将白血细胞图像与基因数据对齐,提升血液病诊断准确率
Genetically Aligned Patient Representations Improve Hematological Diagnosis

- 用自监督预训练+对比学习,把细胞图像与染色体异常、突变数据对齐
- 在急性髓系白血病患者上,诊断性能优于传统病理模型
- 可直接检索疾病和基因变异,适合临床辅助诊断场景
多模态对齐组织病理编码器与转录组及基因组数据已被证明能显著提升下游诊断任务表现。血液学细胞学的独特之处在于,视觉单细胞评估常与细胞遗传学和分子遗传学结合用于血液癌诊断。本研究提出一种框架,将单个白血细胞图像与染色体异常(核型)及靶向基因面板的体细胞突变对齐。训练策略采用两阶段方法:(i) 使用iBOT头在超过1500名患者的队列上进行自监督、仅视觉的Transformer聚合器预训练;(ii) 在急性髓系白血病患者上通过监督对比损失实现基因对齐。所提出的基因对齐患者编码器在血液学诊断任务中表现更优,超越了滑动级别病理基础模型。此外,该模型提供开箱即用的疾病和基因变异检索能力。将基因数据融入患者编码器提升了表示质量,构建了一个契合临床诊断流程的多模态血液学专用AI框架,为未来研究铺平道路。代码与模型权重可在https://github.com/marrlab/GenBloom获取。
原文摘要 · Abstract (English)
Multimodal alignment of histopathology encoders with transcriptomic and genomic data has been shown to significantly improve performance in downstream diagnostic tasks. Hematological cytology is unique in that visual single-cell evaluation is often paired with cytogenetics and molecular genetics for blood cancer diagnosis. In this study, we present a framework to align single white blood cell images with chromosomal aberrations (karyotype) and somatic mutations from targeted gene panels. Our training strategy follows a two-stage approach: (i) self-supervised, vision-only pretraining of a transformer aggregator using an iBOT head on a cohort of over 1500 patients, and (ii) genetic alignment via supervised contrastive loss on acute myeloid leukemia patients. Our genetically aligned patient encoder improves hematological diagnostic tasks, outperforming slide-level histopathology foundation models. Additionally, the model provides off-the-shelf retrieval capabilities for diseases and genetic alterations. Incorporating genetic data into patient encoders increases the quality of patient representations, providing a framework that aligns with clinical diagnostic workflows and paves the way for future multimodal hematology-specific AI. The code and model weights are available at https://github.com/marrlab/GenBloom.
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