@datagrok/proteomics 1.0.1 → 1.2.1

package/src/parsers/spectronaut-parser.ts

@@ -0,0 +1,604 @@
+import * as grok from 'datagrok-api/grok';
+import * as DG from 'datagrok-api/dg';
+import {SEMTYPE} from '../utils/proteomics-types';
+import {
+  log2TransformColumns, copyAsLog2Columns, detectLog2Status,
+  addPrimaryColumnIfNeeded,
+} from './shared-utils';
+import {setGroups} from '../analysis/experiment-setup';
+import {resolveGeneLabels} from '../utils/gene-label-resolver';
+
+/** Required Spectronaut columns for detection. */
+const REQUIRED_COLUMNS = ['R.Condition', 'R.Replicate', 'PG.ProteinGroups'];
+
+/** Protein-group quantity column candidates, in preference order. `PG.IBAQ` is the
+ * historical Spectronaut export; modern long-form reports use `PG.Quantity` (MaxLFQ
+ * or top-N peptide sum). Both are constant per (protein-group, run). */
+const QUANTITY_COLUMNS = ['PG.IBAQ', 'PG.Quantity'];
+
+/** Result of pivoting Spectronaut long-format data. */
+interface PivotResult {
+  proteinMap: Map<string, Map<string, number>>;
+  sampleKeys: string[];
+  sampleFileNames: Map<string, string>;
+  organisms: Map<string, string>;
+  /** Phase 16 SPC seed (D-01): earliest observed R.RunDate as ISO-8601, null if absent/unparseable. */
+  earliestRunDate?: string | null;
+  /** Phase 16 SPC seed (D-01): first non-empty R.InstrumentMethod cell, null if absent. */
+  firstInstrumentMethod?: string | null;
+}
+
+/** Tries to parse a raw R.RunDate cell into a comparable epoch-ms; returns
+ *  null when the value is empty or `Date` cannot parse it. */
+function tryParseRunDate(raw: string): number | null {
+  if (!raw || raw.trim().length === 0) return null;
+  const t = Date.parse(raw);
+  return Number.isNaN(t) ? null : t;
+}
+
+/** Pivots Spectronaut long-format rows into protein -> sample -> quantity map.
+ * Filters CON__/REV__ proteins and rows exceeding q-value threshold.
+ * Non-numeric q-values (e.g., 'Profiled', 'NaN') are treated as passing. */
+function pivotSpectronaut(
+  longDf: DG.DataFrame,
+  quantityColName: string,
+  qValueThreshold: number,
+): PivotResult {
+  const condCol = longDf.col('R.Condition')!;
+  const replCol = longDf.col('R.Replicate')!;
+  const protCol = longDf.col('PG.ProteinGroups')!;
+  const ibaqCol = longDf.col(quantityColName)!;
+  const qvalCol = longDf.col('EG.Qvalue');
+  const fileCol = longDf.col('R.FileName');
+  const orgCol = longDf.col('PG.Organisms');
+  // Phase 16 SPC-seed columns (D-01): OPTIONAL; never added to REQUIRED_COLUMNS
+  // so v1.3 inputs without them still parse.
+  const runDateCol = longDf.col('R.RunDate');
+  const instrMethodCol = longDf.col('R.InstrumentMethod');
+
+  const proteinMap = new Map<string, Map<string, number>>();
+  const sampleSet = new Set<string>();
+  const sampleFileNames = new Map<string, string>();
+  const organisms = new Map<string, string>();
+  let earliestRunDateMs: number | null = null;
+  let earliestRunDateIso: string | null = null;
+  let firstInstrumentMethod: string | null = null;
+
+  for (let i = 0; i < longDf.rowCount; i++) {
+    // Q-value filter: numeric values > threshold are excluded; non-numeric pass
+    if (qvalCol) {
+      if (qvalCol.isNone(i)) {
+        // null q-value: treat as passing
+      } else {
+        const raw = qvalCol.get(i);
+        const qval = Number(raw);
+        if (!isNaN(qval) && qval > qValueThreshold)
+          continue;
+      }
+    }
+
+    const protein = protCol.get(i) as string;
+    if (!protein) continue;
+    if (protein.startsWith('CON__') || protein.startsWith('REV__')) continue;
+
+    const condition = String(condCol.get(i));
+    const replicate = String(replCol.get(i));
+    const sampleKey = `${condition}_${replicate}`;
+    sampleSet.add(sampleKey);
+
+    if (!proteinMap.has(protein))
+      proteinMap.set(protein, new Map<string, number>());
+
+    // First-encountered value wins (PG.IBAQ is constant per protein+sample)
+    if (!proteinMap.get(protein)!.has(sampleKey) && !ibaqCol.isNone(i))
+      proteinMap.get(protein)!.set(sampleKey, Number(ibaqCol.get(i)));
+
+    if (fileCol && !sampleFileNames.has(sampleKey) && !fileCol.isNone(i))
+      sampleFileNames.set(sampleKey, fileCol.get(i) as string);
+    if (orgCol && !organisms.has(protein) && !orgCol.isNone(i))
+      organisms.set(protein, orgCol.get(i) as string);
+
+    // SPC seed: single-pass accumulators (Plan 16-04 Perf Decision Option A).
+    if (runDateCol && !runDateCol.isNone(i)) {
+      const raw = String(runDateCol.get(i));
+      const ms = tryParseRunDate(raw);
+      if (ms !== null && (earliestRunDateMs === null || ms < earliestRunDateMs)) {
+        earliestRunDateMs = ms;
+        earliestRunDateIso = new Date(ms).toISOString();
+      }
+    }
+    if (instrMethodCol && firstInstrumentMethod === null && !instrMethodCol.isNone(i)) {
+      const raw = String(instrMethodCol.get(i));
+      if (raw.trim().length > 0) firstInstrumentMethod = raw;
+    }
+  }
+
+  return {
+    proteinMap,
+    sampleKeys: Array.from(sampleSet).sort(),
+    sampleFileNames,
+    organisms,
+    earliestRunDate: earliestRunDateIso,
+    firstInstrumentMethod,
+  };
+}
+
+/** Builds wide protein-by-sample DataFrame from pivot result. */
+function buildWideDataFrame(result: PivotResult): DG.DataFrame {
+  const proteins = Array.from(result.proteinMap.keys());
+  const n = proteins.length;
+
+  const proteinCol = DG.Column.fromStrings('PG.ProteinGroups', proteins);
+  proteinCol.semType = SEMTYPE.PROTEIN_ID;
+
+  const cols: DG.Column[] = [proteinCol];
+
+  // Add organisms column if any were collected
+  if (result.organisms.size > 0) {
+    const orgValues = proteins.map((p) => result.organisms.get(p) ?? '');
+    const orgCol = DG.Column.fromStrings('PG.Organisms', orgValues);
+    cols.push(orgCol);
+  }
+
+  for (const sampleKey of result.sampleKeys) {
+    const values = new Float32Array(n);
+    for (let i = 0; i < n; i++) {
+      const sampleMap = result.proteinMap.get(proteins[i])!;
+      values[i] = sampleMap.has(sampleKey) ? sampleMap.get(sampleKey)! : DG.FLOAT_NULL;
+    }
+    const col = DG.Column.fromFloat32Array(sampleKey, values);
+    col.semType = SEMTYPE.INTENSITY;
+    if (result.sampleFileNames.has(sampleKey))
+      col.setTag('spectronaut.fileName', result.sampleFileNames.get(sampleKey)!);
+    cols.push(col);
+  }
+
+  return DG.DataFrame.fromColumns(cols);
+}
+
+/** Auto-populates experimental groups from R.Condition when exactly 2 conditions exist.
+ * Groups use log2-prefixed column names for downstream analysis compatibility. */
+function autoPopulateGroups(df: DG.DataFrame, sampleKeys: string[]): void {
+  const conditionMap = new Map<string, string[]>();
+  for (const key of sampleKeys) {
+    const lastUnderscore = key.lastIndexOf('_');
+    const condition = key.substring(0, lastUnderscore);
+    if (!conditionMap.has(condition))
+      conditionMap.set(condition, []);
+    conditionMap.get(condition)!.push(`log2(${key})`);
+  }
+
+  const conditions = Array.from(conditionMap.keys());
+  if (conditions.length === 2) {
+    setGroups(df, {
+      group1: {name: conditions[0], columns: conditionMap.get(conditions[0])!},
+      group2: {name: conditions[1], columns: conditionMap.get(conditions[1])!},
+    });
+  }
+}
+
+/** Shared post-pivot tail for BOTH the text and streaming Spectronaut paths.
+ *
+ * Builds the wide DataFrame, derives the primary protein column, detects/applies
+ * the log2 transform, sets the `proteomics.*` tags, and auto-populates the two
+ * experimental groups. `parseSpectronautText` and `parseSpectronautStream` both
+ * end by handing their `PivotResult` here, so their output is byte-identical in
+ * shape, semTypes, log2 columns, tags, and groups (R3).
+ *
+ * NOTE: this is the verbatim former tail of `parseSpectronautText` extracted
+ * unchanged — do not edit tag strings, semType assignments, the log2 branch, or
+ * column construction here without re-locking the existing Spectronaut tests. */
+async function finalizeSpectronaut(result: PivotResult): Promise<DG.DataFrame> {
+  // Build wide DataFrame
+  const df = buildWideDataFrame(result);
+
+  // Parse semicolon-delimited protein groups into primary column
+  addPrimaryColumnIfNeeded(df, 'PG.ProteinGroups', 'Primary Protein ID', SEMTYPE.PROTEIN_ID);
+
+  // Get intensity column names (the sample columns)
+  const intensityColNames = result.sampleKeys;
+
+  // Detect log2 status
+  const log2Status = detectLog2Status(df, intensityColNames);
+
+  if (log2Status.isLog2) {
+    // Pre-normalized: copy as log2 columns without transformation
+    copyAsLog2Columns(df, intensityColNames);
+  } else {
+    // Raw: apply log2 transformation, keeping originals
+    log2TransformColumns(df, intensityColNames);
+  }
+
+  // Spectronaut always performs its own normalization regardless of export format
+  df.setTag('proteomics.preNormalized', 'true');
+
+  // Tag source
+  df.setTag('proteomics.source', 'spectronaut');
+
+  // Auto-populate groups from R.Condition
+  autoPopulateGroups(df, result.sampleKeys);
+
+  await resolveGeneLabels(df);
+
+  return df;
+}
+
+/** Mirrors duckdb `nullstr=['','NaN','NA']` + `TRY_CAST(... AS DOUBLE)` from
+ * tools/spectronaut-aggregate.sql. Returns `null` for the duckdb null tokens
+ * and for anything that is not a finite number; otherwise the parsed number.
+ *
+ * This is intentionally STRICTER than `pivotSpectronaut`'s loose
+ * `Number(raw)`/`isNaN` (which treats `''` as `0` via `Number('')`): the
+ * streaming path must match the duckdb D-04 golden oracle exactly. The two
+ * paths only diverge on degenerate inputs (`''` q-value/quantity) that the
+ * real Spectronaut exports and the synthetic fixture never contain — the text
+ * path stays byte-identical because it does not route precursor reports. */
+function tryCastDouble(s: string | null | undefined): number | null {
+  if (s === null || s === undefined) return null;
+  const t = s.trim();
+  if (t === '' || t === 'NaN' || t === 'NA') return null;
+  const n = Number(t);
+  return Number.isFinite(n) ? n : null;
+}
+
+/** Outcome of feeding one already-split streamed data line to `handleFields`:
+ *
+ * - `'kept'`      — the row was aggregated into `agg` (counts toward `rowCount`).
+ * - `'malformed'` — the row is structurally unparseable (too few tab-separated
+ *                   fields). ONLY this category is surfaced to the user as
+ *                   "malformed/unparseable line(s)".
+ * - `'filtered'`  — the row was dropped by a correct, by-design duckdb-parity
+ *                   filter (empty `PG.ProteinGroups`, CON__/REV__ decoy/
+ *                   contaminant, numeric `EG.Qvalue` > threshold, or both
+ *                   numeric casts null). This is NOT malformed and is SILENT —
+ *                   exactly as the text path (`pivotSpectronaut`) is for the
+ *                   identical drops.
+ */
+type LineOutcome = 'kept' | 'malformed' | 'filtered';
+
+/** Per-(protein × condition × replicate) running aggregate accumulated by the
+ * streaming path. Mirrors the duckdb GROUP BY: `max(quantity)`, `min(qvalue)`,
+ * first-non-null `R.FileName` / `PG.Organisms`. */
+interface AggRow {
+  protein: string;
+  condition: string;
+  replicate: string;
+  maxQuantity: number;
+  minQvalue: number;
+  fileName: string | null;
+  organism: string | null;
+}
+
+/** Group-key field separator. ASCII Unit Separator (0x1F) is not a TSV-legal
+ * character, so it cannot collide with any condition/replicate/protein value. */
+const AGG_KEY_SEP = '\x1f';
+
+/** Folds the streaming aggregate map into the same `PivotResult` shape that
+ * `pivotSpectronaut` produces, so `finalizeSpectronaut` is path-agnostic.
+ * `sampleKey` MUST be `${condition}_${replicate}` to match `pivotSpectronaut`
+ * (L65) and `autoPopulateGroups`'s `lastIndexOf('_')` split. */
+function aggToPivotResult(agg: Map<string, AggRow>): PivotResult {
+  const proteinMap = new Map<string, Map<string, number>>();
+  const sampleSet = new Set<string>();
+  const sampleFileNames = new Map<string, string>();
+  const organisms = new Map<string, string>();
+
+  for (const row of agg.values()) {
+    // Never-set groups (no surviving numeric quantity) carry -Infinity; skip
+    // them exactly as duckdb would emit no quantity for an all-null group.
+    if (!Number.isFinite(row.maxQuantity)) continue;
+
+    const sampleKey = `${row.condition}_${row.replicate}`;
+    sampleSet.add(sampleKey);
+
+    if (!proteinMap.has(row.protein))
+      proteinMap.set(row.protein, new Map<string, number>());
+    proteinMap.get(row.protein)!.set(sampleKey, row.maxQuantity);
+
+    if (row.fileName !== null && !sampleFileNames.has(sampleKey))
+      sampleFileNames.set(sampleKey, row.fileName);
+    if (row.organism !== null && !organisms.has(row.protein))
+      organisms.set(row.protein, row.organism);
+  }
+
+  return {
+    proteinMap,
+    sampleKeys: Array.from(sampleSet).sort(),
+    sampleFileNames,
+    organisms,
+  };
+}
+
+/** Streams a precursor/fragment-level Spectronaut long-format TSV `File` and
+ * single-pass aggregates it down to the same wide protein-by-sample DataFrame
+ * `parseSpectronautText` produces — without ever materializing the whole file
+ * as a string (the V8 ~512 MB string ceiling is why a 2.6 GB report OOMs the
+ * text path). Only state retained is the bounded carry-over line buffer and the
+ * aggregate Map keyed by (protein × condition × replicate); raw input rows are
+ * NEVER buffered (T-12-05).
+ *
+ * Filter / aggregate parity with tools/spectronaut-aggregate.sql:
+ * - drop empty / `CON__` / `REV__` `PG.ProteinGroups`
+ * - drop a row only if `tryCastDouble(EG.Qvalue) > threshold` (null/non-numeric
+ *   passes — duckdb `IS NULL OR <= 0.01`)
+ * - per group: `max(tryCastDouble(quantity))`, `min(tryCastDouble(EG.Qvalue))`,
+ *   first-non-null `R.FileName` / `PG.Organisms`
+ * - the DMD↔WT `R.Condition` flip in the SQL is REFERENCE-FILE-ONLY and is
+ *   deliberately NOT ported here (RESEARCH Pitfall 1).
+ *
+ * Malformed lines (too few fields, or both numeric casts null) are skipped and
+ * counted (duckdb `ignore_errors=true` parity), surfaced via the progress
+ * message rather than aborting. A `TaskBarProgressIndicator` advances by
+ * bytes-read and an explicit `setTimeout(0)` macrotask yield runs on a ~16 ms
+ * cadence so the tab stays responsive (T-12-09; the stream-read await alone
+ * does not yield on OS-buffered data). */
+export async function parseSpectronautStream(
+  file: File, qValueThreshold: number = 0.01,
+): Promise<DG.DataFrame> {
+  const pi = DG.TaskBarProgressIndicator.create('Streaming Spectronaut report...');
+  try {
+    const reader = file.stream()
+      .pipeThrough(new TextDecoderStream('utf-8'))
+      .getReader();
+
+    const agg = new Map<string, AggRow>();
+    let buffer = '';
+    let headerParsed = false;
+    let colIdx: Map<string, number> = new Map();
+    let protI = -1; let condI = -1; let repI = -1;
+    let qvalI = -1; let qtyI = -1; let fileI = -1; let orgI = -1;
+    // Phase 16 SPC seed (D-01) — OPTIONAL columns, never required.
+    let runDateI = -1; let instrMethodI = -1;
+    let expectedFields = 0;
+    let earliestRunDateMs: number | null = null;
+    let earliestRunDateIso: string | null = null;
+    let firstInstrumentMethod: string | null = null;
+
+    let bytesRead = 0;
+    let rowCount = 0;
+    // Structurally unparseable lines (too few tab-separated fields). ONLY this
+    // counter feeds the user-facing "malformed line(s)" message.
+    let malformed = 0;
+    // Rows dropped by a correct by-design duckdb-parity filter (CON__/REV__ or
+    // numeric q > threshold). Tracked for completeness but SILENT to the user —
+    // the text path (pivotSpectronaut) drops the identical rows with no message.
+    let filtered = 0;
+    let lastYield = performance.now();
+    const fileSize = Math.max(1, file.size);
+
+    /** Aggregate one already-split data line into `agg` (parity with the
+     * duckdb WHERE + GROUP BY). Returns a discriminated outcome:
+     * `'malformed'` for a structurally unparseable row (too few tab-separated
+     * fields), `'filtered'` for a correct by-design duckdb-parity drop (empty
+     * `PG.ProteinGroups`, CON__/REV__ decoy/contaminant, numeric `EG.Qvalue` >
+     * threshold, or both numeric casts null), `'kept'` once the row is
+     * aggregated. Empty-protein and both-casts-null are duckdb-silent drops
+     * that the text path (`pivotSpectronaut`) also drops without messaging —
+     * categorizing them `'filtered'` keeps streaming↔text user-message parity.
+     * The predicates below are duckdb-parity-correct and UNCHANGED — only the
+     * outcome value carries the malformed-vs-filtered distinction. */
+    const handleFields = (f: string[]): LineOutcome => {
+      if (f.length < expectedFields) return 'malformed';
+      const protein = f[protI];
+      // Drop empty / decoy / contaminant protein groups — all silent, matching
+      // `pivotSpectronaut`'s `if (!protein) continue` + CON__/REV__ skip.
+      if (!protein) return 'filtered';
+      if (protein.startsWith('CON__') || protein.startsWith('REV__')) return 'filtered';
+
+      const q = qvalI >= 0 ? tryCastDouble(f[qvalI]) : null;
+      // duckdb: (qvalue IS NULL OR qvalue <= threshold) — null/non-numeric pass.
+      if (q !== null && q > qValueThreshold) return 'filtered';
+
+      const qty = tryCastDouble(f[qtyI]);
+      // Both numeric casts null → unusable for aggregation; drop silently
+      // (duckdb `ignore_errors` semantics — the text path likewise omits this row).
+      if (qty === null && q === null) return 'filtered';
+
+      const condition = f[condI] ?? '';
+      const replicate = f[repI] ?? '';
+      const key = protein + AGG_KEY_SEP + condition + AGG_KEY_SEP + replicate;
+      let row = agg.get(key);
+      if (row === undefined) {
+        row = {
+          protein, condition, replicate,
+          maxQuantity: -Infinity, minQvalue: Infinity,
+          fileName: null, organism: null,
+        };
+        agg.set(key, row);
+      }
+      if (qty !== null && qty > row.maxQuantity) row.maxQuantity = qty;
+      if (q !== null && q < row.minQvalue) row.minQvalue = q;
+      if (row.fileName === null && fileI >= 0) {
+        const fn = f[fileI];
+        if (fn) row.fileName = fn;
+      }
+      if (row.organism === null && orgI >= 0) {
+        const og = f[orgI];
+        if (og) row.organism = og;
+      }
+      // Phase 16 SPC seed (D-01) — accumulate inline so the streaming-path adds
+      // no second pass over the file.
+      if (runDateI >= 0) {
+        const rd = f[runDateI];
+        if (rd) {
+          const ms = tryParseRunDate(rd);
+          if (ms !== null && (earliestRunDateMs === null || ms < earliestRunDateMs)) {
+            earliestRunDateMs = ms;
+            earliestRunDateIso = new Date(ms).toISOString();
+          }
+        }
+      }
+      if (instrMethodI >= 0 && firstInstrumentMethod === null) {
+        const im = f[instrMethodI];
+        if (im && im.trim().length > 0) firstInstrumentMethod = im;
+      }
+      return 'kept';
+    };
+
+    /** Parse the first complete line as the header; resolve column indices and
+     * the single quantity column once, matching the text-path validation. */
+    const parseHeader = (line: string): void => {
+      const cols = line.split('\t');
+      colIdx = new Map();
+      for (let i = 0; i < cols.length; i++)
+        colIdx.set(cols[i], i);
+      for (const colName of REQUIRED_COLUMNS) {
+        if (!colIdx.has(colName))
+          throw new Error(`Missing required Spectronaut column: ${colName}`);
+      }
+      const quantityColName = QUANTITY_COLUMNS.find((n) => colIdx.has(n));
+      if (!quantityColName) {
+        throw new Error(`Missing protein-group quantity column ` +
+          `(expected one of ${QUANTITY_COLUMNS.join(', ')})`);
+      }
+      protI = colIdx.get('PG.ProteinGroups')!;
+      condI = colIdx.get('R.Condition')!;
+      repI = colIdx.get('R.Replicate')!;
+      qtyI = colIdx.get(quantityColName)!;
+      qvalI = colIdx.has('EG.Qvalue') ? colIdx.get('EG.Qvalue')! : -1;
+      fileI = colIdx.has('R.FileName') ? colIdx.get('R.FileName')! : -1;
+      orgI = colIdx.has('PG.Organisms') ? colIdx.get('PG.Organisms')! : -1;
+      // Phase 16 SPC seed: optional indices, contribute to expectedFields ONLY
+      // when present so v1.3 headers without them still parse.
+      runDateI = colIdx.has('R.RunDate') ? colIdx.get('R.RunDate')! : -1;
+      instrMethodI = colIdx.has('R.InstrumentMethod') ? colIdx.get('R.InstrumentMethod')! : -1;
+      // Highest index we read; a shorter split means a truncated/malformed row.
+      expectedFields = Math.max(
+        protI, condI, repI, qtyI, qvalI, fileI, orgI, runDateI, instrMethodI,
+      ) + 1;
+      headerParsed = true;
+    };
+
+    while (true) {
+      const {value, done} = await reader.read();
+      if (done) break;
+      bytesRead += value.length;
+      buffer += value;
+
+      let nl: number;
+      while ((nl = buffer.indexOf('\n')) >= 0) {
+        let line = buffer.slice(0, nl);
+        buffer = buffer.slice(nl + 1);
+        if (line.endsWith('\r')) line = line.slice(0, -1);
+        if (!headerParsed) {
+          if (line.length === 0) continue;
+          parseHeader(line);
+          continue;
+        }
+        if (line.length === 0) continue;
+        switch (handleFields(line.split('\t'))) {
+        case 'kept': rowCount++; break;
+        case 'malformed': malformed++; break;
+        case 'filtered': filtered++; break;
+        }
+      }
+
+      // ~16 ms wall-clock yield cadence (RESEARCH Q3 resolution / D-02). The
+      // explicit setTimeout(0) macrotask yield is REQUIRED — await reader.read()
+      // does not reliably yield on OS-buffered data (T-12-09).
+      const now = performance.now();
+      if (now - lastYield >= 16) {
+        const pct = Math.min(99, (bytesRead / fileSize) * 100);
+        // Only the genuine-malformed count is surfaced; by-design-filtered rows
+        // (CON__/REV__, q > threshold) stay silent — text-path-consistent.
+        const msg = malformed > 0
+          ? `${rowCount} rows (${malformed} malformed skipped)`
+          : `${rowCount} rows`;
+        pi.update(pct, msg);
+        await new Promise<void>((r) => setTimeout(r, 0));
+        lastYield = performance.now();
+      }
+    }
+
+    // Flush a trailing partial line (file without a final newline).
+    if (buffer.length > 0) {
+      let line = buffer;
+      if (line.endsWith('\r')) line = line.slice(0, -1);
+      if (line.length > 0) {
+        if (!headerParsed) {
+          parseHeader(line);
+        } else {
+          switch (handleFields(line.split('\t'))) {
+          case 'kept': rowCount++; break;
+          case 'malformed': malformed++; break;
+          case 'filtered': filtered++; break;
+          }
+        }
+      }
+    }
+
+    if (!headerParsed)
+      throw new Error('Missing required Spectronaut column: R.Condition');
+
+    // Genuine-malformed only. By-design-filtered rows (CON__/REV__, q >
+    // threshold) are intentionally SILENT — pivotSpectronaut drops the
+    // identical rows with no message; matching that silence is the locked,
+    // path-consistent UX decision. `filtered` is tracked but never surfaced.
+    void filtered;
+    if (malformed > 0)
+      grok.shell.info(`Spectronaut import: skipped ${malformed} malformed line(s)`);
+
+    const pivot = aggToPivotResult(agg);
+    pivot.earliestRunDate = earliestRunDateIso;
+    pivot.firstInstrumentMethod = firstInstrumentMethod;
+    const df = await finalizeSpectronaut(pivot);
+    // Phase 16 D-01: write the `proteomics.spc_run_meta_seed` tag when either
+    // capture was made (streaming path).
+    applySpcRunMetaSeed(df, pivot);
+    return df;
+  } finally {
+    pi.close();
+  }
+}
+
+/** Parses Spectronaut long-format TSV text into a wide protein-by-sample DataFrame.
+ *
+ * Applies:
+ * - Q-value filtering (default threshold 0.01; non-numeric q-values pass)
+ * - CON__/REV__ contaminant/decoy filtering
+ * - Long-to-wide pivot using PG.IBAQ (preferred) or PG.Quantity (newer exports)
+ *   as protein-level intensity
+ * - Semantic type assignment (PROTEIN_ID, INTENSITY)
+ * - Log2 transformation (or copy if pre-normalized)
+ * - Auto-group population from R.Condition when exactly 2 conditions
+ * - Pre-normalization detection and tagging */
+export async function parseSpectronautText(text: string, qValueThreshold: number = 0.01): Promise<DG.DataFrame> {
+  // Parse long-format TSV
+  const longDf = DG.DataFrame.fromCsv(text, {delimiter: '\t'});
+
+  // Validate required columns
+  for (const colName of REQUIRED_COLUMNS) {
+    if (!longDf.col(colName))
+      throw new Error(`Missing required Spectronaut column: ${colName}`);
+  }
+
+  // Pick the protein-group quantity column (PG.IBAQ preferred, PG.Quantity accepted).
+  const quantityColName = QUANTITY_COLUMNS.find((n) => longDf.col(n) !== null);
+  if (!quantityColName) {
+    throw new Error(`Missing protein-group quantity column ` +
+      `(expected one of ${QUANTITY_COLUMNS.join(', ')})`);
+  }
+
+  // Pivot long-to-wide with filtering
+  const result = pivotSpectronaut(longDf, quantityColName, qValueThreshold);
+
+  // Shared post-pivot tail (identical for the streaming path).
+  const df = await finalizeSpectronaut(result);
+  // Phase 16 D-01: write the `proteomics.spc_run_meta_seed` tag when either
+  // capture was made (text path).
+  applySpcRunMetaSeed(df, result);
+  return df;
+}
+
+/** Phase 16 D-01: Attach the SPC run-meta seed to the parsed df when either
+ *  R.RunDate or R.InstrumentMethod was captured. Plan 16-05's Annotate
+ *  Experiment dialog reads this seed to prefill its two new inputs. */
+function applySpcRunMetaSeed(df: DG.DataFrame, result: PivotResult): void {
+  const hasDate = result.earliestRunDate != null;
+  const hasInstr = result.firstInstrumentMethod != null;
+  if (!hasDate && !hasInstr) return;
+  df.setTag('proteomics.spc_run_meta_seed', JSON.stringify({
+    instrument_id: result.firstInstrumentMethod ?? '',
+    acquisition_datetime: result.earliestRunDate ?? '',
+  }));
+}