Mercurial > repos > peterjc > samtools_bam2fq

changeset 4:8ac1057b1a7d draft

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Uploaded v0.0.2a, fixed typo
author peterjc
date Tue, 04 Nov 2014 07:13:44 -0500
parents 14ff32f355f0
children fc1637bbe838
files tools/samtools_bam2fq/samtools_bam2fq.xml
diffstat 1 files changed, 1 insertions(+), 1 deletions(-) [+]
line wrap: on
line diff
--- a/tools/samtools_bam2fq/samtools_bam2fq.xml	Tue Nov 04 07:11:58 2014 -0500
+++ b/tools/samtools_bam2fq/samtools_bam2fq.xml	Tue Nov 04 07:13:44 2014 -0500
@@ -103,7 +103,7 @@
 
 By default this will pre-sort your SAM/BAM file by read name and split your
 reads into an interlaced FASTQ file for paired reads, and a separate FASTQ
-file for singlton reads. A naive conversion is also offered which gives a
+file for singleton reads. A naive conversion is also offered which gives a
 single FASTQ file with the reads ordered as in the input SAM/BAM file.
 
 It is quite common to wish to remap high-throughput sequencing data. If you