Expert is there any existing SNP/Indel Simulator for NGS reads?
The principle the tool does something like taking any reference genome, pick positions randomly in that genome and begin to introduce SNP or indels in that position. Finally the tool should give reads given from the variant genome above with certain depth, and location of SNP/Indel is introduced in the reads fasta header.
The principle the tool does something like taking any reference genome, pick positions randomly in that genome and begin to introduce SNP or indels in that position. Finally the tool should give reads given from the variant genome above with certain depth, and location of SNP/Indel is introduced in the reads fasta header.
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