Cleaner handling of reverse quality columns
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@ -6,6 +6,7 @@ from .solexapairend import iterOnAligment
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from .shifted_ali cimport Ali_shifted
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from obitools3.dms.capi.obiview cimport Obiview_p, QUALITY_COLUMN, NUC_SEQUENCE_COLUMN, \
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REVERSE_SEQUENCE_COLUMN, REVERSE_QUALITY_COLUMN, \
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obi_set_qual_int_with_elt_idx_and_col_p_in_view, \
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obi_set_str_with_elt_idx_and_col_p_in_view
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@ -13,7 +14,6 @@ from obitools3.dms.capi.obidmscolumn cimport OBIDMS_column_p
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from obitools3.dms.view.view cimport View
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from obitools3.dms.column.column cimport Column
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from obitools3.commands.ngsfilter import REVERSE_SEQ_COLUMN_NAME, REVERSE_QUALITY_COLUMN_NAME
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from math import log10
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@ -233,7 +233,7 @@ def buildConsensus(ali, seq, ref_tags=None):
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seq[b'mode']=b'alignment'
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for tag in ref_tags:
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if tag != REVERSE_SEQ_COLUMN_NAME and tag != REVERSE_QUALITY_COLUMN_NAME and \
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if tag != REVERSE_SEQUENCE_COLUMN and tag != REVERSE_QUALITY_COLUMN and \
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tag != NUC_SEQUENCE_COLUMN and tag != QUALITY_COLUMN:
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seq[tag] = ref_tags[tag]
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@ -254,7 +254,7 @@ def buildJoinedSequence(ali, reverse, seq, forward=None):
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seq[b"mode"]=b"joined"
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seq[b"pairedend_limit"]=len(forward)
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for tag in forward:
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if tag != REVERSE_SEQ_COLUMN_NAME and tag != REVERSE_QUALITY_COLUMN_NAME:
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if tag != REVERSE_SEQUENCE_COLUMN and tag != REVERSE_QUALITY_COLUMN:
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seq[tag] = forward[tag]
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return seq
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