This paper explores a simple and efficient baseline for person re-identification (ReID). Person re-identification (ReID) with deep neural networks has made progress and achieved high performance in recent years. However, many state-of-the-arts methods design complex network structure and concatenate multi-branch features. In the literature, some effective training tricks are briefly appeared in several papers or source codes. This paper will collect and evaluate these effective training tricks in person ReID. By combining these tricks together, the model achieves 94.5% rank-1 and 85.9% mAP on Market1501 with only using global features. Our codes and models are available at https://github.com/michuanhaohao/reid-strong-baseline * Equal contributions. This work was partially done when Hao Luo and Xingyu Liao were interns at Megvii Inc. (a) Market1501 (b) DukeMTMC-reID
This study explores a simple but strong baseline for person re-identification (ReID). Person ReID with deep neural networks has progressed and achieved high performance in recent years. However, many state-of-the-art methods design complex network structures and concatenate multi-branch features. In the literature, some effective training tricks briefly appear in several papers or source codes. The present study collects and evaluates these effective training tricks in person ReID. By combining these tricks, the model achieves 94.5% rank-1 and 85.9% mean average precision on Market1501 with only using the global features of ResNet50. The performance surpasses all existing global-and part-based baselines in person ReID. We propose a novel neck structure named as batch normalization neck (BNNeck). BNNeck adds a batch normalization layer after global pooling layer to separate metric and classification losses into two different feature spaces because we observe they are inconsistent in one embedding space. Extended experiments show that BNNeck can boost the baseline, and our baseline can improve the performance of existing stateof-the-art methods. Our codes and models are available at: https://github.com/michuanhaohao/reid-strong-baseline
General Instance Re-identification is a very important task in the computer vision, which can be widely used in many practical applications, such as person/vehicle reidentification, face recognition, wildlife protection, commodity tracing, and snapshop, etc.. To meet the increasing application demand for general instance re-identification, we present FastReID as a widely used software system in JD AI Research. In FastReID, highly modular and extensible design makes it easy for the researcher to achieve new research ideas. Friendly manageable system configuration and engineering deployment functions allow practitioners to quickly deploy models into productions. We have implemented some state-of-the-art projects, including person reid, partial re-id, cross-domain re-id and vehicle re-id, and plan to release these pre-trained models on multiple benchmark datasets. FastReID is by far the most general and high-performance toolbox that supports single and multiple GPU servers, you can reproduce our project results very easily and are very welcome to use it, the code and models are available at https: https://github.com/ JDAI-CV/fast-reid.
Background: Next-generation sequencing (NGS) technologies have fostered an unprecedented proliferation of highthroughput sequencing projects and a concomitant development of novel algorithms for the assembly of short reads. However, numerous technical or computational challenges in de novo assembly still remain, although many new ideas and solutions have been suggested to tackle the challenges in both experimental and computational settings. Results: In this review, we first briefly introduce some of the major challenges faced by NGS sequence assembly. Then, we analyze the characteristics of various sequencing platforms and their impact on assembly results. After that, we classify de novo assemblers according to their frameworks (overlap graph-based, de Bruijn graph-based and string graph-based), and introduce the characteristics of each assembly tool and their adaptation scene. Next, we introduce in detail the solutions to the main challenges of de novo assembly of next generation sequencing data, single-cell sequencing data and single molecule sequencing data. At last, we discuss the application of SMS long reads in solving problems encountered in NGS assembly. Conclusions: This review not only gives an overview of the latest methods and developments in assembly algorithms, but also provides guidelines to determine the optimal assembly algorithm for a given input sequencing data type.
The National Genomics Data Center (NGDC), part of the China National Center for Bioinformation (CNCB), provides a family of database resources to support global academic and industrial communities. With the explosive accumulation of multi-omics data generated at an unprecedented rate, CNCB-NGDC constantly expands and updates core database resources by big data archive, integrative analysis and value-added curation. In the past year, efforts have been devoted to integrating multiple omics data, synthesizing the growing knowledge, developing new resources and upgrading a set of major resources. Particularly, several database resources are newly developed for infectious diseases and microbiology (MPoxVR, KGCoV, ProPan), cancer-trait association (ASCancer Atlas, TWAS Atlas, Brain Catalog, CCAS) as well as tropical plants (TCOD). Importantly, given the global health threat caused by monkeypox virus and SARS-CoV-2, CNCB-NGDC has newly constructed the monkeypox virus resource, along with frequent updates of SARS-CoV-2 genome sequences, variants as well as haplotypes. All the resources and services are publicly accessible at https://ngdc.cncb.ac.cn.
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