Wenjiang Deng

发表

A fast detection of fusion genes from paired-end RNA-seq data

Y. Pawitan, S. Calza, T. Vu, 2018, BMC Genomics.

Reproducibility of Methods to Detect Differentially Expressed Genes from Single-Cell RNA Sequencing

Y. Pawitan, T. Vu, Wenjiang Deng, 2020, Frontiers in Genetics.

Accumulation of potential driver genes with genomic alterations predicts survival of high-risk neuroblastoma patients

Y. Pawitan, Leming Shi, C. Suo, 2018, Biology Direct.

Quantification of mutant–allele expression at isoform level in cancer from RNA-seq data

Y. Pawitan, T. Vu, Wenjiang Deng, 2022, NAR Genomics and Bioinformatics.

Fusion Gene Detection Using Whole-Exome Sequencing Data in Cancer Patients

Y. Pawitan, J. Lindberg, T. Vu, 2022, Frontiers in Genetics.

A fast detection of fusion genes from paired-end RNA-seq data

Y. Pawitan, S. Calza, T. Vu, 2018, BMC Genomics.

The transcriptome‐wide landscape of molecular subtype‐specific mRNA expression profiles in acute myeloid leukemia

Y. Pawitan, O. Kallioniemi, B. Seashore-Ludlow, 2021, American journal of hematology.

Alternating EM algorithm for a bilinear model in isoform quantification from RNA-seq data

Krishna R. Kalari, Yudi Pawitan, Liewei Wang, 2019, Bioinform..

Accumulation of potential driver genes with genomic alterations predicts survival of high-risk neuroblastoma patients

Y. Pawitan, Leming Shi, C. Suo, 2018, Biology direct.

Single extracellular vesicle surface protein‐based blood assay identifies potential biomarkers for detection and screening of five cancers

Kelin Xu, Wenjiang Deng, H. Yuan, 2024, Molecular oncology.