Author

Zhanqing Li

BGI Group (China)ORCID 0000-0001-6737-382XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Ao CheniD· 2 shared Hanjie Shen· 2 shared Lin Wang· 2 shared Pengjuan Liu· 2 shared Qiaoling LiiD· 2 shared Radoje Drmanac· 2 shared Snezana Drmanac· 2 shared Xinming LiangiD· 2 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Ao ChenORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintDec 20, 2019

Advanced Whole Genome Sequencing Using an Entirely PCR-free Massively Parallel Sequencing Workflow

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.

4 citations

whole-genome sequencingmachine learning (classical)

𝕏 PostBluesky

GenomicsBMC GenomicsPeer-reviewedMar 13, 2019

Reliable Multiplex Sequencing with Rare Index Mis-Assignment on DNB-Based NGS Platform

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.

70 citations

whole-genome sequencingexperimental assay

𝕏 PostBluesky