Your search for returned 17 results

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Resource

GenomeVIP: a cloud platform for genomic variant discovery and interpretation

  • First Published May 18, 2017
Method

Identification of complex genomic rearrangements in cancers using CouGaR

  • First Published November 14, 2016
Research

Characteristics of de novo structural changes in the human genome

  • First Published April 16, 2015
Resource

Alignathon: a competitive assessment of whole-genome alignment methods

  • First Published October 1, 2014
Method

iReckon: Simultaneous isoform discovery and abundance estimation from RNA-seq data

  • First Published November 29, 2012
Resource

MuSiC: Identifying mutational significance in cancer genomes

  • First Published July 3, 2012
Resource

Detecting copy number variation with mated short reads

  • First Published August 30, 2010
Resource

Multiple whole-genome alignments without a reference organism

  • First Published January 28, 2009
RESOURCE

PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data

  • First Published April 6, 2007
Methods

Automated Whole-Genome Multiple Alignment of Rat, Mouse, and Human

  • First Published April 1, 2004
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