From 1227c7ad2d8b2420649ecf6a36133543752c3f13 Mon Sep 17 00:00:00 2001 From: kyros Date: Tue, 28 Nov 2023 16:31:58 -0500 Subject: [PATCH] Corrected spelling typos in README. --- README.md | 2 +- 1 file changed, 1 insertion(+), 1 deletion(-) diff --git a/README.md b/README.md index 5067e69..5055852 100644 --- a/README.md +++ b/README.md @@ -12,7 +12,7 @@ To build from a source release, download the source zip or tar.gz, unpack it, ch With most new data sets you can use gentle quality trimming and adapter clipping. -You often don't need leading and traling clipping. Also in general setting the keepBothReads to True can be useful when working with paired end data, you will keep even redunfant information but this likely makes your pipelines more manageable. Note the additional :2 in front of the True (for keepBothReads) - this is the minimum adapter length in palindrome mode, you can even set this to 1. (Default is a very conservative 8) +You often don't need leading and trailing clipping. Also in general setting the keepBothReads to True can be useful when working with paired end data, you will keep even redundant information but this likely makes your pipelines more manageable. Note the additional :2 in front of the True (for keepBothReads) - this is the minimum adapter length in palindrome mode, you can even set this to 1. (Default is a very conservative 8) If you have questions please don't hesitate to contact us, this is not necessarily one size fits all. (e.g. RNAseq expression analysis vs DNA assembly).