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6.6 years ago
PK
▴
130
I am trying to get new coordinated for my sequencing file so i tried to align my new version of the genomic file (TB927_v5.1). I used smalt to get sam file. I converted my sam file into bam file using this command:
samtools view -h -b -S out.sam > out.bam
Next, i used to multicuv
bedtools multicov -bams out.bam -bed merged.bed >nucleolus.txt
to get read counts but it shows
Could not find indexes
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