跳到正文
研踪PaperTrail
← 研踪 PaperTrail

arXiv:2611.11745 · v1

Reproducible quantum clustering for single-cell transcriptome atlases

首次提交 2026-11-09 09:31
版本更新 2026-11-09 09:31
雷达观测 2026-11-10 13:18
arXiv ↗PDF ↗

摘要

Current single-cell clustering pipelines discard most genes and can yield inconsistent clusters across random seeds. We introduce KQE-2, a training-free hybrid quantum-classical framework for reproducible whole-transcriptome clustering. KQE-2 maps cells into entanglement-free quantum states, enabling exact feature evaluation on classical hardware and direct checks on a quantum processor. Theoretically, we prove that removing entanglement is necessary and sufficient to bound single-qubit feature variance locally. Practically, while retraining scVI shifted 14% of cells and altered rare-type markers and drug targets, KQE-2 delivered identical biology across runs. On standard highly variable genes, the quantum encoding alone raised accuracy on a developing cortex from 0.61 to 0.79. KQE-2 scales to 11.4 million nuclei on one server, outperforming the compared methods on eight of ten complete atlases (and within the best method's run-to-run range on two), and leads on six even under standard downstream clustering.

作者备注:28 pages; 5 figures and 1 table in the main text; 5 Extended Data figures, 5 Extended Data tables; Supplementary Information with 2 figures and 15 tables

AI 论文解读

基于摘要 · 非全文审阅

此版本尚未生成 AI 解读。解读由后台任务生成并按论文版本保存,登录后共享已有结果。

版本差异

目前只观测到一个版本,无法比较变化。之后收录新版本时,会在这里对照标题、作者、分类和摘要。

观测到的版本

相邻记录可能跳过中间版本;首次发现 v2 及以上也会标为版本更新。

v1 · 2026-11-09 09:31 · 最新观测版本

Reproducible quantum clustering for single-cell transcriptome atlases

Current single-cell clustering pipelines discard most genes and can yield inconsistent clusters across random seeds. We introduce KQE-2, a training-free hybrid quantum-classical framework for reproducible whole-transcriptome clustering. KQE-2 maps cells into entanglement-free quantum states, enabling exact feature evaluation on classical hardware and direct checks on a quantum processor. Theoretically, we prove that removing entanglement is necessary and sufficient to bound single-qubit feature variance locally. Practically, while retraining scVI shifted 14% of cells and altered rare-type markers and drug targets, KQE-2 delivered identical biology across runs. On standard highly variable genes, the quantum encoding alone raised accuracy on a developing cortex from 0.61 to 0.79. KQE-2 scales to 11.4 million nuclei on one server, outperforming the compared methods on eight of ten complete atlases (and within the best method's run-to-run range on two), and leads on six even under standard downstream clustering.

查看此版本解读 →查看此版本原文 ↗