Mapping and Variant calling
I need to do mapping and variant calling , so I need fastq files and reference fasta file and I don't know how to take and where to take the sequence files(disease related to human). Is there any reference? Because I am new to this.
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lakhujanivijay
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ttananthi97 •
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ttananthi97 •
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It looks like you are working or trying to work with human samples. For variant calling, first you should have some samples in your hand; either you generate NGS data for your own samples or you may be interested to work with already available databases like SRA.
check this one out
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