convert bam to sam: $ samtools view -h -o out.sam in.bam
convert sam to bam: $ samtools view -bT .faFILE samfile
sort the bam: $ samtools sort Example.bam Example.sorted
view a specific region(must be properly indexed while indexing depends on sorting):
$ samtools view Example.bam chr17:220-300
Print the header of bam
samtools view -H in.bam
The end of sam file has the bowtie parameters used.
sam to fastq
cat samplename.nomapping.sam | grep -v ^@ | awk '{print "@"$1"\n"$10"\n+\n"$11}' > unmapped/samplename.fastq
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