Author
Complete Genomics (United States)
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
4 papers
Recent·Most cited
Snezana Drmanac, Matthew J. Callow, Linsu Chen…·Radoje Drmanac
The paper introduces a new sequencing chemistry (CoolMPS) that improves signal intensity and eliminates scar interference in massively parallel sequencing.
Hanjie Shen, Pengjuan Liu, Zhanqing Li…·Radoje Drmanac
This paper demonstrates that PCR-free whole genome sequencing using the DNBSEQ platform and machine learning variant calling significantly reduces InDel errors and improves variant calling performance.
Ou Wang, Robert G. Chin, Xiaofang Cheng…·Brock A. Peters
This paper introduces stLFR, a low-cost method for long DNA sequencing that enables accurate variant calling, haplotyping, and de novo assembly.
Qiaoling Li, Xia Zhao, Wenwei Zhang…·Yuan Jiang
The paper evaluates index mis-assignment rates on DNB-based sequencing platforms and finds they are exceptionally low, suggesting reliable multiplex sequencing.