Method
Optimal marker genes for c-separated cell types with SepSolve
- First Published October 9, 2025
Method
Partial alignment of multislice spatially resolved transcriptomics data
- First Published August 8, 2023
Method
Linear-time cluster ensembles of large-scale single-cell RNA-seq and multimodal data
- First Published February 24, 2021
Method
Reconstruction of clone- and haplotype-specific cancer genome karyotypes from bulk tumor samples
- First Published September 4, 2020
Method
Single-cell sequencing data reveal widespread recurrence and loss of mutational hits in the life histories of tumors
- First Published October 13, 2017
Resource
GenomeVIP: a cloud platform for genomic variant discovery and interpretation
- First Published May 18, 2017
Method
Read clouds uncover variation in complex regions of the human genome
- First Published August 18, 2015
Method
Discovery of recurrent structural variants in nasopharyngeal carcinoma
- First Published November 8, 2013
Research
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes
- First Published March 11, 2013