# HG changeset patch
# User peterjc
# Date 1415103224 18000
# Node ID 8ac1057b1a7d6fe90826d78849595b1ce307d100
# Parent  14ff32f355f0001db2d9d30728130332323f3bcc
Uploaded v0.0.2a, fixed typo

diff -r 14ff32f355f0 -r 8ac1057b1a7d tools/samtools_bam2fq/samtools_bam2fq.xml
--- 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