switch to version 3.0.1b4

primer would be missed

python/obitools3/commands/ngsfilter.pyx

@@ -322,7 +322,7 @@ cdef tuple annotate(sequences, infos, no_tags, verbose=False):
         sequences[0] = sequences[0][directmatch[1][2]:]
     else:
         sequences[1] = sequences[1][directmatch[1][2]:]
-        sequences[0][REVERSE_SEQUENCE_COLUMN] = sequences[1].seq           # used by alignpairedend tool
+        sequences[0][REVERSE_SEQUENCE_COLUMN] = sequences[1].seq      # used by alignpairedend tool
         sequences[0][REVERSE_QUALITY_COLUMN] = sequences[1].quality   # used by alignpairedend tool
     
     if directmatch[0].forward:
@@ -369,7 +369,7 @@ cdef tuple annotate(sequences, infos, no_tags, verbose=False):
                 sequences[0] = sequences[0][:r[1]]
             else:
                 sequences[1] = sequences[1][:r[1]]
-                sequences[0][REVERSE_SEQUENCE_COLUMN] = sequences[1].seq           # used by alignpairedend tool
+                sequences[0][REVERSE_SEQUENCE_COLUMN] = sequences[1].seq      # used by alignpairedend tool
                 sequences[0][REVERSE_QUALITY_COLUMN] = sequences[1].quality   # used by alignpairedend tool
         # do the same on the other seq
         if first_match_first_seq: 
@@ -394,7 +394,7 @@ cdef tuple annotate(sequences, infos, no_tags, verbose=False):
             seq_to_match = sequences[0]
         reversematch = []
         # Compute begin
-        begin=directmatch[1][2]+1  # end of match + 1 on the same sequence
+        #begin=directmatch[1][2]+1  # end of match + 1 on the same sequence -- No, already cut out forward primer        
         # Try reverse matching on the other sequence:
         new_seq = True
         pattern = 0
@@ -408,7 +408,7 @@ cdef tuple annotate(sequences, infos, no_tags, verbose=False):
                 primer=p
             # Saving original primer as 4th member of the tuple to serve as correct key in infos dict even if it might have been reversed complemented
             # (3rd member already used by directmatch)
-            reversematch.append((primer, primer(seq_to_match, same_sequence=not new_seq, pattern=pattern, begin=begin), None, p))
+            reversematch.append((primer, primer(seq_to_match, same_sequence=not new_seq, pattern=pattern, begin=0), None, p))
             new_seq = False
             pattern+=1
         # Choose match closer to the end of the sequence

python/obitools3/commands/uniq.pyx

@@ -354,8 +354,8 @@ cdef uniq_sequences(View_NUC_SEQS view, View_NUC_SEQS o_view, ProgressBar pb, di
         key = mergedKeys[k]
         merged_col_name = mergedKeys_m[k]
         
-        if merged_infos[merged_col_name]['nb_elts'] == 1:
-            raise Exception("Can't merge information from a tag with only one element (e.g. one sample ; don't use -m option)")
+#        if merged_infos[merged_col_name]['nb_elts'] == 1:
+#            raise Exception("Can't merge information from a tag with only one element (e.g. one sample ; don't use -m option)")
         
         if merged_col_name in view:
             i_col = view[merged_col_name]

python/obitools3/parsers/tab.pyx

@@ -8,7 +8,7 @@ Created on feb 20th 2018
 
 import types
 from obitools3.utils cimport __etag__
-
+from obitools3.utils cimport str2bytes
 
 def tabIterator(lineiterator, 
                 bint header = False,
@@ -75,7 +75,7 @@ def tabIterator(lineiterator,
                 continue
             else:
                 # TODO ??? default column names? like R?
-                keys = [i for i in range(len(line.split(sep)))]
+                keys = [str2bytes(str(i)) for i in range(len(line.split(sep)))]
                 
         while skipped < skip :
             line = next(iterator)

python/obitools3/version.py

@@ -1,5 +1,5 @@
 major = 3
 minor = 0
-serial= '1b2'
+serial= '1b4'
 
 version ="%d.%d.%s" % (major,minor,serial)