Research
Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps
- First Published November 1, 2024
Research
Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles
- First Published May 16, 2013
Research
NAHR-mediated copy-number variants in a clinical population: Mechanistic insights into both genomic disorders and Mendelizing traits
- First Published May 8, 2013
Letter
Functional diversity for REST (NRSF) is defined by in vivo binding affinity hierarchies at the DNA sequence level
- First Published April 28, 2009
LETTER
Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets
- First Published February 7, 2008
ARTICLE
Butyrate mediates decrease of histone acetylation centered on transcription start sites and down-regulation of associated genes
- First Published June 13, 2007
ARTICLE
The landscape of histone modifications across 1% of the human genome in five human cell lines
- First Published June 13, 2007
Methods
Identifying gene regulatory elements by genomic microarray mapping of DNaseI hypersensitive sites
- First Published September 8, 2006
LETTER
The portability of tagSNPs across populations: A worldwide survey
- First Published February 8, 2006
RESOURCE
Complete MHC Haplotype Sequencing for Common Disease Gene Mapping
- First Published May 12, 2004