Quantifying the distribution of feature values over data represented in arbitrary dimensional spaces.
Enrique R SebastianJulio EsparzaLiset Menendez de la PridaPublished in: PLoS computational biology (2024)
Identifying the structured distribution (or lack thereof) of a given feature over a point cloud is a general research question. In the neuroscience field, this problem arises while investigating representations over neural manifolds (e.g., spatial coding), in the analysis of neurophysiological signals (e.g., sensory coding) or in anatomical image segmentation. We introduce the Structure Index (SI) as a directed graph-based metric to quantify the distribution of feature values projected over data in arbitrary D-dimensional spaces (defined from neurons, time stamps, pixels, genes, etc). The SI is defined from the overlapping distribution of data points sharing similar feature values in a given neighborhood of the cloud. Using arbitrary data clouds, we show how the SI provides quantification of the degree and directionality of the local versus global organization of feature distribution. SI can be applied to both scalar and vectorial features permitting quantification of the relative contribution of related variables. When applied to experimental studies of head-direction cells, it is able to retrieve consistent feature structure from both the high- and low-dimensional representations, and to disclose the local and global structure of the angle and speed represented in different brain regions. Finally, we provide two general-purpose examples (sound and image categorization), to illustrate the potential application to arbitrary dimensional spaces. Our method provides versatile applications in the neuroscience and data science fields.
Keyphrases
- deep learning
- machine learning
- electronic health record
- big data
- artificial intelligence
- convolutional neural network
- working memory
- neural network
- gene expression
- room temperature
- public health
- cell death
- spinal cord
- social media
- multiple sclerosis
- transcription factor
- cell cycle arrest
- drug induced
- endoplasmic reticulum stress
- genome wide identification