Starting /dee2/code/volunteer_pipeline.sh SRR6941583
    current disk space = 1551432118272
    free memory = 1599734672 
SRR6941583 SRAfilesize
fc1d0aca48aabd8c2a118d5f0be67f3b  SRR6941583.sra
SRR6941583.sra file validated
SRR6941583 is single end
SRR6941583 is conventional basespace
SRR6941583 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR6941583_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	101
%GC	47
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	33.13825	34.0	33.0	34.0	32.0	34.0
2	33.25625	34.0	33.0	34.0	32.0	34.0
3	32.68425	34.0	33.0	34.0	30.0	34.0
4	33.13075	34.0	33.0	34.0	32.0	34.0
5	33.15725	34.0	33.0	34.0	31.0	34.0
6	36.94175	38.0	37.0	38.0	36.0	38.0
7	37.31575	38.0	38.0	38.0	37.0	38.0
8	37.5425	38.0	38.0	38.0	37.0	38.0
9	37.55675	38.0	38.0	38.0	37.0	38.0
10-11	37.4795	38.0	38.0	38.0	37.0	38.0
12-13	37.431125	38.0	38.0	38.0	37.0	38.0
14-15	37.4405	38.0	38.0	38.0	37.0	38.0
16-17	36.258624999999995	38.0	37.5	38.0	32.0	38.0
18-19	36.933125000000004	38.0	38.0	38.0	34.5	38.0
20-21	35.8855	38.0	37.5	38.0	29.5	38.0
22-23	37.060125	38.0	38.0	38.0	35.5	38.0
24-25	37.379125	38.0	38.0	38.0	37.0	38.0
26-27	37.304625	38.0	38.0	38.0	37.0	38.0
28-29	37.37875	38.0	38.0	38.0	37.0	38.0
30-31	37.345875	38.0	38.0	38.0	37.0	38.0
32-33	37.191374999999994	38.0	38.0	38.0	36.5	38.0
34-35	37.02975	38.0	38.0	38.0	36.5	38.0
36-37	36.947	38.0	38.0	38.0	36.0	38.0
38-39	36.9925	38.0	38.0	38.0	36.0	38.0
40-41	36.98775	38.0	38.0	38.0	36.0	38.0
42-43	36.900625000000005	38.0	38.0	38.0	35.5	38.0
44-45	36.747749999999996	38.0	38.0	38.0	35.0	38.0
46-47	36.560375	38.0	38.0	38.0	34.0	38.0
48-49	36.803375	38.0	38.0	38.0	35.0	38.0
50-51	36.515375	38.0	38.0	38.0	34.0	38.0
52-53	36.383750000000006	38.0	38.0	38.0	33.5	38.0
54-55	36.711749999999995	38.0	38.0	38.0	34.5	38.0
56-57	36.6845	38.0	38.0	38.0	34.5	38.0
58-59	36.767250000000004	38.0	38.0	38.0	35.0	38.0
60-61	36.691125	38.0	38.0	38.0	35.0	38.0
62-63	35.931125	38.0	37.0	38.0	31.0	38.0
64-65	35.15712499999999	38.0	36.5	38.0	28.0	38.0
66-67	34.741375000000005	38.0	35.0	38.0	21.5	38.0
68-69	35.3955	38.0	37.0	38.0	28.5	38.0
70-71	34.714124999999996	38.0	35.5	38.0	26.0	38.0
72-73	33.90575	38.0	33.5	38.0	20.0	38.0
74-75	33.35525	37.5	33.0	38.0	15.0	38.0
76-77	33.8245	37.5	33.5	38.0	24.5	38.0
78-79	33.813625	37.5	33.5	38.0	24.5	38.0
80-81	34.271	37.5	34.0	38.0	25.0	38.0
82-83	33.72525	37.0	33.5	38.0	20.0	38.0
84-85	33.415875	37.0	33.0	38.0	19.5	38.0
86-87	33.604875	37.5	33.5	38.0	15.0	38.0
88-89	34.533874999999995	38.0	34.5	38.0	26.0	38.0
90-91	34.926874999999995	38.0	35.0	38.0	27.0	38.0
92-93	34.903375	38.0	36.0	38.0	27.0	38.0
94-95	35.242125	38.0	37.0	38.0	29.0	38.0
96-97	34.072625	38.0	35.5	38.0	24.5	38.0
98-99	32.345875	38.0	34.0	38.0	8.5	38.0
100-101	29.785375000000002	38.0	27.0	38.0	2.0	38.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
3	1.0
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
10	0.0
11	1.0
12	0.0
13	0.0
14	2.0
15	0.0
16	1.0
17	0.0
18	0.0
19	3.0
20	0.0
21	2.0
22	7.0
23	6.0
24	9.0
25	14.0
26	12.0
27	21.0
28	34.0
29	42.0
30	66.0
31	68.0
32	120.0
33	180.0
34	331.0
35	650.0
36	1304.0
37	1126.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	32.800000000000004	24.075	16.900000000000002	26.224999999999998
2	30.207551887971995	32.38309577394349	18.504626156539132	18.904726181545385
3	31.275	19.825	26.75	22.15
4	27.925	30.5	13.4	28.175
5	39.75	18.575	21.375	20.3
6	20.1	38.2	22.900000000000002	18.8
7	43.025000000000006	21.275	20.575	15.125
8	21.2	17.724999999999998	42.875	18.2
9	18.075	43.25	18.2	20.474999999999998
10-11	36.2375	27.8875	19.2625	16.6125
12-13	17.0	17.375	22.45	43.175000000000004
14-15	20.2125	38.1625	26.437500000000004	15.187500000000002
16-17	26.887499999999996	17.6625	40.637499999999996	14.8125
18-19	38.625	22.3125	24.825	14.2375
20-21	14.374999999999998	27.450000000000003	36.6375	21.5375
22-23	32.6625	27.762500000000003	23.5375	16.037499999999998
24-25	31.8625	28.999999999999996	25.0375	14.099999999999998
26-27	40.5625	26.0	19.037499999999998	14.399999999999999
28-29	15.225	40.2625	23.275000000000002	21.2375
30-31	19.85	9.762500000000001	47.5625	22.825
32-33	32.1125	11.525	28.199999999999996	28.1625
34-35	37.075	21.475	24.9125	16.537499999999998
36-37	43.3375	17.2375	27.500000000000004	11.924999999999999
38-39	23.9125	18.3	34.9875	22.8
40-41	23.35	15.6375	21.675	39.3375
42-43	36.025	27.900000000000002	16.9375	19.1375
44-45	53.05	15.275	14.124999999999998	17.549999999999997
46-47	26.8	29.7375	15.462500000000002	28.000000000000004
48-49	19.6125	26.1125	18.0	36.275
50-51	28.050000000000004	24.825	7.95	39.175
52-53	27.55	44.5125	7.062499999999999	20.875
54-55	16.7625	25.4625	21.4875	36.2875
56-57	12.962499999999999	29.95	12.675	44.4125
58-59	22.575	22.025	16.45	38.95
60-61	15.387500000000001	28.349999999999998	24.675	31.587500000000002
62-63	21.1375	21.4375	17.724999999999998	39.7
64-65	16.075	23.3875	27.737499999999997	32.800000000000004
66-67	15.137500000000001	18.387500000000003	27.925	38.550000000000004
68-69	28.875	18.45	20.3625	32.3125
70-71	18.3125	27.825	32.324999999999996	21.5375
72-73	24.325	14.787500000000001	31.974999999999998	28.9125
74-75	19.2625	9.225	27.8125	43.7
76-77	20.7	12.025	44.6	22.675
78-79	19.787499999999998	8.475000000000001	41.875	29.862499999999997
80-81	20.1	9.4625	34.675	35.7625
82-83	28.125	6.9125000000000005	39.675	25.2875
84-85	19.075	8.5875	38.45	33.887499999999996
86-87	18.912499999999998	17.549999999999997	40.362500000000004	23.175
88-89	13.0375	39.025	30.9625	16.975
90-91	8.9	43.275000000000006	30.162499999999998	17.6625
92-93	16.3875	49.3625	22.5125	11.737499999999999
94-95	9.762500000000001	66.5	17.1875	6.550000000000001
96-97	7.825	80.33749999999999	9.625	2.2125
98-99	3.5749999999999997	92.525	3.05	0.8500000000000001
100-101	1.0250000000000001	96.55	1.575	0.8500000000000001
>>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	0.0
18	0.0
19	0.0
20	0.0
21	0.0
22	0.0
23	0.0
24	0.0
25	0.0
26	0.0
27	0.0
28	0.0
29	0.0
30	0.0
31	0.0
32	0.5
33	2.0
34	1.5
35	1.0
36	5.0
37	5.0
38	1.0
39	2.5
40	13.5
41	27.5
42	59.5
43	152.0
44	264.0
45	510.5
46	586.5
47	419.5
48	384.0
49	300.0
50	180.5
51	227.0
52	305.0
53	261.0
54	133.0
55	44.5
56	40.0
57	30.0
58	12.5
59	13.0
60	11.0
61	3.5
62	2.0
63	0.5
64	0.0
65	0.0
66	0.5
67	0.5
68	0.0
69	0.0
70	0.0
71	0.0
72	0.0
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	0.025
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
94-95	0.0
96-97	0.0
98-99	0.0
100-101	0.0
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
101	4000.0
>>END_MODULE
>>Sequence Duplication Levels	warn
#Total Deduplicated Percentage	50.724999999999994
#Duplication Level	Percentage of deduplicated	Percentage of total
1	89.15722030556925	45.225
2	4.2878265155248885	4.35
3	1.4785608674223756	2.25
4	1.1828486939379004	2.4
5	0.5421389847215378	1.375
6	0.4928536224741252	1.5
7	0.4928536224741252	1.7500000000000002
8	0.14785608674223755	0.6
9	0.2957121734844751	1.35
>10	1.3799901429275505	13.775
>50	0.2957121734844751	9.675
>100	0.2464268112370626	15.75
>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
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	157	3.925	No Hit
GAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAG	132	3.3000000000000003	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	129	3.225	No Hit
CTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	109	2.725	RNA PCR Primer, Index 1 (100% over 28bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTGGAATTCTCGGGTGCCAAGG	103	2.5749999999999997	Illumina Small RNA Adapter 2 (100% over 21bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTTGGAATTCTCGGGTG	91	2.275	No Hit
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	66	1.6500000000000001	RNA PCR Primer, Index 1 (100% over 29bp)
TCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTC	65	1.625	RNA PCR Primer, Index 1 (100% over 26bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTGGAATTCTCGGGTGCCAA	57	1.425	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	55	1.375	No Hit
TGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAA	53	1.325	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTTGGAATTCTCGGGTGC	41	1.0250000000000001	No Hit
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTTGGAATTCTCGGGTGCC	39	0.975	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTGGAATTCTCGGGTGCCA	35	0.8750000000000001	No Hit
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTGGAATTCTCGGGTGCCA	30	0.75	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTTGGAATTCTCGGGTGCCAAG	30	0.75	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTTGGAATTCTCGGGTGCCA	30	0.75	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGG	28	0.7000000000000001	Illumina Small RNA Adapter 2 (100% over 21bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGGAATTCTCGGGTGC	22	0.5499999999999999	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATATGGAATTCTCGGGTGCCAAG	22	0.5499999999999999	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTGGAATTCTCGGGTGCCAAGG	22	0.5499999999999999	Illumina Small RNA Adapter 2 (100% over 21bp)
TCCGTCGTAGTCTAGGTGGTTAGGATACTCTGGAATTCTCGGGTGCCAAG	21	0.525	No Hit
CGGTCGAGGGCACGCCTGCCTGGGCGTCACGCTGGAATTCTCGGGTGCCA	18	0.44999999999999996	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGTGGAATTCTCGGGTGCC	18	0.44999999999999996	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCTGGAATTCTCGGGTGC	17	0.42500000000000004	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATGGAATTCTCGGGTGCCAAGGA	17	0.42500000000000004	RNA PCR Primer, Index 1 (100% over 22bp)
TAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAG	17	0.42500000000000004	RNA PCR Primer, Index 1 (100% over 29bp)
GAAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTGC	16	0.4	No Hit
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTTGGAATTCTCGGGTGC	16	0.4	No Hit
TCCTCAGTAGCTCAGTGGTAGAGCGGTCGGCTTGGAATTCTCGGGTGCCA	14	0.35000000000000003	No Hit
TTGACAGAAGAGAGTGAGCACTGGAATTCTCGGGTGCCAAGGAACTCCAG	13	0.325	RNA PCR Primer, Index 1 (100% over 29bp)
GGGTGTTTGGTCTAGTGGTATGATTCTCGCTTGGAATTCTCGGGTGCCAA	11	0.27499999999999997	No Hit
CATCGAGTAGACCTTGTTATTGTGAGATGGAATTCTCGGGTGCCAAGGAA	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 23bp)
CATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAAC	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 24bp)
GAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGTCAC	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 33bp)
ATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACT	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 25bp)
AGAAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTG	10	0.25	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCTGGAATTCTCGGGTGCCAAGG	10	0.25	Illumina Small RNA Adapter 2 (100% over 21bp)
TGTCGTGCCAATTCAACATAAACCCCTGGAATTCTCGGGTGCCAAGGAAC	10	0.25	RNA PCR Primer, Index 1 (100% over 24bp)
GAACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 26bp)
TCGGACCAGGCTTCGATCCCTTGGAATTCTCGGGTGCCAAGGAACTCCAG	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 29bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTAATGGAATTCTCGGGTGC	9	0.22499999999999998	No Hit
ACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCCA	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 28bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAATGGAATTCTCGGGTG	9	0.22499999999999998	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTATGGAATTCTCGGGTGCCAA	9	0.22499999999999998	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTGGAATTCTCGGGTG	8	0.2	No Hit
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTTGGAATTCTCGGGTGC	8	0.2	No Hit
AGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGG	8	0.2	Illumina Small RNA Adapter 2 (100% over 21bp)
TCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 24bp)
AGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTCC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 27bp)
CGAACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACT	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 25bp)
TGTCGTGCCAATTCAACATAAACCCTGGAATTCTCGGGTGCCAAGGAACT	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 25bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCAATGGAATTCTCGGGTGCC	7	0.17500000000000002	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGCCAAGGATGGAATTCTC	7	0.17500000000000002	No Hit
ACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 31bp)
CTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCCAG	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 29bp)
TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCGTACGATCTCGTATGC	7	0.17500000000000002	RNA PCR Primer, Index 22 (100% over 50bp)
CAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 26bp)
CACGACTCTCGGCAACGGATATCTCGGCTCTTGGAATTCTCGGGTGCCAA	6	0.15	No Hit
GGGATTGTAGTTCAATTGGACAGAGCACCGCCCTGGAATTCTCGGGTGCC	6	0.15	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAAATGGAATTCTCGGGT	6	0.15	No Hit
GACACGACTCTCGGCAACGGATATCTCGGCTTGGAATTCTCGGGTGCCAA	6	0.15	No Hit
TGACAGAAGAGAGTGAGCACTGGAATTCTCGGGTGCCAAGGAACTCCAGT	6	0.15	RNA PCR Primer, Index 1 (100% over 30bp)
GGCGGATGTAGCCAAGTGGTTCAAGGCAGTGGATTTGGAATTCTCGGGTG	6	0.15	No Hit
GACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAAC	6	0.15	RNA PCR Primer, Index 1 (100% over 24bp)
CCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCC	6	0.15	RNA PCR Primer, Index 1 (100% over 27bp)
ACGAACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAAC	6	0.15	RNA PCR Primer, Index 1 (100% over 24bp)
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTGTTGGAATTCTCGGGT	6	0.15	No Hit
AGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGC	5	0.125	No Hit
GCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTCCA	5	0.125	RNA PCR Primer, Index 1 (100% over 28bp)
AACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
ATATTGGGTAGGTTGTGGTATTTCATTGCTATGGAATTCTCGGGTGCCAA	5	0.125	No Hit
AACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGTCACC	5	0.125	RNA PCR Primer, Index 2 (100% over 34bp)
GGTAGTTCGACCGCGGAATTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	5	0.125	RNA PCR Primer, Index 1 (100% over 31bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTAAATGGAATTCTCGGGTGCC	5	0.125	No Hit
AACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGT	5	0.125	RNA PCR Primer, Index 1 (100% over 30bp)
GGGATTGTAGTTCAATTGGTGAGAGCACCGCCCTGGAATTCTCGGGTGCC	5	0.125	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGGAATTCTCGGGTGCCAA	5	0.125	No Hit
TGAACCTTGGGGAAAAGCCGCCTTGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
>>END_MODULE
>>Adapter Content	fail
#Position	Illumina Universal Adapter	Illumina Small RNA 3' Adapter	Illumina Small RNA 5' Adapter	Nextera Transposase Sequence	SOLID Small RNA Adapter
1	0.0	0.225	0.0	0.0	0.0
2	0.0	0.225	0.0	0.0	0.0
3	0.0	0.225	0.0	0.0	0.0
4	0.0	0.225	0.0	0.0	0.0
5	0.0	0.225	0.0	0.0	0.0
6	0.0	0.225	0.0	0.0	0.0
7	0.0	0.25	0.0	0.0	0.0
8	0.0	0.275	0.0	0.0	0.0
9	0.0	0.275	0.0	0.0	0.0
10-11	0.0	0.275	0.0	0.0	0.0
12-13	0.0	0.30000000000000004	0.0	0.0	0.0
14-15	0.0	0.38749999999999996	0.0	0.0	0.0
16-17	0.0	0.825	0.0	0.0	0.0
18-19	0.0	1.6875	0.0	0.0	0.0
20-21	0.0	3.2	0.0	0.0	0.0
22-23	0.0	11.9625	0.0	0.0	0.0
24-25	0.0	26.862499999999997	0.0	0.0	0.0
26-27	0.0	40.125	0.0	0.0	0.0
28-29	0.0	43.9	0.0	0.0	0.0
30-31	0.0	56.9375	0.0	0.0	0.0
32-33	0.0	71.425	0.0	0.0	0.0
34-35	0.0	85.8625	0.0	0.0	0.0
36-37	0.0	93.9125	0.0	0.0	0.0
38-39	0.0	95.9	0.0	0.0	0.0
40-41	0.0	96.5875	0.0	0.0	0.0
42-43	0.0	97.2625	0.0	0.0	0.0
44-45	0.0	97.5125	0.0	0.0	0.0
46-47	0.0	97.675	0.0	0.0	0.0
48-49	0.0	97.725	0.0	0.0	0.0
50-51	0.0	97.725	0.0	0.0	0.0
52-53	0.0	97.725	0.0	0.0	0.0
54-55	0.0	97.725	0.0	0.0	0.0
56-57	0.0	97.725	0.0	0.0	0.0
58-59	0.0	97.725	0.0	0.0	0.0
60-61	0.0	97.725	0.0	0.0	0.0
62-63	0.0	97.725	0.0	0.0	0.0
64-65	0.0	97.725	0.0	0.0	0.0
66-67	0.0	97.725	0.0	0.0	0.0
68-69	0.0	97.725	0.0	0.0	0.0
70-71	0.0	97.725	0.0	0.0	0.0
72-73	0.0	97.725	0.0	0.0	0.0
74-75	0.0	97.725	0.0	0.0	0.0
76-77	0.0	97.725	0.0	0.0	0.0
78-79	0.0	97.725	0.0	0.0	0.0
80-81	0.0	97.7375	0.0	0.0	0.0
82-83	0.0	97.75	0.0	0.0	0.0
84-85	0.0	97.7625	0.0	0.0	0.0
86-87	0.0	97.775	0.0	0.0	0.0
88-89	0.0	97.775	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGATGTA	20	1.5392321E-5	95.00001	4
GATGTAG	20	1.5392321E-5	95.00001	5
TAGCCAA	20	1.5392321E-5	95.00001	9
GGATTGT	40	5.456968E-12	95.00001	2
CGGATGT	20	1.5392321E-5	95.00001	3
GATTGTA	40	5.456968E-12	95.00001	3
ATTGTAG	40	5.456968E-12	95.00001	4
TGTAGCC	20	1.5392321E-5	95.00001	7
ATGTAGC	20	1.5392321E-5	95.00001	6
GTAGCCA	20	1.5392321E-5	95.00001	8
GGCGGAT	20	1.5392321E-5	95.00001	1
GTAGACC	60	0.0	95.0	7
TTGTAGT	45	0.0	95.0	5
AGTAGAC	60	0.0	95.0	6
TAGTTCA	50	0.0	95.0	8
GAGTAGA	60	0.0	95.0	5
CGAGTAG	60	0.0	95.0	4
AGACCTT	60	0.0	95.0	9
ATCGAGT	60	0.0	95.0	2
TCGAGTA	60	0.0	95.0	3
>>END_MODULE
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261630 READS because READLEN < 1
Read 261630 spots for SRR6941583.sra
Written 261630 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
Rejected 261618 READS because READLEN < 1
Read 261618 spots for SRR6941583.sra
Written 261618 spots for SRR6941583.sra
SRR ids: ['SRR6941583.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_vhwh7mkf
SRR6941583.sra spots: 5232372
blocks: [[1, 261618], [261619, 523236], [523237, 784854], [784855, 1046472], [1046473, 1308090], [1308091, 1569708], [1569709, 1831326], [1831327, 2092944], [2092945, 2354562], [2354563, 2616180], [2616181, 2877798], [2877799, 3139416], [3139417, 3401034], [3401035, 3662652], [3662653, 3924270], [3924271, 4185888], [4185889, 4447506], [4447507, 4709124], [4709125, 4970742], [4970743, 5232372]]
SRR6941583 file size 1249716
SRR6941583 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 SRR6941583 SRR6941583_1.fastq
Input file:	SRR6941583_1.fastq
trimmed:	SRR6941583-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
Fri Dec  6 12:08:45 2024 >> started

Fri Dec  6 12:08:49 2024 >> done (3.737s)
5232372 reads processed; of these:
     63 ( 0.00%) short reads filtered out after trimming by size control
      7 ( 0.00%) empty reads filtered out after trimming by size control
5232302 (100.00%) reads available; of these:
 619638 (11.84%) trimmed reads available after processing
4612664 (88.16%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	     10	  0.00%
 19	      7	  0.00%
 20	      6	  0.00%
 21	      9	  0.00%
 22	     11	  0.00%
 23	      8	  0.00%
 24	     14	  0.00%
 25	     17	  0.00%
 26	     16	  0.00%
 27	     22	  0.00%
 28	     18	  0.00%
 29	     50	  0.00%
 30	     43	  0.00%
 31	     45	  0.00%
 32	     68	  0.00%
 33	     35	  0.00%
 34	     71	  0.00%
 35	     48	  0.00%
 36	     43	  0.00%
 37	     44	  0.00%
 38	     43	  0.00%
 39	     55	  0.00%
 40	     74	  0.00%
 41	     65	  0.00%
 42	     68	  0.00%
 43	     73	  0.00%
 44	     48	  0.00%
 45	     95	  0.00%
 46	     95	  0.00%
 47	     89	  0.00%
 48	     64	  0.00%
 49	     68	  0.00%
 50	     40	  0.00%
 51	     72	  0.00%
 52	     40	  0.00%
 53	     59	  0.00%
 54	     67	  0.00%
 55	     70	  0.00%
 56	     76	  0.00%
 57	     97	  0.00%
 58	    100	  0.00%
 59	    109	  0.00%
 60	    128	  0.00%
 61	    136	  0.00%
 62	    128	  0.00%
 63	    110	  0.00%
 64	    124	  0.00%
 65	    116	  0.00%
 66	    156	  0.00%
 67	    210	  0.00%
 68	    270	  0.01%
 69	    278	  0.01%
 70	    358	  0.01%
 71	    354	  0.01%
 72	    519	  0.01%
 73	    855	  0.02%
 74	   2490	  0.05%
 75	   1825	  0.03%
 76	    884	  0.02%
 77	    415	  0.01%
 78	    493	  0.01%
 79	    460	  0.01%
 80	    497	  0.01%
 81	    481	  0.01%
 82	    603	  0.01%
 83	    714	  0.01%
 84	   1173	  0.02%
 85	   1637	  0.03%
 86	   1931	  0.04%
 87	   2263	  0.04%
 88	   2529	  0.05%
 89	   3444	  0.07%
 90	   3995	  0.08%
 91	   6045	  0.12%
 92	   8489	  0.16%
 93	  14395	  0.28%
 94	  25092	  0.48%
 95	  54869	  1.05%
 96	  60387	  1.15%
 97	  73968	  1.41%
 98	  91647	  1.75%
 99	 151502	  2.90%
100	 101516	  1.94%
101	4612664	 88.16%
5232302 reads passed initial QC


criterion=sequence-density
sequence-density=97.65
sequence-density-rank=1
fanout-score=21.75
fanout-score-rank=1
prefix-density=97.94
prefix-fanout=21.7
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCGTACGATCTCGTATGCCGTCTTCTGCTTGAAAAA


criterion=fanout-score
sequence-density=97.65
sequence-density-rank=1
fanout-score=21.75
fanout-score-rank=1
prefix-density=97.94
prefix-fanout=21.7
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCGTACGATCTCGTATGCCGTCTTCTGCTTGAAAAA
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:
    1 (100.00%) aligned 0 times
    0 (0.00%) aligned exactly 1 time
    0 (0.00%) aligned >1 times
0.00% overall alignment rate
Adapter seq not found in reference. Now shuffling file before clipping
skewer v0.2.2 [April 4, 2016]
COMMAND LINE:	skewer -f sanger -l 18 -t 20 -x TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCGTACGATCTCGTATGCCGTCTTCTGCTTGAAAAA -o SRR6941583 -
Input file:	STDIN
trimmed:	SRR6941583-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCGTACGATCTCGTATGCCGTCTTCTGCTTGA
-- maximum error ratio allowed (-r):	0.100
-- maximum indel error ratio allowed (-d):	0.030
-- minimum read length allowed after trimming (-l):	18
-- file format (-f):		Sanger/Illumina 1.8+ FASTQ 
-- minimum overlap length for adapter detection (-k):	3
-- number of concurrent threads (-t):	20
Fri Dec  6 12:09:05 2024 >> started

Fri Dec  6 12:09:11 2024 >> done (5.823s)
5125520 reads processed; of these:
  56536 ( 1.10%) short reads filtered out after trimming by size control
  16740 ( 0.33%) empty reads filtered out after trimming by size control
5052244 (98.57%) reads available; of these:
5021306 (99.39%) trimmed reads available after processing
  30938 ( 0.61%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  19829	  0.39%
 19	  45972	  0.91%
 20	  58707	  1.16%
 21	 286905	  5.68%
 22	 263171	  5.21%
 23	 148587	  2.94%
 24	1003025	 19.85%
 25	 136926	  2.71%
 26	 117033	  2.32%
 27	  94129	  1.86%
 28	 102677	  2.03%
 29	 324856	  6.43%
 30	 538584	 10.66%
 31	 325730	  6.45%
 32	 372537	  7.37%
 33	 430845	  8.53%
 34	 275395	  5.45%
 35	 252519	  5.00%
 36	  84939	  1.68%
 37	  41030	  0.81%
 38	  20231	  0.40%
 39	  13357	  0.26%
 40	  18352	  0.36%
 41	  18030	  0.36%
 42	  14014	  0.28%
 43	   3326	  0.07%
 44	   3605	  0.07%
 45	   3316	  0.07%
 46	    977	  0.02%
 47	   1432	  0.03%
 48	    505	  0.01%
 49	    205	  0.00%
 50	     98	  0.00%
 51	     81	  0.00%
 52	     33	  0.00%
 53	     51	  0.00%
 54	     45	  0.00%
 55	     29	  0.00%
 56	     32	  0.00%
 57	     31	  0.00%
 58	     29	  0.00%
 59	     32	  0.00%
 60	     26	  0.00%
 61	     28	  0.00%
 62	     27	  0.00%
 63	     17	  0.00%
 64	     19	  0.00%
 65	     19	  0.00%
 66	     34	  0.00%
 67	     38	  0.00%
 68	     45	  0.00%
 69	     56	  0.00%
 70	     57	  0.00%
 71	     44	  0.00%
 72	     50	  0.00%
 73	     44	  0.00%
 74	     48	  0.00%
 75	     54	  0.00%
 76	     62	  0.00%
 77	    147	  0.00%
 78	     54	  0.00%
 79	     60	  0.00%
 80	    210	  0.00%
 81	    102	  0.00%
 82	    124	  0.00%
 83	    119	  0.00%
 84	     60	  0.00%
 85	     65	  0.00%
 86	     75	  0.00%
 87	    104	  0.00%
 88	     65	  0.00%
 89	     83	  0.00%
 90	     97	  0.00%
 91	    142	  0.00%
 92	    157	  0.00%
 93	    208	  0.00%
 94	    270	  0.01%
 95	    316	  0.01%
 96	    292	  0.01%
 97	    393	  0.01%
 98	    765	  0.02%
 99	    736	  0.01%
100	    727	  0.01%
101	  24998	  0.49%


criterion=sequence-density
sequence-density=13.88
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=14
prefix-density=0.00
prefix-fanout=1.0
sequence=CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAA


criterion=fanout-score
sequence-density=0.33
sequence-density-rank=14
fanout-score=41.72
fanout-score-rank=1
prefix-density=13.55
prefix-fanout=1.0
sequence=ATTGTGAGAATAAAAA
                                 Started job on |	Dec 06 12:09:29
                             Started mapping on |	Dec 06 12:09:29
                                    Finished on |	Dec 06 12:09:47
       Mapping speed, Million of reads per hour |	1031.81

                          Number of input reads |	5159026
                      Average input read length |	30
                                    UNIQUE READS:
                   Uniquely mapped reads number |	848451
                        Uniquely mapped reads % |	16.45%
                          Average mapped length |	25.03
                       Number of splices: Total |	21594
            Number of splices: Annotated (sjdb) |	1936
                       Number of splices: GT/AG |	20847
                       Number of splices: GC/AG |	657
                       Number of splices: AT/AC |	3
               Number of splices: Non-canonical |	87
                      Mismatch rate per base, % |	1.07%
                         Deletion rate per base |	0.01%
                        Deletion average length |	1.28
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.17
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	3442788
             % of reads mapped to multiple loci |	66.73%
        Number of reads mapped to too many loci |	618311
             % of reads mapped to too many loci |	11.99%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	4.05%
                     % of reads unmapped: other |	0.79%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	867787	867787	867787
N_multimapping	3442788	3442788	3442788
N_noFeature	577768	676908	745018
N_ambiguous	8764	3952	611
UnstrandedReadsAssigned:261919 PositiveStrandReadsAssigned:167591 NegativeStrandReadsAssigned:102822
Dataset is classified unstranded
MeadianReadLen=29 20thPercentileLength=24 echo kmer=19
SRR6941583 Starting Kallisto single end mapping to ensembl reference transcriptome. kmer=19

[quant] fragment length distribution is truncated gaussian with mean = 100, sd = 20
[index] k-mer length: 19
[index] number of targets: 52,972
[index] number of k-mers: 65,492,969
[index] number of equivalence classes: 320,172
[quant] running in single-end mode
[quant] will process file 1: SRR6941583-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 5,159,026 reads, 2,226,141 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 942 rounds

  52973 SRR6941583.ke.tsv
  35125 SRR6941583.se.tsv
  88098 total
==> SRR6941583.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	0	0
PNS24243	293	194	2	1.97945
KQK14069	1603	1504	6.49906	0.829695
KQK14071	474	375	0	0

==> SRR6941583.se.tsv <==
BRADI_1g14170v3	6
BRADI_1g53295v3	3
BRADI_1g59795v3	2
BRADI_1g07683v3	0
BRADI_1g00485v3	2
BRADI_1g20270v3	2
BRADI_1g74790v3	10
BRADI_1g09890v3	14
BRADI_1g77505v3	1
BRADI_1g48960v3	0
SRR6941583 completed mapping pipeline successfully
