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A deconvolution framework that uses single-cell sequencing plus a small benchmark data set for accurate analysis of cell type ratios in complex tissue samples

  • First Published November 25, 2024

Deep sequencing of short capped RNAs reveals novel families of noncoding RNAs

  • First Published August 12, 2022

Comparative transcriptomics of primary cells in vertebrates

  • First Published July 27, 2020

Read clouds uncover variation in complex regions of the human genome

  • First Published August 18, 2015

The frequent evolutionary birth and death of functional promoters in mouse and human

  • First Published July 30, 2015

Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing

  • First Published March 27, 2014

Discovery of recurrent structural variants in nasopharyngeal carcinoma

  • First Published November 8, 2013

Genome evolution during progression to breast cancer

  • First Published April 8, 2013

The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes

  • First Published March 11, 2013
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