计算机科学
压缩(物理)
数据压缩
编码(内存)
质谱法
二进制数
压缩传感
压缩比
图像压缩
特征(语言学)
人工智能
数据挖掘
空间分析
足迹
延迟(音频)
图像分辨率
模式识别(心理学)
计算机数据存储
蛋白质组学
算法
内存占用
还原(数学)
钥匙(锁)
计算机硬件
数据压缩比
实时计算
代谢组学
质谱成像
蛋白质基因组学
错误发现率
作者
Shuochao Li,Hongping Sheng,Pengyuan Du,Jingying Chen,Xixi Wang,Junjie Tong,Jiahua Hong,Xiaohan Jing,Miaoshan Lu,Changbin Brad Yu
标识
DOI:10.1021/acs.jproteome.5c00423
摘要
Abstract Mass spectrometry imaging has emerged as a pivotal tool in spatial metabolomics, yet its reliance on the imzML format poses critical challenges in data storage, transmission, and computational efficiency. While imzML ensures cross-platform compatibility, its lower compressed binary architecture results in large file sizes and high parsing overhead, hindering cloud-based analysis and real-time visualization. This study introduces an enhanced Aird compression format optimized for spatial metabolomics through two innovations: (1) a dynamic combinatorial compression algorithm for integer-based encoding of m/z and intensity data; (2) a coordinate-separation storage strategy for rapid spatial indexing. Experimental validation on 47 public datasets demonstrated significant performance gains. Compared to imzML, Aird achieved a 70% reduction in storage footprint (mean compression ratio: 30.03%) while maintaining near-lossless data precision (F1-score = 99.26% at 0.1 ppm m/z tolerance). For high-precision-controlled datasets, Aird accelerated loading speeds by 15-fold in MZmine. The Aird format overcomes crucial bottlenecks in spatial metabolomics by harmonizing storage efficiency, computational speed, and analytical precision, reducing I/O latency for large cohorts. By achieving near-native feature detection accuracy, Aird establishes a robust infrastructure for translational applications, including disease biomarker discovery and pharmacokinetic imaging.
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