Author

Rui Han

BGI Group (China)ORCID 0000-0001-6358-4689Unclaimed ORCID profile · follow to get notified of new preprints

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Rui Han2 papers · China Institute of Water Resources and Hydropower Research

Biology Disciplines

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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2

Frequent Co-Authors

Yaoshen WangiD· 2 shared Chang Shi· 1 shared Chaonan ShiiD· 1 shared Chunna Fan· 1 shared Fengxia LiuiD· 1 shared Hongmei ZhuiD· 1 shared Hongyun ZhangiD· 1 shared Hui HuangiD· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenomics

Yaoshen WangORCID

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2 papers

Recent·Most cited

GenomicsBMC Medical GenomicsPeer-reviewedApr 13, 2021

Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders

Yan Sun, Fengxia Liu, Chunna Fan…·Zhiyu Peng

This study evaluates the sensitivity and coverage of clinical whole-genome sequencing (WGS) for detecting genetic variants, finding that 40X mean depth achieves high sensitivity for SNVs and indels but not 100%.

40 citationstop 4%

humanwhole-genome sequencing

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BioinformaticsbioRxivPreprintSep 7, 2018

SCDT: Detecting CNVs of low chimeric ratio in cf-DNA

Zhaoyang Qian, Xiaofeng Wang, Chang Shi…·Hongmei Zhu

SCDT detects sub-chromosome CNVs in cf-DNA with high sensitivity and specificity using GC correction and segmentation algorithms.

DOI 10.1101/411256

humanwhole-genome sequencing

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