You analyze sequence data by mapping it against a reference genome sequence (in this case yeast).
Sequence data = ERR000004.fastq (you already have it).
You know where the yeast genome index is to search against.
After bowtie2 search resulting sam file has information about where each read aligns to the reference genome.
Sequence data = ERR000004.fastq (you already have it).
You know where the yeast genome index is to search against.
After bowtie2 search resulting sam file has information about where each read aligns to the reference genome.
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