Simulates common DNA variants and generates sequencing reads for mixture genomes. Features; 1. Simulates both germline and somatic variants, 2. Generates reads corresponding to heterogeneous genomes and produces tumor-normal matched samples, 3. Simulates correlations among SNPs, among CNVs/CNAs based on HMM models, 4. Simulates broad and focal CNV/CNA events.
DNA, Genomics, DNA mutation, Sequencing
If you find errors, please report here.