Starting /dee2/code/volunteer_pipeline.sh ERR6133396
    current disk space = 1547477929984
    free memory = 1434837284 
ERR6133396 SRAfilesize
17605d6ed57f0b89ac90efaa93d2261f  ERR6133396.sra
ERR6133396.sra file validated
ERR6133396 is single end
ERR6133396 is conventional basespace
ERR6133396 read1 length is 70-93 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	ERR6133396_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	28.744	33.0	27.0	33.0	15.0	37.0
2	33.1235	33.0	33.0	37.0	27.0	37.0
3	33.536	37.0	33.0	37.0	27.0	37.0
4	33.67775	37.0	33.0	37.0	27.0	37.0
5	33.8175	37.0	33.0	37.0	27.0	37.0
6	34.253	37.0	33.0	37.0	27.0	37.0
7	35.242	37.0	33.0	37.0	27.0	40.0
8	35.18925	37.0	33.0	40.0	27.0	40.0
9	35.31125	37.0	33.0	37.0	33.0	40.0
10-11	35.213375	37.0	33.0	38.5	27.0	40.0
12-13	34.9755	37.0	33.0	37.0	27.0	40.0
14-15	35.044375	37.0	33.0	37.0	27.0	40.0
16-17	34.911875	37.0	33.0	37.0	27.0	40.0
18-19	34.783375	37.0	33.0	37.0	27.0	40.0
20-21	34.056124999999994	37.0	33.0	37.0	24.5	40.0
22-23	33.5415	37.0	33.0	37.0	22.0	40.0
24-25	33.325500000000005	37.0	33.0	37.0	22.0	40.0
26-27	32.836749999999995	37.0	33.0	37.0	22.0	40.0
28-29	32.609625	33.0	33.0	37.0	22.0	40.0
30-31	32.397625	33.0	33.0	37.0	22.0	40.0
32-33	31.984875	33.0	30.0	37.0	22.0	40.0
34-35	31.203125	33.0	27.0	37.0	15.0	40.0
36-37	30.8265	33.0	27.0	37.0	15.0	38.5
38-39	30.80225	33.0	27.0	37.0	15.0	37.0
40-41	31.00175	33.0	27.0	37.0	18.5	38.5
42-43	30.806375	33.0	27.0	37.0	15.0	40.0
44-45	30.620125	33.0	27.0	37.0	18.5	38.5
46-47	29.955125000000002	33.0	27.0	37.0	15.0	37.0
48-49	29.714375	33.0	27.0	37.0	15.0	37.0
50-51	29.33175	33.0	27.0	37.0	15.0	37.0
52-53	29.098125	33.0	27.0	37.0	15.0	37.0
54-55	29.193	33.0	27.0	37.0	15.0	37.0
56-57	28.509625	33.0	27.0	35.0	15.0	37.0
58-59	28.257125000000002	33.0	24.5	33.0	15.0	37.0
60-61	27.84675	33.0	24.5	33.0	15.0	37.0
62-63	27.472	33.0	22.0	33.0	15.0	37.0
64-65	27.025375	33.0	22.0	33.0	10.5	37.0
66-67	26.693375	27.0	22.0	33.0	6.0	37.0
68-69	25.928	27.0	18.5	33.0	10.5	35.0
70-71	27.845399084295032	33.0	27.0	33.0	15.0	35.0
72-73	28.289697077586624	33.0	27.0	33.0	15.0	37.0
74-75	27.997444334740162	33.0	27.0	33.0	15.0	37.0
76-77	27.930489889877386	33.0	27.0	33.0	15.0	37.0
78-79	27.095654608247735	33.0	24.5	33.0	6.0	37.0
80-81	26.206651604147368	33.0	22.0	33.0	4.0	37.0
82-83	25.36662057256556	33.0	22.0	33.0	2.0	37.0
84-85	24.935966626685545	33.0	18.5	33.0	2.0	37.0
86-87	23.960695187165776	30.0	15.0	33.0	2.0	35.0
88-89	23.40681818181818	30.0	10.5	33.0	2.0	33.0
90-91	21.997593582887703	27.0	2.0	33.0	2.0	33.0
92-93	20.74077540106952	27.0	2.0	33.0	2.0	33.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
20	104.0
21	160.0
22	145.0
23	155.0
24	178.0
25	211.0
26	251.0
27	263.0
28	239.0
29	253.0
30	256.0
31	247.0
32	269.0
33	262.0
34	288.0
35	258.0
36	251.0
37	184.0
38	26.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	69.125	8.475000000000001	8.6	13.8
2	52.349999999999994	23.0	14.975	9.675
3	33.725	35.099999999999994	17.849999999999998	13.325000000000001
4	24.3	32.35	22.35	21.0
5	28.9	23.849999999999998	28.025	19.225
6	15.2	40.300000000000004	25.974999999999998	18.525
7	36.7	27.05	18.9	17.349999999999998
8	24.45	25.650000000000002	24.9	25.0
9	20.275000000000002	34.825	26.075	18.825
10-11	21.224999999999998	28.962500000000002	32.0375	17.775
12-13	19.725	31.724999999999998	26.875	21.675
14-15	18.5625	35.6375	27.237499999999997	18.5625
16-17	25.2125	28.6625	22.5	23.625
18-19	23.724999999999998	23.5875	33.625	19.0625
20-21	26.387500000000003	23.175	31.874999999999996	18.5625
22-23	29.362500000000004	21.0	31.25	18.387500000000003
24-25	22.037499999999998	24.55	30.2375	23.175
26-27	25.4	23.150000000000002	28.999999999999996	22.45
28-29	22.037499999999998	29.562500000000004	30.7375	17.6625
30-31	32.25	24.9	24.887500000000003	17.962500000000002
32-33	26.75	22.912499999999998	27.6	22.7375
34-35	20.825	36.3125	24.025	18.8375
36-37	26.924999999999997	26.1125	23.6375	23.325000000000003
38-39	33.5125	21.9625	26.337500000000002	18.1875
40-41	22.5875	23.4625	35.5375	18.4125
42-43	27.474999999999998	29.599999999999998	25.6125	17.3125
44-45	24.75	25.2	31.0375	19.0125
46-47	27.2625	23.8375	25.587500000000002	23.3125
48-49	26.0625	23.075000000000003	27.425	23.4375
50-51	20.875	30.349999999999998	25.837500000000002	22.9375
52-53	21.837500000000002	25.45	24.8125	27.900000000000002
54-55	21.55	24.925	31.45	22.075
56-57	26.9625	30.0375	25.2	17.8
58-59	20.8625	30.562499999999996	29.562500000000004	19.0125
60-61	31.0125	25.5375	25.7375	17.712500000000002
62-63	19.8125	26.1125	31.587500000000002	22.4875
64-65	19.175	37.6	25.4	17.825
66-67	25.362499999999997	30.9	25.025	18.712500000000002
68-69	19.5875	25.8625	29.562500000000004	24.9875
70-71	22.28900576008014	29.539193588780364	24.655647382920108	23.516153268219384
72-73	25.355838266784232	25.64554729814838	30.369064113868244	18.629550321199144
74-75	26.42131979695431	30.063451776649746	25.926395939086294	17.588832487309645
76-77	21.565863659661712	23.449513070220398	25.909789851358276	29.07483341875961
78-79	25.449838187702266	29.009708737864077	27.28802588996764	18.25242718446602
80-81	20.75816993464052	36.993464052287585	25.084967320261438	17.163398692810457
82-83	23.48044397463002	25.726744186046513	25.21141649048626	25.581395348837212
84-85	20.89671737389912	26.75473712303176	32.2257806244996	20.12276487856952
86-87	20.588235294117645	30.04010695187166	24.665775401069517	24.705882352941178
88-89	18.836898395721924	27.018716577540108	31.44385026737968	22.70053475935829
90-91	25.04010695187166	31.390374331550802	24.31818181818182	19.25133689839572
92-93	18.422459893048128	29.906417112299465	29.53208556149733	22.13903743315508
>>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	0.0
13	0.0
14	0.0
15	0.0
16	0.0
17	2.0
18	4.0
19	4.0
20	2.0
21	1.5
22	4.0
23	6.5
24	6.5
25	9.0
26	13.0
27	16.0
28	25.0
29	31.0
30	30.0
31	38.5
32	45.5
33	54.0
34	71.5
35	86.0
36	116.5
37	184.0
38	223.5
39	199.5
40	219.5
41	229.5
42	217.0
43	231.0
44	219.0
45	191.5
46	143.0
47	116.0
48	113.0
49	109.0
50	113.0
51	113.0
52	109.5
53	138.0
54	264.5
55	259.0
56	119.0
57	78.0
58	55.5
59	32.5
60	25.5
61	23.5
62	20.5
63	11.5
64	7.0
65	7.5
66	8.0
67	7.0
68	7.5
69	8.5
70	6.5
71	4.0
72	2.0
73	0.0
74	0.0
75	0.0
76	0.0
77	0.0
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	14.0
71	7.0
72	19.0
73	13.0
74	14.0
75	20.0
76	22.0
77	19.0
78	19.0
79	21.0
80	14.0
81	23.0
82	22.0
83	19.0
84	14.0
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	3740.0
>>END_MODULE
>>Sequence Duplication Levels	warn
#Total Deduplicated Percentage	68.75
#Duplication Level	Percentage of deduplicated	Percentage of total
1	91.85454545454546	63.14999999999999
2	3.272727272727273	4.5
3	1.6363636363636365	3.375
4	0.8727272727272728	2.4
5	0.6181818181818182	2.125
6	0.32727272727272727	1.35
7	0.14545454545454545	0.7000000000000001
8	0.36363636363636365	2.0
9	0.0	0.0
>10	0.8363636363636363	10.775
>50	0.03636363636363636	1.325
>100	0.03636363636363636	8.3
>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	332	8.3	No Hit
GGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAA	53	1.325	No Hit
GGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGG	42	1.05	No Hit
CAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGATAT	29	0.7250000000000001	No Hit
GGGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAA	29	0.7250000000000001	No Hit
CAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTG	29	0.7250000000000001	No Hit
CAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCT	26	0.65	No Hit
TACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTT	23	0.575	No Hit
TCTCATGGAGAGTTCGATCCTGGCTCAGGATGAACGCTGGCGGCATGCTT	23	0.575	No Hit
CAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTC	22	0.5499999999999999	No Hit
GGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAATGGATTC	19	0.475	No Hit
GTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAG	19	0.475	No Hit
TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGA	19	0.475	No Hit
GGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTC	18	0.44999999999999996	No Hit
GTATTAGTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCT	16	0.4	No Hit
GGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCG	15	0.375	No Hit
CAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTT	13	0.325	No Hit
GGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCA	13	0.325	No Hit
GGATTTGTTAAATCAAATCCTTGGTTTAATAACGAACGGTGTTAACTTAC	13	0.325	No Hit
GTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTT	11	0.27499999999999997	No Hit
GTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCT	11	0.27499999999999997	No Hit
GGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGT	11	0.27499999999999997	No Hit
GTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAA	10	0.25	No Hit
GGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAA	10	0.25	No Hit
GGAAAAGAAAGCAAAAGCGATTCCCGTAGTAGCGGCGAGCGAAATGGGAG	10	0.25	No Hit
GGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAA	8	0.2	No Hit
GCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATC	8	0.2	No Hit
GCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCT	8	0.2	No Hit
CTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGT	8	0.2	No Hit
GGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCT	8	0.2	No Hit
GGGGTTGTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTG	8	0.2	No Hit
GTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAA	8	0.2	No Hit
GAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCTG	8	0.2	No Hit
AACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGA	8	0.2	No Hit
CGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAA	8	0.2	No Hit
GGGTTGTTTGGGAATGCAGCCCAAATCGGGCGGTAGACTCCGTCCAAGGC	7	0.17500000000000002	No Hit
AACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCG	7	0.17500000000000002	No Hit
AGTCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAA	7	0.17500000000000002	No Hit
GGGTGAGAGCCCCGTCCGGCCCGGACCCTGTCGCCCCACGAGGCGCCGTC	7	0.17500000000000002	No Hit
TAGTCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTA	6	0.15	No Hit
ATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGG	6	0.15	No Hit
GATAGTCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGC	6	0.15	No Hit
GTAATGCACGAACGTAATGCTCACAACTTCCCTCTAGATCTAGCTGCTCT	6	0.15	No Hit
GATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAACGTAA	6	0.15	No Hit
GGAGTATCCTTGATATATAAATATATAGATAAATAGATTTAAATGGAAAA	6	0.15	No Hit
GAAGGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGC	6	0.15	No Hit
GAACGTAATGCTCACAACTTCCCTCTAGATCTAGCTGCTCTTGAAGTTCC	6	0.15	No Hit
GCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGT	6	0.15	No Hit
GGGTATCCATGCCAGGTGTTATACCAGTAGCTTCAGGTGGTATTCATGTT	5	0.125	No Hit
GGAGTCCTGAACTAGCCGCAGCTTGTGAAGTATGGAAGGCGATCAAATTC	5	0.125	No Hit
GGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAAC	5	0.125	No Hit
GGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTGTACAAGCTCGTAA	5	0.125	No Hit
GTAACGAAGGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCA	5	0.125	No Hit
GGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTT	5	0.125	No Hit
GGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAA	5	0.125	No Hit
GTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGGT	5	0.125	No Hit
GATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAAT	5	0.125	No Hit
GGCCTGTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCG	5	0.125	No Hit
GAAGCCTGTGTACAAGCTCGTAACGAAGGGCGCGATCTTGCTCGTGAAGG	5	0.125	No Hit
GTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCC	5	0.125	No Hit
GTCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGG	5	0.125	No Hit
GTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGGTATGGA	5	0.125	No Hit
GGGGAGTTGAAAATAAGCATAGATCCGGAGATTCCCAAATAGGTCAACCT	5	0.125	No Hit
GGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTA	5	0.125	No Hit
TCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCT	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	0.0	0.0	0.0	0.0	0.0
70-71	0.0	0.0	0.0	0.0	0.0
72-73	0.0	0.0	0.0	0.0	0.0
74-75	0.0	0.0	0.0	0.0	0.0
76-77	0.0	0.0	0.0	0.0	0.0
78-79	0.0	0.0	0.0	0.0	0.0
80-81	0.0	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
AGAGCAA	35	5.5606506E-8	73.60714	4
GGAGAGC	40	1.4029138E-7	64.40625	2
GGGAGAG	40	1.4029138E-7	64.40625	1
CAATACA	40	1.4029138E-7	64.40625	8
GAGCAAT	40	1.4029138E-7	64.40625	5
AATACAA	40	1.4029138E-7	64.40625	9
AGCAATA	40	1.4029138E-7	64.40625	6
GCAATAC	45	3.1700074E-7	57.250004	7
GAGAGCA	45	3.1700074E-7	57.250004	3
TGCTGCT	30	2.6342168E-6	42.9375	22-23
GCTGCTA	30	2.6342168E-6	42.9375	22-23
TGCTAGG	30	2.6342168E-6	42.9375	24-25
CTGCTAG	30	2.6342168E-6	42.9375	24-25
GTGCTGC	30	2.6342168E-6	42.9375	20-21
AAAAAAA	25	0.001695651	37.135136	86-87
GCTAGGC	35	7.600218E-6	36.80357	26-27
AGGCGAA	35	7.600218E-6	36.80357	28-29
CTAGGCG	35	7.600218E-6	36.80357	26-27
TACAAGC	35	7.600218E-6	36.80357	10-11
AAGCGTT	35	7.600218E-6	36.80357	14-15
>>END_MODULE
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25928 READS because READLEN < 1
Read 25928 spots for ERR6133396.sra
Written 25928 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
Rejected 25913 READS because READLEN < 1
Read 25913 spots for ERR6133396.sra
Written 25913 spots for ERR6133396.sra
SRR ids: ['ERR6133396.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_hjcqtyys
ERR6133396.sra spots: 518275
blocks: [[1, 25913], [25914, 51826], [51827, 77739], [77740, 103652], [103653, 129565], [129566, 155478], [155479, 181391], [181392, 207304], [207305, 233217], [233218, 259130], [259131, 285043], [285044, 310956], [310957, 336869], [336870, 362782], [362783, 388695], [388696, 414608], [414609, 440521], [440522, 466434], [466435, 492347], [492348, 518275]]
ERR6133396 file size 113173
ERR6133396 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 ERR6133396 ERR6133396_1.fastq
Input file:	ERR6133396_1.fastq
trimmed:	ERR6133396-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 03:04:04 2024 >> started

Sat Dec  7 03:04:05 2024 >> done (0.717s)
518275 reads processed; of these:
     8 ( 0.00%) short reads filtered out after trimming by size control
     1 ( 0.00%) empty reads filtered out after trimming by size control
518266 (100.00%) reads available; of these:
137843 (26.60%) trimmed reads available after processing
380423 (73.40%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	     2	  0.00%
 19	     2	  0.00%
 20	     0	  0.00%
 21	     0	  0.00%
 22	     1	  0.00%
 23	     1	  0.00%
 24	     1	  0.00%
 25	     0	  0.00%
 26	     0	  0.00%
 27	     1	  0.00%
 28	     1	  0.00%
 29	    22	  0.00%
 30	     0	  0.00%
 31	     1	  0.00%
 32	     1	  0.00%
 33	     2	  0.00%
 34	     1	  0.00%
 35	     0	  0.00%
 36	     2	  0.00%
 37	     1	  0.00%
 38	     7	  0.00%
 39	     6	  0.00%
 40	     4	  0.00%
 41	     6	  0.00%
 42	     4	  0.00%
 43	     6	  0.00%
 44	     7	  0.00%
 45	    17	  0.00%
 46	    19	  0.00%
 47	    20	  0.00%
 48	    26	  0.01%
 49	    41	  0.01%
 50	    50	  0.01%
 51	    63	  0.01%
 52	   101	  0.02%
 53	   146	  0.03%
 54	   217	  0.04%
 55	   271	  0.05%
 56	   380	  0.07%
 57	   562	  0.11%
 58	   431	  0.08%
 59	   492	  0.09%
 60	   661	  0.13%
 61	   717	  0.14%
 62	   789	  0.15%
 63	   859	  0.17%
 64	   956	  0.18%
 65	   964	  0.19%
 66	  1052	  0.20%
 67	  1046	  0.20%
 68	   910	  0.18%
 69	   929	  0.18%
 70	  3011	  0.58%
 71	  3129	  0.60%
 72	  3717	  0.72%
 73	  3970	  0.77%
 74	  4201	  0.81%
 75	  4584	  0.88%
 76	  4789	  0.92%
 77	  5480	  1.06%
 78	  5652	  1.09%
 79	  5742	  1.11%
 80	  6216	  1.20%
 81	  7037	  1.36%
 82	  7446	  1.44%
 83	  7912	  1.53%
 84	  8739	  1.69%
 85	  6887	  1.33%
 86	  7120	  1.37%
 87	  7886	  1.52%
 88	  9727	  1.88%
 89	  9971	  1.92%
 90	 10736	  2.07%
 91	 11258	  2.17%
 92	  9899	  1.91%
 93	351359	 67.80%
518266 reads passed initial QC


criterion=sequence-density
sequence-density=2.51
sequence-density-rank=1
fanout-score=2.06
fanout-score-rank=23
prefix-density=2.58
prefix-fanout=2.0
sequence=CAAGGCTAAATAC


criterion=fanout-score
sequence-density=0.13
sequence-density-rank=20
fanout-score=102.81
fanout-score-rank=1
prefix-density=12.54
prefix-fanout=1.0
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 03:04:24
                             Started mapping on |	Dec 07 03:04:25
                                    Finished on |	Dec 07 03:04:31
       Mapping speed, Million of reads per hour |	310.96

                          Number of input reads |	518266
                      Average input read length |	89
                                    UNIQUE READS:
                   Uniquely mapped reads number |	183372
                        Uniquely mapped reads % |	35.38%
                          Average mapped length |	88.31
                       Number of splices: Total |	8222
            Number of splices: Annotated (sjdb) |	6466
                       Number of splices: GT/AG |	7796
                       Number of splices: GC/AG |	131
                       Number of splices: AT/AC |	6
               Number of splices: Non-canonical |	289
                      Mismatch rate per base, % |	0.87%
                         Deletion rate per base |	0.04%
                        Deletion average length |	1.74
                        Insertion rate per base |	0.02%
                       Insertion average length |	1.85
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	292490
             % of reads mapped to multiple loci |	56.44%
        Number of reads mapped to too many loci |	12544
             % of reads mapped to too many loci |	2.42%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	5.37%
                     % of reads unmapped: other |	0.39%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	42404	42404	42404
N_multimapping	292490	292490	292490
N_noFeature	17495	19543	175440
N_ambiguous	7142	1253	40
UnstrandedReadsAssigned:158735 PositiveStrandReadsAssigned:162576 NegativeStrandReadsAssigned:7892
Dataset is classified positive stranded
MeadianReadLen=93 20thPercentileLength=86 echo kmer=81
ERR6133396 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: ERR6133396-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 518,266 reads, 320,913 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 725 rounds

  52973 ERR6133396.ke.tsv
  35125 ERR6133396.se.tsv
  88098 total
==> ERR6133396.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	4	11.8369
PNS24243	293	194	0	0
KQK14069	1603	1504	2	5.39902
KQK14071	474	375	0	0

==> ERR6133396.se.tsv <==
BRADI_1g14170v3	2
BRADI_1g53295v3	3
BRADI_1g59795v3	0
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	3
BRADI_1g74790v3	4
BRADI_1g09890v3	0
BRADI_1g77505v3	4
BRADI_1g48960v3	0
ERR6133396 completed mapping pipeline successfully
