2025年累计影响因子超过100！赛陆助力科研团队成效卓著

赛陆自成立以来，科研助力成效显著：截至2025年9月，赛陆测序平台及相关技术产品已助力全球科研团队发表多篇高质量SCI论文，包括Science、Nature Methods、Genomics Proteomics Bioinformatics等国内国际核心期刊，累计影响因子突破100分，篇均影响因子达10.9分。这些成果得益于国内外顶尖学者们对赛陆产品的专业认可，合作机构涵盖浙江大学、复旦大学、香港中文大学、中山大学、四川大学、四川大学华西医院、哈尔滨工业大学、厦门大学、西湖大学、山东第一医科大学、广州国家实验室，以及哈佛大学、墨尔本大学等国内外知名高校、科研院所和医院。

从基础科研到临床应用，从疾病机制探索到遗传学研究，赛陆测序平台在全基因组测序（WGS）、全外显子组测序（WES）、16S rRNA扩增子测序、转录组学、单细胞组学、空间转录组学等多个前沿领域展现出卓越的技术实力，为生命科学的探索和临床实践提供了坚实的支撑。赛陆测序平台及空间转录组技术正以卓越的性能和丰富的应用场景，为全球科研工作者提供强大助力。

1. “Evaluation of 10 different pipelines for bacterial single-nucleotide variant detection.”Infectious Microbes and Diseases, 2023, 5, 172.

2. “Systematic comparison of sequencing-based spatial transcriptomic methods.”Nature Methods, 2024, 21, 1743.

3. “Cryo-EM reveals mechanisms of natural RNA multivalency.”Science, 2025, 388, 6746.

4. “Concomitant T315I and E459K mutations in chronic myeloid leukemia: A case report.”Oncology Letters, 2025, 30, 410.

5. “A heterozygous nonsense mutation in the FGB gene (c.1299G>A) causes congenital fibrinogen disorder across four consecutive generations.”Thrombosis Journal, 2025, 23, 63.

6. “YanHuang paternal genomic resource suggested a weakly-differentiated multi-source admixture model for the formation of Han's founding ancestral lineages.”Genomics Proteomics Bioinformatics, 2025, qzaf049.

7. “AUTS2 disruption underlies radioulnar synostosis and skeletal dysmorphogenesis: Evidence from four unrelated cases.”Journal of Medical Genetics, 2025, 110886.

8. “lmpact of different DNA enrichment methods on 16S rRNA amplicon based and nanopore metagenomic sequencingbased microbial investigation of low biomass samples.”Frontiers of Environmental Science &Engineering, 2025, 19, 140.

9. “COCA-seq: genome-wide mapping of O-GlcNAc-associated open chromatin.”Acta Biochimica et Biophysica Sinica, Accepted.

10. “Identification of hub genes associated with severe COPD via WGCNA and immune infiltration analysis.” Scientific Reports, Accepted