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Method

Comparative Annotation Toolkit (CAT)—simultaneous clade and personal genome annotation

  • First Published June 8, 2018
Corrigendum

Corrigendum: Discovery and genotyping of structural variation from long-read haploid genome sequence data

  • First Published January 2, 2018
Resource

GenomeVIP: a cloud platform for genomic variant discovery and interpretation

  • First Published May 18, 2017
Research

Discovery and genotyping of structural variation from long-read haploid genome sequence data

  • First Published November 28, 2016
Research

Characteristics of de novo structural changes in the human genome

  • First Published April 16, 2015
Resource

MuSiC: Identifying mutational significance in cancer genomes

  • First Published July 3, 2012
RESOURCE

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

  • First Published April 6, 2007
LETTER

Characterization and predictive discovery of evolutionarily conserved mammalian alternative promoters

  • First Published January 8, 2007
METHODS

Generalized Gap Model for Bacterial Artificial Chromosome Clone Fingerprint Mapping and Shotgun Sequencing

  • First Published December 1, 2002
RESOURCE

Assembly, Annotation, and Integration of UNIGENE Clusters into the Human Genome Draft

  • First Published April 11, 2001
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