Starting /dee2/code/volunteer_pipeline.sh ERR6133391
    current disk space = 1547242577920
    free memory = 1599395212 
ERR6133391 SRAfilesize
284be7974384fd56e834655f8807f97e  ERR6133391.sra
ERR6133391.sra file validated
ERR6133391 is single end
ERR6133391 is conventional basespace
ERR6133391 read1 length is 70-93 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	ERR6133391_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	70-93
%GC	45
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	36.90125	37.0	37.0	37.0	37.0	37.0
2	36.7965	37.0	37.0	37.0	37.0	37.0
3	36.5655	37.0	37.0	37.0	37.0	37.0
4	36.10225	37.0	37.0	37.0	33.0	37.0
5	35.9755	37.0	37.0	37.0	33.0	37.0
6	36.24125	37.0	37.0	37.0	33.0	37.0
7	38.20475	40.0	37.0	40.0	37.0	40.0
8	38.11975	40.0	37.0	40.0	33.0	40.0
9	38.19725	40.0	37.0	40.0	37.0	40.0
10-11	38.18575	40.0	37.0	40.0	37.0	40.0
12-13	38.221125	40.0	37.0	40.0	37.0	40.0
14-15	38.081	40.0	37.0	40.0	37.0	40.0
16-17	38.02575	40.0	37.0	40.0	35.0	40.0
18-19	37.98975	40.0	37.0	40.0	33.0	40.0
20-21	37.86	40.0	37.0	40.0	33.0	40.0
22-23	37.718875	40.0	37.0	40.0	33.0	40.0
24-25	37.56125	40.0	37.0	40.0	33.0	40.0
26-27	37.5005	38.5	37.0	40.0	33.0	40.0
28-29	37.29275	37.0	37.0	40.0	33.0	40.0
30-31	37.21925	37.0	37.0	40.0	33.0	40.0
32-33	36.992375	37.0	37.0	40.0	33.0	40.0
34-35	36.913375	37.0	37.0	40.0	33.0	40.0
36-37	36.807	37.0	37.0	40.0	33.0	40.0
38-39	36.89575	37.0	37.0	40.0	33.0	40.0
40-41	37.191874999999996	37.0	37.0	40.0	33.0	40.0
42-43	37.13175	37.0	37.0	40.0	33.0	40.0
44-45	36.953374999999994	37.0	37.0	40.0	33.0	40.0
46-47	36.765125	37.0	37.0	40.0	33.0	40.0
48-49	36.668875	37.0	37.0	40.0	33.0	40.0
50-51	36.52575	37.0	37.0	40.0	33.0	40.0
52-53	36.36075	37.0	37.0	37.0	33.0	40.0
54-55	36.053125	37.0	37.0	37.0	33.0	40.0
56-57	35.888000000000005	37.0	37.0	37.0	33.0	40.0
58-59	35.781625000000005	37.0	37.0	37.0	33.0	40.0
60-61	35.642125	37.0	35.0	37.0	33.0	37.0
62-63	35.353375	37.0	33.0	37.0	33.0	37.0
64-65	35.084125	37.0	33.0	37.0	33.0	37.0
66-67	35.00125	37.0	33.0	37.0	33.0	37.0
68-69	34.15275	35.0	33.0	37.0	30.0	37.0
70-71	34.288412593984965	37.0	33.0	37.0	33.0	37.0
72-73	34.49474011399835	37.0	33.0	37.0	30.0	37.0
74-75	34.6403258319979	37.0	33.0	37.0	33.0	37.0
76-77	34.61093219996769	37.0	33.0	37.0	33.0	37.0
78-79	34.79624173921059	37.0	33.0	37.0	33.0	37.0
80-81	34.51382983841464	37.0	33.0	37.0	30.0	37.0
82-83	34.04914244040627	37.0	33.0	37.0	27.0	37.0
84-85	34.20760142309372	37.0	33.0	37.0	30.0	37.0
86-87	34.28509916492693	37.0	33.0	37.0	30.0	37.0
88-89	34.26748434237996	37.0	33.0	37.0	33.0	37.0
90-91	33.64418058455115	37.0	33.0	37.0	27.0	37.0
92-93	33.66453549060543	37.0	33.0	37.0	27.0	37.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
20	4.0
21	9.0
22	9.0
23	8.0
24	17.0
25	17.0
26	27.0
27	33.0
28	37.0
29	47.0
30	62.0
31	71.0
32	102.0
33	139.0
34	184.0
35	361.0
36	849.0
37	1037.0
38	941.0
39	46.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	80.625	5.525	4.9	8.95
2	58.025000000000006	24.349999999999998	11.275	6.35
3	33.25	36.575	17.025000000000002	13.15
4	33.575	26.974999999999998	19.225	20.225
5	23.425	31.724999999999998	25.75	19.1
6	19.675	37.25	26.400000000000002	16.675
7	34.425	30.225	19.825	15.525
8	30.55	28.65	23.849999999999998	16.950000000000003
9	26.174999999999997	24.95	28.749999999999996	20.125
10-11	25.0	27.725	27.275	20.0
12-13	28.0625	24.9375	28.812500000000004	18.1875
14-15	21.8875	26.525	31.087500000000002	20.5
16-17	24.224999999999998	30.5375	26.974999999999998	18.2625
18-19	23.6375	26.387500000000003	26.8625	23.1125
20-21	25.887500000000003	26.05	27.8875	20.175
22-23	27.55	23.125	28.475	20.849999999999998
24-25	26.650000000000002	23.65	27.987499999999997	21.712500000000002
26-27	25.637500000000003	25.087500000000002	29.6375	19.6375
28-29	25.7125	26.724999999999998	27.4125	20.150000000000002
30-31	26.2625	25.087500000000002	27.2625	21.3875
32-33	24.175	26.687499999999996	28.712500000000002	20.424999999999997
34-35	25.724999999999998	24.525	28.5875	21.1625
36-37	25.0	24.4875	29.1125	21.4
38-39	25.474999999999998	25.674999999999997	28.962500000000002	19.8875
40-41	26.4125	24.675	28.1	20.8125
42-43	24.1125	27.8625	28.249999999999996	19.775000000000002
44-45	23.6625	25.224999999999998	29.4375	21.675
46-47	24.4875	24.3875	27.987499999999997	23.1375
48-49	24.2	25.8	29.512500000000003	20.4875
50-51	25.374999999999996	25.662499999999998	28.0875	20.875
52-53	26.174999999999997	25.912499999999998	26.9625	20.95
54-55	23.8125	27.8875	27.4125	20.8875
56-57	24.0	26.387500000000003	29.599999999999998	20.0125
58-59	23.400000000000002	24.875	29.212500000000002	22.5125
60-61	24.474999999999998	24.6875	29.612500000000004	21.224999999999998
62-63	22.787499999999998	27.575	30.3875	19.25
64-65	23.974999999999998	26.2125	29.862499999999997	19.950000000000003
66-67	25.7125	26.875	28.425	18.987499999999997
68-69	23.674999999999997	26.087500000000002	29.525000000000002	20.7125
70-71	24.60575719649562	24.96871088861076	28.86107634543179	21.564455569461828
72-73	26.040487866214008	24.971708789136173	28.32893247831007	20.658870866339747
74-75	22.943558592761327	26.208554796254113	30.017717033662368	20.830169577322195
76-77	23.009412363266343	27.194098193843807	28.669549732892396	21.126939709997455
78-79	24.55893633341856	25.70953720276144	29.21247762720532	20.519048836614676
80-81	23.740359897172237	27.76349614395887	29.13881748071979	19.3573264781491
82-83	25.36888428682371	24.566399171628266	30.49443437742687	19.57028216412115
84-85	24.18198409594577	24.53395906661452	30.36110024768609	20.922956589753618
86-87	21.88152400835073	26.52661795407098	32.2286012526096	19.363256784968684
88-89	21.933716075156575	29.318893528183715	30.532359081419624	18.215031315240083
90-91	24.112734864300624	27.38778705636743	28.97964509394572	19.51983298538622
92-93	23.434237995824635	27.805323590814197	28.927453027139876	19.832985386221296
>>END_MODULE
>>Per sequence GC content	warn
#GC Content	Count
0	0.0
1	0.0
2	0.0
3	0.0
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
10	0.0
11	0.0
12	0.0
13	0.0
14	0.0
15	0.0
16	0.5
17	7.5
18	7.5
19	2.5
20	4.0
21	3.5
22	2.0
23	3.0
24	3.5
25	1.5
26	4.0
27	11.5
28	12.5
29	10.5
30	21.0
31	45.0
32	58.0
33	73.0
34	93.0
35	90.0
36	108.5
37	140.5
38	149.0
39	153.0
40	179.0
41	200.5
42	200.5
43	200.0
44	192.0
45	181.0
46	210.0
47	214.5
48	174.0
49	170.5
50	176.0
51	171.0
52	149.0
53	130.0
54	119.5
55	96.0
56	71.5
57	60.0
58	61.5
59	54.5
60	42.0
61	34.5
62	31.0
63	32.0
64	31.0
65	31.0
66	24.5
67	11.5
68	9.0
69	9.5
70	7.5
71	7.0
72	3.5
73	1.5
74	2.5
75	1.5
76	1.0
77	0.5
78	0.0
79	0.0
80	0.5
81	0.5
82	0.0
83	0.0
84	0.0
85	0.0
86	0.0
87	0.0
88	0.0
89	0.0
90	0.0
91	0.0
92	0.0
93	0.0
94	0.0
95	0.0
96	0.0
97	0.0
98	0.0
99	0.0
100	0.0
>>END_MODULE
>>Per base N content	pass
#Base	N-Count
1	0.0
2	0.0
3	0.0
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
10-11	0.0
12-13	0.0
14-15	0.0
16-17	0.0
18-19	0.0
20-21	0.0
22-23	0.0
24-25	0.0
26-27	0.0
28-29	0.0
30-31	0.0
32-33	0.0
34-35	0.0
36-37	0.0
38-39	0.0
40-41	0.0
42-43	0.0
44-45	0.0
46-47	0.0
48-49	0.0
50-51	0.0
52-53	0.0
54-55	0.0
56-57	0.0
58-59	0.0
60-61	0.0
62-63	0.0
64-65	0.0
66-67	0.0
68-69	0.0
70-71	0.0
72-73	0.0
74-75	0.0
76-77	0.0
78-79	0.0
80-81	0.0
82-83	0.0
84-85	0.0
86-87	0.0
88-89	0.0
90-91	0.0
92-93	0.0
>>END_MODULE
>>Sequence Length Distribution	warn
#Length	Count
70	10.0
71	7.0
72	13.0
73	14.0
74	10.0
75	10.0
76	10.0
77	11.0
78	8.0
79	11.0
80	12.0
81	17.0
82	8.0
83	20.0
84	7.0
85	0.0
86	0.0
87	0.0
88	0.0
89	0.0
90	0.0
91	0.0
92	0.0
93	3832.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	83.975
#Duplication Level	Percentage of deduplicated	Percentage of total
1	94.10538850848467	79.025
2	3.632033343256922	6.1
3	0.6549568323905924	1.6500000000000001
4	0.4763322417386127	1.6
5	0.3274784161952962	1.375
6	0.029770765108663295	0.15
7	0.17862459065197975	1.05
8	0.029770765108663295	0.2
9	0.029770765108663295	0.22499999999999998
>10	0.5358737719559392	8.625
>50	0.0	0.0
>100	0.0	0.0
>500	0.0	0.0
>1k	0.0	0.0
>5k	0.0	0.0
>10k+	0.0	0.0
>>END_MODULE
>>Overrepresented sequences	warn
#Sequence	Count	Percentage	Possible Source
GGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGT	36	0.8999999999999999	No Hit
GGGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGG	36	0.8999999999999999	No Hit
GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGC	29	0.7250000000000001	No Hit
GGGGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTG	27	0.675	No Hit
GAAGGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGC	25	0.625	No Hit
GGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAA	22	0.5499999999999999	No Hit
TACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTT	21	0.525	No Hit
GTATTTAGCCTTGCAAGGTGGTCCTTGCTGATTCACACGGGATTCCACGT	20	0.5	No Hit
GGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGGG	17	0.42500000000000004	No Hit
GGAGTATCCTTGATATATAAATATATAGATAAATAGATTTAAATGGAAAA	16	0.4	No Hit
GGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAAA	14	0.35000000000000003	No Hit
GGGCATTCGTATTTCATAGTCAGAGGTGAAATTCTTGGATTTATGAAAGA	14	0.35000000000000003	No Hit
GGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTG	14	0.35000000000000003	No Hit
GGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGCCGC	12	0.3	No Hit
GGAGGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAA	12	0.3	No Hit
GGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTT	10	0.25	No Hit
GGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTGTACAAGCTCGTAA	10	0.25	No Hit
GGGGAAGTACACCAGCGACGGCGAGGCCGCCGCCGCCAAGGAAGGCATGT	10	0.25	No Hit
GTATGGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATACTATCGATTA	9	0.22499999999999998	No Hit
TAGTTTCCACCGCCTGTCCAGGGTTGAGCCCTGGGATTTGACGGCGGACT	8	0.2	No Hit
GGAGTCCTGAACTAGCCGCAGCTTGTGAAGTATGGAAGGCGATCAAATTC	7	0.17500000000000002	No Hit
GAAGTATGGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATACTATCGA	7	0.17500000000000002	No Hit
GAGGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAAT	7	0.17500000000000002	No Hit
GGGAATCGATCGTGATTTAGAACCTGTTCTTTACATGAACCCTCTTAACT	7	0.17500000000000002	No Hit
AACGAAGGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGC	7	0.17500000000000002	No Hit
GGTTTTGAAAAGGGAATCGATCGTGATTTAGAACCTGTTCTTTACATGAA	7	0.17500000000000002	No Hit
GTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGCCGCA	6	0.15	No Hit
GGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAATCG	5	0.125	No Hit
GGGAGTATTATGAAAGGAGATTAATCATAGATTATCAAAAACCCTAGAAA	5	0.125	No Hit
GAAGGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTG	5	0.125	No Hit
GGGCCTGTTATCTCTATCAATATGATTCTAATTCGTCAGATATTATTTAT	5	0.125	No Hit
CAGCTAATCGAGTGGCTTTAGAAGCCTGTGTACAAGCTCGTAACGAAGGG	5	0.125	No Hit
GGGGGTCGCAGTGACCAGGCCCGGGCGACTGTTTACCAAAAACACAGGTC	5	0.125	No Hit
GATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGGGG	5	0.125	No Hit
GTAACGAAGGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCA	5	0.125	No Hit
GGGCCGGGTATCTCTCTGCATGTACGTATGCCTGTAATGTACGTAGCTAC	5	0.125	No Hit
GACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTA	5	0.125	No Hit
GAATCGATCGTGATTTAGAACCTGTTCTTTACATGAACCCTCTTAACTAA	5	0.125	No Hit
>>END_MODULE
>>Adapter Content	pass
#Position	Illumina Universal Adapter	Illumina Small RNA 3' Adapter	Illumina Small RNA 5' Adapter	Nextera Transposase Sequence	SOLID Small RNA Adapter
1	0.0	0.0	0.0	0.0	0.0
2	0.0	0.0	0.0	0.0	0.0
3	0.0	0.0	0.0	0.0	0.0
4	0.0	0.0	0.0	0.0	0.0
5	0.0	0.0	0.0	0.0	0.0
6	0.0	0.0	0.0	0.0	0.0
7	0.0	0.0	0.0	0.0	0.0
8	0.0	0.0	0.0	0.0	0.0
9	0.0	0.0	0.0	0.0	0.0
10-11	0.0	0.0	0.0	0.0	0.0
12-13	0.0	0.0	0.0	0.0	0.0
14-15	0.0	0.0	0.0	0.0	0.0
16-17	0.0	0.0	0.0	0.0	0.0
18-19	0.0	0.0	0.0	0.0	0.0
20-21	0.0	0.0	0.0	0.0	0.0
22-23	0.0	0.0	0.0	0.0	0.0
24-25	0.0	0.0	0.0	0.0	0.0
26-27	0.0	0.0	0.0	0.0	0.0
28-29	0.0	0.0	0.0	0.0	0.0
30-31	0.0	0.0	0.0	0.0	0.0
32-33	0.0	0.0	0.0	0.0	0.0
34-35	0.0	0.0	0.0	0.0	0.0
36-37	0.0	0.0	0.0	0.0	0.0
38-39	0.0	0.0	0.0	0.0	0.0
40-41	0.0125	0.0	0.0	0.0	0.0
42-43	0.025	0.0	0.0	0.0	0.0
44-45	0.025	0.0	0.0	0.0	0.0
46-47	0.025	0.0	0.0	0.0	0.0
48-49	0.025	0.0	0.0	0.0	0.0
50-51	0.025	0.0	0.0	0.0	0.0
52-53	0.025	0.0	0.0	0.0	0.0
54-55	0.025	0.0	0.0	0.0	0.0
56-57	0.025	0.0	0.0	0.0	0.0
58-59	0.025	0.0	0.0	0.0	0.0
60-61	0.025	0.0	0.0	0.0	0.0
62-63	0.025	0.0	0.0	0.0	0.0
64-65	0.025	0.0	0.0	0.0	0.0
66-67	0.025	0.0	0.0	0.0	0.0
68-69	0.025	0.0	0.0	0.0	0.0
70-71	0.025	0.0	0.0	0.0	0.0
72-73	0.025	0.0	0.0	0.0	0.0
74-75	0.025	0.0	0.0	0.0	0.0
76-77	0.025	0.0	0.0	0.0	0.0
78-79	0.025	0.0	0.0	0.0	0.0
80-81	0.025	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	pass
>>END_MODULE
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440606 READS because READLEN < 1
Read 440606 spots for ERR6133391.sra
Written 440606 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
Rejected 440603 READS because READLEN < 1
Read 440603 spots for ERR6133391.sra
Written 440603 spots for ERR6133391.sra
SRR ids: ['ERR6133391.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_0di1o6p0
ERR6133391.sra spots: 8812063
blocks: [[1, 440603], [440604, 881206], [881207, 1321809], [1321810, 1762412], [1762413, 2203015], [2203016, 2643618], [2643619, 3084221], [3084222, 3524824], [3524825, 3965427], [3965428, 4406030], [4406031, 4846633], [4846634, 5287236], [5287237, 5727839], [5727840, 6168442], [6168443, 6609045], [6609046, 7049648], [7049649, 7490251], [7490252, 7930854], [7930855, 8371457], [8371458, 8812063]]
ERR6133391 file size 1945661
ERR6133391 completed basic pipeline successfully
skewer v0.2.2 [April 4, 2016]
COMMAND LINE:	skewer -f sanger -l 18 -q 10 -k inf -t 20 -o ERR6133391 ERR6133391_1.fastq
Input file:	ERR6133391_1.fastq
trimmed:	ERR6133391-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	AGATCGGAAGAGCACACGTCTGAACTCCAGTCAC
-- maximum error ratio allowed (-r):	0.100
-- maximum indel error ratio allowed (-d):	0.030
-- end quality threshold (-q):		10
-- minimum read length allowed after trimming (-l):	18
-- file format (-f):		Sanger/Illumina 1.8+ FASTQ 
-- minimum overlap length for adapter detection (-k):	inf
-- number of concurrent threads (-t):	20
Sat Dec  7 02:50:24 2024 >> started

Sat Dec  7 02:50:29 2024 >> done (4.450s)
8812063 reads processed; of these:
    680 ( 0.01%) short reads filtered out after trimming by size control
     17 ( 0.00%) empty reads filtered out after trimming by size control
8811366 (99.99%) reads available; of these:
 361546 ( 4.10%) trimmed reads available after processing
8449820 (95.90%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	     65	  0.00%
 19	     75	  0.00%
 20	     46	  0.00%
 21	     19	  0.00%
 22	     42	  0.00%
 23	     19	  0.00%
 24	     34	  0.00%
 25	     25	  0.00%
 26	     26	  0.00%
 27	     30	  0.00%
 28	     33	  0.00%
 29	     38	  0.00%
 30	     27	  0.00%
 31	     29	  0.00%
 32	     67	  0.00%
 33	     25	  0.00%
 34	     20	  0.00%
 35	     24	  0.00%
 36	     19	  0.00%
 37	     40	  0.00%
 38	     97	  0.00%
 39	    136	  0.00%
 40	    255	  0.00%
 41	     53	  0.00%
 42	     51	  0.00%
 43	     55	  0.00%
 44	     64	  0.00%
 45	     80	  0.00%
 46	    155	  0.00%
 47	    259	  0.00%
 48	    417	  0.00%
 49	   2714	  0.03%
 50	    804	  0.01%
 51	    939	  0.01%
 52	    878	  0.01%
 53	   1045	  0.01%
 54	   1169	  0.01%
 55	   1412	  0.02%
 56	   1520	  0.02%
 57	   1800	  0.02%
 58	   1772	  0.02%
 59	   2034	  0.02%
 60	   2548	  0.03%
 61	   2075	  0.02%
 62	   2304	  0.03%
 63	   3117	  0.04%
 64	   2811	  0.03%
 65	   2890	  0.03%
 66	   3324	  0.04%
 67	   3623	  0.04%
 68	   4508	  0.05%
 69	   2178	  0.02%
 70	  29385	  0.33%
 71	  30629	  0.35%
 72	  38335	  0.44%
 73	  32505	  0.37%
 74	  33513	  0.38%
 75	  36405	  0.41%
 76	  30996	  0.35%
 77	  32344	  0.37%
 78	  38531	  0.44%
 79	  40070	  0.45%
 80	  36281	  0.41%
 81	  36157	  0.41%
 82	  42990	  0.49%
 83	  55484	  0.63%
 84	  41395	  0.47%
 85	  14610	  0.17%
 86	  16545	  0.19%
 87	  19745	  0.22%
 88	  24231	  0.27%
 89	  24158	  0.27%
 90	  32454	  0.37%
 91	  37125	  0.42%
 92	  40620	  0.46%
 93	7999068	 90.78%
8811366 reads passed initial QC


criterion=sequence-density
sequence-density=0.24
sequence-density-rank=1
fanout-score=7.17
fanout-score-rank=23
prefix-density=0.60
prefix-fanout=2.8
sequence=GCCGCCGCCGCCAAGGAAGGCATGTTCGTCAAGAACTACAGCTACTGATCCTAATCGCATCAAGCTTCAACGCCTGTGAGTGAAAACCAGTGATGAGAGTGCTGCTGCTAGCTAGCGCCGGCATTGATGAGCTTGAGAGGGCACTGTAGCCAGTGTGTCAGTCGTTGTTAAATTACAGGTTGAGATCATCAGCGTACTCCGATGGGAGGTGGACATCAGAAAGTATACTGTGTTTTACCACCCTAATTAAGTAAACAACTTTTGGAATGGTGATCATCTTACTGTTTTAAATAAATCTGTTTCAGA


criterion=fanout-score
sequence-density=0.01
sequence-density-rank=35
fanout-score=298.18
fanout-score-rank=1
prefix-density=0.53
prefix-fanout=7.1
sequence=GAAGAAGAAAAGTTTTCTCAACATGGGGAGGAAGTCCCTCCGAAATTTGATTTGTTATTGTATTGTAAGGGGCTTTTTTAGTATTTATCTAAAGGAAGGAACAAACGAGGATAAGATAAAATTGCTTTAAATTTATTTTGCCCAAGTGGGATATATGGCATACTATTCTTTCCATTTTCATCTTTTTTTCTATTCCACTCCATCTAGATATAAGAAAGAACCCAATGCAATGAAATTCCACTAATATACAATACAAAAAAGAAGAATAGATACAGGGTCTCAAACCTTGCTATAGAGTTTTTGCTT
                                 Started job on |	Dec 07 02:50:46
                             Started mapping on |	Dec 07 02:50:47
                                    Finished on |	Dec 07 02:50:59
       Mapping speed, Million of reads per hour |	2643.41

                          Number of input reads |	8811366
                      Average input read length |	91
                                    UNIQUE READS:
                   Uniquely mapped reads number |	6509419
                        Uniquely mapped reads % |	73.88%
                          Average mapped length |	91.29
                       Number of splices: Total |	314146
            Number of splices: Annotated (sjdb) |	254232
                       Number of splices: GT/AG |	295742
                       Number of splices: GC/AG |	6971
                       Number of splices: AT/AC |	86
               Number of splices: Non-canonical |	11347
                      Mismatch rate per base, % |	0.47%
                         Deletion rate per base |	0.03%
                        Deletion average length |	1.84
                        Insertion rate per base |	0.02%
                       Insertion average length |	1.96
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	1978423
             % of reads mapped to multiple loci |	22.45%
        Number of reads mapped to too many loci |	88585
             % of reads mapped to too many loci |	1.01%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	2.54%
                     % of reads unmapped: other |	0.13%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	323524	323524	323524
N_multimapping	1978423	1978423	1978423
N_noFeature	335655	396919	6209556
N_ambiguous	259717	20983	848
UnstrandedReadsAssigned:5914047 PositiveStrandReadsAssigned:6091517 NegativeStrandReadsAssigned:299015
Dataset is classified positive stranded
MeadianReadLen=93 20thPercentileLength=93 echo kmer=89
ERR6133391 Starting Kallisto single end mapping to ensembl reference transcriptome. kmer=31

[quant] fragment length distribution is truncated gaussian with mean = 100, sd = 20
[index] k-mer length: 31
[index] number of targets: 52,972
[index] number of k-mers: 66,720,672
[index] number of equivalence classes: 111,837
[quant] running in single-end mode
[quant] will process file 1: ERR6133391-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 8,811,366 reads, 7,361,923 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,116 rounds

  52973 ERR6133391.ke.tsv
  35125 ERR6133391.se.tsv
  88098 total
==> ERR6133391.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	0	0
PNS24249	1928	1829	0	0
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	185	24.9114
PNS24243	293	194	0	0
KQK14069	1603	1504	130	15.9689
KQK14071	474	375	0	0

==> ERR6133391.se.tsv <==
BRADI_1g14170v3	130
BRADI_1g53295v3	108
BRADI_1g59795v3	62
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	89
BRADI_1g74790v3	57
BRADI_1g09890v3	0
BRADI_1g77505v3	199
BRADI_1g48960v3	0
ERR6133391 completed mapping pipeline successfully
