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ServicesKorbel Group

High-throughput sequencing

CopySeq Discovery and copy-number genotyping of genomic structural variants
DELLY Integrated split-read and paired-end based structural variant discovery in massively parallel sequencing data
PEMer Discovery of genomic structural variants by high-throughput and massive paired-end mapping

Sequence Analysis

BreakSeq Nucleotide-resolution genotyping of structural variants in personal genomics data

Miscellaneous

BreakPtr Mapping copy-number variation with high-density oligonucleotide tiling arrays.

PEMer Discovery of genomic structural variants by high-throughput and massive paired-end mapping