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Long-read single-cell RNA sequencing enables the study of cancer subclone-specific genotypes and phenotypes in chronic lymphocytic leukemia

  • First Published February 18, 2025

Differences in molecular sampling and data processing explain variation among single-cell and single-nucleus RNA-seq experiments

  • First Published February 14, 2024

A Bayesian framework to study tumor subclone–specific expression by combining bulk DNA and single-cell RNA sequencing data

  • First Published January 9, 2024

Read clouds uncover variation in complex regions of the human genome

  • First Published August 18, 2015

Parente2: a fast and accurate method for detecting identity by descent

  • First Published October 1, 2014

Genome evolution during progression to breast cancer

  • First Published April 8, 2013

Ubiquitous heterogeneity and asymmetry of the chromatin environment at regulatory elements

  • First Published September 5, 2012

Linking disease associations with regulatory information in the human genome

  • First Published September 5, 2012

ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia

  • First Published September 5, 2012

Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomes

  • First Published January 12, 2010
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