RESOURCE
Haplotype sorting using human fosmid clone end-sequence pairs
- First Published October 3, 2008
Methods
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
- First Published October 5, 2007
RESOURCE
PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data
- First Published April 6, 2007
RESOURCE
EAnnot: A genome annotation tool using experimental evidence
- First Published December 1, 2004