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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 |
| commit | bccf1f3d8833d637dd4de46dcd9cf59a91e571a3 (patch) | |
| tree | 4b99afa2ba7bc43c10df5c88762aa754131da2ba /academic/cutadapt | |
| parent | dc248e8bc1c21a5fa51f6b69000221c60c86c775 (diff) | |
| download | slackbuilds-bccf1f3d8833d637dd4de46dcd9cf59a91e571a3.tar.gz | |
academic/cutadapt: Fix README.
Diffstat (limited to 'academic/cutadapt')
| -rw-r--r-- | academic/cutadapt/README | 4 |
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 |