How convert a fastQ file to a Sam/Bam file
Hello, I need call some snps, and in the programs that I use will need the input file in .bam, but my files are in .fastq
Can someone help me?
I use ubuntu os
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You need a reference genome against which you are going to align the reads against depending on your organism, an aligner tool that depends on your technology (like bwa mem, bowtie2).
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what is the organism that you work with?