Method
Partial alignment of multislice spatially resolved transcriptomics data
- First Published August 8, 2023
Method
Targeted single-cell RNA sequencing of transcription factors enhances the identification of cell types and trajectories
- First Published May 19, 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
Corrigendum
Corrigendum: Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells
- First Published September 1, 2015
Research
The clustering of functionally related genes contributes to CNV-mediated disease
- First Published April 17, 2015
Research
Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells
- First Published March 19, 2015
Research
Natural genetic variation caused by small insertions and deletions in the human genome
- First Published April 1, 2011