Simulates single nucleotide polymorphism (SNP), insertions and deletions (indels), and copy number variation (CNV).
Biology, Genetics, DNA polymorphism
Pattnaik S, Gupta S, Rao AA, Panda B "SInC: an accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence data." BMC Bioinformatics 2014 https://doi.org/10.1186/1471-2105-15-40
PMID: 24495296
PMCID: PMC3926339
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