Author

Weiying Liu

Shanghai Jiao Tong UniversityORCID 0000-0001-5152-8663Unclaimed 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:benchmarking· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Chie FurihataiD· 1 shared Masamitsu HonmaiD· 1 shared Mikihiko NaitoiD· 1 shared Suresh Thiruppathi· 1 shared Takayoshi SuzukiiD· 1 shared Xinyue You· 1 shared Yang LuaniD· 1 shared Yiyi CaoiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperGenomics

Chie FurihataORCID

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1 paper

Recent·Most cited

GenomicsArchives of ToxicologyPeer-reviewedJul 31, 2020

Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequencing (PECC-Seq) revealed end-repair derived artifacts as residual errors

Xinyue You, Suresh Thiruppathi, Weiying Liu…·Takayoshi Suzuki

The paper introduces PECC-Seq, a PCR-free method for detecting low-frequency mutations, and identifies end-repair artifacts as a major source of sequencing errors.

30 citations

humanwhole-genome sequencing

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