Starting /dee2/code/volunteer_pipeline.sh ERR6133411
    current disk space = 1547524263936
    free memory = 1603316056 
ERR6133411 SRAfilesize
43abbe4cc9fc5f4a0de469fe7357388b  ERR6133411.sra
ERR6133411.sra file validated
ERR6133411 is single end
ERR6133411 is conventional basespace
ERR6133411 read1 length is 70-93 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	ERR6133411_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	fail
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	30.035	33.0	27.0	33.0	15.0	37.0
2	33.76375	37.0	33.0	37.0	27.0	37.0
3	33.79425	37.0	33.0	37.0	27.0	37.0
4	33.83175	37.0	33.0	37.0	27.0	37.0
5	34.09975	37.0	33.0	37.0	27.0	37.0
6	34.0675	37.0	33.0	37.0	27.0	37.0
7	35.3375	37.0	33.0	37.0	27.0	40.0
8	35.21425	37.0	33.0	40.0	27.0	40.0
9	35.5955	37.0	33.0	40.0	33.0	40.0
10-11	35.318124999999995	37.0	33.0	40.0	30.0	40.0
12-13	35.2755	37.0	33.0	38.5	30.0	40.0
14-15	35.1055	37.0	33.0	37.0	27.0	40.0
16-17	34.840625	37.0	33.0	37.0	27.0	40.0
18-19	34.6935	37.0	33.0	37.0	27.0	40.0
20-21	34.032125	37.0	33.0	37.0	24.5	40.0
22-23	34.016375	37.0	33.0	37.0	27.0	40.0
24-25	33.689750000000004	37.0	33.0	37.0	24.5	40.0
26-27	33.214375000000004	37.0	33.0	37.0	22.0	40.0
28-29	32.831374999999994	37.0	33.0	37.0	22.0	40.0
30-31	32.72725	33.0	33.0	37.0	22.0	40.0
32-33	32.292500000000004	33.0	30.0	37.0	22.0	40.0
34-35	31.55775	33.0	27.0	37.0	15.0	40.0
36-37	31.201625	33.0	27.0	37.0	15.0	38.5
38-39	31.499	33.0	27.0	37.0	22.0	40.0
40-41	31.331125	33.0	27.0	37.0	22.0	40.0
42-43	30.730875	33.0	27.0	37.0	15.0	40.0
44-45	30.578875	33.0	27.0	37.0	15.0	37.0
46-47	30.087	33.0	27.0	37.0	15.0	37.0
48-49	30.022624999999998	33.0	27.0	37.0	15.0	37.0
50-51	29.546	33.0	27.0	37.0	15.0	37.0
52-53	29.426625	33.0	27.0	37.0	15.0	37.0
54-55	29.250875	33.0	27.0	37.0	15.0	37.0
56-57	28.438375	33.0	27.0	33.0	15.0	37.0
58-59	28.4055	33.0	27.0	33.0	15.0	37.0
60-61	28.369	33.0	27.0	33.0	15.0	37.0
62-63	27.9375	33.0	22.0	33.0	15.0	37.0
64-65	27.083750000000002	30.0	22.0	33.0	10.5	37.0
66-67	26.64375	27.0	22.0	33.0	6.0	37.0
68-69	26.208875	27.0	22.0	33.0	10.5	35.0
70-71	28.092242924528303	33.0	27.0	33.0	15.0	37.0
72-73	28.423566846600185	33.0	27.0	33.0	15.0	37.0
74-75	28.468848815140994	33.0	27.0	33.0	15.0	37.0
76-77	28.189784185404704	33.0	27.0	33.0	15.0	37.0
78-79	27.353249005438272	33.0	24.5	33.0	6.0	37.0
80-81	26.429369352546345	33.0	22.0	33.0	6.0	37.0
82-83	25.751884088168524	33.0	22.0	33.0	2.0	37.0
84-85	25.137275200568638	33.0	22.0	33.0	2.0	37.0
86-87	24.279676985195152	30.0	15.0	33.0	2.0	37.0
88-89	23.409825033647376	30.0	10.5	33.0	2.0	35.0
90-91	22.05343203230148	27.0	2.0	33.0	2.0	33.0
92-93	20.74912516823688	27.0	2.0	33.0	2.0	33.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
20	92.0
21	119.0
22	151.0
23	163.0
24	171.0
25	195.0
26	198.0
27	256.0
28	237.0
29	296.0
30	243.0
31	272.0
32	292.0
33	289.0
34	295.0
35	289.0
36	236.0
37	173.0
38	33.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	68.4	8.674999999999999	8.475000000000001	14.45
2	50.175000000000004	23.5	14.975	11.35
3	34.5	34.725	18.15	12.625
4	25.7	32.5	21.6	20.200000000000003
5	27.400000000000002	25.3	28.249999999999996	19.05
6	17.25	40.275	25.474999999999998	17.0
7	36.075	26.3	21.0	16.625
8	24.175	25.95	24.725	25.15
9	21.0	33.625	26.724999999999998	18.65
10-11	21.7	29.175	31.387500000000003	17.7375
12-13	21.85	29.7375	26.05	22.3625
14-15	19.7375	34.25	27.487499999999997	18.525
16-17	25.05	27.250000000000004	24.3125	23.3875
18-19	24.4375	23.7375	32.675	19.15
20-21	25.087500000000002	24.525	30.65	19.7375
22-23	28.237499999999997	22.287499999999998	30.7375	18.7375
24-25	22.037499999999998	24.5375	29.775000000000002	23.65
26-27	26.387500000000003	23.5375	28.275	21.8
28-29	22.625	29.375	29.4	18.6
30-31	32.1125	23.8125	25.324999999999996	18.75
32-33	27.224999999999998	24.7375	25.5375	22.5
34-35	20.8125	33.7875	25.900000000000002	19.5
36-37	27.1125	25.275	24.45	23.1625
38-39	31.775	22.325	26.437500000000004	19.4625
40-41	23.05	23.9875	34.525	18.4375
42-43	27.275	30.1875	24.6125	17.925
44-45	25.3	25.15	30.7375	18.8125
46-47	27.6125	24.5625	25.224999999999998	22.6
48-49	25.337500000000002	24.0625	27.2625	23.3375
50-51	21.2	30.225	25.887500000000003	22.6875
52-53	21.462500000000002	26.6	24.2375	27.700000000000003
54-55	21.712500000000002	24.775	31.3	22.2125
56-57	26.025	29.675	26.137500000000003	18.1625
58-59	21.4	29.4875	30.3	18.8125
60-61	30.075000000000003	25.387500000000003	26.2875	18.25
62-63	19.7625	26.187500000000004	32.3875	21.6625
64-65	21.7	35.25	25.337500000000002	17.712500000000002
66-67	24.637500000000003	31.137500000000003	25.8	18.425
68-69	21.1875	24.2875	29.875	24.65
70-71	21.46708463949843	29.442006269592476	26.583072100313483	22.50783699059561
72-73	25.894550512074847	25.565811101277024	29.902642559109875	18.636995827538247
74-75	26.77797603874586	29.35253632424165	26.051491205709915	17.817996431302575
76-77	20.996395468589082	23.892893923789906	26.15859938208033	28.952111225540676
78-79	26.01795238714713	29.07506179263692	27.045661506439444	17.861324313776507
80-81	22.27481919789612	36.09467455621302	24.77317554240631	16.85733070348455
82-83	24.56163655685441	25.425079702444208	26.115834218916046	23.897449521785337
84-85	21.385420861860652	27.292253993824673	32.138542086186064	19.183783058128608
86-87	20.430686406460296	30.484522207267833	25.383580080753703	23.701211305518168
88-89	20.69986541049798	27.33512786002692	30.134589502018844	21.83041722745626
90-91	25.491251682368777	31.372812920592192	25.19515477792732	17.94078061911171
92-93	19.43472409152086	29.811574697173622	28.627187079407808	22.12651413189771
>>END_MODULE
>>Per sequence GC content	fail
#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	0.5
13	0.5
14	0.0
15	0.0
16	0.0
17	5.5
18	7.5
19	3.0
20	2.5
21	5.0
22	5.5
23	5.0
24	5.5
25	8.0
26	13.5
27	18.5
28	21.0
29	19.5
30	29.0
31	46.0
32	58.5
33	68.0
34	69.0
35	85.5
36	118.5
37	184.0
38	227.5
39	207.5
40	205.5
41	211.5
42	181.5
43	158.0
44	164.5
45	157.0
46	146.0
47	135.0
48	119.5
49	125.5
50	123.5
51	126.5
52	131.5
53	151.0
54	256.5
55	249.0
56	129.0
57	92.5
58	67.0
59	34.0
60	24.0
61	23.5
62	17.0
63	12.0
64	13.0
65	7.0
66	3.0
67	4.0
68	9.0
69	11.0
70	8.5
71	8.0
72	5.5
73	1.5
74	0.5
75	0.5
76	0.5
77	0.5
78	0.0
79	0.0
80	0.0
81	0.0
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	25.0
71	12.0
72	17.0
73	14.0
74	18.0
75	20.0
76	20.0
77	18.0
78	25.0
79	21.0
80	15.0
81	21.0
82	20.0
83	20.0
84	19.0
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	3715.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	73.02499999999999
#Duplication Level	Percentage of deduplicated	Percentage of total
1	92.1944539541253	67.325
2	3.560424512153372	5.2
3	1.4720985963711057	3.225
4	0.6846970215679562	2.0
5	0.5135227661759671	1.875
6	0.23964395754878468	1.05
7	0.20540910647038688	1.05
8	0.23964395754878468	1.4000000000000001
9	0.13693940431359122	0.8999999999999999
>10	0.7189318726463539	8.475000000000001
>50	0.0	0.0
>100	0.034234851078397806	7.5
>500	0.0	0.0
>1k	0.0	0.0
>5k	0.0	0.0
>10k+	0.0	0.0
>>END_MODULE
>>Overrepresented sequences	fail
#Sequence	Count	Percentage	Possible Source
GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGC	300	7.5	No Hit
GGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAA	36	0.8999999999999999	No Hit
TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGA	23	0.575	No Hit
GGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAATGGATTC	21	0.525	No Hit
CAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTG	21	0.525	No Hit
TACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTT	20	0.5	No Hit
TCTCATGGAGAGTTCGATCCTGGCTCAGGATGAACGCTGGCGGCATGCTT	20	0.5	No Hit
GGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTC	19	0.475	No Hit
CAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTC	18	0.44999999999999996	No Hit
GTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAG	18	0.44999999999999996	No Hit
CAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGATAT	15	0.375	No Hit
GGGTTGTTTGGGAATGCAGCCCAAATCGGGCGGTAGACTCCGTCCAAGGC	14	0.35000000000000003	No Hit
CAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCT	14	0.35000000000000003	No Hit
GGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGT	13	0.325	No Hit
GGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCG	12	0.3	No Hit
GGGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGG	12	0.3	No Hit
GGAGTATCCTTGATATATAAATATATAGATAAATAGATTTAAATGGAAAA	12	0.3	No Hit
GATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAAT	11	0.27499999999999997	No Hit
GTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTT	10	0.25	No Hit
GGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGG	10	0.25	No Hit
GGATTTGTTAAATCAAATCCTTGGTTTAATAACGAACGGTGTTAACTTAC	10	0.25	No Hit
TCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCT	10	0.25	No Hit
CAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTT	9	0.22499999999999998	No Hit
GGGAATGCAGCCCAAATCGGGCGGTAGACTCCGTCCAAGGCTAAATACAG	9	0.22499999999999998	No Hit
GGGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAA	9	0.22499999999999998	No Hit
GGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCT	9	0.22499999999999998	No Hit
GGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTT	8	0.2	No Hit
GAAGCCTGTGTACAAGCTCGTAACGAAGGGCGCGATCTTGCTCGTGAAGG	8	0.2	No Hit
GGGGTTGTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTG	8	0.2	No Hit
GGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAA	8	0.2	No Hit
GTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCT	8	0.2	No Hit
CGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAA	8	0.2	No Hit
GGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTA	8	0.2	No Hit
GGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAA	7	0.17500000000000002	No Hit
GGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTG	7	0.17500000000000002	No Hit
GGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGGG	7	0.17500000000000002	No Hit
GCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCT	7	0.17500000000000002	No Hit
GTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAA	7	0.17500000000000002	No Hit
GGAGGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAA	7	0.17500000000000002	No Hit
GTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAATGGATTCA	6	0.15	No Hit
GTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAA	6	0.15	No Hit
GGGAGTATTATGAAAGGAGATTAATCATAGATTATCAAAAACCCTAGAAA	6	0.15	No Hit
GAAGGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTG	6	0.15	No Hit
GGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCA	6	0.15	No Hit
GAAGGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGC	6	0.15	No Hit
GGAAAAGAAAGCAAAAGCGATTCCCGTAGTAGCGGCGAGCGAAATGGGAG	6	0.15	No Hit
GGTATTAGTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATC	5	0.125	No Hit
GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGACGCGGTTGAGTGCCGC	5	0.125	No Hit
GGGTGAGTAACGCGTAAGAACCTGCCCTTGGGAGGGGAACAACAACTGGA	5	0.125	No Hit
CAACTCTCGTTCTTTACACTTCTTCTTGGCTGCTTGGCCTGTAGTAGGAA	5	0.125	No Hit
GGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAATCG	5	0.125	No Hit
GAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAAT	5	0.125	No Hit
GGTTGTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAG	5	0.125	No Hit
GTATGGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATACTATCGATTA	5	0.125	No Hit
CTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGT	5	0.125	No Hit
GGCCTGTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCG	5	0.125	No Hit
GTATTAGTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCT	5	0.125	No Hit
CGGGTTGTTTGGGAATGCAGCCCAAATCGGGCGGTAGACTCCGTCCAAGG	5	0.125	No Hit
GGGGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTG	5	0.125	No Hit
GCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCA	5	0.125	No Hit
GGGTGAGAGCCCCGTCCGGCCCGGACCCTGTCGCCCCACGAGGCGCCGTC	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	0.05	0.0	0.0	0.0	0.0
74-75	0.05	0.0	0.0	0.0	0.0
76-77	0.05	0.0	0.0	0.0	0.0
78-79	0.05	0.0	0.0	0.0	0.0
80-81	0.05	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGAGAGC	50	1.8189894E-12	77.94	2
GGGAGAG	50	1.8189894E-12	77.94	1
GCAATAC	60	0.0	72.166664	7
CAATACA	60	0.0	72.166664	8
GAGCAAT	60	0.0	72.166664	5
AATACAA	60	0.0	72.166664	9
AGCAATA	65	0.0	66.61539	6
AGAGCAA	60	5.456968E-12	64.95	4
GAGAGCA	65	1.2732926E-11	59.953846	3
CATCACT	55	4.9112714E-11	40.37296	82-83
ATCACTA	55	4.9112714E-11	40.37296	84-85
CACTAGC	55	4.9112714E-11	40.37296	86-87
TCACTAG	55	4.9112714E-11	40.37296	84-85
ACTAGCT	55	4.9112714E-11	40.37296	86-87
GCATCAC	55	4.9112714E-11	40.37296	82-83
AGCATCA	50	9.313226E-10	39.96923	80-81
AAGCATC	45	1.7329512E-8	39.47578	80-81
CCAGTAG	50	1.0586518E-9	39.46329	68-69
TCCAGTA	50	1.0586518E-9	39.46329	68-69
GTCCAGT	50	1.0586518E-9	39.46329	66-67
>>END_MODULE
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108821 READS because READLEN < 1
Read 108821 spots for ERR6133411.sra
Written 108821 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
Rejected 108819 READS because READLEN < 1
Read 108819 spots for ERR6133411.sra
Written 108819 spots for ERR6133411.sra
SRR ids: ['ERR6133411.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_ksmyhwmc
ERR6133411.sra spots: 2176382
blocks: [[1, 108819], [108820, 217638], [217639, 326457], [326458, 435276], [435277, 544095], [544096, 652914], [652915, 761733], [761734, 870552], [870553, 979371], [979372, 1088190], [1088191, 1197009], [1197010, 1305828], [1305829, 1414647], [1414648, 1523466], [1523467, 1632285], [1632286, 1741104], [1741105, 1849923], [1849924, 1958742], [1958743, 2067561], [2067562, 2176382]]
ERR6133411 file size 477692
ERR6133411 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 ERR6133411 ERR6133411_1.fastq
Input file:	ERR6133411_1.fastq
trimmed:	ERR6133411-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 03:34:36 2024 >> started

Sat Dec  7 03:34:37 2024 >> done (1.214s)
2176382 reads processed; of these:
     30 ( 0.00%) short reads filtered out after trimming by size control
      5 ( 0.00%) empty reads filtered out after trimming by size control
2176347 (100.00%) reads available; of these:
 574979 (26.42%) trimmed reads available after processing
1601368 (73.58%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      8	  0.00%
 19	     13	  0.00%
 20	      9	  0.00%
 21	      2	  0.00%
 22	      4	  0.00%
 23	      1	  0.00%
 24	      2	  0.00%
 25	      5	  0.00%
 26	      2	  0.00%
 27	      2	  0.00%
 28	     23	  0.00%
 29	     47	  0.00%
 30	      3	  0.00%
 31	      4	  0.00%
 32	     13	  0.00%
 33	     13	  0.00%
 34	      4	  0.00%
 35	      4	  0.00%
 36	      8	  0.00%
 37	      9	  0.00%
 38	     14	  0.00%
 39	     24	  0.00%
 40	     34	  0.00%
 41	     21	  0.00%
 42	     23	  0.00%
 43	     31	  0.00%
 44	     32	  0.00%
 45	     43	  0.00%
 46	     59	  0.00%
 47	     95	  0.00%
 48	    146	  0.01%
 49	    198	  0.01%
 50	    252	  0.01%
 51	    322	  0.01%
 52	    477	  0.02%
 53	    704	  0.03%
 54	    987	  0.05%
 55	   1207	  0.06%
 56	   1707	  0.08%
 57	   2516	  0.12%
 58	   1813	  0.08%
 59	   2176	  0.10%
 60	   2586	  0.12%
 61	   3039	  0.14%
 62	   3428	  0.16%
 63	   3722	  0.17%
 64	   3848	  0.18%
 65	   4187	  0.19%
 66	   4284	  0.20%
 67	   4448	  0.20%
 68	   3882	  0.18%
 69	   3906	  0.18%
 70	  14315	  0.66%
 71	  14495	  0.67%
 72	  17150	  0.79%
 73	  17648	  0.81%
 74	  18358	  0.84%
 75	  19741	  0.91%
 76	  21066	  0.97%
 77	  23707	  1.09%
 78	  24547	  1.13%
 79	  25685	  1.18%
 80	  26784	  1.23%
 81	  30600	  1.41%
 82	  32417	  1.49%
 83	  33677	  1.55%
 84	  37860	  1.74%
 85	  28656	  1.32%
 86	  29615	  1.36%
 87	  32803	  1.51%
 88	  40349	  1.85%
 89	  41862	  1.92%
 90	  44079	  2.03%
 91	  46910	  2.16%
 92	  40952	  1.88%
 93	1462684	 67.21%
2176347 reads passed initial QC


criterion=sequence-density
sequence-density=2.94
sequence-density-rank=1
fanout-score=2.09
fanout-score-rank=29
prefix-density=3.02
prefix-fanout=2.0
sequence=CAAGGCTAAATAC


criterion=fanout-score
sequence-density=0.12
sequence-density-rank=20
fanout-score=95.70
fanout-score-rank=1
prefix-density=11.15
prefix-fanout=1.1
sequence=CCTAGATGGCTCAAGTCCAGTAG
Potential 3prime adapter identified. Now checking if in reference sequence
Warning: gzbuffer added in zlib v1.2.3.5. Unable to change buffer size from default of 8192.
1 reads; of these:
  1 (100.00%) were unpaired; of these:
    0 (0.00%) aligned 0 times
    0 (0.00%) aligned exactly 1 time
    1 (100.00%) aligned >1 times
100.00% overall alignment rate
Potential adapter found in reference sequence. Continuing without clipping.
                                 Started job on |	Dec 07 03:34:51
                             Started mapping on |	Dec 07 03:34:51
                                    Finished on |	Dec 07 03:34:57
       Mapping speed, Million of reads per hour |	1305.81

                          Number of input reads |	2176347
                      Average input read length |	89
                                    UNIQUE READS:
                   Uniquely mapped reads number |	892526
                        Uniquely mapped reads % |	41.01%
                          Average mapped length |	88.46
                       Number of splices: Total |	38833
            Number of splices: Annotated (sjdb) |	31655
                       Number of splices: GT/AG |	37504
                       Number of splices: GC/AG |	781
                       Number of splices: AT/AC |	47
               Number of splices: Non-canonical |	501
                      Mismatch rate per base, % |	0.68%
                         Deletion rate per base |	0.02%
                        Deletion average length |	1.42
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.33
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	1123552
             % of reads mapped to multiple loci |	51.63%
        Number of reads mapped to too many loci |	63357
             % of reads mapped to too many loci |	2.91%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	3.94%
                     % of reads unmapped: other |	0.52%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	160269	160269	160269
N_multimapping	1123552	1123552	1123552
N_noFeature	75031	83822	853614
N_ambiguous	36014	5840	191
UnstrandedReadsAssigned:781481 PositiveStrandReadsAssigned:802864 NegativeStrandReadsAssigned:38721
Dataset is classified positive stranded
MeadianReadLen=93 20thPercentileLength=84 echo kmer=79
ERR6133411 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: ERR6133411-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 2,176,347 reads, 1,393,392 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 938 rounds

  52973 ERR6133411.ke.tsv
  35125 ERR6133411.se.tsv
  88098 total
==> ERR6133411.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	14	9.56905
PNS24243	293	194	0	0
KQK14069	1603	1504	7	4.3646
KQK14071	474	375	0	0

==> ERR6133411.se.tsv <==
BRADI_1g14170v3	7
BRADI_1g53295v3	12
BRADI_1g59795v3	8
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	14
BRADI_1g74790v3	7
BRADI_1g09890v3	0
BRADI_1g77505v3	15
BRADI_1g48960v3	0
ERR6133411 completed mapping pipeline successfully
