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Resource

Benchmarking small-variant genotyping in polyploids

  • First Published December 29, 2021
Research

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

  • First Published March 11, 2013
Resource

Dindel: Accurate indel calls from short-read data

  • First Published October 27, 2010
Resource

Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads

  • First Published October 27, 2010
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

Massive turnover of functional sequence in human and other mammalian genomes

  • First Published August 6, 2010
Method

Genome assembly quality: Assessment and improvement using the neutral indel model

  • First Published March 19, 2010
Letter

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

  • First Published August 24, 2009
LETTER

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

  • First Published July 14, 2008
Methods

Uncertainty in homology inferences: Assessing and improving genomic sequence alignment

  • First Published December 11, 2007
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