Starting /dee2/code/volunteer_pipeline.sh SRR6941538
    current disk space = 1551545425920
    free memory = 1607239636 
SRR6941538 SRAfilesize
17b53adae5eec905a28e3252a9e15075  SRR6941538.sra
SRR6941538.sra file validated
SRR6941538 is single end
SRR6941538 is conventional basespace
SRR6941538 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR6941538_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	46
>>END_MODULE
>>Per base sequence quality	fail
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	32.975	34.0	33.0	34.0	32.0	34.0
2	33.17525	34.0	33.0	34.0	32.0	34.0
3	32.351	34.0	33.0	34.0	28.0	34.0
4	32.85725	34.0	33.0	34.0	32.0	34.0
5	32.994	34.0	33.0	34.0	31.0	34.0
6	36.884	38.0	37.0	38.0	36.0	38.0
7	37.20525	38.0	38.0	38.0	36.0	38.0
8	37.309	38.0	38.0	38.0	37.0	38.0
9	37.47225	38.0	38.0	38.0	37.0	38.0
10-11	37.405625	38.0	38.0	38.0	37.0	38.0
12-13	37.296875	38.0	38.0	38.0	37.0	38.0
14-15	37.349500000000006	38.0	38.0	38.0	37.0	38.0
16-17	36.253	38.0	37.5	38.0	31.5	38.0
18-19	36.84425	38.0	38.0	38.0	34.5	38.0
20-21	35.66974999999999	38.0	37.0	38.0	30.5	38.0
22-23	36.856375	38.0	37.5	38.0	33.5	38.0
24-25	37.341499999999996	38.0	38.0	38.0	37.0	38.0
26-27	37.269625000000005	38.0	38.0	38.0	37.0	38.0
28-29	37.363375000000005	38.0	38.0	38.0	37.0	38.0
30-31	37.318875	38.0	38.0	38.0	37.0	38.0
32-33	37.23425	38.0	38.0	38.0	37.0	38.0
34-35	37.159625	38.0	38.0	38.0	37.0	38.0
36-37	37.057625	38.0	38.0	38.0	36.5	38.0
38-39	37.163	38.0	38.0	38.0	37.0	38.0
40-41	37.01775	38.0	38.0	38.0	36.5	38.0
42-43	36.949875000000006	38.0	38.0	38.0	36.0	38.0
44-45	36.9845	38.0	38.0	38.0	36.0	38.0
46-47	36.9075	38.0	38.0	38.0	36.0	38.0
48-49	36.989875	38.0	38.0	38.0	36.5	38.0
50-51	36.76375	38.0	38.0	38.0	35.5	38.0
52-53	36.719375	38.0	38.0	38.0	35.5	38.0
54-55	36.885000000000005	38.0	38.0	38.0	36.0	38.0
56-57	36.855625	38.0	38.0	38.0	35.5	38.0
58-59	37.03725	38.0	38.0	38.0	36.0	38.0
60-61	37.054500000000004	38.0	38.0	38.0	36.0	38.0
62-63	36.645125	38.0	38.0	38.0	34.5	38.0
64-65	36.4745	38.0	37.5	38.0	34.0	38.0
66-67	36.151624999999996	38.0	37.0	38.0	31.5	38.0
68-69	36.688125	38.0	38.0	38.0	35.0	38.0
70-71	36.210875	38.0	37.0	38.0	32.0	38.0
72-73	36.182	38.0	37.0	38.0	33.0	38.0
74-75	35.972875	38.0	37.0	38.0	31.5	38.0
76-77	35.849999999999994	38.0	37.0	38.0	32.0	38.0
78-79	35.738	38.0	37.0	38.0	30.0	38.0
80-81	36.164500000000004	38.0	38.0	38.0	34.0	38.0
82-83	36.2415	38.0	38.0	38.0	34.0	38.0
84-85	36.295125	38.0	38.0	38.0	34.0	38.0
86-87	36.053250000000006	38.0	38.0	38.0	34.0	38.0
88-89	36.0475	38.0	38.0	38.0	34.0	38.0
90-91	35.9705	38.0	38.0	38.0	34.0	38.0
92-93	35.757374999999996	38.0	38.0	38.0	33.5	38.0
94-95	35.306125	38.0	38.0	38.0	32.5	38.0
96-97	32.54425	38.0	35.0	38.0	8.5	38.0
98-99	29.30725	38.0	24.5	38.0	2.0	38.0
100-101	25.665125	38.0	2.0	38.0	2.0	38.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
2	1.0
3	0.0
4	0.0
5	0.0
6	0.0
7	0.0
8	1.0
9	0.0
10	0.0
11	0.0
12	0.0
13	1.0
14	0.0
15	0.0
16	0.0
17	1.0
18	0.0
19	5.0
20	3.0
21	3.0
22	3.0
23	5.0
24	6.0
25	13.0
26	17.0
27	31.0
28	54.0
29	38.0
30	42.0
31	52.0
32	76.0
33	109.0
34	216.0
35	532.0
36	824.0
37	1967.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	35.25	27.725	16.6	20.424999999999997
2	34.150000000000006	25.825	17.5	22.525000000000002
3	29.5	18.2	24.375	27.925
4	32.225	24.6	18.425	24.75
5	41.05	21.85	20.175	16.925
6	22.925	32.25	22.875	21.95
7	35.475	20.724999999999998	28.225	15.575
8	27.6	17.4	37.6	17.4
9	22.6	35.425000000000004	27.325	14.649999999999999
10-11	36.6125	25.587500000000002	16.85	20.95
12-13	19.675	15.425	25.3	39.6
14-15	21.637500000000003	37.762499999999996	23.5375	17.0625
16-17	28.712500000000002	15.950000000000001	38.15	17.1875
18-19	38.7	21.8125	22.5	16.9875
20-21	16.925	26.625	34.825	21.625
22-23	28.9	29.7875	23.7125	17.599999999999998
24-25	30.775000000000002	29.25	23.599999999999998	16.375
26-27	40.362500000000004	22.037499999999998	20.5625	17.0375
28-29	18.575	38.9625	22.325	20.1375
30-31	21.3625	10.7375	46.6625	21.2375
32-33	30.2625	14.85	29.912499999999998	24.975
34-35	36.7375	19.787499999999998	26.687499999999996	16.7875
36-37	42.2875	16.025	26.700000000000003	14.9875
38-39	24.05	18.4375	33.7375	23.775
40-41	26.887499999999996	16.0875	21.4875	35.5375
42-43	34.0375	29.062500000000004	18.862499999999997	18.0375
44-45	51.0125	14.9875	12.75	21.25
46-47	25.6	32.4	15.262500000000001	26.737499999999997
48-49	22.325	24.9125	18.725	34.0375
50-51	26.3625	25.662499999999998	9.7875	38.1875
52-53	27.175	42.1	7.9750000000000005	22.75
54-55	16.025	27.537499999999998	21.7375	34.699999999999996
56-57	13.625000000000002	33.6625	14.95	37.762499999999996
58-59	22.575	25.7125	23.1125	28.599999999999998
60-61	10.237499999999999	21.525	33.324999999999996	34.9125
62-63	10.1875	23.4125	19.3875	47.0125
64-65	13.525	28.012500000000003	31.4625	27.0
66-67	13.65	16.9625	35.8875	33.5
68-69	18.925	20.95	26.3	33.825
70-71	12.075	21.75	37.5375	28.6375
72-73	18.862499999999997	11.6125	34.637499999999996	34.887499999999996
74-75	15.675	9.7125	29.925	44.6875
76-77	20.0375	12.687499999999998	44.824999999999996	22.45
78-79	18.5	8.975	39.2	33.324999999999996
80-81	21.5625	9.0875	33.575	35.775
82-83	25.5625	6.6000000000000005	41.4	26.437500000000004
84-85	18.0375	9.625	40.862500000000004	31.474999999999998
86-87	19.925	17.837500000000002	39.65	22.5875
88-89	14.0375	38.8875	27.287499999999998	19.787499999999998
90-91	9.8375	42.8625	31.387500000000003	15.9125
92-93	15.975	50.9875	21.925	11.1125
94-95	9.725	65.9875	16.775000000000002	7.512499999999999
96-97	7.75	77.6625	10.7875	3.8
98-99	4.075	87.7875	5.0874999999999995	3.05
100-101	2.1875	90.2375	4.237500000000001	3.3375000000000004
>>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	0.0
33	2.5
34	4.5
35	5.0
36	10.0
37	10.0
38	7.0
39	10.5
40	19.0
41	35.0
42	83.0
43	179.0
44	446.0
45	573.5
46	442.0
47	362.0
48	286.5
49	233.5
50	362.0
51	353.5
52	195.0
53	131.0
54	67.5
55	49.0
56	32.5
57	20.5
58	39.5
59	31.5
60	3.5
61	2.5
62	1.5
63	1.0
64	0.5
65	0.0
66	0.0
67	0.0
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	0.0
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
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	53.15
#Duplication Level	Percentage of deduplicated	Percentage of total
1	88.00564440263405	46.775
2	4.985888993414863	5.3
3	2.257761053621825	3.5999999999999996
4	0.8466603951081844	1.7999999999999998
5	0.6114769520225777	1.625
6	0.7996237064910631	2.55
7	0.23518344308560676	0.8750000000000001
8	0.18814675446848542	0.8
9	0.28222013170272814	1.35
>10	1.5051740357478833	20.4
>50	0.18814675446848542	6.275
>100	0.09407337723424271	8.649999999999999
>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
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGG	232	5.800000000000001	Illumina Small RNA Adapter 2 (100% over 21bp)
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	114	2.85	RNA PCR Primer, Index 1 (100% over 29bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	91	2.275	No Hit
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTTGGAATTCTCGGGTGC	56	1.4000000000000001	No Hit
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTTGGAATTCTCGGGTGCC	53	1.325	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTGGAATTCTCGGGTGCCAA	51	1.275	No Hit
CGGTCGAGGGCACGCCTGCCTGGGCGTCACGCTGGAATTCTCGGGTGCCA	50	1.25	No Hit
GAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAG	47	1.175	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	44	1.0999999999999999	No Hit
TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACAGTTCCATCTCGTATGC	40	1.0	RNA PCR Primer, Index 14 (100% over 50bp)
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTTGGAATTCTCGGGTGCCA	40	1.0	No Hit
ACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCCA	37	0.9249999999999999	RNA PCR Primer, Index 1 (100% over 28bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTGGAATTCTCGGGTGCCA	37	0.9249999999999999	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTTGGAATTCTCGGGTGCCAAG	34	0.8500000000000001	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTGGAATTCTCGGGTGCCAAGG	34	0.8500000000000001	Illumina Small RNA Adapter 2 (100% over 21bp)
CTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	32	0.8	RNA PCR Primer, Index 1 (100% over 28bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTTGGAATTCTCGGGTGC	32	0.8	No Hit
GAACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTC	30	0.75	RNA PCR Primer, Index 1 (100% over 26bp)
AACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCC	30	0.75	RNA PCR Primer, Index 1 (100% over 27bp)
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTTGGAATTCTCGGGTGC	30	0.75	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTGGAATTCTCGGGTGCCAAGG	29	0.7250000000000001	Illumina Small RNA Adapter 2 (100% over 21bp)
ACCTGCTCTGATACCATGTTGTGATGGAATTCTCGGGTGCCAAGGAACTC	27	0.675	RNA PCR Primer, Index 1 (100% over 26bp)
TCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTC	25	0.625	RNA PCR Primer, Index 1 (100% over 26bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTTGGAATTCTCGGGTG	24	0.6	No Hit
TGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAA	23	0.575	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCTGGAATTCTCGGGTGC	22	0.5499999999999999	No Hit
GCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGGA	19	0.475	RNA PCR Primer, Index 1 (100% over 22bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	15	0.375	No Hit
GGGTGTTTGGTCTAGTGGTATGATTCTCGCTTGGAATTCTCGGGTGCCAA	14	0.35000000000000003	No Hit
AGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGG	14	0.35000000000000003	Illumina Small RNA Adapter 2 (100% over 21bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTGATGGAATTCTCGGGTG	12	0.3	No Hit
TTGACAGAAGAGAGTGAGCACTGGAATTCTCGGGTGCCAAGGAACTCCAG	12	0.3	RNA PCR Primer, Index 1 (100% over 29bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTGGAATTCTCGGGTGCCA	11	0.27499999999999997	No Hit
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTGTTGGAATTCTCGGGT	11	0.27499999999999997	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTATGGAATTCTCGGGTGCCAA	11	0.27499999999999997	No Hit
TTCGGACCAGGCTTCATTCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	10	0.25	RNA PCR Primer, Index 1 (100% over 29bp)
GTCCTGCGGCAAAATAGCTCGATGCCAGAATTGGAATTCTCGGGTGCCAA	10	0.25	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATATGGAATTCTCGGGTGCCAAG	10	0.25	No Hit
TCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAAC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 24bp)
AGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTCC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 27bp)
GGCGGATGTAGCCAAGAGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGG	9	0.22499999999999998	Illumina Small RNA Adapter 2 (100% over 21bp)
GTCGTTGTAGTATAGTGGTAAGTATTCCCGCCTTGGAATTCTCGGGTGCC	9	0.22499999999999998	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGCCAAGGATGGAATTCTC	9	0.22499999999999998	No Hit
TGTCGTGCCAATTCAACATAAACCCCTGGAATTCTCGGGTGCCAAGGAAC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 24bp)
TCCGTCGTAGTCTAGGTGGTTAGGATACTCTGGAATTCTCGGGTGCCAAG	8	0.2	No Hit
TGTCGTGCCAATTCAACATAAACCCCTTGGAATTCTCGGGTGCCAAGGAA	8	0.2	RNA PCR Primer, Index 1 (100% over 23bp)
TGCCACGATCCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAAT	8	0.2	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGTGGAATTCTCGGGTGCC	8	0.2	No Hit
AGGGATGTAGCGCAGCTGGAATTCTCGGGTGCCAAGGAACTCCAGTCACA	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 34bp)
AATATTGGGTAGGTTGTGGTATTTCATTGCTTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
GGCGGATGTAGCCAAGTGGACCAAGGCAGTGGAATTCTCGGGTGCCAAGG	7	0.17500000000000002	Illumina Small RNA Adapter 2 (100% over 21bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACCTGGAATTCTCGGGTGCC	7	0.17500000000000002	No Hit
CTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCA	7	0.17500000000000002	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGTGGAATTCTCGGGTGCCAAGGA	6	0.15	RNA PCR Primer, Index 1 (100% over 22bp)
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTGCTGGAATTCTCGGGT	6	0.15	No Hit
GAAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTGC	6	0.15	No Hit
TAGAACTCCACATCCTTGGCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
TCGGACCAGGCTTCATTCCCTTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTGGAATTCTCGGGTG	6	0.15	No Hit
TAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
CCTGTGCCTGCCTCTTCCATTTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
CTCTGATGATGATCAAACTAATACTTTCGTTCTTCTGGAATTCTCGGGTG	6	0.15	No Hit
TCCCGTGCTGTAAAATAACTGATTTGCCTATCTGATCTGGAATTCTCGGG	6	0.15	No Hit
GCGTCTGTAGTCCAACGGTTAGGATAATTGCCTTCTGGAATTCTCGGGTG	6	0.15	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCAATGGAATTCTCGGGTGCC	6	0.15	No Hit
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTGGAATTCTCGGGTGCC	6	0.15	No Hit
CACGACTCTCGGCAACGGATATCTCGGCTTGGAATTCTCGGGTGCCAAGG	6	0.15	Illumina Small RNA Adapter 2 (100% over 21bp)
CTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
CAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTC	6	0.15	RNA PCR Primer, Index 1 (100% over 26bp)
TCGCTTGGTGCAGATCGGGACTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
CATCGAGTAGACCTTGTTATTGTGAGAATAAATGGAATTCTCGGGTGCCA	5	0.125	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATGGAATTCTCGGGTGCCAAGGA	5	0.125	RNA PCR Primer, Index 1 (100% over 22bp)
TGAAGCTGCCAGCATGATCTGATGGAATTCTCGGGTGCCAAGGAACTCCA	5	0.125	RNA PCR Primer, Index 1 (100% over 28bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCAAAATCTTGGAATTCT	5	0.125	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGGAATTCTCGGGTGC	5	0.125	No Hit
TCCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGT	5	0.125	No Hit
CCCTATAGAACTCCACATCCTTGGAATTCTCGGGTGCCAAGGAACTCCAG	5	0.125	RNA PCR Primer, Index 1 (100% over 29bp)
CATCGAGTAGACCTTGTTATTGTGAGATGGAATTCTCGGGTGCCAAGGAA	5	0.125	RNA PCR Primer, Index 1 (100% over 23bp)
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTGTGGAATTCTCGGGTG	5	0.125	No Hit
ACGAACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTAATGGAATTCTCGGGTGCCA	5	0.125	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGGAATTCTCGGGTGCCAA	5	0.125	No Hit
CCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACT	5	0.125	RNA PCR Primer, Index 1 (100% over 25bp)
>>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	1.3	0.0	0.0	0.0
2	0.0	1.3	0.0	0.0	0.0
3	0.0	1.3	0.0	0.0	0.0
4	0.0	1.3	0.0	0.0	0.0
5	0.0	1.3	0.0	0.0	0.0
6	0.0	1.3	0.0	0.0	0.0
7	0.0	1.3	0.0	0.0	0.0
8	0.0	1.3	0.0	0.0	0.0
9	0.0	1.325	0.0	0.0	0.0
10-11	0.0	1.325	0.0	0.0	0.0
12-13	0.0	1.3625	0.0	0.0	0.0
14-15	0.0	1.5	0.0	0.0	0.0
16-17	0.0	1.9375	0.0	0.0	0.0
18-19	0.0	2.5	0.0	0.0	0.0
20-21	0.0	3.75	0.0	0.0	0.0
22-23	0.0	13.462499999999999	0.0	0.0	0.0
24-25	0.0	27.7	0.0	0.0	0.0
26-27	0.0	40.474999999999994	0.0	0.0	0.0
28-29	0.0	44.45	0.0	0.0	0.0
30-31	0.0	59.224999999999994	0.0	0.0	0.0
32-33	0.0	71.4125	0.0	0.0	0.0
34-35	0.0	83.55	0.0	0.0	0.0
36-37	0.0	91.5125	0.0	0.0	0.0
38-39	0.0	94.4125	0.0	0.0	0.0
40-41	0.0	95.5125	0.0	0.0	0.0
42-43	0.0	96.4375	0.0	0.0	0.0
44-45	0.0	96.9375	0.0	0.0	0.0
46-47	0.0	97.17500000000001	0.0	0.0	0.0
48-49	0.0	97.275	0.0	0.0	0.0
50-51	0.0	97.275	0.0	0.0	0.0
52-53	0.0	97.3	0.0	0.0	0.0
54-55	0.0	97.3	0.0	0.0	0.0
56-57	0.0	97.3	0.0	0.0	0.0
58-59	0.0	97.3	0.0	0.0	0.0
60-61	0.0	97.3	0.0	0.0	0.0
62-63	0.0	97.3	0.0	0.0	0.0
64-65	0.0	97.3	0.0	0.0	0.0
66-67	0.0	97.3	0.0	0.0	0.0
68-69	0.0	97.3	0.0	0.0	0.0
70-71	0.0	97.3	0.0	0.0	0.0
72-73	0.0	97.3	0.0	0.0	0.0
74-75	0.0	97.3	0.0	0.0	0.0
76-77	0.0	97.3	0.0	0.0	0.0
78-79	0.0	97.3	0.0	0.0	0.0
80-81	0.0	97.3	0.0	0.0	0.0
82-83	0.0	97.3	0.0	0.0	0.0
84-85	0.0	97.3	0.0	0.0	0.0
86-87	0.0	97.3	0.0	0.0	0.0
88-89	0.0	97.3	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
TTGTAGT	20	1.5392321E-5	95.00001	5
GGATTGT	20	1.5392321E-5	95.00001	2
GATTGTA	20	1.5392321E-5	95.00001	3
ATTGTAG	20	1.5392321E-5	95.00001	4
GGGATTG	20	1.5392321E-5	95.00001	1
GGCGGAT	20	1.5392321E-5	95.00001	1
TGGTCTA	15	6.142176E-4	95.0	8
GTAGACC	15	6.142176E-4	95.0	7
AGTAGAC	15	6.142176E-4	95.0	6
GGACCAG	25	3.8289727E-7	95.0	3
GGTCTAG	15	6.142176E-4	95.0	9
CGGACCA	25	3.8289727E-7	95.0	2
TCGGACC	25	3.8289727E-7	95.0	1
TAGTTCA	30	9.458745E-9	95.0	8
GAGTAGA	15	6.142176E-4	95.0	5
AGGCTTC	25	3.8289727E-7	95.0	8
GGCTTCA	25	3.8289727E-7	95.0	9
CGAGTAG	15	6.142176E-4	95.0	4
CAGGCTT	25	3.8289727E-7	95.0	7
AGACCTT	15	6.142176E-4	95.0	9
>>END_MODULE
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230604 READS because READLEN < 1
Read 230604 spots for SRR6941538.sra
Written 230604 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
Rejected 230591 READS because READLEN < 1
Read 230591 spots for SRR6941538.sra
Written 230591 spots for SRR6941538.sra
SRR ids: ['SRR6941538.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_3_xfuab7
SRR6941538.sra spots: 4611833
blocks: [[1, 230591], [230592, 461182], [461183, 691773], [691774, 922364], [922365, 1152955], [1152956, 1383546], [1383547, 1614137], [1614138, 1844728], [1844729, 2075319], [2075320, 2305910], [2305911, 2536501], [2536502, 2767092], [2767093, 2997683], [2997684, 3228274], [3228275, 3458865], [3458866, 3689456], [3689457, 3920047], [3920048, 4150638], [4150639, 4381229], [4381230, 4611833]]
SRR6941538 file size 1101247
SRR6941538 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 SRR6941538 SRR6941538_1.fastq
Input file:	SRR6941538_1.fastq
trimmed:	SRR6941538-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 10:31:26 2024 >> started

Fri Dec  6 10:31:29 2024 >> done (3.180s)
4611833 reads processed; of these:
     81 ( 0.00%) short reads filtered out after trimming by size control
     18 ( 0.00%) empty reads filtered out after trimming by size control
4611734 (100.00%) reads available; of these:
1049620 (22.76%) trimmed reads available after processing
3562114 (77.24%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      3	  0.00%
 19	      3	  0.00%
 20	      8	  0.00%
 21	     12	  0.00%
 22	      8	  0.00%
 23	     11	  0.00%
 24	      9	  0.00%
 25	     19	  0.00%
 26	     39	  0.00%
 27	     38	  0.00%
 28	     51	  0.00%
 29	     62	  0.00%
 30	     66	  0.00%
 31	     40	  0.00%
 32	     41	  0.00%
 33	     34	  0.00%
 34	     40	  0.00%
 35	     34	  0.00%
 36	     32	  0.00%
 37	     28	  0.00%
 38	     34	  0.00%
 39	     45	  0.00%
 40	     45	  0.00%
 41	     44	  0.00%
 42	     30	  0.00%
 43	     39	  0.00%
 44	     20	  0.00%
 45	     28	  0.00%
 46	     31	  0.00%
 47	     26	  0.00%
 48	     33	  0.00%
 49	     34	  0.00%
 50	     28	  0.00%
 51	     32	  0.00%
 52	     16	  0.00%
 53	     22	  0.00%
 54	     23	  0.00%
 55	     20	  0.00%
 56	     31	  0.00%
 57	     24	  0.00%
 58	     27	  0.00%
 59	     20	  0.00%
 60	     41	  0.00%
 61	     43	  0.00%
 62	     36	  0.00%
 63	     46	  0.00%
 64	     48	  0.00%
 65	     45	  0.00%
 66	     71	  0.00%
 67	    107	  0.00%
 68	    215	  0.00%
 69	    277	  0.01%
 70	    557	  0.01%
 71	    487	  0.01%
 72	    857	  0.02%
 73	   2206	  0.05%
 74	  15477	  0.34%
 75	   9630	  0.21%
 76	   2852	  0.06%
 77	    733	  0.02%
 78	    872	  0.02%
 79	    860	  0.02%
 80	   1098	  0.02%
 81	   1140	  0.02%
 82	   1402	  0.03%
 83	   1790	  0.04%
 84	   2547	  0.06%
 85	   2831	  0.06%
 86	   2901	  0.06%
 87	   3102	  0.07%
 88	   3859	  0.08%
 89	   5527	  0.12%
 90	  10217	  0.22%
 91	  11909	  0.26%
 92	  12925	  0.28%
 93	  23838	  0.52%
 94	  44400	  0.96%
 95	 137164	  2.97%
 96	 123863	  2.69%
 97	 116638	  2.53%
 98	 207004	  4.49%
 99	 217355	  4.71%
100	  81420	  1.77%
101	3562114	 77.24%
4611734 reads passed initial QC


criterion=sequence-density
sequence-density=97.83
sequence-density-rank=1
fanout-score=28.80
fanout-score-rank=1
prefix-density=97.02
prefix-fanout=28.8
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACAGTTCCATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA


criterion=fanout-score
sequence-density=97.83
sequence-density-rank=1
fanout-score=28.80
fanout-score-rank=1
prefix-density=97.02
prefix-fanout=28.8
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACAGTTCCATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACAGTTCCATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA -o SRR6941538 -
Input file:	STDIN
trimmed:	SRR6941538-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACAGTTCCATCTCGTATGCCGTCTTCTGCTTGA
-- 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 10:31:38 2024 >> started

Fri Dec  6 10:31:44 2024 >> done (5.777s)
4517617 reads processed; of these:
  52729 ( 1.17%) short reads filtered out after trimming by size control
  57873 ( 1.28%) empty reads filtered out after trimming by size control
4407015 (97.55%) reads available; of these:
4382663 (99.45%) trimmed reads available after processing
  24352 ( 0.55%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  12964	  0.29%
 19	  35530	  0.81%
 20	  47821	  1.09%
 21	 343525	  7.79%
 22	 171034	  3.88%
 23	 138824	  3.15%
 24	 886298	 20.11%
 25	 114249	  2.59%
 26	  92965	  2.11%
 27	  77887	  1.77%
 28	 112857	  2.56%
 29	 464881	 10.55%
 30	 310031	  7.03%
 31	 242587	  5.50%
 32	 281172	  6.38%
 33	 305716	  6.94%
 34	 257276	  5.84%
 35	 173334	  3.93%
 36	 108103	  2.45%
 37	  56661	  1.29%
 38	  26961	  0.61%
 39	  18406	  0.42%
 40	  24568	  0.56%
 41	  29340	  0.67%
 42	  18931	  0.43%
 43	   5717	  0.13%
 44	  13881	  0.31%
 45	   5406	  0.12%
 46	   1394	  0.03%
 47	   1562	  0.04%
 48	    629	  0.01%
 49	    316	  0.01%
 50	    187	  0.00%
 51	    178	  0.00%
 52	    105	  0.00%
 53	     68	  0.00%
 54	     44	  0.00%
 55	     30	  0.00%
 56	     21	  0.00%
 57	     33	  0.00%
 58	     18	  0.00%
 59	     18	  0.00%
 60	     18	  0.00%
 61	     22	  0.00%
 62	      5	  0.00%
 63	     10	  0.00%
 64	     13	  0.00%
 65	     13	  0.00%
 66	     15	  0.00%
 67	     15	  0.00%
 68	     24	  0.00%
 69	     28	  0.00%
 70	     45	  0.00%
 71	     26	  0.00%
 72	     36	  0.00%
 73	     40	  0.00%
 74	     49	  0.00%
 75	     67	  0.00%
 76	     59	  0.00%
 77	    167	  0.00%
 78	     49	  0.00%
 79	     89	  0.00%
 80	    204	  0.00%
 81	     99	  0.00%
 82	    144	  0.00%
 83	    177	  0.00%
 84	     82	  0.00%
 85	     74	  0.00%
 86	    134	  0.00%
 87	    176	  0.00%
 88	     87	  0.00%
 89	     92	  0.00%
 90	     96	  0.00%
 91	    166	  0.00%
 92	    187	  0.00%
 93	    212	  0.00%
 94	    259	  0.01%
 95	    305	  0.01%
 96	    311	  0.01%
 97	    326	  0.01%
 98	    616	  0.01%
 99	    432	  0.01%
100	    463	  0.01%
101	  20055	  0.46%


criterion=sequence-density
sequence-density=8.65
sequence-density-rank=1
fanout-score=1.00
fanout-score-rank=6
prefix-density=0.05
prefix-fanout=1.0
sequence=GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGTGAATCC


criterion=fanout-score
sequence-density=0.19
sequence-density-rank=26
fanout-score=58.39
fanout-score-rank=1
prefix-density=6.19
prefix-fanout=1.8
sequence=GTGAGAATTCTAAAAA
                                 Started job on |	Dec 06 10:31:57
                             Started mapping on |	Dec 06 10:31:57
                                    Finished on |	Dec 06 10:32:11
       Mapping speed, Million of reads per hour |	1157.43

                          Number of input reads |	4501132
                      Average input read length |	30
                                    UNIQUE READS:
                   Uniquely mapped reads number |	1077288
                        Uniquely mapped reads % |	23.93%
                          Average mapped length |	25.87
                       Number of splices: Total |	4729
            Number of splices: Annotated (sjdb) |	1568
                       Number of splices: GT/AG |	4517
                       Number of splices: GC/AG |	138
                       Number of splices: AT/AC |	2
               Number of splices: Non-canonical |	72
                      Mismatch rate per base, % |	0.13%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.56
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.04
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	2576222
             % of reads mapped to multiple loci |	57.23%
        Number of reads mapped to too many loci |	652528
             % of reads mapped to too many loci |	14.50%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	3.68%
                     % of reads unmapped: other |	0.65%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	847622	847622	847622
N_multimapping	2576222	2576222	2576222
N_noFeature	735006	888072	920312
N_ambiguous	9789	5709	211
UnstrandedReadsAssigned:332493 PositiveStrandReadsAssigned:183507 NegativeStrandReadsAssigned:156765
Dataset is classified unstranded
MeadianReadLen=29 20thPercentileLength=24 echo kmer=19
SRR6941538 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: SRR6941538-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 4,501,132 reads, 2,281,910 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 918 rounds

  52973 SRR6941538.ke.tsv
  35125 SRR6941538.se.tsv
  88098 total
==> SRR6941538.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	0	0
PNS24249	1928	1829	3	0.216096
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	0	0
PNS24243	293	194	0	0
KQK14069	1603	1504	0	0
KQK14071	474	375	1.1038	0.387792

==> SRR6941538.se.tsv <==
BRADI_1g14170v3	60
BRADI_1g53295v3	0
BRADI_1g59795v3	2
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	0
BRADI_1g74790v3	6
BRADI_1g09890v3	0
BRADI_1g77505v3	2
BRADI_1g48960v3	0
SRR6941538 completed mapping pipeline successfully
