Hello!
I'm working on somatic variant identification from cancer samples. So, I try to simulate Illumina paired-end read with known variants...
3 results in 0.0021 seconds.
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The problem with sensitivity analysis of somatic variant caller
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MNase-seq reads simulation method
I'm now analyzing MNase-seq data. But I'm confusing about the simulation method of MNase-seq reads. Because MNase has cut bias for AT-rich sequence. So... -
Simulating structural variants
I have been trying to generate simulated reads from an interchromosomal breakpoint for some time now. I'm quite puzzled by what I am generating however....Last edited by saraki; 02-02-2015, 04:52 AM.
