4 results in 0.0021 seconds.
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Recommendations for CNV calling algorithms/programs to benchmark
I want to benchmark the time/resource use and breakpoint accuracy of CNV callers on multiple individual NGS data at 30x-100x coverage at specific CNVs.... -
Mate-pair sequence structural variants
I was given a mate-pair whole genome dataset that was sequenced on a SOLID 5500xl. I was interested in knowing if anyone has had any experience in doing... -
na12878 ground truth SVs
Hi,
Are there any available ground truth SV sets for the individual na12878 beyond what is presented in additional material of "Mapping... -
Delly output
Hi,
I am new to using Delly, and trying to figure out what it's output means in human terms so that I can write a script to annotate it. Here is...
