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Diffstat (limited to 'sci-biology/abyss/files/abyss-1.3.6-samtoafg.patch')
-rw-r--r--sci-biology/abyss/files/abyss-1.3.6-samtoafg.patch40
1 files changed, 40 insertions, 0 deletions
diff --git a/sci-biology/abyss/files/abyss-1.3.6-samtoafg.patch b/sci-biology/abyss/files/abyss-1.3.6-samtoafg.patch
new file mode 100644
index 000000000000..cb7dfb08a84d
--- /dev/null
+++ b/sci-biology/abyss/files/abyss-1.3.6-samtoafg.patch
@@ -0,0 +1,40 @@
+Hello,
+
+I see Shaun Jackmans' (abyss-)sam2afg script is available within the
+Amos source repository. I find this very useful for coercing output from
+assemblers which which don't track read location into amos by remapping
+reads against the assembly and converting to afg - not ideal but better
+than nothing when you don't have the 'real' read locations to work with.
+
+This fails, however when reads are aligned with 'bwa mem', which can
+output multi-part alignments. sam2afg checks for reuse of the same read
+id (presumably to prevent the generation of non-unique eid values),
+consequently encountering multiple alignments for a read causes it to die.
+
+The following one-line patch allows sam2afg to skip these secondary
+alignments present in 'bwa mem' output, provided bwa mem has been run
+with the '-M' argument which sets the SAM 'secondary alignment' flag on
+the alignments in question.
+
+Hopefully this will also be of use to others...
+
+Best Regards,
+James
+
+--
+Dr. James Abbott
+Lead Bioinformatician
+Bioinformatics Support Service
+Imperial College, London
+
+
+--- abyss-1.3.6/bin/abyss-samtoafg.ori 2015-05-23 23:43:46.797747928 +0200
++++ abyss-1.3.6/bin/abyss-samtoafg 2015-05-23 23:44:09.227747743 +0200
+@@ -105,6 +105,7 @@
+ die unless defined $qqual;
+
+ $tstart--; # convert to zero-based coordinate
++ next if $flag & 0x100; # secondary alignment
+ $qid .= "/1" if $flag & 0x40; #FREAD1
+ $qid .= "/2" if $flag & 0x80; #FREAD2
+