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"cells": [
{
"cell_type": "markdown",
"id": "7215a5aa",
"metadata": {},
"source": [
"# ICD-Codable Sentence Classification β Weak Supervision + Bio_ClinicalBERT\n",
"\n",
"**CSCE 633 Final Project**\n",
"\n",
"Binary classifier for *\"does this clinical text chunk contain ICD-codable medical information?\"* The 20 provided labels are themselves BERT-generated and noisy, so we treat them as one weak source among several rather than gold ground truth.\n",
"\n",
"## Pipeline\n",
"\n",
"1. **Mine MIMIC-III** (`NOTEEVENTS.csv`) for ~10k discharge-summary chunks shaped like the test inputs\n",
"2. **Apply labeling functions** β heuristics that vote `1`, `0`, or abstain on each chunk\n",
"3. **Aggregate with Snorkel's `LabelModel`** to get probabilistic training labels that account for LF accuracy and correlation\n",
"4. **Fine-tune Bio_ClinicalBERT** on the soft labels (binary cross-entropy)\n",
"5. **Predict** on `test{01,02,03}_text_only.csv` β write Gradescope-shaped CSVs\n",
"\n",
"The 20 provided labels are **never used for training**, only as a sanity-check oracle (with the caveat that they are themselves noisy).\n",
"\n",
"## Run order\n",
"\n",
"Run cells top to bottom. Cells in **Section 1** must be edited to point at your local MIMIC-III install. Cells in **Section 6** (training) need a GPU; everything else runs comfortably on CPU.\n"
]
},
{
"cell_type": "markdown",
"id": "43774d01",
"metadata": {},
"source": [
"## Section 0 β Install dependencies\n",
"\n",
"Run this once. If you're on Colab, this also installs Snorkel and the right transformers version.\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "5085c1bb",
"metadata": {},
"outputs": [],
"source": [
"# !pip install -q numpy pandas scikit-learn snorkel torch transformers datasets pyarrow tqdm\n",
"# Uncomment above on first run. Comment out afterwards to skip the slow pip step.\n"
]
},
{
"cell_type": "markdown",
"id": "2515e3dd",
"metadata": {},
"source": [
"## Section 1 β Configuration\n",
"\n",
"**Edit the paths below before running.**\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "76f6aacd",
"metadata": {},
"outputs": [],
"source": [
"from pathlib import Path\n",
"\n",
"# ----- EDIT THESE -----------------------------------------------------------\n",
"MIMIC_NOTEEVENTS_PATH = Path(\"./noteevents.csv\") # <-- EDIT\n",
"PROJECT_FILES_DIR = Path(\"./project_files\") # contains the provided test/train CSVs\n",
"# ---------------------------------------------------------------------------\n",
"\n",
"# Working directories (created automatically)\n",
"WORK_DIR = Path(\"./icd_work\")\n",
"DATA_DIR = WORK_DIR / \"data\"\n",
"OUTPUT_DIR = WORK_DIR / \"outputs\"\n",
"MODEL_DIR = OUTPUT_DIR / \"bert_model\"\n",
"for d in (DATA_DIR, OUTPUT_DIR):\n",
" d.mkdir(parents=True, exist_ok=True)\n",
"\n",
"# Cached intermediate artifacts\n",
"MIMIC_CHUNKS_PATH = DATA_DIR / \"mimic_chunks.parquet\"\n",
"LF_VOTES_PATH = DATA_DIR / \"lf_votes.npy\"\n",
"SOFT_LABELS_PATH = DATA_DIR / \"soft_labels.npy\"\n",
"TRAINING_SET_PATH = DATA_DIR / \"training_set.parquet\"\n",
"\n",
"# Mining hyperparameters\n",
"N_MIMIC_NOTES_TO_SCAN = 6000\n",
"CHUNK_TARGET_WORDS = 110\n",
"CHUNK_MIN_WORDS = 40\n",
"CHUNK_MAX_WORDS = 180\n",
"CHUNKS_PER_NOTE_CAP = 8\n",
"RANDOM_SEED = 42\n",
"\n",
"# Snorkel\n",
"LABEL_MODEL_EPOCHS = 500\n",
"LABEL_MODEL_LR = 0.01\n",
"DROP_ALL_ABSTAIN = True\n",
"\n",
"# Bio_ClinicalBERT\n",
"BERT_MODEL_NAME = \"emilyalsentzer/Bio_ClinicalBERT\"\n",
"MAX_SEQ_LEN = 256\n",
"BATCH_SIZE = 16\n",
"EVAL_BATCH_SIZE = 32\n",
"LEARNING_RATE = 2e-5\n",
"NUM_EPOCHS = 3\n",
"WARMUP_RATIO = 0.1\n",
"WEIGHT_DECAY = 0.01\n",
"\n",
"# Decision threshold for binary prediction at inference time\n",
"DECISION_THRESHOLD = 0.5\n",
"\n",
"print(f\"MIMIC NOTEEVENTS: {MIMIC_NOTEEVENTS_PATH} exists={MIMIC_NOTEEVENTS_PATH.exists()}\")\n",
"print(f\"Project files: {PROJECT_FILES_DIR} exists={PROJECT_FILES_DIR.exists()}\")\n",
"print(f\"Work dir: {WORK_DIR.resolve()}\")\n"
]
},
{
"cell_type": "markdown",
"id": "76fed1d0",
"metadata": {},
"source": [
"## Section 2 β Labeling functions\n",
"\n",
"Each LF takes a chunk of clinical text and votes:\n",
"\n",
"* `1` β contains ICD-codable medical info (positive)\n",
"* `0` β does NOT contain ICD-codable medical info (negative)\n",
"* `-1` β abstain\n",
"\n",
"**Design philosophy.** Each LF encodes ONE narrow, interpretable signal. Snorkel's `LabelModel` learns each LF's accuracy from agreement statistics across many examples, so noisy LFs are fine as long as they're better than random and not perfectly correlated.\n",
"\n",
"**Signals observed in the 20 training examples:**\n",
"\n",
"*Positive cues:* `Discharge Diagnosis:` sections, `# DiagnosisName:` problem-list markers, past-tense treatment narratives, dense diagnosis vocabulary\n",
"\n",
"*Negative cues:* mostly numbers + lab units, imaging-finding narratives (\"arteriogram shows...\"), pharmacy dispensing lines (`Disp:*N Tablet(s)*`), microbiology susceptibility tables, vital-sign clusters\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "737b0baf",
"metadata": {},
"outputs": [],
"source": [
"import re\n",
"import numpy as np\n",
"\n",
"ABSTAIN = -1\n",
"NEG = 0\n",
"POS = 1\n",
"\n",
"# ---------------------------------------------------------------------------\n",
"# Vocabulary\n",
"# ---------------------------------------------------------------------------\n",
"DIAGNOSIS_TERMS = [\n",
" # cardio\n",
" \"myocardial infarction\", \"MI\", \"STEMI\", \"NSTEMI\", \"CAD\",\n",
" \"coronary artery disease\", \"cardiogenic shock\", \"atrial fibrillation\",\n",
" \"afib\", \"CHF\", \"heart failure\", \"cardiomyopathy\", \"endocarditis\",\n",
" \"pericarditis\", \"hypertension\", \"HTN\", \"hyperlipidemia\", \"hypercalcemia\",\n",
" \"hyperparathyroidism\", \"hypothyroidism\",\n",
" # renal\n",
" \"ESRD\", \"CKD\", \"AKI\", \"acute kidney injury\", \"chronic kidney disease\",\n",
" \"renal failure\", \"nephropathy\",\n",
" # pulm\n",
" \"pneumonia\", \"COPD\", \"asthma\", \"pulmonary embolism\", \"PE\", \"ARDS\",\n",
" \"respiratory failure\", \"atelectasis\",\n",
" # neuro\n",
" \"stroke\", \"CVA\", \"SAH\", \"subarachnoid hemorrhage\", \"ICH\", \"seizure\",\n",
" \"hydrocephalus\", \"aneurysm\", \"encephalopathy\", \"dementia\",\n",
" # GI\n",
" \"GI bleed\", \"cirrhosis\", \"pancreatitis\", \"cholecystitis\", \"hepatitis\",\n",
" \"obstruction\",\n",
" # endo\n",
" \"diabetes\", \"DM\", \"DKA\", \"hyperglycemia\", \"hypoglycemia\",\n",
" # heme/onc\n",
" \"anemia\", \"thrombocytopenia\", \"leukemia\", \"lymphoma\", \"neutropenia\",\n",
" # infectious\n",
" \"sepsis\", \"bacteremia\", \"UTI\", \"cellulitis\", \"osteomyelitis\", \"MRSA\",\n",
" \"MSSA\", \"abscess\",\n",
" # trauma / orthopedic\n",
" \"fracture\", \"femur fracture\", \"hip fracture\", \"motor vehicle crash\",\n",
" \"MVC\", \"MVA\",\n",
" # other\n",
" \"paraplegia\", \"gangrene\", \"ulcer\", \"intracranial hypertension\",\n",
" \"pyrexia\",\n",
"]\n",
"\n",
"_DX_RE = re.compile(\n",
" r\"\\b(\" + \"|\".join(re.escape(t.lower()) for t in DIAGNOSIS_TERMS) + r\")\\b\",\n",
" re.IGNORECASE,\n",
")\n",
"\n",
"POSITIVE_SECTION_PATTERNS = [\n",
" r\"discharge diagnosis\\s*:\",\n",
" r\"primary diagnosis\\s*:\",\n",
" r\"secondary diagnosis\\s*:\",\n",
" r\"chief complaint\\s*:\",\n",
" r\"history of present illness\\s*:\",\n",
" r\"past medical history\\s*:\",\n",
" r\"discharge instructions\\s*:\",\n",
" r\"hospital course\\s*:\",\n",
" r\"active issues\\s*:\",\n",
" r\"problem list\\s*:\",\n",
" r\"assessment and plan\\s*:\",\n",
" r\"admitting diagnosis\\s*:\",\n",
"]\n",
"_POS_SECTION_RE = re.compile(\"|\".join(POSITIVE_SECTION_PATTERNS), re.IGNORECASE)\n",
"\n",
"_PROBLEM_MARKER_RE = re.compile(r\"(^|\\n)\\s*#\\s*[A-Za-z][^:\\n]{1,60}:\")\n",
"\n",
"_NEG_SECTION_RE = re.compile(\n",
" r\"(reason for( this)? examination|comparison\\s*:|technique\\s*:|indication\\s*:)\",\n",
" re.IGNORECASE,\n",
")\n",
"\n",
"_DISP_RE = re.compile(r\"disp\\s*:\\s*\\*\\s*\\d\", re.IGNORECASE)\n",
"\n",
"_LAB_UNITS_RE = re.compile(\n",
" r\"\\b(mg/d[lL]|mEq/L|K/uL|mmol/L|g/d[lL]|mcg/mL|ng/mL|IU/L|U/L|\"\n",
" r\"mm\\s*Hg|bpm|%)\\b\"\n",
")\n",
"\n",
"_VITALS_CLUSTER_RE = re.compile(\n",
" r\"\\b(BP|HR|RR|Sat|SpO2|T|Temp)\\b\\s*\\d\", re.IGNORECASE\n",
")\n",
"\n",
"_IMAGING_MEASUREMENT_RE = re.compile(r\"\\b\\d+(\\.\\d+)?\\s*(mm|cm)\\b\", re.IGNORECASE)\n",
"\n",
"_RAD_TECHNIQUE_RE = re.compile(\n",
" r\"\\b(microcatheter|microwire|guidewire|french catheter|ultrasoft|\"\n",
" r\"target coil|arteriogram|fluoroscop)\", re.IGNORECASE\n",
")\n",
"\n",
"_RAD_NARRATIVE_RE = re.compile(\n",
" r\"\\b(catheterized|filming|coiled|embolization|arteriogram shows|\"\n",
" r\"injection|exchanged out|advanced|deployed)\\b\",\n",
" re.IGNORECASE,\n",
")\n",
"\n",
"_DISCHARGE_COND_RE = re.compile(\n",
" r\"(mental status\\s*:|level of consciousness\\s*:|activity status\\s*:)\",\n",
" re.IGNORECASE,\n",
")\n",
"\n",
"\n",
"def _word_count(text):\n",
" return len(text.split())\n",
"\n",
"\n",
"def _digit_density(text):\n",
" toks = text.split()\n",
" if not toks:\n",
" return 0.0\n",
" digity = sum(\n",
" 1 for t in toks\n",
" if sum(c.isdigit() for c in t) >= max(1, len(t) // 2)\n",
" )\n",
" return digity / len(toks)\n"
]
},
{
"cell_type": "markdown",
"id": "24ce62fe",
"metadata": {},
"source": [
"### Section 2.1 β The labeling functions themselves\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "21cf1c4d",
"metadata": {},
"outputs": [],
"source": [
"# ====== Positive LFs ========================================================\n",
"\n",
"def lf_discharge_diagnosis_section(text):\n",
" \"\"\"Discharge / primary / secondary / admitting diagnosis sections.\"\"\"\n",
" if re.search(r\"(discharge|primary|secondary|admitting)\\s+diagnosis\\s*:\",\n",
" text, re.IGNORECASE):\n",
" return POS\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_problem_list_marker(text):\n",
" \"\"\"'# CAD:', '# ESRD on HD:' style problem-list entries.\"\"\"\n",
" if len(_PROBLEM_MARKER_RE.findall(text)) >= 1:\n",
" return POS\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_positive_section_header(text):\n",
" \"\"\"Any of several diagnosis/HPI/PMH/course headers.\"\"\"\n",
" if _POS_SECTION_RE.search(text):\n",
" return POS\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_diagnosis_vocabulary_dense(text):\n",
" \"\"\"Multiple distinct named diagnoses β codable.\"\"\"\n",
" hits = set(m.group(0).lower() for m in _DX_RE.finditer(text))\n",
" if len(hits) >= 2:\n",
" return POS\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_diagnosis_vocabulary_any(text):\n",
" \"\"\"At least one named diagnosis β weak positive signal.\"\"\"\n",
" if _DX_RE.search(text):\n",
" return POS\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_treatment_narrative(text):\n",
" \"\"\"Past-tense treatment/procedure narrative.\"\"\"\n",
" patterns = [\n",
" r\"\\bwas (started|continued|treated|given|placed|admitted|transferred|dialyzed|extubated|intubated|weaned)\\b\",\n",
" r\"\\bunderwent\\b\",\n",
" r\"\\bs/p\\s+\\w+\",\n",
" r\"\\bstatus\\s+post\\b\",\n",
" ]\n",
" hits = sum(1 for p in patterns if re.search(p, text, re.IGNORECASE))\n",
" if hits >= 2:\n",
" return POS\n",
" return ABSTAIN\n",
"\n",
"\n",
"# ====== Negative LFs ========================================================\n",
"\n",
"def lf_lab_unit_density(text):\n",
" \"\"\"Lots of lab units relative to length β mostly lab data β negative.\"\"\"\n",
" n_units = len(_LAB_UNITS_RE.findall(text))\n",
" n_words = _word_count(text)\n",
" if n_words == 0:\n",
" return ABSTAIN\n",
" if n_units >= 4 and n_units / n_words > 0.04:\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_high_digit_density(text):\n",
" \"\"\"If >25% of tokens are mostly digits, it's mostly numerical data.\"\"\"\n",
" if _digit_density(text) > 0.25:\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_dispensing_line(text):\n",
" \"\"\"'Disp:*N Tablet(s)*' lines are pharmacy fulfillment, not diagnoses.\"\"\"\n",
" if len(_DISP_RE.findall(text)) >= 2:\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_radiology_technique(text):\n",
" \"\"\"Pure radiology technique / device mechanics β describes procedure\n",
" machinery, not a codable diagnosis. Allows DX vocab to coexist.\"\"\"\n",
" tech_hits = len(_RAD_TECHNIQUE_RE.findall(text))\n",
" narrative_hits = len(_RAD_NARRATIVE_RE.findall(text))\n",
" if tech_hits + narrative_hits >= 3:\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_imaging_measurements_only(text):\n",
" \"\"\"Lots of mm/cm measurements with no diagnosis vocabulary.\"\"\"\n",
" n_meas = len(_IMAGING_MEASUREMENT_RE.findall(text))\n",
" has_dx = bool(_DX_RE.search(text))\n",
" if n_meas >= 4 and not has_dx:\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_negative_section_header(text):\n",
" \"\"\"'COMPARISON:', 'TECHNIQUE:', 'INDICATION:' alone β procedural metadata.\"\"\"\n",
" if _NEG_SECTION_RE.search(text) and not _POS_SECTION_RE.search(text):\n",
" if not _DX_RE.search(text):\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_no_findings_impression(text):\n",
" \"\"\"IMPRESSION sections that are only 'no evidence of...' / 'unchanged'.\"\"\"\n",
" if re.search(r\"\\bimpression\\s*:\", text, re.IGNORECASE):\n",
" if re.search(\n",
" r\"(no evidence|unchanged|stable|no acute|normal appearance|\"\n",
" r\"decreased|no new)\",\n",
" text, re.IGNORECASE,\n",
" ) and not _DX_RE.search(text):\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_discharge_condition_checklist(text):\n",
" \"\"\"'Mental Status: Clear / Activity: Out of bed' checklist content.\"\"\"\n",
" if _DISCHARGE_COND_RE.search(text) and not _DX_RE.search(text):\n",
" if not _POS_SECTION_RE.search(text):\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_imaging_finding_narrative(text):\n",
" \"\"\"Radiology IMPRESSION/FINDINGS narratives describing imaging\n",
" observations rather than asserting a diagnosis.\"\"\"\n",
" finding_cues = re.findall(\n",
" r\"\\b(arteriogram shows|no evidence of|caliber|stable ventricular|\"\n",
" r\"impression\\s*:|comparison\\s*:|widely patent|filling defect|\"\n",
" r\"interval (placement|change)|no acute|appears patent)\\b\",\n",
" text, re.IGNORECASE,\n",
" )\n",
" if len(finding_cues) >= 2 and not _POS_SECTION_RE.search(text):\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_med_adjustment_narrative(text):\n",
" \"\"\"Discharge med-adjustment narratives describe medication changes,\n",
" not diagnoses. Negative IF no diagnosis section is present.\"\"\"\n",
" cues = re.findall(\n",
" r\"\\b(please (stop|continue|start) taking|increase\\s+\\w+\\s+to|\"\n",
" r\"discontinue|decrease\\s+\\w+\\s+to|please have repeat|\"\n",
" r\"the following changes to your)\\b\",\n",
" text, re.IGNORECASE,\n",
" )\n",
" if len(cues) >= 2 and not _POS_SECTION_RE.search(text):\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_med_dispensing_or_dosing_dense(text):\n",
" \"\"\"Numbered medication dispensing/dosing list β strong negative pattern.\"\"\"\n",
" n_sig = len(re.findall(r\"\\bSig\\s*:\", text, re.IGNORECASE))\n",
" n_disp = len(_DISP_RE.findall(text))\n",
" n_numbered = len(re.findall(r\"^\\s*\\d{1,2}\\.\\s\", text, re.MULTILINE))\n",
" if n_sig + n_disp >= 3 or (n_sig >= 2 and n_numbered >= 2):\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_vitals_cluster(text):\n",
" \"\"\"Cluster of vital-sign abbreviations + values β vitals/triage data.\"\"\"\n",
" if len(_VITALS_CLUSTER_RE.findall(text)) >= 3:\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"def lf_micro_susceptibility_table(text):\n",
" \"\"\"Microbiology susceptibility tables β not a diagnosis on their own.\"\"\"\n",
" if re.search(\n",
" r\"(STAPH|STREP|ENTEROCOCC|KLEBSIELLA|E\\.?\\s*COLI|PSEUDOMONAS).{0,300}-{2,}.{0,20}\\b[SRI]\\b\",\n",
" text, re.DOTALL,\n",
" ):\n",
" return NEG\n",
" return ABSTAIN\n",
"\n",
"\n",
"ALL_LFS = [\n",
" lf_discharge_diagnosis_section,\n",
" lf_problem_list_marker,\n",
" lf_positive_section_header,\n",
" lf_diagnosis_vocabulary_dense,\n",
" lf_diagnosis_vocabulary_any,\n",
" lf_treatment_narrative,\n",
" lf_lab_unit_density,\n",
" lf_high_digit_density,\n",
" lf_dispensing_line,\n",
" lf_radiology_technique,\n",
" lf_imaging_measurements_only,\n",
" lf_negative_section_header,\n",
" lf_no_findings_impression,\n",
" lf_discharge_condition_checklist,\n",
" lf_imaging_finding_narrative,\n",
" lf_med_adjustment_narrative,\n",
" lf_med_dispensing_or_dosing_dense,\n",
" lf_vitals_cluster,\n",
" lf_micro_susceptibility_table,\n",
"]\n",
"LF_NAMES = [lf.__name__ for lf in ALL_LFS]\n",
"\n",
"\n",
"def apply_lfs(texts):\n",
" \"\"\"Apply all LFs to a list/Series of texts. Returns (n_texts, n_lfs) array.\"\"\"\n",
" n = len(texts)\n",
" L = np.full((n, len(ALL_LFS)), ABSTAIN, dtype=np.int8)\n",
" for i, t in enumerate(texts):\n",
" for j, lf in enumerate(ALL_LFS):\n",
" try:\n",
" L[i, j] = lf(t)\n",
" except Exception:\n",
" L[i, j] = ABSTAIN\n",
" return L\n",
"\n",
"print(f\"Defined {len(ALL_LFS)} labeling functions\")\n"
]
},
{
"cell_type": "markdown",
"id": "80b43247",
"metadata": {},
"source": [
"### Section 2.2 β Sanity check the LFs on the 20 seed examples\n",
"\n",
"Look at coverage (what fraction of seeds each LF voted on) and agreement (how often the LF was correct *when it voted*). LFs with low coverage but high agreement are gold; LFs with high coverage and ~50% agreement are noise.\n",
"\n",
"**Caveat:** the 20 seed labels are themselves noisy, so disagreement here doesn't necessarily mean the LF is wrong.\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "8fdcf3f7",
"metadata": {},
"outputs": [],
"source": [
"import pandas as pd\n",
"\n",
"seed_df = pd.read_csv(PROJECT_FILES_DIR / \"train_data-text_and_labels.csv\")\n",
"print(f\"Loaded {len(seed_df)} seed examples\")\n",
"print(f\"Label distribution: {seed_df['label'].value_counts().to_dict()}\")\n",
"\n",
"L_seed = apply_lfs(seed_df[\"text\"].tolist())\n",
"y_seed = seed_df[\"label\"].values\n",
"\n",
"print()\n",
"print(f\"{'LF':<42} {'cov':>5} {'agree':>10}\")\n",
"print(\"-\" * 60)\n",
"for j, name in enumerate(LF_NAMES):\n",
" col = L_seed[:, j]\n",
" voting = col != ABSTAIN\n",
" if voting.sum() == 0:\n",
" print(f\"{name:<42} {0:>5d} {'never':>10}\")\n",
" continue\n",
" agree = (col[voting] == y_seed[voting]).mean()\n",
" print(f\"{name:<42} {voting.sum():>5d} {agree:>10.2%}\")\n",
"\n",
"# Quick majority-vote score\n",
"preds_mv = np.where(\n",
" (L_seed == 1).sum(1) > (L_seed == 0).sum(1), 1,\n",
" np.where((L_seed == 0).sum(1) > (L_seed == 1).sum(1), 0, 1)\n",
")\n",
"print(f\"\\nNaive majority-vote agreement with seed labels: {(preds_mv == y_seed).mean():.2%}\")\n"
]
},
{
"cell_type": "markdown",
"id": "d210af95",
"metadata": {},
"source": [
"## Section 3 β Mine MIMIC-III for training chunks\n",
"\n",
"Stream `NOTEEVENTS.csv` (it's ~4GB, can't fit in memory), reservoir-sample notes from `Discharge summary` / `Radiology` / `Physician` categories, then chunk each note into ~110-word excerpts that match the shape of the test inputs.\n",
"\n",
"This cell takes ~5-10 minutes the first time, then caches to `data/mimic_chunks.parquet` so subsequent runs skip it.\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "a4a8fb94",
"metadata": {},
"outputs": [],
"source": [
"import random\n",
"from tqdm.auto import tqdm\n",
"\n",
"NOTE_CATEGORIES = {\"Discharge summary\", \"Radiology\", \"Physician \"}\n",
"\n",
"\n",
"def split_into_blocks(text):\n",
" text = text.replace(\"\\r\\n\", \"\\n\").replace(\"\\r\", \"\\n\")\n",
" text = re.sub(r\"\\n{3,}\", \"\\n\\n\", text)\n",
" return [b.strip() for b in text.split(\"\\n\\n\") if b.strip()]\n",
"\n",
"\n",
"def build_chunks_from_blocks(blocks):\n",
" chunks, cur, cur_words = [], [], 0\n",
" for blk in blocks:\n",
" bw = len(blk.split())\n",
" if bw > CHUNK_MAX_WORDS:\n",
" words = blk.split()\n",
" for i in range(0, len(words), CHUNK_TARGET_WORDS):\n",
" slice_text = \" \".join(words[i : i + CHUNK_TARGET_WORDS])\n",
" if len(slice_text.split()) >= CHUNK_MIN_WORDS:\n",
" chunks.append(slice_text)\n",
" continue\n",
" if cur and cur_words + bw > CHUNK_MAX_WORDS:\n",
" chunk_text = \"\\n\\n\".join(cur)\n",
" if len(chunk_text.split()) >= CHUNK_MIN_WORDS:\n",
" chunks.append(chunk_text)\n",
" cur, cur_words = [], 0\n",
" cur.append(blk)\n",
" cur_words += bw\n",
" if cur_words >= CHUNK_TARGET_WORDS:\n",
" chunks.append(\"\\n\\n\".join(cur))\n",
" cur, cur_words = [], 0\n",
" if cur:\n",
" chunk_text = \"\\n\\n\".join(cur)\n",
" if len(chunk_text.split()) >= CHUNK_MIN_WORDS:\n",
" chunks.append(chunk_text)\n",
" return chunks\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "069c9ee4",
"metadata": {},
"outputs": [],
"source": [
"if MIMIC_CHUNKS_PATH.exists():\n",
" print(f\"Cached chunks found at {MIMIC_CHUNKS_PATH} β skipping mining.\")\n",
" print(\"(Delete that file if you want to re-mine.)\")\n",
" chunks_df = pd.read_parquet(MIMIC_CHUNKS_PATH)\n",
"else:\n",
" if not MIMIC_NOTEEVENTS_PATH.exists():\n",
" raise FileNotFoundError(\n",
" f\"NOTEEVENTS.csv not found at {MIMIC_NOTEEVENTS_PATH}. \"\n",
" \"Edit MIMIC_NOTEEVENTS_PATH in Section 1.\"\n",
" )\n",
"\n",
" print(f\"Streaming {MIMIC_NOTEEVENTS_PATH}...\")\n",
" rng = random.Random(RANDOM_SEED)\n",
" sampled_notes = []\n",
" seen_in_category = 0\n",
"\n",
" reader = pd.read_csv(\n",
" MIMIC_NOTEEVENTS_PATH,\n",
" usecols=[\"ROW_ID\", \"CATEGORY\", \"TEXT\"],\n",
" chunksize=50_000,\n",
" low_memory=False,\n",
" )\n",
"\n",
" for batch in tqdm(reader, desc=\"scanning NOTEEVENTS\"):\n",
" batch = batch[batch[\"CATEGORY\"].isin(NOTE_CATEGORIES)]\n",
" for row_id, text in zip(batch[\"ROW_ID\"], batch[\"TEXT\"]):\n",
" if not isinstance(text, str) or len(text) < 200:\n",
" continue\n",
" seen_in_category += 1\n",
" if len(sampled_notes) < N_MIMIC_NOTES_TO_SCAN:\n",
" sampled_notes.append((int(row_id), text))\n",
" else:\n",
" j = rng.randint(0, seen_in_category - 1)\n",
" if j < N_MIMIC_NOTES_TO_SCAN:\n",
" sampled_notes[j] = (int(row_id), text)\n",
" if seen_in_category > 10 * N_MIMIC_NOTES_TO_SCAN:\n",
" break\n",
"\n",
" print(f\"Sampled {len(sampled_notes)} notes. Chunking...\")\n",
" rows = []\n",
" chunk_id = 0\n",
" for note_id, text in tqdm(sampled_notes, desc=\"chunking\"):\n",
" blocks = split_into_blocks(text)\n",
" chunks = build_chunks_from_blocks(blocks)\n",
" if len(chunks) > CHUNKS_PER_NOTE_CAP:\n",
" chunks = rng.sample(chunks, CHUNKS_PER_NOTE_CAP)\n",
" for c in chunks:\n",
" rows.append({\"chunk_id\": chunk_id, \"note_id\": note_id, \"text\": c})\n",
" chunk_id += 1\n",
"\n",
" chunks_df = pd.DataFrame(rows)\n",
" chunks_df.to_parquet(MIMIC_CHUNKS_PATH, index=False)\n",
" print(f\"Wrote {MIMIC_CHUNKS_PATH}\")\n",
"\n",
"print(f\"\\nTotal chunks: {len(chunks_df):,}\")\n",
"print(\"Word count distribution:\")\n",
"print(chunks_df['text'].str.split().str.len().describe())\n"
]
},
{
"cell_type": "markdown",
"id": "2ef42734",
"metadata": {},
"source": [
"## Section 4 β Apply LFs to mined chunks\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "5fb361a4",
"metadata": {},
"outputs": [],
"source": [
"print(\"Applying labeling functions to mined chunks...\")\n",
"L = apply_lfs(chunks_df[\"text\"].tolist())\n",
"np.save(LF_VOTES_PATH, L)\n",
"print(f\"Saved LF votes β {LF_VOTES_PATH} shape={L.shape}\")\n",
"\n",
"print(\"\\nLF coverage on mined chunks:\")\n",
"print(f\"{'name':<42} {'cov':>6} {'pos':>6} {'neg':>6}\")\n",
"print(\"-\" * 64)\n",
"for j, name in enumerate(LF_NAMES):\n",
" col = L[:, j]\n",
" cov = (col != ABSTAIN).mean()\n",
" pos = (col == 1).mean()\n",
" neg = (col == 0).mean()\n",
" print(f\"{name:<42} {cov:>6.2%} {pos:>6.2%} {neg:>6.2%}\")\n",
"\n",
"abstain_all = (L == ABSTAIN).all(axis=1)\n",
"print(f\"\\nChunks where every LF abstained: {abstain_all.sum():,} ({abstain_all.mean():.2%})\")\n"
]
},
{
"cell_type": "markdown",
"id": "d4cee79e",
"metadata": {},
"source": [
"## Section 5 β Aggregate LF votes with Snorkel's LabelModel\n",
"\n",
"`LabelModel` learns each LF's accuracy *without gold labels* by exploiting agreement/disagreement statistics across all the chunks. The output is a probability `P(label=1 | LF votes)` for each chunk β calibrated soft labels we can train on.\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "929243a2",
"metadata": {},
"outputs": [],
"source": [
"from snorkel.labeling.model import LabelModel\n",
"\n",
"print(\"Fitting Snorkel LabelModel...\")\n",
"label_model = LabelModel(cardinality=2, verbose=False)\n",
"label_model.fit(\n",
" L_train=L,\n",
" n_epochs=LABEL_MODEL_EPOCHS,\n",
" lr=LABEL_MODEL_LR,\n",
" seed=RANDOM_SEED,\n",
")\n",
"\n",
"probs = label_model.predict_proba(L)\n",
"p_pos = probs[:, 1].astype(np.float32)\n",
"np.save(SOFT_LABELS_PATH, p_pos)\n",
"\n",
"# Build training set\n",
"chunks_df = chunks_df.reset_index(drop=True)\n",
"chunks_df[\"soft_label\"] = p_pos\n",
"\n",
"if DROP_ALL_ABSTAIN:\n",
" keep = ~abstain_all\n",
" train_df = chunks_df[keep].reset_index(drop=True)\n",
" print(f\"\\nKept {len(train_df):,} chunks after dropping all-abstain ({(~keep).sum():,} dropped).\")\n",
"else:\n",
" train_df = chunks_df\n",
"\n",
"train_df.to_parquet(TRAINING_SET_PATH, index=False)\n",
"\n",
"# Soft label distribution\n",
"print(\"\\nSoft-label distribution (kept rows):\")\n",
"bins = [0, 0.2, 0.4, 0.5, 0.6, 0.8, 1.01]\n",
"counts, edges = np.histogram(train_df[\"soft_label\"], bins=bins)\n",
"for c, lo, hi in zip(counts, edges[:-1], edges[1:]):\n",
" print(f\" [{lo:.2f}, {hi:.2f}): {c:,}\")\n"
]
},
{
"cell_type": "markdown",
"id": "f555c9ca",
"metadata": {},
"source": [
"### Section 5.1 β Sanity-check LabelModel against the seed examples\n",
"\n",
"Apply LFs to the 20 seeds and run them through the *same fitted* LabelModel. Disagreement is informative but not dispositive β the seed labels are noisy too.\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "639e7e87",
"metadata": {},
"outputs": [],
"source": [
"seed_probs = label_model.predict_proba(L_seed)[:, 1]\n",
"seed_preds = (seed_probs >= 0.5).astype(int)\n",
"\n",
"print(f\"LabelModel agreement with seed labels: {(seed_preds == y_seed).mean():.2%}\")\n",
"print()\n",
"print(\"Per-row LabelModel output:\")\n",
"for i in range(len(seed_df)):\n",
" mark = \"β\" if seed_preds[i] == y_seed[i] else \"β\"\n",
" print(f\" row {i:2d}: seed={y_seed[i]} LM_p={seed_probs[i]:.2f} pred={seed_preds[i]} {mark}\")\n"
]
},
{
"cell_type": "markdown",
"id": "98c56852",
"metadata": {},
"source": [
"## Section 6 β Fine-tune Bio_ClinicalBERT on soft labels\n",
"\n",
"**Key design choice:** train with binary cross-entropy against the *soft* label (probability), not hard 0/1. This preserves LabelModel's uncertainty β chunks where LFs disagreed contribute less gradient signal than chunks where they all agreed.\n",
"\n",
"Bio_ClinicalBERT is downloaded from HuggingFace once and cached locally (~440MB). Fully offline thereafter.\n",
"\n",
"**Runtime:** ~20-40 min on a single GPU. Skip this section if you want to evaluate the rule-based baseline only.\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "5f8e22c6",
"metadata": {},
"outputs": [],
"source": [
"import torch\n",
"from torch.utils.data import Dataset, DataLoader\n",
"from torch.optim import AdamW\n",
"from transformers import (\n",
" AutoTokenizer,\n",
" AutoModelForSequenceClassification,\n",
" get_linear_schedule_with_warmup,\n",
")\n",
"\n",
"device = \"cuda\" if torch.cuda.is_available() else \"cpu\"\n",
"print(f\"Device: {device}\")\n",
"if device == \"cpu\":\n",
" print(\"WARNING: training on CPU will take hours. Consider Colab GPU.\")\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "a2cdfa5d",
"metadata": {},
"outputs": [],
"source": [
"class SoftLabelDataset(Dataset):\n",
" def __init__(self, texts, soft_labels, tokenizer):\n",
" assert len(texts) == len(soft_labels)\n",
" self.texts = texts\n",
" self.labels = soft_labels.astype(np.float32)\n",
" self.tokenizer = tokenizer\n",
"\n",
" def __len__(self):\n",
" return len(self.texts)\n",
"\n",
" def __getitem__(self, idx):\n",
" enc = self.tokenizer(\n",
" self.texts[idx],\n",
" truncation=True,\n",
" padding=\"max_length\",\n",
" max_length=MAX_SEQ_LEN,\n",
" return_tensors=\"pt\",\n",
" )\n",
" return {\n",
" \"input_ids\": enc[\"input_ids\"].squeeze(0),\n",
" \"attention_mask\": enc[\"attention_mask\"].squeeze(0),\n",
" \"soft_label\": torch.tensor(self.labels[idx], dtype=torch.float32),\n",
" }\n",
"\n",
"\n",
"def soft_bce_loss(logits, soft_labels):\n",
" \"\"\"Binary cross-entropy against soft targets. logits is (B, 2).\"\"\"\n",
" logit_pos = logits[:, 1] - logits[:, 0]\n",
" return torch.nn.functional.binary_cross_entropy_with_logits(\n",
" logit_pos, soft_labels\n",
" )\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "b00bc3bf",
"metadata": {},
"outputs": [],
"source": [
"# Optional: drop low-confidence rows (soft label in [0.4, 0.6])\n",
"FILTER_CONFIDENT = False\n",
"VAL_FRAC = 0.1\n",
"\n",
"torch.manual_seed(RANDOM_SEED)\n",
"np.random.seed(RANDOM_SEED)\n",
"\n",
"train_df_use = train_df.copy()\n",
"if FILTER_CONFIDENT:\n",
" before = len(train_df_use)\n",
" train_df_use = train_df_use[\n",
" (train_df_use[\"soft_label\"] < 0.4) | (train_df_use[\"soft_label\"] > 0.6)\n",
" ].reset_index(drop=True)\n",
" print(f\"Filtered to confident rows: {before:,} β {len(train_df_use):,}\")\n",
"\n",
"perm = np.random.permutation(len(train_df_use))\n",
"n_val = max(200, int(len(train_df_use) * VAL_FRAC))\n",
"val_idx, train_idx = perm[:n_val], perm[n_val:]\n",
"train_split = train_df_use.iloc[train_idx].reset_index(drop=True)\n",
"val_split = train_df_use.iloc[val_idx].reset_index(drop=True)\n",
"print(f\"train: {len(train_split):,} val: {len(val_split):,}\")\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "0fbbdc3f",
"metadata": {},
"outputs": [],
"source": [
"print(f\"Loading {BERT_MODEL_NAME} (downloads ~440MB on first call)...\")\n",
"tokenizer = AutoTokenizer.from_pretrained(BERT_MODEL_NAME)\n",
"model = AutoModelForSequenceClassification.from_pretrained(\n",
" BERT_MODEL_NAME, num_labels=2\n",
").to(device)\n",
"print(\"Loaded.\")\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "03d73e16",
"metadata": {},
"outputs": [],
"source": [
"train_ds = SoftLabelDataset(\n",
" train_split[\"text\"].tolist(), train_split[\"soft_label\"].values, tokenizer,\n",
")\n",
"val_ds = SoftLabelDataset(\n",
" val_split[\"text\"].tolist(), val_split[\"soft_label\"].values, tokenizer,\n",
")\n",
"train_loader = DataLoader(train_ds, batch_size=BATCH_SIZE, shuffle=True, num_workers=2)\n",
"val_loader = DataLoader(val_ds, batch_size=EVAL_BATCH_SIZE, shuffle=False, num_workers=2)\n",
"\n",
"optimizer = AdamW(model.parameters(), lr=LEARNING_RATE, weight_decay=WEIGHT_DECAY)\n",
"total_steps = len(train_loader) * NUM_EPOCHS\n",
"scheduler = get_linear_schedule_with_warmup(\n",
" optimizer,\n",
" num_warmup_steps=int(WARMUP_RATIO * total_steps),\n",
" num_training_steps=total_steps,\n",
")\n",
"\n",
"\n",
"@torch.no_grad()\n",
"def evaluate_model(model, loader, device):\n",
" model.eval()\n",
" all_probs, all_targets, losses = [], [], []\n",
" for batch in loader:\n",
" input_ids = batch[\"input_ids\"].to(device)\n",
" attn_mask = batch[\"attention_mask\"].to(device)\n",
" soft = batch[\"soft_label\"].to(device)\n",
" out = model(input_ids=input_ids, attention_mask=attn_mask)\n",
" loss = soft_bce_loss(out.logits, soft)\n",
" losses.append(loss.item())\n",
" probs = torch.softmax(out.logits, dim=-1)[:, 1]\n",
" all_probs.append(probs.cpu().numpy())\n",
" all_targets.append(soft.cpu().numpy())\n",
" probs = np.concatenate(all_probs)\n",
" targets = np.concatenate(all_targets)\n",
" hard_targets = (targets >= 0.5).astype(int)\n",
" hard_preds = (probs >= 0.5).astype(int)\n",
" acc = (hard_preds == hard_targets).mean()\n",
" return {\"loss\": float(np.mean(losses)), \"acc_vs_hard_target\": float(acc)}\n",
"\n",
"\n",
"best_val = float(\"inf\")\n",
"MODEL_DIR.mkdir(parents=True, exist_ok=True)\n",
"\n",
"for epoch in range(1, NUM_EPOCHS + 1):\n",
" model.train()\n",
" losses = []\n",
" pbar = tqdm(train_loader, desc=f\"epoch {epoch} train\")\n",
" for batch in pbar:\n",
" input_ids = batch[\"input_ids\"].to(device)\n",
" attn_mask = batch[\"attention_mask\"].to(device)\n",
" soft = batch[\"soft_label\"].to(device)\n",
" optimizer.zero_grad()\n",
" out = model(input_ids=input_ids, attention_mask=attn_mask)\n",
" loss = soft_bce_loss(out.logits, soft)\n",
" loss.backward()\n",
" torch.nn.utils.clip_grad_norm_(model.parameters(), 1.0)\n",
" optimizer.step()\n",
" scheduler.step()\n",
" losses.append(loss.item())\n",
" pbar.set_postfix(loss=np.mean(losses[-50:]))\n",
"\n",
" metrics = evaluate_model(model, val_loader, device)\n",
" print(\n",
" f\"epoch {epoch} train_loss={np.mean(losses):.4f} \"\n",
" f\"val_loss={metrics['loss']:.4f} \"\n",
" f\"val_acc_vs_hard={metrics['acc_vs_hard_target']:.4f}\"\n",
" )\n",
" if metrics[\"loss\"] < best_val:\n",
" best_val = metrics[\"loss\"]\n",
" model.save_pretrained(MODEL_DIR)\n",
" tokenizer.save_pretrained(MODEL_DIR)\n",
" print(f\" β³ saved checkpoint to {MODEL_DIR}\")\n",
"\n",
"print(f\"\\nDone. Best val loss: {best_val:.4f}. Model in {MODEL_DIR}\")\n"
]
},
{
"cell_type": "markdown",
"id": "063feb95",
"metadata": {},
"source": [
"## Section 7 β Generate Gradescope predictions\n",
"\n",
"Predicts on `test{01,02,03}_text_only.csv` and writes Gradescope-shaped CSVs to `outputs/test{NN}-pred.csv` (columns: `row_id`, `prediction`).\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "692c68cd",
"metadata": {},
"outputs": [],
"source": [
"@torch.no_grad()\n",
"def predict_probs(model, tokenizer, texts, device):\n",
" model.eval()\n",
" probs = []\n",
" for start in tqdm(range(0, len(texts), EVAL_BATCH_SIZE), desc=\"predict\"):\n",
" batch_texts = texts[start : start + EVAL_BATCH_SIZE]\n",
" enc = tokenizer(\n",
" batch_texts,\n",
" truncation=True,\n",
" padding=True,\n",
" max_length=MAX_SEQ_LEN,\n",
" return_tensors=\"pt\",\n",
" ).to(device)\n",
" out = model(**enc)\n",
" p1 = torch.softmax(out.logits, dim=-1)[:, 1].cpu().numpy()\n",
" probs.append(p1)\n",
" return np.concatenate(probs)\n",
"\n",
"\n",
"def predict_test_file(test_path, out_path, model, tokenizer, device):\n",
" df = pd.read_csv(test_path)\n",
" if \"text\" not in df.columns or \"row_id\" not in df.columns:\n",
" raise ValueError(f\"{test_path} missing required columns\")\n",
" probs = predict_probs(model, tokenizer, df[\"text\"].astype(str).tolist(), device)\n",
" preds = (probs >= DECISION_THRESHOLD).astype(int)\n",
" out_df = pd.DataFrame({\"row_id\": df[\"row_id\"].astype(int), \"prediction\": preds})\n",
" out_df.to_csv(out_path, index=False)\n",
" print(f\" {out_path.name}: {preds.sum()}/{len(preds)} positive β {out_path}\")\n",
" return out_df\n",
"\n",
"\n",
"# Reload from disk to ensure we're using the saved best checkpoint\n",
"print(f\"Loading model from {MODEL_DIR}...\")\n",
"tokenizer = AutoTokenizer.from_pretrained(MODEL_DIR)\n",
"model = AutoModelForSequenceClassification.from_pretrained(MODEL_DIR).to(device)\n",
"\n",
"for n in (\"01\", \"02\", \"03\"):\n",
" in_path = PROJECT_FILES_DIR / f\"test{n}_text_only.csv\"\n",
" out_path = OUTPUT_DIR / f\"test{n}-pred.csv\"\n",
" if not in_path.exists():\n",
" print(f\" skipped {in_path} (not found)\")\n",
" continue\n",
" predict_test_file(in_path, out_path, model, tokenizer, device)\n"
]
},
{
"cell_type": "markdown",
"id": "475bdc40",
"metadata": {},
"source": [
"## Section 8 β BERT diagnostics on the 20 seed examples\n",
"\n",
"Sanity check the trained BERT against the noisy seed labels. Disagreement is informative both ways:\n",
"\n",
"* Model wrong on a seed β maybe the LFs+aggregation steered it incorrectly\n",
"* Model \"wrong\" but you agree with it on inspection β the seed label was wrong\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "21d35f6c",
"metadata": {},
"outputs": [],
"source": [
"seed_bert_probs = predict_probs(\n",
" model, tokenizer, seed_df[\"text\"].astype(str).tolist(), device,\n",
")\n",
"seed_bert_preds = (seed_bert_probs >= DECISION_THRESHOLD).astype(int)\n",
"\n",
"print(f\"BERT agreement with (noisy) seed labels: {(seed_bert_preds == y_seed).mean():.2%}\")\n",
"print(f\"\\nConfusion (rows=seed, cols=pred):\")\n",
"for s in (0, 1):\n",
" row = [int(((y_seed == s) & (seed_bert_preds == p)).sum()) for p in (0, 1)]\n",
" print(f\" seed={s}: pred=0:{row[0]:3d} pred=1:{row[1]:3d}\")\n",
"\n",
"print(\"\\nPer-row breakdown:\")\n",
"for i in range(len(seed_df)):\n",
" mark = \"β\" if seed_bert_preds[i] == y_seed[i] else \"β\"\n",
" print(f\" row {i:2d}: seed={y_seed[i]} bert_p={seed_bert_probs[i]:.3f} pred={seed_bert_preds[i]} {mark}\")\n"
]
},
{
"cell_type": "markdown",
"id": "ea5b48f7",
"metadata": {},
"source": [
"## Section 9 β Approach 1 baseline: pure rule-based (LF majority vote)\n",
"\n",
"For the report's *negative results / iterative exploration* section. Quantifies how much of the test signal is captured by handwritten heuristics alone, before any ML. Writes separate `outputs/test{NN}-pred-rulebased.csv` files.\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "f8f2555c",
"metadata": {},
"outputs": [],
"source": [
"def majority_vote(L):\n",
" \"\"\"Per row: count POS vs NEG votes; ties / all-abstain β predict 1.\"\"\"\n",
" pos_votes = (L == 1).sum(axis=1)\n",
" neg_votes = (L == 0).sum(axis=1)\n",
" return np.where(pos_votes >= neg_votes, 1, 0).astype(int)\n",
"\n",
"\n",
"for n in (\"01\", \"02\", \"03\"):\n",
" in_path = PROJECT_FILES_DIR / f\"test{n}_text_only.csv\"\n",
" out_path = OUTPUT_DIR / f\"test{n}-pred-rulebased.csv\"\n",
" if not in_path.exists():\n",
" print(f\" skipped {in_path}\")\n",
" continue\n",
" df = pd.read_csv(in_path)\n",
" L_test = apply_lfs(df[\"text\"].astype(str).tolist())\n",
" preds = majority_vote(L_test)\n",
" out = pd.DataFrame({\"row_id\": df[\"row_id\"].astype(int), \"prediction\": preds})\n",
" out.to_csv(out_path, index=False)\n",
" print(f\" {out_path.name}: {preds.sum()}/{len(preds)} positive\")\n"
]
},
{
"cell_type": "markdown",
"id": "df0adafd",
"metadata": {},
"source": [
"## Section 10 β Compare rule baseline vs. trained BERT\n",
"\n",
"Cross-check how often the two disagree on the test sets. Big disagreement = BERT is doing something the rules can't capture (good β that's why we trained it). Tiny disagreement = the rules already capture most of the signal (also useful information for the report).\n"
]
},
{
"cell_type": "code",
"execution_count": null,
"id": "c11af3b4",
"metadata": {},
"outputs": [],
"source": [
"for n in (\"01\", \"02\", \"03\"):\n",
" rule_path = OUTPUT_DIR / f\"test{n}-pred-rulebased.csv\"\n",
" bert_path = OUTPUT_DIR / f\"test{n}-pred.csv\"\n",
" if not rule_path.exists() or not bert_path.exists():\n",
" continue\n",
" r = pd.read_csv(rule_path)[\"prediction\"].values\n",
" b = pd.read_csv(bert_path)[\"prediction\"].values\n",
" agree = (r == b).mean()\n",
" print(f\"test{n}: rule_pos={r.sum()}, bert_pos={b.sum()}, agreement={agree:.2%}\")\n"
]
},
{
"cell_type": "markdown",
"id": "d95f57cb",
"metadata": {},
"source": [
"## Notes for the report\n",
"\n",
"* **Soft-label BCE training** is the technically interesting bit β the model learns from LabelModel's calibrated uncertainty rather than thresholded hard labels. Mention this; it differentiates the work from a vanilla Snorkel pipeline.\n",
"* **The 20 seed labels are noisy** (themselves BERT-generated). Frame any \"agreement with seed\" numbers as agreement, not accuracy.\n",
"* **Negative results are explicitly rewarded** by the rubric. Include the rule-based baseline (Section 9), the BERT model (Section 7), and ideally one variant: e.g., BERT trained on the 20 seeds *directly* (no MIMIC, no Snorkel) β likely overfits and is much worse, which is informative. You can build that variant by skipping Sections 3-5 and replacing `train_df` in Section 6 with a dataframe of just the 20 seeds.\n",
"* **Related work** to read for the report: CAML (Mullenbach et al. 2018) for ICD coding on MIMIC-III, Snorkel (Ratner et al.) for weak supervision theory, ClinicalBERT / Bio_ClinicalBERT for the encoder choice, SetFit for the few-shot baseline you could optionally add.\n"
]
}
],
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|