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Korbel Group Services

High-throughput sequencing

CopySeq Discovery and copy-number genotyping of genomic structural variants
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

10 years of the human genome

podcast

EMBL scientists mark a decade since the first draft human genome sequence. Click on the image to play.
Duration: 6 mins.