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| Metric | Value |
|---|---|
| Base Model | openai/gpt-oss-20b |
| Architecture | Mixture-of-Experts Transformer |
| Total Parameters | ~14.3B (pruned from 21B) |
| Original Experts per Layer | 32 |
| Pruned Experts per Layer | 21 |
| Layers | 24 |
| Top-k Routing | 4 |
| Context Length | 128K tokens |
| Attention Heads | 64 (Query), 8 (Key-Value) |
| Residual Dimension | 2880 |
| Attention Pattern | Alternating dense & sliding window (128 tokens) |
| Positional Encoding | RoPE (Rotary Position Embedding) |
| Normalization | RMSNorm |
| Precision | BF16 |
| License | Apache 2.0 |
| Specialization | Health Or Medicine |
1from transformers import AutoModelForCausalLM, AutoTokenizer
2import torch
3
4# Load the specialized model on CPU
5model = AutoModelForCausalLM.from_pretrained(
6 "AmanPriyanshu/gpt-oss-14.3b-specialized-health_or_medicine-pruned-moe-only-21-experts",
7 torch_dtype=torch.bfloat16,
8 device_map="cpu",
9 trust_remote_code=True
10)
11tokenizer = AutoTokenizer.from_pretrained("AmanPriyanshu/gpt-oss-14.3b-specialized-health_or_medicine-pruned-moe-only-21-experts")
12
13# Generate with the model
14messages = [
15 {"role": "user", "content": "What are the main functions of the human heart?"}
16]
17
18inputs = tokenizer.apply_chat_template(
19 messages,
20 add_generation_prompt=True,
21 return_tensors="pt",
22 return_dict=True,
23 reasoning_effort="medium"
24)
25
26# Ensure inputs are on the same device as model
27inputs = {k: v.to(model.device) for k, v in inputs.items()}
28
29outputs = model.generate(
30 **inputs,
31 max_new_tokens=512,
32 do_sample=True,
33 temperature=0.1,
34 top_p=0.9,
35 pad_token_id=tokenizer.eos_token_id,
36 eos_token_id=tokenizer.eos_token_id
37)
38
39# Decode only the generated part
40input_length = inputs['input_ids'].shape[1]
41response_tokens = outputs[0][input_length:]
42response = tokenizer.decode(response_tokens, skip_special_tokens=True)
43print(response)1from transformers import AutoModelForCausalLM, AutoTokenizer
2import torch
3
4# Check MPS availability and load model
5device = "mps" if torch.backends.mps.is_available() else "cpu"
6
7model = AutoModelForCausalLM.from_pretrained(
8 "AmanPriyanshu/gpt-oss-14.3b-specialized-health_or_medicine-pruned-moe-only-21-experts",
9 torch_dtype=torch.float16, # Better MPS compatibility
10 device_map=device,
11 trust_remote_code=True,
12 low_cpu_mem_usage=True
13)
14tokenizer = AutoTokenizer.from_pretrained("AmanPriyanshu/gpt-oss-14.3b-specialized-health_or_medicine-pruned-moe-only-21-experts")
15
16# Generate with the model
17messages = [
18 {"role": "user", "content": "What are the main functions of the human heart?"}
19]
20
21inputs = tokenizer.apply_chat_template(
22 messages,
23 add_generation_prompt=True,
24 return_tensors="pt",
25 return_dict=True,
26 reasoning_effort="medium"
27)
28
29# Move inputs to model device
30inputs = {k: v.to(model.device) if isinstance(v, torch.Tensor) else v for k, v in inputs.items()}
31
32# Use torch.no_grad for MPS stability
33with torch.no_grad():
34 outputs = model.generate(
35 **inputs,
36 max_new_tokens=512,
37 do_sample=True,
38 temperature=0.1,
39 top_p=0.9,
40 pad_token_id=tokenizer.eos_token_id,
41 eos_token_id=tokenizer.eos_token_id,
42 use_cache=True
43 )
44
45# Decode only the generated part
46input_length = inputs['input_ids'].shape[1]
47response_tokens = outputs[0][input_length:]
48response = tokenizer.decode(response_tokens, skip_special_tokens=True)
49print(response)1device_map="auto" # Will automatically use GPU if available
2torch_dtype=torch.bfloat16 # or torch.float16<|channel|>analysis<|message|>Need concise answer.<|end|><|start|>assistant<|channel|>final<|message|>The human heart performs three core functions that keep the body alive and functioning:
| Function | What it does | How it works |
|----------|--------------|--------------|
| **Pumping** | Moves blood throughout the body | The left ventricle contracts to push oxygen‑rich blood into the aorta; the right ventricle pumps de‑oxygenated blood into the pulmonary artery. |
| **Circulation** | Delivers oxygen, nutrients, hormones, and removes waste | Blood travels through arteries → capillaries → veins, exchanging substances with tissues. |
| **Regulation** | Maintains blood pressure and flow | The heart’s intrinsic pacemaker (SA node) sets rhythm; autonomic nerves and hormones adjust rate and force of contraction to meet the body’s needs. |
Together, these functions keep tissues supplied with oxygen and nutrients while removing metabolic waste, enabling the body to function and respond to changing demands.<|return|><|channel|>analysis<|message|>Need concise explanation.<|end|><|start|>assistant<|channel|>final<|message|>**Bacteria vs. Viruses – the key differences**
| Feature | Bacteria | Viruses |
|--------|----------|--------|
| **Size** | Microscopic, 0.5–5 µm (visible under a microscope) | 20–200 nm (too small for a light microscope) |
| **Structure** | Complex, cell‑like structure: cell wall, membrane, cytoplasm, organelles (e.g., ribosomes) | Very simple: a nucleic acid genome (DNA or RNA) surrounded by a protein coat (capsid); some have a lipid envelope |
| **Life Cycle** | Independent life form; can grow, divide, and reproduce on their own (metabolism, energy production) | Not a living organism on its own; must infect a host cell and hijack its machinery to replicate |
| **Reproduction** | Divide by binary (or sometimes more complex) cell division (mitosis‑like) | Replicate by copying their genome inside a host cell, then assembling new virions |
| **Genetic Material** | DNA (usually double‑stranded) | DNA or RNA (single‑ or double‑stranded) |
| **Infection Mechanism** | Can colonize or invade tissues, produce toxins, or cause inflammation; often spread by contact, food, water, vectors | Attach to specific host receptors, enter cells, use host enzymes to replicate; often cause cell lysis or dormancy |
| **Treatment** | Antibiotics (target cell wall, protein synthesis, DNA replication, etc.) | Antiviral drugs (target viral enzymes or replication steps); vaccines; no antibiotics work |
| **Evolutionary Complexity** | More complex genomes, can exchange genes via plasmids, conjugation, etc. | Simpler genomes; evolve mainly by mutation and recombination |
| **Examples** | *Staphylococcus aureus*, *E. coli*, *Bacillus subtilis* | Influenza virus, HIV, SARS‑CoV‑2, HPV |
**Bottom line:**
Bacteria are true, independent microorganisms that can live and reproduce on their own, whereas viruses are essentially “parasite‑like” particles that need a host cell to make copies of themselves. This fundamental difference shapes how they cause disease, how we diagnose them, and how we treat or prevent infections.<|return|><|channel|>analysis<|message|>Need concise answer.<|end|><|start|>assistant<|channel|>final<|message|>**Diabetes mellitus** is a chronic metabolic disorder in which the body cannot regulate blood glucose properly. The two main types—Type 1 and Type 2—share many symptoms but differ in underlying causes.
---
## 1. Symptoms (common to both types)
| Symptom | Typical Onset | Why it Happens |
|---------|---------------|----------------|
| **Polyuria** (excessive urination) | Often first sign | High blood glucose spills into urine, pulling water with it (osmotic diuresis). |
| **Polydipsia** (excessive thirst) | Usually follows polyuria | Loss of fluid through urine leads to dehydration; kidneys signal thirst. |
| **Polyphagia** (increased hunger) | Common in Type 1; variable in Type 2 | Cells can’t get glucose → body signals “need more food.” |
| **Weight loss** | More pronounced in Type 1 | Body breaks down fat and muscle for energy when glucose can’t be used. |
| **Fatigue / weakness** | Early symptom | Energy deficit from impaired glucose utilization. |
| **Blurred vision** | Can appear early | Hyperglycemia causes fluid shifts in the lens, altering its shape. |
| **Slow‑healing cuts or infections** | Later symptom | High glucose impairs immune function and tissue repair. |
| **Numbness or tingling in extremities** | Later symptom | Chronic hyperglycemia damages nerves (diabetic neuropathy). |
| **Frequent infections (e.g., urinary, skin, oral)** | Later symptom | Impaired immune response. |
> **Note:** In Type 2 diabetes, many people are asymptomatic for years; early signs may be subtle (e.g., mild fatigue, occasional blurred vision).
---
## 2. Causes
| Type | Primary Cause | Key Risk Factors |
|------|---------------|-----------------|
| **Type 1** | Autoimmune destruction of pancreatic β‑cells → insulin deficiency | Genetic predisposition, viral infections (e.g., enteroviruses), environmental triggers, early childhood onset |
| **Type 2** | Insulin resistance + relative insulin deficiency | Obesity, sedentary lifestyle, poor diet, family history, age ≥45, certain ethnicities (African‑American, Hispanic, Native American, Asian), gestational diabetes history |
| **Gestational** | Hormonal changes during pregnancy → insulin resistance1@misc{priyanshu2025gptoss,
2 title={{GPT-OSS MoE Expert Fingerprinting: Analyzing Expert Activation Patterns in Mixture of Experts Models}},
3 author={Priyanshu, Aman and Vijay, Supriti},
4 year={2025},
5 howpublished={\url{https://amanpriyanshu.github.io/GPT-OSS-MoE-ExpertFingerprinting/}},
6 note={Interactive analysis tool for expert activation patterns in MoE architectures}
7}