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author B. Watson <yalhcru@gmail.com>2016-11-14 15:50:57 -0500
committer Willy Sudiarto Raharjo <willysr@slackbuilds.org>2016-11-15 21:41:38 +0700
commitbccf1f3d8833d637dd4de46dcd9cf59a91e571a3 (patch)
tree4b99afa2ba7bc43c10df5c88762aa754131da2ba /academic
parentdc248e8bc1c21a5fa51f6b69000221c60c86c775 (diff)
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academic/cutadapt: Fix README.
Diffstat (limited to 'academic')
-rw-r--r--academic/cutadapt/README4
1 files changed, 2 insertions, 2 deletions
diff --git a/academic/cutadapt/README b/academic/cutadapt/README
index a558d53867..723e302b49 100644
--- a/academic/cutadapt/README
+++ b/academic/cutadapt/README
@@ -5,10 +5,10 @@ and other types of unwanted sequence from your high-throughput
sequencing reads.
Cleaning your data in this way is often required: Reads from small-RNA
-sequencing contain the 3’ sequencing adapter because the read is
+sequencing contain the 3' sequencing adapter because the read is
longer than the molecule that is sequenced. Amplicon reads start with
a primer sequence. Poly-A tails are useful for pulling out RNA from
-your sample, but often you don’t want them to be in your reads.
+your sample, but often you don't want them to be in your reads.
Cutadapt helps with these trimming tasks by finding the adapter or
primer sequences in an error-tolerant way. It can also modify and