Author

Yi Dai

Chinese Academy of Medical Sciences & Peking Union Medical CollegeORCID 0000-0002-2696-0179Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Yi Dai1 paper · Centro Internacional de Mejoramiento de Maíz Y Trigo

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Lijie SongiD· 2 shared Xiaoru Yang· 2 shared Xunzhe Yang· 2 shared Yunmei CheniD· 2 shared Zhiyu PengiD· 2 shared Zhonghua WangiD· 2 shared Ziying YangiD· 2 shared Depeng WangiD· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Lijie SongORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 21, 2023

Whole genome and transcriptome sequencing in neuromuscular disorders: a diagnostic and health economic analysis

Ziying Yang, Xiaoru Yang, Yunmei Chen…·Yi Dai

This paper evaluates the clinical and cost-effectiveness of combining whole-genome and RNA sequencing for diagnosing neuromuscular disorders in patients with negative whole-exome results.

DOI 10.1101/2023.12.21.23300182

humanwhole-exome sequencing

Genetic & Genomic MedicinemedRxivPreprintApr 22, 2023

Systematic evaluation of the two main blood-based RNA-seq approaches for Mendelian disease diagnosis

Ziying Yang, Xiaoru Yang, Yunmei Chen…·Yi Dai

This study evaluates two RNA-seq methods for Mendelian disease diagnosis using blood samples, finding polyA-selection outperforms rRNA depletion in detecting disease-related genes and variants.

2 citations

humanbulk RNA-seq

GenomicsJournal of Medical GeneticsPeer-reviewedSep 10, 2019

Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD)

Yi Dai, Pidong Li, Zhiqiang Wang…·Kai Wang

This paper develops a single-molecule optical mapping method for quantitative D4Z4 repeat analysis in FSHD, showing concordance with Southern blot and improved haplotype resolution.

80 citations

humanexperimental assay