Denoiser version: 1.9.1
SFF files: fasta_sff/blue.txt
Fasta file: demultiplexed/blue_demultiplexed.fna
Preprocess dir: None
Primer sequence: GAGTTTGATCMTGGCTCAG
Running on cluster: False
Num CPUs: 1
Squeeze Seqs: True
tmpdir: denoised/blue/
percent_id threshold: 0.97
Minimal sequence coverage for first phase: 1
Low cut-off: 3.75
High cut-off: 4.50
Error profile: /usr/local/lib/python2.7/dist-packages/qiime/support_files/denoiser/Data/FLX_error_profile.dat
Maximal number of iteration: None

Sequences in barcode mapping: 5765
Truncated flowgrams written: 5765
Filter flowgrams by prefix matching
Prefix matching: removed 2985 out of 5765 seqs
Remaining number of sequences: 2780
Clustersize	#
1:		2114
2:		372
3:		131
4:		49
5:		40
6:		18
7:		6
8:		4
9:		3
10:		4
11:		2
12:		3
13:		3
14:		3
15:		3
19:		2
21:		2
24:		1
25:		1
27:		1
28:		3
29:		1
30:		1
31:		1
36:		1
40:		1
43:		1
78:		1
105:		1
108:		1
127:		1
129:		1
132:		1
152:		1
177:		1
228:		1
Round 1:
Rounds remaining in worst case: 666
Filtering with IIN13JX02GWPTO: 2780 flowgrams