Author

Fanwei Zeng

University of CopenhagenORCID 0000-0003-2508-0011Unclaimed ORCID profile · follow to get notified of new preprints

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Fanwei Zeng2 papers · BGI Genomics

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Fengxia LiuiD· 1 shared Fengyu Wu· 1 shared Gang ZouiD· 1 shared Jia ZhouiD· 1 shared Jian WangiD· 1 shared Jun You SuniD· 1 shared Lipei LiuiD· 1 shared Luming SuniD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Fengxia LiuORCID

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1 paper

Recent·Most cited

GenomicsbioRxivPreprintAug 22, 2020

Comprehensive genome sequencing analysis as a promising option in the prenatal diagnosis of fetal structural anomalies: a prospective study.

Jia Zhou, Ziying Yang, Jun You Sun…·Luming Sun

This study evaluates genome sequencing as a first-line prenatal diagnostic tool, finding it more comprehensive than CMA plus exome sequencing in detecting genetic anomalies and nongenetic factors.

DOI 10.1101/2020.08.22.260893

humanwhole-genome sequencing

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