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Research

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

  • First Published February 14, 2024
Research

Coexpression patterns define epigenetic regulators associated with neurological dysfunction

  • First Published March 11, 2019
Research

Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms

  • First Published February 14, 2013
Method

Copy number variation detection and genotyping from exome sequence data

  • First Published May 14, 2012
Method

Computational analysis of genome-wide DNA methylation during the differentiation of human embryonic stem cells along the endodermal lineage

  • First Published August 27, 2010
Research

Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome

  • First Published March 22, 2010
Letter

Complex selection on 5′ splice sites in intron-rich organisms

  • First Published September 10, 2009
Letter

Deeply conserved chordate noncoding sequences preserve genome synteny but do not drive gene duplicate retention

  • First Published August 24, 2009
Methods

Rapid whole-genome mutational profiling using next-generation sequencing technologies

  • First Published September 4, 2008
LETTER

Early vertebrate whole genome duplications were predated by a period of intense genome rearrangement

  • First Published July 14, 2008
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