Repository 'naive_variant_caller'
hg clone https://toolshed.g2.bx.psu.edu/repos/blankenberg/naive_variant_caller

Changeset 10:907b40517289 (2015-03-31)
Previous changeset 9:4fab5fce1adb (2015-03-31) Next changeset 11:8af4e7a4d041 (2015-09-17)
Commit message:
Fix typo ("with with") in readme.
modified:
README.rst
b
diff -r 4fab5fce1adb -r 907b40517289 README.rst
--- a/README.rst Tue Mar 31 11:11:15 2015 -0400
+++ b/README.rst Tue Mar 31 11:19:47 2015 -0400
b
@@ -54,7 +54,7 @@
 
     The number of genotype calls to make at each reported position.
 
-Only write out positions with with possible alternate alleles:
+Only write out positions with possible alternate alleles:
 
     When set, only positions which have at least one non-reference nucleotide which passes declare filters will be present in the output.