Inference of differentiation trajectories by transfer learning across biological processes.

Cell systems Pub Date : 2024-01-17 Epub Date: 2023-12-20 DOI:10.1016/j.cels.2023.12.002
Gaurav Jumde, Bastiaan Spanjaard, Jan Philipp Junker
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Abstract

Stem cells differentiate into distinct fates by transitioning through a series of transcriptional states. Current computational approaches allow reconstruction of differentiation trajectories from single-cell transcriptomics data, but it remains unknown to what degree differentiation can be predicted across biological processes. Here, we use transfer learning to infer differentiation processes and quantify predictability in early embryonic development and adult hematopoiesis. Overall, we find that non-linear methods outperform linear approaches, and we achieved the best predictions with a custom variational autoencoder that explicitly models changes in transcriptional variance. We observed a high accuracy of predictions in embryonic development, but we found somewhat lower agreement with the real data in adult hematopoiesis. We demonstrate that this discrepancy can be explained by a higher degree of concordant transcriptional processes along embryonic differentiation compared with adult homeostasis. In summary, we establish a framework for quantifying and exploiting predictability of cellular differentiation trajectories.

Abstract Image

通过跨生物过程的迁移学习推断分化轨迹。
干细胞通过一系列转录状态的转换分化成不同的命运。目前的计算方法可以从单细胞转录组学数据重建分化轨迹,但在多大程度上可以预测整个生物过程的分化仍是未知数。在这里,我们利用迁移学习来推断早期胚胎发育和成体造血的分化过程并量化可预测性。总体而言,我们发现非线性方法优于线性方法,而且我们使用定制的变异自动编码器实现了最佳预测,该编码器明确地模拟了转录方差的变化。在胚胎发育过程中,我们观察到了较高的预测准确率,但在成人造血过程中,我们发现与真实数据的一致性略低。我们证明,这种差异可以用胚胎分化过程中转录过程的一致性高于成体平衡过程来解释。总之,我们建立了一个量化和利用细胞分化轨迹可预测性的框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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