",
+    )
+
+    command_line_args = parser.parse_args()
+
+    return command_line_args
+
+
+# ====================================================================================
+
+grok = "clusters" in globals()
+
+if not grok:
+    # We are not in Datagrok - need to parse command line arguments
+    args = parse_command_line_args()
+    clusters = args.clusters
+    num_sequences = args.sequences
+    motif_length = args.motif_length
+    max_variants_position = args.max_variants_position
+    random_length = args.random_length
+    dispersion = args.dispersion
+    alphabet_key = args.alphabet
+    disable_cliffs = args.disable_cliffs
+    cliff_probability = args.cliff_probability
+    cliff_strength = args.cliff_strength
+
+alphabet: alphabet_type = alphabets[alphabet_key].split(",") if alphabet_key in alphabets else alphabet_key.split(",")
+
+# Running sequence generator
+header, data = generate_sequences(
+    clusters,
+    num_sequences,
+    motif_length,
+    max_variants_position,
+    random_length,
+    dispersion,
+    alphabet,
+    not disable_cliffs,
+    cliff_probability,
+    cliff_strength,
+)
+
+if grok:
+    # Exporting data to Datagrok as a pandas dataframe
+    import pandas as pd
+
+    sequences = pd.DataFrame.from_records(data, columns=header)
+else:
+    # Writing results to stdout - no need to work with big and heavy Pandas
+    import csv
+
+    csv_writer = csv.writer(sys.stdout, delimiter="\t", quoting=csv.QUOTE_MINIMAL)
+    csv_writer.writerow(header)
+    for line in data:
+        csv_writer.writerow(line)

package/src/analysis/sequence-diversity-viewer.ts

@@ -12,15 +12,17 @@ import {updateDivInnerHTML} from '../utils/ui-utils';
 import {Subject} from 'rxjs';
 
 export class SequenceDiversityViewer extends SequenceSearchBaseViewer {
+  diverseColumnLabel: string | null; // Use postfix Label to prevent activating table column selection editor
+
   renderMolIds: number[] | null = null;
   columnNames = [];
   computeCompleted = new Subject<boolean>();
 
   constructor() {
     super('diversity');
+    this.diverseColumnLabel = this.string('diverseColumnLabel', null);
   }
 
-
   async render(computeData = true): Promise<void> {
     if (!this.beforeRender())
       return;
@@ -29,14 +31,15 @@ export class SequenceDiversityViewer extends SequenceSearchBaseViewer {
         const monomericMols = await getMonomericMols(this.moleculeColumn);
         //need to create df to calculate fingerprints
         const monomericMolsDf = DG.DataFrame.fromColumns([monomericMols]);
-        this.renderMolIds =
-        await grok.functions.call('Chem:callChemDiversitySearch', {
+        this.renderMolIds = await grok.functions.call('Chem:callChemDiversitySearch', {
           col: monomericMols,
           metricName: this.distanceMetric,
           limit: this.limit,
           fingerprint: this.fingerprint
         });
-        const resCol = DG.Column.string('sequence', this.renderMolIds!.length)
+        const diverseColumnName: string = this.diverseColumnLabel != null ? this.diverseColumnLabel :
+          `diverse (${this.moleculeColumnName})`;
+        const resCol = DG.Column.string(diverseColumnName, this.renderMolIds!.length)
           .init((i) => this.moleculeColumn?.get(this.renderMolIds![i]));
         resCol.semType = DG.SEMTYPE.MACROMOLECULE;
         this.tags.forEach((tag) => resCol.setTag(tag, this.moleculeColumn!.getTag(tag)));

package/src/analysis/sequence-similarity-viewer.ts

@@ -11,13 +11,15 @@ import {Subject} from 'rxjs';
 import {TAGS as bioTAGS, getSplitter} from '@datagrok-libraries/bio/src/utils/macromolecule';
 
 export class SequenceSimilarityViewer extends SequenceSearchBaseViewer {
+  cutoff: number;
   hotSearch: boolean;
+  similarColumnLabel: string | null; // Use postfix Label to prevent activating table column selection editor
+
   sketchedMolecule: string = '';
   curIdx: number = 0;
   molCol: DG.Column | null = null;
   idxs: DG.Column | null = null;
   scores: DG.Column | null = null;
-  cutoff: number;
   gridSelect: boolean = false;
   targetMoleculeIdx: number = 0;
   computeCompleted = new Subject<boolean>();
@@ -26,6 +28,7 @@ export class SequenceSimilarityViewer extends SequenceSearchBaseViewer {
     super('similarity');
     this.cutoff = this.float('cutoff', 0.01, {min: 0, max: 1});
     this.hotSearch = this.bool('hotSearch', true);
+    this.similarColumnLabel = this.string('similarColumnLabel', null);
   }
 
   init(): void {
@@ -54,7 +57,9 @@ export class SequenceSimilarityViewer extends SequenceSearchBaseViewer {
         });
         this.idxs = df.getCol('indexes');
         this.scores = df.getCol('score');
-        this.molCol = DG.Column.string('sequence',
+        const similarColumnName: string = this.similarColumnLabel != null ? this.similarColumnLabel :
+          `similar (${this.moleculeColumnName})`;
+        this.molCol = DG.Column.string(similarColumnName,
           this.idxs!.length).init((i) => this.moleculeColumn?.get(this.idxs?.get(i)));
         this.molCol.semType = DG.SEMTYPE.MACROMOLECULE;
         this.tags.forEach((tag) => this.molCol!.setTag(tag, this.moleculeColumn!.getTag(tag)));

package/src/demo/bio01-similarity-diversity.ts

@@ -6,8 +6,10 @@ import {_package} from '../package';
 import {DemoScript} from '@datagrok-libraries/tutorials/src/demo-script';
 import {delay} from '@datagrok-libraries/utils/src/test';
 import {handleError} from './utils';
+import {SequenceDiversityViewer} from '../analysis/sequence-diversity-viewer';
+import {SequenceSimilarityViewer} from '../analysis/sequence-similarity-viewer';
 
-const dataFn = 'data/sample_FASTA_DNA.csv';
+const dataFn: string = 'data/sample_FASTA_DNA.csv';
 
 export async function demoBio01UI() {
   let view: DG.TableView;
@@ -17,21 +19,34 @@ export async function demoBio01UI() {
     const demoScript = new DemoScript('Demo', 'Sequence similarity / diversity search');
     await demoScript
       .step(`Loading DNA notation 'fasta'`, async () => {
+        grok.shell.windows.showContextPanel = false;
+        grok.shell.windows.showProperties = false;
+
         df = await _package.files.readCsv(dataFn);
         view = grok.shell.addTableView(df);
+
+        view.grid.columns.byName('id')!.width = 0;
+        view.grid.columns.byName('sequence')!.width = 500;
+        // TODO: Fix column width
       }, {
         description: `Load dataset with macromolecules of 'fasta' notation, 'DNA' alphabet.`,
-        delay: 1600
+        delay: 1200
       })
       .step('Sequence similarity search', async () => {
-        const simViewer = await df.plot.fromType('Sequence Similarity Search') as DG.Viewer;
+        const simViewer = await df.plot.fromType('Sequence Similarity Search', {
+          moleculeColumnName: 'sequence',
+          similarColumnLabel: 'Similar to current',
+        }) as SequenceSimilarityViewer;
         view.dockManager.dock(simViewer, DG.DOCK_TYPE.RIGHT, null, 'Similarity search', 0.35);
       }, {
         description: `Add 'Sequence Similarity Search' viewer.`,
         delay: 1600
       })
       .step('Sequence diversity search', async () => {
-        const divViewer = await df.plot.fromType('Sequence Diversity Search') as DG.Viewer;
+        const divViewer = await df.plot.fromType('Sequence Diversity Search', {
+          moleculeColumnName: 'sequence',
+          diverseColumnLabel: 'Top diverse sequences of all data'
+        }) as SequenceDiversityViewer;
         view.dockManager.dock(divViewer, DG.DOCK_TYPE.DOWN, null, 'Diversity search', 0.27);
       }, {
         description: `Add 'Sequence Deversity Search' viewer.`,

package/src/demo/bio01a-hierarchical-clustering-and-sequence-space.ts

@@ -36,6 +36,9 @@ export async function demoBio01aUI() {
         ]);
         view = grok.shell.addTableView(df);
         view.grid.props.rowHeight = 22;
+
+        grok.shell.windows.showContextPanel = false;
+        grok.shell.windows.showProperties = false;
       }, {
         description: `Load dataset with macromolecules of 'fasta' notation, 'DNA' alphabet.`,
         delay: 1600,

package/src/demo/bio01b-hierarchical-clustering-and-activity-cliffs.ts

@@ -29,6 +29,9 @@ export async function demoBio01bUI() {
     const demoScript = new DemoScript('Demo', '');
     await demoScript
       .step(`Loading DNA notation \'fasta\'`, async () => {
+        grok.shell.windows.showContextPanel = false;
+        grok.shell.windows.showProperties = false;
+
         [df, treeHelper, dendrogramSvc] = await Promise.all([
           _package.files.readCsv(dataFn),
           getTreeHelper(),

package/src/demo/bio05-helm-msa-sequence-space.ts

@@ -28,6 +28,9 @@ export async function demoBio05UI(): Promise<void> {
     await demoScript
       .step(`Loading peptides notation 'HELM'`, async () => {
         view = grok.shell.addTableView(df = await _package.files.readCsv(helmFn));
+
+        grok.shell.windows.showContextPanel = false;
+        grok.shell.windows.showProperties = false;
       }, {
         description: 'Load dataset with macromolecules of \'Helm\' notation.',
         delay: 1600,
@@ -44,15 +47,6 @@ export async function demoBio05UI(): Promise<void> {
         description: 'Multiple sequence alignment (MSA) performed with PepSeA tool operating on non-natural aminoacids as well.',
         delay: 1600,
       })
-      .step('Composition analysis on MSA results', async () => {
-        wlViewer = await df.plot.fromType('WebLogo', {
-          sequenceColumnName: msaHelmColName
-        }) as DG.Viewer & IWebLogoViewer;
-        view.dockManager.dock(wlViewer, DG.DOCK_TYPE.DOWN, null, 'Composition analysis', 0.2);
-      }, {
-        description: 'Composition analysis allows to reveal functional features of sequences like motifs, or variable loops.',
-        delay: 1600,
-      })
       .step('Building sequence space', async () => {
         const method: string = 'UMAP';
         ssViewer = (await sequenceSpaceTopMenu(df, msaHelmCol,
@@ -62,6 +56,16 @@ export async function demoBio05UI(): Promise<void> {
         description: 'Reduce sequence space dimensionality to display on 2D representation.',
         delay: 1600
       })
+      .step('Composition analysis on MSA results', async () => {
+        wlViewer = await df.plot.fromType('WebLogo', {
+          sequenceColumnName: msaHelmColName,
+          maxHeight: 50,
+        }) as DG.Viewer & IWebLogoViewer;
+        view.dockManager.dock(wlViewer, DG.DOCK_TYPE.DOWN, null, 'Composition analysis', 0.2);
+      }, {
+        description: 'Composition analysis allows to reveal functional features of sequences like motifs, or variable loops.',
+        delay: 1600,
+      })
       .start();
   } catch (err: any) {
     handleError(err);

package/src/package.ts

@@ -49,6 +49,7 @@ import {demoBio01bUI} from './demo/bio01b-hierarchical-clustering-and-activity-c
 import {demoBio05UI} from './demo/bio05-helm-msa-sequence-space';
 import {checkInputColumnUI} from './utils/check-input-column';
 import {multipleSequenceAlignmentUI} from './utils/multiple-sequence-alignment-ui';
+import { runKalign } from './utils/multiple-sequence-alignment';
 
 export const _package = new DG.Package();
 
@@ -411,10 +412,21 @@ export async function toAtomicLevel(df: DG.DataFrame, macroMolecule: DG.Column):
 //top-menu: Bio | Alignment | MSA...
 //name: MSA...
 //tags: bio, panel
-export function multipleSequenceAlignmentAny(): void {
+export function multipleSequenceAlignmentDialog(): void {
   multipleSequenceAlignmentUI();
 }
 
+//name: Multiple Sequence Alignment
+//description: Multiple sequence alignment
+//tags: bio
+//input: column sequenceCol {semType: Macromolecule}
+//input: column clustersCol
+//output: column result
+export async function alignSequences(sequenceCol: DG.Column<string> | null = null,
+  clustersCol: DG.Column | null = null): Promise<DG.Column<string>> {
+  return multipleSequenceAlignmentUI({col: sequenceCol, clustersCol});
+}
+
 //top-menu: Bio | Structure | Composition Analysis
 //name: Composition Analysis
 //meta.icon: files/icons/composition-analysis.svg

package/src/tests/checkInputColumn-tests.ts

@@ -15,7 +15,7 @@ seq3,
 seq4`;
 
   test('testMsaPos', async () => {
-    const func: DG.Func = DG.Func.find({package: 'Bio', name: 'multipleSequenceAlignmentAny'})[0];
+    const func: DG.Func = DG.Func.find({package: 'Bio', name: 'multipleSequenceAlignmentDialog'})[0];
     const funcInputColumnProperty: DG.Property = func.inputs.find((i) => i.name == 'sequence')!;
 
     const k = 11;
@@ -67,7 +67,7 @@ seq4`;
   });
 
   test('testGetActionFunctionMeta', async () => {
-    const func: DG.Func = DG.Func.find({package: 'Bio', name: 'multipleSequenceAlignmentAny'})[0];
+    const func: DG.Func = DG.Func.find({package: 'Bio', name: 'multipleSequenceAlignmentDialog'})[0];
     const sequenceInput: DG.Property = func.inputs.find((i) => i.name == 'sequence')!;
     const k = 11;
   });

package/src/tests/msa-tests.ts

@@ -138,7 +138,7 @@ async function _testMSAOnColumn(
   if (alphabet)
     expect(srcSeqCol.getTag(bioTAGS.alphabet), alphabet);
 
-  const msaSeqCol = await multipleSequenceAlignmentUI(srcSeqCol, pepseaMethod);
+  const msaSeqCol = await multipleSequenceAlignmentUI({col: srcSeqCol, pepsea: {method: pepseaMethod}});
   expect(msaSeqCol.semType, DG.SEMTYPE.MACROMOLECULE);
   expect(msaSeqCol.getTag(DG.TAGS.UNITS), tgtNotation);
   expect(msaSeqCol.getTag(bioTAGS.aligned), ALIGNMENT.SEQ_MSA);

package/src/tests/renderers-test.ts

@@ -3,7 +3,7 @@ import * as DG from 'datagrok-api/dg';
 
 import {after, before, category, delay, expect, test} from '@datagrok-libraries/utils/src/test';
 
-import {importFasta, multipleSequenceAlignmentAny} from '../package';
+import {importFasta} from '../package';
 import {convertDo} from '../utils/convert';
 import * as C from '../utils/constants';
 import {generateLongSequence, generateManySequences, performanceTest} from './utils/sequences-generators';
@@ -146,7 +146,7 @@ category('renderers', () => {
     expect(srcSeqCol.getTag(bioTAGS.alphabet), ALPHABET.PT);
     expect(srcSeqCol.getTag(DG.TAGS.CELL_RENDERER), 'sequence');
 
-    const msaSeqCol = await multipleSequenceAlignmentUI(srcSeqCol);
+    const msaSeqCol = await multipleSequenceAlignmentUI({col: srcSeqCol});
     tv.grid.invalidate();
 
     expect(msaSeqCol.semType, DG.SEMTYPE.MACROMOLECULE);

package/src/utils/cell-renderer.ts

@@ -57,9 +57,9 @@ export class MacromoleculeSequenceCellRenderer extends DG.GridCellRenderer {
 
   get cellType(): string { return 'sequence'; }
 
-  get defaultHeight(): number { return 30; }
+  get defaultHeight(): number | null { return 30; }
 
-  get defaultWidth(): number { return 230; }
+  get defaultWidth(): number | null { return 230; }
 
   onClick(gridCell: DG.GridCell, e: MouseEvent): void {
     const colTemp: TempType = gridCell.cell.column.temp;
@@ -350,7 +350,7 @@ export function drawMoleculeDifferenceOnCanvas(
   g.restore();
 }
 
-interface IComparedSequences{
+interface IComparedSequences {
   subParts1: string[];
   subParts2: string[];
 }
@@ -401,6 +401,6 @@ function fillShorterSequence(subParts1: string[], subParts2: string[]): ICompare
     return numIdenticalStart > numIdenticalEnd ? subparts.concat(emptyMonomersArray) : emptyMonomersArray.concat(subparts);
   }
 
-  subParts1.length > subParts2.length ?  subParts2 = concatWithEmptyVals(subParts2) : subParts1 = concatWithEmptyVals(subParts1);
+  subParts1.length > subParts2.length ? subParts2 = concatWithEmptyVals(subParts2) : subParts1 = concatWithEmptyVals(subParts1);
   return {subParts1: subParts1, subParts2: subParts2};
 }