Your search for returned 27 results

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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
Corrigendum

Corrigendum: Functional annotation of human long noncoding RNAs via molecular phenotyping

  • First Published September 14, 2020
Method

Reconstruction of clone- and haplotype-specific cancer genome karyotypes from bulk tumor samples

  • First Published September 4, 2020
Resource

Functional annotation of human long noncoding RNAs via molecular phenotyping

  • First Published July 27, 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

De novo discovery of mutated driver pathways in cancer

  • First Published June 7, 2011
Methods

Decoding the fine-scale structure of a breast cancer genome and transcriptome

  • First Published February 3, 2006
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