Author

Lingtong Hao

Harvard UniversityORCID 0000-0002-0360-6177Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Lingtong Hao1 paper

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:whole-exome sequencing· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Carrie L. Blout ZawatskyiD· 1 shared Changlin LiuiD· 1 shared Cheng LiiD· 1 shared Christina Anne Austin-TseiD· 1 shared Heather Mason‐SuaresiD· 1 shared Heidi L. RehmiD· 1 shared Kalotina MachiniiD· 1 shared Lihua CaoiD· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Carrie L. Blout ZawatskyORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedJun 10, 2021

A Framework for Automated Gene Selection in Genomic Screening

Lorena Lazo de la Vega, W. Yu, Kalotina Machini…·Matthew S. Lebo

This paper proposes a framework for automated gene selection in genomic screening, creating gene lists with strong disease associations and demonstrating their utility in healthy genome screening.

9 citations

humanwhole-exome sequencing

𝕏 PostBluesky

BioinformaticsbioRxivPreprintMar 5, 2019

GVC: A superfast and universal genomic variant caller

Zhongbo Zhang, Longhui Yin, Lingtong Hao…·Shaoping Ling

GVC is a fast and universal genomic variant caller that detects SNV, sINDEL, and SV from whole-genome/exome sequencing data with high sensitivity and precision.

3 citations

humanwhole-genome sequencing

𝕏 PostBluesky