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Research

Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing

  • First Published October 29, 2024
Research

A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities

  • First Published October 29, 2024
Methods

Accurate and reliable high-throughput detection of copy number variation in the human genome

  • First Published November 22, 2006
REVIEW

Copy number variation: New insights in genome diversity

  • First Published June 29, 2006
METHODS

DASH-2: Flexible, Low-Cost, and High-Throughput SNP Genotyping by Dynamic Allele-Specific Hybridization on Membrane Arrays

  • First Published May 1, 2003
METHODS

iFRET: An Improved Fluorescence System for DNA-Melting Analysis

  • First Published September 1, 2002
METHODS

Robust and Accurate Single Nucleotide Polymorphism Genotyping by Dynamic Allele-Specific Hybridization (DASH): Design Criteria and Assay Validation

  • First Published January 1, 2001
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