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Resource

GenomeVIP: a cloud platform for genomic variant discovery and interpretation

  • First Published May 18, 2017
Resource

Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly

  • First Published April 10, 2017
Method

Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomes

  • First Published December 16, 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

Assemblathon 1: A competitive assessment of de novo short read assembly methods

  • First Published September 16, 2011
Method

Revealing the genetic structure of a trait by sequencing a population under selection

  • First Published March 21, 2011
Resource

ABySS: A parallel assembler for short read sequence data

  • First Published February 27, 2009
RESOURCE

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

  • First Published April 6, 2007
METHODS

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

  • First Published December 1, 2002
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