Starting /dee2/code/volunteer_pipeline.sh ERR6133398
    current disk space = 1547668152320
    free memory = 1603274732 
ERR6133398 SRAfilesize
3e305ec3126f267c580596ad142aebd2  ERR6133398.sra
ERR6133398.sra file validated
ERR6133398 is single end
ERR6133398 is conventional basespace
ERR6133398 read1 length is 70-93 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	ERR6133398_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	44
>>END_MODULE
>>Per base sequence quality	fail
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	29.28525	33.0	27.0	33.0	15.0	37.0
2	33.58375	33.0	33.0	37.0	27.0	37.0
3	33.7495	37.0	33.0	37.0	27.0	37.0
4	33.8755	37.0	33.0	37.0	27.0	37.0
5	34.106	37.0	33.0	37.0	27.0	37.0
6	34.29525	37.0	33.0	37.0	27.0	37.0
7	35.36775	37.0	33.0	40.0	27.0	40.0
8	35.179	37.0	33.0	40.0	27.0	40.0
9	35.354	37.0	33.0	40.0	27.0	40.0
10-11	35.313375	37.0	33.0	37.0	30.0	40.0
12-13	35.113625	37.0	33.0	37.0	27.0	40.0
14-15	35.186125000000004	37.0	33.0	37.0	27.0	40.0
16-17	34.78	37.0	33.0	37.0	27.0	40.0
18-19	34.662375	37.0	33.0	37.0	27.0	40.0
20-21	33.96025	37.0	33.0	37.0	24.5	40.0
22-23	33.788	37.0	33.0	37.0	27.0	40.0
24-25	33.262125	37.0	33.0	37.0	22.0	40.0
26-27	33.241625	37.0	33.0	37.0	22.0	40.0
28-29	32.74575	37.0	33.0	37.0	22.0	40.0
30-31	32.591875	35.0	33.0	37.0	22.0	40.0
32-33	32.106625	33.0	33.0	37.0	22.0	40.0
34-35	31.361125	33.0	27.0	37.0	15.0	40.0
36-37	31.021875	33.0	27.0	37.0	15.0	37.0
38-39	31.342750000000002	33.0	27.0	37.0	22.0	38.5
40-41	31.318375000000003	33.0	27.0	37.0	22.0	38.5
42-43	31.03975	33.0	27.0	37.0	15.0	40.0
44-45	30.679875	33.0	27.0	37.0	15.0	38.5
46-47	30.154	33.0	27.0	37.0	15.0	37.0
48-49	29.98475	33.0	27.0	37.0	15.0	37.0
50-51	29.492125	33.0	27.0	37.0	15.0	37.0
52-53	29.251625	33.0	27.0	37.0	15.0	37.0
54-55	29.225875000000002	33.0	27.0	37.0	15.0	37.0
56-57	28.536875	33.0	27.0	35.0	15.0	37.0
58-59	28.30325	33.0	27.0	33.0	15.0	37.0
60-61	28.089624999999998	33.0	27.0	33.0	15.0	37.0
62-63	27.596375000000002	33.0	22.0	33.0	15.0	37.0
64-65	27.12325	33.0	22.0	33.0	10.5	37.0
66-67	26.819625000000002	30.0	22.0	33.0	10.5	37.0
68-69	26.394125000000003	27.0	22.0	33.0	10.5	35.0
70-71	28.09386884267404	33.0	27.0	33.0	15.0	37.0
72-73	28.692402572519768	33.0	27.0	33.0	15.0	37.0
74-75	28.664572953086044	33.0	27.0	33.0	15.0	37.0
76-77	28.199389659746842	33.0	27.0	33.0	15.0	37.0
78-79	27.40382583788673	33.0	24.5	33.0	10.5	37.0
80-81	26.7442753699045	33.0	22.0	33.0	6.0	37.0
82-83	26.168161510473723	33.0	22.0	33.0	2.0	37.0
84-85	25.284362887914817	33.0	18.5	33.0	2.0	37.0
86-87	24.24477895307838	30.0	15.0	33.0	2.0	37.0
88-89	23.723216707350147	30.0	10.5	33.0	2.0	37.0
90-91	22.66870084079197	27.0	2.0	33.0	2.0	37.0
92-93	21.249389747762407	27.0	2.0	33.0	2.0	33.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
20	80.0
21	108.0
22	137.0
23	153.0
24	209.0
25	220.0
26	210.0
27	237.0
28	236.0
29	263.0
30	283.0
31	270.0
32	296.0
33	276.0
34	298.0
35	269.0
36	234.0
37	181.0
38	40.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	70.72500000000001	7.675	6.7250000000000005	14.875
2	53.075	24.2	14.7	8.025
3	32.125	36.75	18.05	13.075000000000001
4	27.500000000000004	28.7	22.625	21.175
5	26.474999999999998	25.6	29.4	18.525
6	17.375	37.824999999999996	26.3	18.5
7	35.15	26.700000000000003	21.525	16.625
8	23.849999999999998	27.250000000000004	27.375	21.525
9	21.7	32.85	28.275	17.175
10-11	22.7125	28.487499999999997	30.8125	17.9875
12-13	21.1625	30.062499999999996	27.9375	20.837500000000002
14-15	19.725	33.3625	27.9375	18.975
16-17	24.3125	28.3875	24.3625	22.9375
18-19	23.400000000000002	24.5	32.6875	19.412499999999998
20-21	25.45	23.6625	30.9625	19.925
22-23	27.975	23.1625	28.625	20.2375
24-25	22.4625	25.6125	29.5875	22.3375
26-27	24.1625	24.5	29.9375	21.4
28-29	22.475	28.775000000000002	29.562500000000004	19.1875
30-31	28.4125	26.387500000000003	26.3625	18.8375
32-33	26.05	23.7	28.4	21.85
34-35	21.6875	33.650000000000006	25.5375	19.125
36-37	25.387500000000003	26.05	25.337500000000002	23.225
38-39	30.125	23.425	27.3625	19.0875
40-41	23.3875	24.2875	32.875	19.45
42-43	26.0	29.375	26.75	17.875
44-45	23.9875	26.7125	30.2125	19.0875
46-47	25.162499999999998	25.412499999999998	25.900000000000002	23.525
48-49	24.175	25.525	28.3375	21.9625
50-51	22.0625	29.575000000000003	26.087500000000002	22.275
52-53	21.7375	27.0625	26.0	25.2
54-55	21.925	26.0	31.112499999999997	20.962500000000002
56-57	25.412499999999998	30.075000000000003	25.837500000000002	18.675
58-59	22.4625	28.9	28.6125	20.025000000000002
60-61	27.925	26.974999999999998	27.3375	17.7625
62-63	20.5875	26.924999999999997	31.374999999999996	21.1125
64-65	20.5	35.3	26.474999999999998	17.724999999999998
66-67	24.45	29.049999999999997	27.275	19.225
68-69	19.9875	27.55	28.425	24.0375
70-71	22.458954756235116	28.6878054894097	27.045995738814387	21.807244015540796
72-73	24.564063684609554	26.29517311094263	30.224917867071017	18.915845337376798
74-75	25.379415890830252	29.28197933936998	26.42520086723632	18.91340390256345
76-77	21.807415036045313	25.16735324407827	26.544799176107105	26.48043254376931
78-79	24.084653336795636	28.551025707608414	27.888860036354195	19.475460919241755
80-81	20.089461912906195	35.718984344165236	27.035916326799104	17.15563741612946
82-83	23.427505330490405	26.945628997867804	25.652985074626866	23.973880597014926
84-85	20.76414202781153	26.04293236127987	32.334278385311194	20.85864722559741
86-87	20.88418768646596	29.888798481149987	26.471385950637377	22.755627881746676
88-89	19.9484675888256	28.044480607540006	29.509085977759696	22.497965825874694
90-91	24.003254678600488	32.072145375644155	25.07458638459452	18.850013561160836
92-93	19.338215351234066	31.1364252780038	28.22077569839978	21.304583672362355
>>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	0.5
16	1.0
17	3.5
18	3.5
19	2.0
20	3.0
21	4.5
22	5.5
23	5.0
24	7.5
25	9.5
26	10.0
27	16.5
28	29.5
29	35.0
30	35.5
31	50.0
32	63.0
33	59.5
34	76.5
35	99.0
36	119.5
37	191.0
38	231.0
39	208.0
40	216.5
41	211.5
42	210.5
43	236.5
44	219.0
45	191.5
46	174.5
47	146.5
48	116.5
49	113.0
50	114.0
51	107.0
52	112.5
53	132.0
54	226.5
55	216.5
56	102.0
57	76.0
58	55.0
59	34.0
60	23.5
61	17.5
62	13.5
63	8.0
64	11.0
65	10.5
66	7.0
67	3.5
68	4.0
69	7.5
70	5.5
71	3.0
72	3.0
73	3.0
74	2.0
75	0.5
76	0.0
77	0.0
78	0.5
79	0.5
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	21.0
71	15.0
72	14.0
73	16.0
74	27.0
75	13.0
76	20.0
77	15.0
78	16.0
79	34.0
80	17.0
81	25.0
82	30.0
83	17.0
84	33.0
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	3687.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	72.425
#Duplication Level	Percentage of deduplicated	Percentage of total
1	91.81912323092854	66.5
2	3.8660683465654127	5.6000000000000005
3	1.2426648256817396	2.7
4	0.9319986192613048	2.7
5	0.3451846738004833	1.25
6	0.3451846738004833	1.5
7	0.1380738695201933	0.7000000000000001
8	0.3106662064204349	1.7999999999999998
9	0.2416292716603383	1.575
>10	0.7248878149810148	10.100000000000001
>50	0.0	0.0
>100	0.03451846738004832	5.575
>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	223	5.575	No Hit
GGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGG	46	1.15	No Hit
GGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAA	41	1.0250000000000001	No Hit
CAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTC	27	0.675	No Hit
GGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTC	26	0.65	No Hit
GGGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAA	25	0.625	No Hit
CAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCT	23	0.575	No Hit
GGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAATGGATTC	19	0.475	No Hit
CAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGATAT	18	0.44999999999999996	No Hit
CAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTG	18	0.44999999999999996	No Hit
GGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAA	17	0.42500000000000004	No Hit
GTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAG	17	0.42500000000000004	No Hit
GGGTTGTTTGGGAATGCAGCCCAAATCGGGCGGTAGACTCCGTCCAAGGC	15	0.375	No Hit
GGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAA	15	0.375	No Hit
GGCCTGTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCG	14	0.35000000000000003	No Hit
GGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCT	13	0.325	No Hit
GTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCT	13	0.325	No Hit
GTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTT	12	0.3	No Hit
GTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAA	12	0.3	No Hit
GGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGT	12	0.3	No Hit
GGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCA	11	0.27499999999999997	No Hit
GGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTG	10	0.25	No Hit
GCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGGTATG	9	0.22499999999999998	No Hit
GGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCG	9	0.22499999999999998	No Hit
GCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCT	9	0.22499999999999998	No Hit
GGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAA	9	0.22499999999999998	No Hit
AACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCG	9	0.22499999999999998	No Hit
GTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCC	9	0.22499999999999998	No Hit
GGATTTGTTAAATCAAATCCTTGGTTTAATAACGAACGGTGTTAACTTAC	9	0.22499999999999998	No Hit
GGTATTAGTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATC	8	0.2	No Hit
GGGAATGCAGCCCAAATCGGGCGGTAGACTCCGTCCAAGGCTAAATACAG	8	0.2	No Hit
GGAGTTGAAAATAAGCATAGATCCGGAGATTCCCAAATAGGTCAACCTTT	8	0.2	No Hit
GGGGTTGTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTG	8	0.2	No Hit
GTATTAGTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCT	8	0.2	No Hit
TACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTT	8	0.2	No Hit
GGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGCCGC	8	0.2	No Hit
GGGTGAGAGCCCCGTCCGGCCCGGACCCTGTCGCCCCACGAGGCGCCGTC	8	0.2	No Hit
GGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTA	8	0.2	No Hit
CACGAACGTAATGCTCACAACTTCCCTCTAGATCTAGCTGCTCTTGAAGT	7	0.17500000000000002	No Hit
GGAGGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAA	7	0.17500000000000002	No Hit
TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGA	7	0.17500000000000002	No Hit
GGAAAAGAAAGCAAAAGCGATTCCCGTAGTAGCGGCGAGCGAAATGGGAG	7	0.17500000000000002	No Hit
GGAGTCCTGAACTAGCCGCAGCTTGTGAAGTATGGAAGGCGATCAAATTC	6	0.15	No Hit
CGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGGTAT	6	0.15	No Hit
CAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTT	6	0.15	No Hit
GGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTG	6	0.15	No Hit
TATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAG	6	0.15	No Hit
GGGTTGTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGA	6	0.15	No Hit
GGAGTATCCTTGATATATAAATATATAGATAAATAGATTTAAATGGAAAA	6	0.15	No Hit
GTCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAAT	6	0.15	No Hit
GGGGAGTTGAAAATAAGCATAGATCCGGAGATTCCCAAATAGGTCAACCT	6	0.15	No Hit
GAACGTAATGCTCACAACTTCCCTCTAGATCTAGCTGCTCTTGAAGTTCC	6	0.15	No Hit
GCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATC	5	0.125	No Hit
GGGTGAGTAACGCGTAAGAACCTGCCCTTGGGAGGGGAACAACAACTGGA	5	0.125	No Hit
GGAGGGTGAGAGCCCCGTCCGGCCCGGACCCTGTCGCCCCACGAGGCGCC	5	0.125	No Hit
GAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAAT	5	0.125	No Hit
GTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGCCGCA	5	0.125	No Hit
TGGGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGA	5	0.125	No Hit
GCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCA	5	0.125	No Hit
GAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCTG	5	0.125	No Hit
CAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAACGTAATGCTCACA	5	0.125	No Hit
TCTCATGGAGAGTTCGATCCTGGCTCAGGATGAACGCTGGCGGCATGCTT	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	0.0	0.0	0.0	0.0	0.0
42-43	0.0	0.0	0.0	0.0	0.0
44-45	0.0	0.0	0.0	0.0	0.0
46-47	0.0	0.0	0.0	0.0	0.0
48-49	0.0	0.0	0.0	0.0	0.0
50-51	0.0	0.0	0.0	0.0	0.0
52-53	0.0	0.0	0.0	0.0	0.0
54-55	0.0	0.0	0.0	0.0	0.0
56-57	0.0	0.0	0.0	0.0	0.0
58-59	0.0	0.0	0.0	0.0	0.0
60-61	0.0	0.0	0.0	0.0	0.0
62-63	0.0	0.0	0.0	0.0	0.0
64-65	0.0	0.0	0.0	0.0	0.0
66-67	0.0	0.0	0.0	0.0	0.0
68-69	0.0125	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	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GCAATAC	50	6.8852205E-7	51.1725	7
CAATACA	50	6.8852205E-7	51.1725	8
AGCAATA	50	6.8852205E-7	51.1725	6
ATCACTA	25	2.1884507E-5	48.735714	84-85
AGTTGAA	15	0.008949027	48.735714	82-83
CACTAGC	30	1.0802269E-6	48.735714	86-87
ACTAGCT	25	2.1884507E-5	48.735714	86-87
GCATCAC	30	1.0802269E-6	48.735714	82-83
GGAGTTG	15	0.008949027	48.735714	80-81
GGGGAGT	15	0.00920708	48.390068	78-79
GGAGAGC	45	2.3852977E-5	47.381943	2
GGGAGAG	45	2.3852977E-5	47.381943	1
GAGCAAT	55	1.3292338E-6	46.520454	5
AATACAA	55	1.3292338E-6	46.520454	9
GAGAGCA	50	4.446852E-5	42.643753	3
AAGCATC	35	3.1242216E-6	41.77347	80-81
CATCACT	30	6.425731E-5	40.613094	82-83
AGCATCA	30	6.425731E-5	40.613094	80-81
CCGAAAG	35	4.195088E-6	40.05675	76-77
TCACTAG	25	0.0013295984	38.98857	84-85
>>END_MODULE
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67767 READS because READLEN < 1
Read 67767 spots for ERR6133398.sra
Written 67767 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
Rejected 67764 READS because READLEN < 1
Read 67764 spots for ERR6133398.sra
Written 67764 spots for ERR6133398.sra
SRR ids: ['ERR6133398.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_stp_fuss
ERR6133398.sra spots: 1355283
blocks: [[1, 67764], [67765, 135528], [135529, 203292], [203293, 271056], [271057, 338820], [338821, 406584], [406585, 474348], [474349, 542112], [542113, 609876], [609877, 677640], [677641, 745404], [745405, 813168], [813169, 880932], [880933, 948696], [948697, 1016460], [1016461, 1084224], [1084225, 1151988], [1151989, 1219752], [1219753, 1287516], [1287517, 1355283]]
ERR6133398 file size 296259
ERR6133398 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 ERR6133398 ERR6133398_1.fastq
Input file:	ERR6133398_1.fastq
trimmed:	ERR6133398-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 03:11:51 2024 >> started

Sat Dec  7 03:11:52 2024 >> done (1.037s)
1355283 reads processed; of these:
     19 ( 0.00%) short reads filtered out after trimming by size control
      3 ( 0.00%) empty reads filtered out after trimming by size control
1355261 (100.00%) reads available; of these:
 344873 (25.45%) trimmed reads available after processing
1010388 (74.55%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      2	  0.00%
 19	     18	  0.00%
 20	      4	  0.00%
 21	      2	  0.00%
 22	      4	  0.00%
 23	      0	  0.00%
 24	      1	  0.00%
 25	      4	  0.00%
 26	      2	  0.00%
 27	      2	  0.00%
 28	     14	  0.00%
 29	     28	  0.00%
 30	      5	  0.00%
 31	      0	  0.00%
 32	     11	  0.00%
 33	      1	  0.00%
 34	      6	  0.00%
 35	      1	  0.00%
 36	      4	  0.00%
 37	      4	  0.00%
 38	     15	  0.00%
 39	     18	  0.00%
 40	     17	  0.00%
 41	      9	  0.00%
 42	     11	  0.00%
 43	     19	  0.00%
 44	     18	  0.00%
 45	     32	  0.00%
 46	     39	  0.00%
 47	     63	  0.00%
 48	    103	  0.01%
 49	    125	  0.01%
 50	    183	  0.01%
 51	    232	  0.02%
 52	    295	  0.02%
 53	    415	  0.03%
 54	    564	  0.04%
 55	    747	  0.06%
 56	   1001	  0.07%
 57	   1484	  0.11%
 58	   1053	  0.08%
 59	   1267	  0.09%
 60	   1478	  0.11%
 61	   1769	  0.13%
 62	   1952	  0.14%
 63	   2113	  0.16%
 64	   2308	  0.17%
 65	   2452	  0.18%
 66	   2416	  0.18%
 67	   2637	  0.19%
 68	   2320	  0.17%
 69	   2361	  0.17%
 70	   9054	  0.67%
 71	   9544	  0.70%
 72	  10868	  0.80%
 73	  11412	  0.84%
 74	  11717	  0.86%
 75	  12576	  0.93%
 76	  13480	  0.99%
 77	  14919	  1.10%
 78	  15422	  1.14%
 79	  16178	  1.19%
 80	  17232	  1.27%
 81	  20185	  1.49%
 82	  21366	  1.58%
 83	  21400	  1.58%
 84	  24436	  1.80%
 85	  17399	  1.28%
 86	  17979	  1.33%
 87	  20097	  1.48%
 88	  23948	  1.77%
 89	  25158	  1.86%
 90	  26490	  1.95%
 91	  28454	  2.10%
 92	  24613	  1.82%
 93	 911705	 67.27%
1355261 reads passed initial QC


criterion=sequence-density
sequence-density=3.96
sequence-density-rank=1
fanout-score=2.04
fanout-score-rank=26
prefix-density=4.06
prefix-fanout=2.0
sequence=CAAGGCTAAATAC


criterion=fanout-score
sequence-density=0.12
sequence-density-rank=15
fanout-score=76.44
fanout-score-rank=1
prefix-density=8.84
prefix-fanout=1.1
sequence=CCGCACCCTAGCTGGCTAAAGTC
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 03:12:17
                             Started mapping on |	Dec 07 03:12:17
                                    Finished on |	Dec 07 03:12:24
       Mapping speed, Million of reads per hour |	696.99

                          Number of input reads |	1355261
                      Average input read length |	89
                                    UNIQUE READS:
                   Uniquely mapped reads number |	551610
                        Uniquely mapped reads % |	40.70%
                          Average mapped length |	88.32
                       Number of splices: Total |	22538
            Number of splices: Annotated (sjdb) |	18231
                       Number of splices: GT/AG |	21533
                       Number of splices: GC/AG |	455
                       Number of splices: AT/AC |	23
               Number of splices: Non-canonical |	527
                      Mismatch rate per base, % |	0.84%
                         Deletion rate per base |	0.04%
                        Deletion average length |	1.70
                        Insertion rate per base |	0.02%
                       Insertion average length |	1.88
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	677191
             % of reads mapped to multiple loci |	49.97%
        Number of reads mapped to too many loci |	51621
             % of reads mapped to too many loci |	3.81%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	4.88%
                     % of reads unmapped: other |	0.65%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	126460	126460	126460
N_multimapping	677191	677191	677191
N_noFeature	53242	59260	527225
N_ambiguous	22440	4047	121
UnstrandedReadsAssigned:475928 PositiveStrandReadsAssigned:488303 NegativeStrandReadsAssigned:24264
Dataset is classified positive stranded
MeadianReadLen=93 20thPercentileLength=84 echo kmer=79
ERR6133398 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: ERR6133398-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 1,355,261 reads, 866,478 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 848 rounds

  52973 ERR6133398.ke.tsv
  35125 ERR6133398.se.tsv
  88098 total
==> ERR6133398.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	6	6.62205
PNS24243	293	194	0	0
KQK14069	1603	1504	5	5.03405
KQK14071	474	375	0	0

==> ERR6133398.se.tsv <==
BRADI_1g14170v3	5
BRADI_1g53295v3	7
BRADI_1g59795v3	8
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	12
BRADI_1g74790v3	4
BRADI_1g09890v3	0
BRADI_1g77505v3	14
BRADI_1g48960v3	0
ERR6133398 completed mapping pipeline successfully
