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agwe started a topic Calling structural variants (CNVs) with single-end reads

in Genomic Resequencing

06-07-2011, 03:47 AM
Calling structural variants (CNVs) with single-end reads

Hi,

I would like to hear if anyone tried calling structural variants using single-end data. It seems that most of the tools available for...

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quinlana started a topic Hydra: SV discovery in unique and duplicated sequence

in Bioinformatics

03-30-2010, 09:47 AM
Hydra: SV discovery in unique and duplicated sequence

Hi all,

I recently released HYDRA, a new algorithm I've developed for detecting structural variation (SV) breakpoints using paired-end...

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