Joint imputation and deconvolution of gene expression across spatial transcriptomics platforms
- First Published November 17, 2025
Partial alignment of multislice spatially resolved transcriptomics data
- First Published August 8, 2023
Reconstruction of clone- and haplotype-specific cancer genome karyotypes from bulk tumor samples
- First Published September 4, 2020
netNMF-sc: leveraging gene–gene interactions for imputation and dimensionality reduction in single-cell expression analysis
- First Published January 28, 2020
Single-cell sequencing data reveal widespread recurrence and loss of mutational hits in the life histories of tumors
- First Published October 13, 2017
GenomeVIP: a cloud platform for genomic variant discovery and interpretation
- First Published May 18, 2017
Read clouds uncover variation in complex regions of the human genome
- First Published August 18, 2015
Discovery of recurrent structural variants in nasopharyngeal carcinoma
- First Published November 8, 2013
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes
- First Published March 11, 2013