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Calling structural variants (CNVs) with single-end reads
(Topic in the Genomic Resequencing forum)
01-18-2016, 08:30 AM
Handling duplicates and other biases in Haloplex enriched targeted sequencing data
(Topic in the General forum)
01-27-2014, 04:44 PM
Mate-pair alignment for structural variation analysis
(Topic in the Bioinformatics forum)
07-30-2010, 01:38 AM
Question concering deletions and inversions inferred from PE-sequencing
(Topic in the Genomic Resequencing forum)
05-09-2011, 01:18 AM
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