Sparse Recovery Of Imaging Transcriptomics Data

John P. Bryan, B. Cleary, Samouil L. Farhi, Yonina C. Eldar
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引用次数: 4

Abstract

Imaging transcriptomics (IT) techniques enable characterization of gene expression in cells in their native context by imaging barcoded mRNA probes with single molecule resolution. However, the need to acquire many rounds of high-magnification imaging data limits the throughput and impact of existing methods. We propose an algorithm for decoding lower magnification IT data than that used in standard experimental workflows. Our approach, Joint Sparse method for Imaging Transcriptomics (JSIT), incorporates codebook knowledge and sparsity assumptions into an optimization problem. Using simulated low-magnification data, we demonstrate that JSIT enables improved throughput and recovery performance over standard decoding methods.
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成像转录组学数据的稀疏恢复
成像转录组学(IT)技术通过单分子分辨率成像条形码mRNA探针,能够在细胞的天然环境中表征基因表达。然而,需要获取多轮高倍率成像数据限制了现有方法的吞吐量和影响。我们提出了一种解码比标准实验工作流程中使用的低倍率IT数据的算法。我们的方法,成像转录组学联合稀疏方法(JSIT),将代码本知识和稀疏性假设纳入优化问题。使用模拟的低倍率数据,我们证明了JSIT能够比标准解码方法提高吞吐量和恢复性能。
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