Author

Hai Lin

Indiana University IndianapolisORCID 0000-0003-3376-1247Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Hai Lin2 papers · Shenzhen University

Biology Disciplines

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Bioinformatics· 1 Molecular Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Yunlong LiuiD· 3 shared Jill L. ReiteriD· 2 shared Joseph IpeiD· 2 shared Katherine A. GallawayiD· 2 shared Todd C. SkaariD· 2 shared Alison GoateiD· 1 shared Andrew J. Wallace· 1 shared Andy B. CheniD· 1 shared

Activity by Year

2018-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 34 mutual co-author links

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3 shared papersNeuroscience

Yunlong LiuORCID

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3 papers

Recent·Most cited

NeuroscienceMolecular PsychiatryPeer-reviewedSep 2, 2019

Allele-Specific Expression and High-Throughput Reporter Assay Reveal Functional Variants in Human Brains with Alcohol Use Disorders

Xi Rao, Kriti S. Thapa, Andy B. Chen…·Yunlong Liu

The paper identifies functional variants in human brains with alcohol use disorders by combining allele-specific expression analysis with high-throughput reporter assays.

39 citations

humanbulk RNA-seq

𝕏 PostBluesky

BioinformaticsbioRxivPreprintJan 9, 2019

RegSNPs-Intron: A Computational Framework For Prioritizing Intronic Single Nucleotide Variants in Human Genetic Disease

Hai Lin, Katherine A. Gallaway, Rudong Li…·Yunlong Liu

The paper develops regSNPs-intron, a random forest classifier to prioritize intronic SNVs for disease, validated using ASSET-seq functional assays.

1 citation

humanwhole-genome sequencing

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Molecular BiologyGenome ResearchPeer-reviewedMay 1, 2018

HNRNPA1 promotes recognition of splice site decoys by U2AF2 in vivo

Jonathan M. Howard, Hai Lin, Andrew J. Wallace…·Jeremy R. Sanford

The paper investigates how HNRNPA1 influences U2AF2 RNA binding in vivo, showing it shifts U2AF2 to decoy splice site sequences and affects exon skipping.

36 citations

humanexperimental assay

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