# Clique-like Point Cloud Registration: A Flexible Sampling Registration Method Based on Clique-like for Low-Overlapping Point Cloud

**Authors:** Xinrui Huang, Xiaorong Gao, Jinlong Li, Lin Luo

PMC · DOI: 10.3390/s24175499 · Sensors (Basel, Switzerland) · 2024-08-24

## TL;DR

This paper introduces CL-PCR, a new 3D point cloud registration method that improves accuracy and robustness in low-overlap scenarios using clique-like sampling.

## Contribution

The novel CL-PCR method uses clique-like subsets to enhance registration accuracy and robustness in low-overlap point cloud scenarios.

## Key findings

- CL-PCR outperforms state-of-the-art methods on the 3DMatch/3DLoMatch datasets.
- Fast-CL-PCRv1 achieves superior registration performance using FPFH and FCGF descriptors.
- The method demonstrates robustness and practicality with real-world data.

## Abstract

Three-dimensional point cloud registration is a critical task in 3D perception for sensors that aims to determine the optimal alignment between two point clouds by finding the best transformation. Existing methods like RANSAC and its variants often face challenges, such as sensitivity to low overlap rates, high computational costs, and susceptibility to outliers, leading to inaccurate results, especially in complex or noisy environments. In this paper, we introduce a novel 3D registration method, CL-PCR, inspired by the concept of maximal cliques and built upon the SC2-PCR framework. Our approach allows for the flexible use of smaller sampling subsets to extract more local consensus information, thereby generating accurate pose hypotheses even in scenarios with low overlap between point clouds. This method enhances robustness against low overlap and reduces the influence of outliers, addressing the limitations of traditional techniques. First, we construct a graph matrix to represent the compatibility relationships among the initial correspondences. Next, we build clique-likes subsets of various sizes within the graph matrix, each representing a consensus set. Then, we compute the transformation hypotheses for the subsets using the SVD algorithm and select the best hypothesis for registration based on evaluation metrics. Extensive experiments demonstrate the effectiveness of CL-PCR. In comparison experiments on the 3DMatch/3DLoMatch datasets using both FPFH and FCGF descriptors, our Fast-CL-PCRv1 outperforms state-of-the-art algorithms, achieving superior registration performance. Additionally, we validate the practicality and robustness of our method with real-world data.

## Full-text entities

- **Genes:** TECR (trans-2,3-enoyl-CoA reductase) [NCBI Gene 9524] {aka GPSN2, MRT14, SC2, TER}
- **Diseases:** TE (OMIM:614922), SD (MESH:D012735), NC (OMIM:617025), DD (MESH:C536170), injury to people or property (MESH:C000719191)

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC11397900/full.md

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Source: https://tomesphere.com/paper/PMC11397900