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README.md

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@@ -217,6 +217,9 @@ Take a fasta file with a bunch of short scaffolds, e.g., labeled `>Scaffold12345
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samtools faidx genome.fa && grep -v Scaffold genome.fa.fai | cut -f1 | xargs -n1 samtools faidx genome.fa > genome.noscaffolds.fa
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python -c "f = open('file.txt', 'r'); f.seek(0); file = f.readlines(); print file"
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## find, xargs, and GNU parallel
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[[back to top](#contents)]

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