Starting /dee2/code/volunteer_pipeline.sh SRR6941567
    current disk space = 1551509868544
    free memory = 1604689520 
SRR6941567 SRAfilesize
f3b08ce9139cf065beab08ce754d4e82  SRR6941567.sra
SRR6941567.sra file validated
SRR6941567 is single end
SRR6941567 is conventional basespace
SRR6941567 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR6941567_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	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	33.146	34.0	33.0	34.0	32.0	34.0
2	33.29675	34.0	33.0	34.0	32.0	34.0
3	32.8395	34.0	33.0	34.0	31.0	34.0
4	33.117	34.0	33.0	34.0	32.0	34.0
5	33.1605	34.0	33.0	34.0	31.0	34.0
6	36.94	38.0	37.0	38.0	36.0	38.0
7	37.31725	38.0	38.0	38.0	37.0	38.0
8	37.498	38.0	38.0	38.0	37.0	38.0
9	37.50825	38.0	38.0	38.0	37.0	38.0
10-11	37.441375	38.0	38.0	38.0	37.0	38.0
12-13	37.400375	38.0	38.0	38.0	37.0	38.0
14-15	37.442875	38.0	38.0	38.0	37.0	38.0
16-17	36.175250000000005	38.0	37.5	38.0	31.5	38.0
18-19	36.8665	38.0	38.0	38.0	33.5	38.0
20-21	35.950874999999996	38.0	37.5	38.0	30.5	38.0
22-23	37.094625	38.0	38.0	38.0	36.0	38.0
24-25	37.393249999999995	38.0	38.0	38.0	37.0	38.0
26-27	37.399875	38.0	38.0	38.0	37.0	38.0
28-29	37.397125	38.0	38.0	38.0	37.0	38.0
30-31	37.367625000000004	38.0	38.0	38.0	37.0	38.0
32-33	37.223875	38.0	38.0	38.0	36.5	38.0
34-35	37.168125	38.0	38.0	38.0	37.0	38.0
36-37	37.12725	38.0	38.0	38.0	36.5	38.0
38-39	37.093125	38.0	38.0	38.0	36.5	38.0
40-41	37.049375	38.0	38.0	38.0	36.0	38.0
42-43	37.06875	38.0	38.0	38.0	36.0	38.0
44-45	37.06375	38.0	38.0	38.0	36.0	38.0
46-47	36.908125	38.0	38.0	38.0	36.0	38.0
48-49	37.001000000000005	38.0	38.0	38.0	36.0	38.0
50-51	36.83325000000001	38.0	38.0	38.0	35.5	38.0
52-53	36.82825	38.0	38.0	38.0	36.0	38.0
54-55	36.9025	38.0	38.0	38.0	36.0	38.0
56-57	36.97	38.0	38.0	38.0	36.0	38.0
58-59	37.065749999999994	38.0	38.0	38.0	36.5	38.0
60-61	37.072	38.0	38.0	38.0	36.0	38.0
62-63	36.91725	38.0	38.0	38.0	36.0	38.0
64-65	36.53775	38.0	37.5	38.0	34.5	38.0
66-67	36.456	38.0	37.5	38.0	34.0	38.0
68-69	36.656625000000005	38.0	38.0	38.0	34.5	38.0
70-71	36.310625	38.0	37.5	38.0	33.0	38.0
72-73	36.12875	38.0	37.0	38.0	32.0	38.0
74-75	36.16975	38.0	37.0	38.0	33.0	38.0
76-77	36.04625	38.0	37.5	38.0	32.0	38.0
78-79	36.14125	38.0	37.5	38.0	33.5	38.0
80-81	36.385999999999996	38.0	38.0	38.0	34.0	38.0
82-83	36.38225	38.0	38.0	38.0	34.5	38.0
84-85	36.325125	38.0	38.0	38.0	34.0	38.0
86-87	36.128375000000005	38.0	38.0	38.0	34.0	38.0
88-89	36.195875	38.0	38.0	38.0	34.0	38.0
90-91	36.165875	38.0	38.0	38.0	34.0	38.0
92-93	36.031125	38.0	38.0	38.0	34.0	38.0
94-95	35.7115	38.0	38.0	38.0	33.0	38.0
96-97	34.172125	38.0	36.5	38.0	22.0	38.0
98-99	31.963875	38.0	35.0	38.0	2.0	38.0
100-101	29.2135	38.0	25.0	38.0	2.0	38.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
9	1.0
10	0.0
11	0.0
12	0.0
13	0.0
14	0.0
15	0.0
16	2.0
17	0.0
18	0.0
19	0.0
20	1.0
21	3.0
22	3.0
23	4.0
24	6.0
25	16.0
26	13.0
27	21.0
28	46.0
29	26.0
30	35.0
31	55.0
32	74.0
33	102.0
34	175.0
35	401.0
36	728.0
37	2288.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	30.25	20.9	13.750000000000002	35.099999999999994
2	27.213606803401703	41.295647823911956	15.232616308154077	16.258129064532266
3	28.475	16.775000000000002	34.1	20.65
4	23.125	28.249999999999996	12.5	36.125
5	47.125	16.8	17.875	18.2
6	18.425	41.15	22.125	18.3
7	46.949999999999996	19.5	19.775000000000002	13.775
8	18.45	14.249999999999998	49.225	18.075
9	16.425	48.15	17.775	17.65
10-11	37.8125	28.712500000000002	18.1875	15.287500000000001
12-13	16.2125	16.175	20.0	47.612500000000004
14-15	18.825	31.8625	34.575	14.7375
16-17	29.9375	18.575	37.3	14.1875
18-19	33.175	26.275	27.537499999999998	13.0125
20-21	14.2625	24.4	43.6625	17.675
22-23	34.2	25.0375	26.637499999999996	14.124999999999998
24-25	32.9375	31.2625	21.1625	14.637500000000001
26-27	38.3	28.3875	18.35	14.9625
28-29	16.675	38.3625	26.5	18.462500000000002
30-31	19.8375	13.212499999999999	43.8625	23.0875
32-33	30.837500000000002	14.85	31.324999999999996	22.9875
34-35	33.375	25.3	26.0	15.325
36-37	36.5375	20.0375	30.6375	12.7875
38-39	23.9125	18.2625	35.925000000000004	21.9
40-41	26.200000000000003	13.3125	25.1875	35.3
42-43	38.2125	21.5375	19.0	21.25
44-45	50.4125	14.0125	17.0125	18.5625
46-47	30.9375	25.8625	14.3375	28.8625
48-49	22.7125	28.962500000000002	16.175	32.15
50-51	29.6875	27.3	8.4375	34.575
52-53	27.762500000000003	43.4625	7.025	21.75
54-55	20.0625	28.175	19.162499999999998	32.6
56-57	12.075	29.2	12.4125	46.3125
58-59	20.200000000000003	25.874999999999996	14.0125	39.9125
60-61	12.562499999999998	29.2875	18.9375	39.2125
62-63	14.025000000000002	31.6875	21.8875	32.4
64-65	15.262500000000001	25.6125	21.4125	37.7125
66-67	12.8	25.75	19.35	42.1
68-69	15.587500000000002	29.7125	22.05	32.65
70-71	9.35	35.212500000000006	32.675	22.7625
72-73	14.149999999999999	22.237499999999997	37.6	26.0125
74-75	16.662499999999998	12.587499999999999	31.7125	39.0375
76-77	19.787499999999998	13.925	41.025	25.2625
78-79	20.724999999999998	11.3625	40.4625	27.450000000000003
80-81	20.4125	9.6875	34.175	35.725
82-83	27.150000000000002	6.575	37.5375	28.7375
84-85	19.0625	6.550000000000001	39.574999999999996	34.8125
86-87	18.099999999999998	12.1	43.05	26.75
88-89	15.6	27.775	35.925000000000004	20.7
90-91	12.5125	33.1875	33.7375	20.5625
92-93	17.575	40.8375	27.6625	13.925
94-95	12.4625	60.5375	19.3875	7.6125
96-97	8.275	76.3125	12.025	3.3875
98-99	4.6125	88.3125	4.6	2.475
100-101	2.0875	92.1875	3.1375	2.5875
>>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	1.5
34	2.5
35	5.5
36	5.5
37	3.5
38	6.5
39	10.5
40	14.0
41	30.5
42	88.0
43	184.5
44	520.5
45	695.5
46	450.5
47	350.5
48	309.0
49	204.0
50	225.0
51	283.0
52	255.5
53	146.5
54	65.5
55	58.0
56	38.0
57	10.0
58	13.0
59	14.0
60	5.0
61	2.0
62	1.0
63	0.5
64	0.0
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	0.05
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	50.4
#Duplication Level	Percentage of deduplicated	Percentage of total
1	87.74801587301587	44.224999999999994
2	4.315476190476191	4.35
3	2.232142857142857	3.375
4	1.3888888888888888	2.8000000000000003
5	0.5952380952380952	1.5
6	0.1984126984126984	0.6
7	0.6448412698412698	2.275
8	0.3472222222222222	1.4000000000000001
9	0.3472222222222222	1.575
>10	1.7857142857142856	17.95
>50	0.2976190476190476	11.774999999999999
>100	0.0992063492063492	8.175
>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
CATCGAGTAGACCTTGTTATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	198	4.95	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTGGAATTCTCGGGTGCCAAGG	129	3.225	Illumina Small RNA Adapter 2 (100% over 21bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTGGAATTCTCGGGTGCCA	98	2.45	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTGGAATTCTCGGGTGCCAA	90	2.25	No Hit
GAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAG	89	2.225	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	76	1.9	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTTGGAATTCTCGGGTG	62	1.55	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTTGGAATTCTCGGGTGC	56	1.4000000000000001	No Hit
CTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	50	1.25	RNA PCR Primer, Index 1 (100% over 28bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTTGGAATTCTCGGGTGCC	46	1.15	No Hit
TGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAA	42	1.05	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTTGGAATTCTCGGGTGCCA	39	0.975	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATATGGAATTCTCGGGTGCCAAG	34	0.8500000000000001	No Hit
TCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTC	31	0.775	RNA PCR Primer, Index 1 (100% over 26bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	30	0.75	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATGGAATTCTCGGGTGCCAAGGA	26	0.65	RNA PCR Primer, Index 1 (100% over 22bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTATGGAATTCTCGGGTGCCAA	26	0.65	No Hit
CAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTC	23	0.575	RNA PCR Primer, Index 1 (100% over 26bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCTGGAATTCTCGGGTGC	22	0.5499999999999999	No Hit
GAAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTGC	22	0.5499999999999999	No Hit
TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGCCAATATCTCGTATGC	21	0.525	RNA PCR Primer, Index 6 (100% over 50bp)
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	20	0.5	RNA PCR Primer, Index 1 (100% over 29bp)
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGTGGAATTCTCGGGTGCC	19	0.475	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTTGGAATTCTCGGGTGCCAAG	17	0.42500000000000004	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTTGGAATTCTCGGGTGCC	17	0.42500000000000004	No Hit
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTTGGAATTCTCGGGTGC	16	0.4	No Hit
CGGTCGAGGGCACGCCTGCCTGGGCGTCACGCTGGAATTCTCGGGTGCCA	16	0.4	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCTGGAATTCTCGGGTGCCAAGG	16	0.4	Illumina Small RNA Adapter 2 (100% over 21bp)
GGGTGTTTGGTCTAGTGGTATGATTCTCGCTTGGAATTCTCGGGTGCCAA	15	0.375	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAATGGAATTCTCGGGTG	14	0.35000000000000003	No Hit
AGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTCC	13	0.325	RNA PCR Primer, Index 1 (100% over 27bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTGGAATTCTCGGGTG	13	0.325	No Hit
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTGGAATTCTCGGGTGCCA	13	0.325	No Hit
CTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCA	12	0.3	No Hit
ACCTGCTCTGATACCATGTTGTGATGGAATTCTCGGGTGCCAAGGAACTC	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 26bp)
GACACGACTCTCGGCAACGGATATCTCGGCTTGGAATTCTCGGGTGCCAA	11	0.27499999999999997	No Hit
AGAAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTG	11	0.27499999999999997	No Hit
AGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGG	11	0.27499999999999997	Illumina Small RNA Adapter 2 (100% over 21bp)
GCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAA	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 23bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGG	10	0.25	Illumina Small RNA Adapter 2 (100% over 21bp)
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTTGGAATTCTCGGGTGC	10	0.25	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGTGAATCTGGAATTC	10	0.25	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGCCAAGGATGGAATTCTC	10	0.25	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTGGAATTCTCGGGTGCCAAGG	10	0.25	Illumina Small RNA Adapter 2 (100% over 21bp)
TTCGGACCAGGCTTCATTCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 29bp)
AACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 27bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCAATGGAATTCTCGGGTGCC	9	0.22499999999999998	No Hit
CATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAAC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 24bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTAATGGAATTCTCGGGTGC	9	0.22499999999999998	No Hit
ACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCCA	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 28bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTAAATGGAATTCTCGGGTG	9	0.22499999999999998	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGGAATTCTCGGGTGC	8	0.2	No Hit
GACACGACTCTCGGCAACGGATATCTGGAATTCTCGGGTGCCAAGGAACT	8	0.2	RNA PCR Primer, Index 1 (100% over 25bp)
TGTCGTGCCAATTCAACATAAACCCCTGGAATTCTCGGGTGCCAAGGAAC	8	0.2	RNA PCR Primer, Index 1 (100% over 24bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTAAAATGGAATTCTCGGGT	8	0.2	No Hit
TTGACAGAAGAGAGTGAGCACTGGAATTCTCGGGTGCCAAGGAACTCCAG	8	0.2	RNA PCR Primer, Index 1 (100% over 29bp)
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGGAATTCTCGGGTGCCAA	8	0.2	No Hit
CCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACT	8	0.2	RNA PCR Primer, Index 1 (100% over 25bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAAATGGAATTCTCGGGT	7	0.17500000000000002	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAATTGGAATTCTCGGGT	7	0.17500000000000002	No Hit
AATATTGGGTAGGTTGTGGTATTTCATTGCTTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
GACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 23bp)
GACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 24bp)
CATCGAGTAGACCTTGTTAATGTGAGAATATGGAATTCTCGGGTGCCAAG	7	0.17500000000000002	No Hit
CATCGAGTAGACCTTGTTATTGTGAGATGGAATTCTCGGGTGCCAAGGAA	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 23bp)
ACGAACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 24bp)
AAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTGCC	7	0.17500000000000002	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTAAATGGAATTCTCGGGTGCC	7	0.17500000000000002	No Hit
CACGACTCTCGGCAACGGATATCTCGGCTTGGAATTCTCGGGTGCCAAGG	7	0.17500000000000002	Illumina Small RNA Adapter 2 (100% over 21bp)
CATCGAGTAGACCTTGTTAATGTGAGAATTCTTGGAATTCTCGGGTGCCA	7	0.17500000000000002	No Hit
ATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACT	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 25bp)
CATCGAGTAGACCTTGTTATTGTGAGAATAAATGGAATTCTCGGGTGCCA	6	0.15	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTATGGAATTCTCGGGTGCC	6	0.15	No Hit
AATATTGGGTAGGTTGTGGTATTTCATTGCTGGAATTCTCGGGTGCCAAG	6	0.15	No Hit
CATCGAGTAGACCTTGATATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	6	0.15	No Hit
TCCGTCGTAGTCTAGGTGGTTAGGATACTGGAATTCTCGGGTGCCAAGGA	5	0.125	RNA PCR Primer, Index 1 (100% over 22bp)
TGAAGCTGCCAGCATGATCTGATGGAATTCTCGGGTGCCAAGGAACTCCA	5	0.125	RNA PCR Primer, Index 1 (100% over 28bp)
CCGTTACTCGGAGGTTCGAATCCTTCCGTCCCAGCCATGGAATTCTCGGG	5	0.125	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTAAAAATGGAATTCTCGGG	5	0.125	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTATGGAATTCTCGGGTGCCAA	5	0.125	No Hit
CATCGAGTAGACCTTGTTAATGTGAGAATTCTGGAATTCTCGGGTGCCAA	5	0.125	No Hit
CAGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTG	5	0.125	No Hit
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTGGAATTCTCGGGTGCC	5	0.125	No Hit
ATGCAGTTACTAATTCATGATCTGGCTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTCAAGGCTGGAATTC	5	0.125	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTAAAAAATGGAATTCTCGG	5	0.125	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAAAAATGGAATTCTCGG	5	0.125	No Hit
>>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	0.65	0.0	0.0	0.0
2	0.0	0.65	0.0	0.0	0.0
3	0.0	0.65	0.0	0.0	0.0
4	0.0	0.65	0.0	0.0	0.0
5	0.0	0.675	0.0	0.0	0.0
6	0.0	0.725	0.0	0.0	0.0
7	0.0	0.725	0.0	0.0	0.0
8	0.0	0.725	0.0	0.0	0.0
9	0.0	0.75	0.0	0.0	0.0
10-11	0.0	0.7625	0.0	0.0	0.0
12-13	0.0	0.825	0.0	0.0	0.0
14-15	0.0	0.925	0.0	0.0	0.0
16-17	0.0	1.125	0.0	0.0	0.0
18-19	0.0	1.6	0.0	0.0	0.0
20-21	0.0	2.7750000000000004	0.0	0.0	0.0
22-23	0.0	8.1375	0.0	0.0	0.0
24-25	0.0	18.6875	0.0	0.0	0.0
26-27	0.0	29.8625	0.0	0.0	0.0
28-29	0.0	35.375	0.0	0.0	0.0
30-31	0.0	49.7875	0.0	0.0	0.0
32-33	0.0	67.7125	0.0	0.0	0.0
34-35	0.0	82.5375	0.0	0.0	0.0
36-37	0.0	91.5875	0.0	0.0	0.0
38-39	0.0	94.30000000000001	0.0	0.0	0.0
40-41	0.0	95.6625	0.0	0.0	0.0
42-43	0.0	96.9	0.0	0.0	0.0
44-45	0.0	97.36250000000001	0.0	0.0	0.0
46-47	0.0	97.4375	0.0	0.0	0.0
48-49	0.0	97.475	0.0	0.0	0.0
50-51	0.0	97.525	0.0	0.0	0.0
52-53	0.0	97.525	0.0	0.0	0.0
54-55	0.0	97.525	0.0	0.0	0.0
56-57	0.0	97.525	0.0	0.0	0.0
58-59	0.0	97.525	0.0	0.0	0.0
60-61	0.0	97.525	0.0	0.0	0.0
62-63	0.0	97.525	0.0	0.0	0.0
64-65	0.0	97.525	0.0	0.0	0.0
66-67	0.0	97.525	0.0	0.0	0.0
68-69	0.0	97.525	0.0	0.0	0.0
70-71	0.0	97.525	0.0	0.0	0.0
72-73	0.0	97.525	0.0	0.0	0.0
74-75	0.0	97.525	0.0	0.0	0.0
76-77	0.0	97.525	0.0	0.0	0.0
78-79	0.0	97.525	0.0	0.0	0.0
80-81	0.0	97.5375	0.0	0.0	0.0
82-83	0.0	97.575	0.0	0.0	0.0
84-85	0.0	97.575	0.0	0.0	0.0
86-87	0.0	97.575	0.0	0.0	0.0
88-89	0.0	97.575	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGATGTA	15	6.142176E-4	95.0	4
GAGCGTA	25	3.8289727E-7	95.0	3
GTAGACC	90	0.0	95.0	7
AGTAGAC	90	0.0	95.0	6
GATGTAG	15	6.142176E-4	95.0	5
TAGCCAA	15	6.142176E-4	95.0	9
CGTAGTT	25	3.8289727E-7	95.0	6
CGGATGT	15	6.142176E-4	95.0	3
GCGGATG	15	6.142176E-4	95.0	2
TAGTTCA	60	0.0	95.0	8
GAGTAGA	90	0.0	95.0	5
TGTAGCC	15	6.142176E-4	95.0	7
CGAGCGT	25	3.8289727E-7	95.0	2
CGAGTAG	90	0.0	95.0	4
AGACCTT	90	0.0	95.0	9
GCGTAGT	25	3.8289727E-7	95.0	5
ATGTAGC	15	6.142176E-4	95.0	6
AGCGTAG	25	3.8289727E-7	95.0	4
TCGAGTA	90	0.0	95.0	3
AGTTCAA	60	0.0	95.0	9
>>END_MODULE
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
Rejected 268783 READS because READLEN < 1
Read 268783 spots for SRR6941567.sra
Written 268783 spots for SRR6941567.sra
SRR ids: ['SRR6941567.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_onta5pb6
SRR6941567.sra spots: 5375660
blocks: [[1, 268783], [268784, 537566], [537567, 806349], [806350, 1075132], [1075133, 1343915], [1343916, 1612698], [1612699, 1881481], [1881482, 2150264], [2150265, 2419047], [2419048, 2687830], [2687831, 2956613], [2956614, 3225396], [3225397, 3494179], [3494180, 3762962], [3762963, 4031745], [4031746, 4300528], [4300529, 4569311], [4569312, 4838094], [4838095, 5106877], [5106878, 5375660]]
SRR6941567 file size 1283999
SRR6941567 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 SRR6941567 SRR6941567_1.fastq
Input file:	SRR6941567_1.fastq
trimmed:	SRR6941567-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 11:35:17 2024 >> started

Fri Dec  6 11:35:20 2024 >> done (3.297s)
5375660 reads processed; of these:
     97 ( 0.00%) short reads filtered out after trimming by size control
     22 ( 0.00%) empty reads filtered out after trimming by size control
5375541 (100.00%) reads available; of these:
 769344 (14.31%) trimmed reads available after processing
4606197 (85.69%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      7	  0.00%
 19	      4	  0.00%
 20	      8	  0.00%
 21	     11	  0.00%
 22	     10	  0.00%
 23	     12	  0.00%
 24	     18	  0.00%
 25	     20	  0.00%
 26	     24	  0.00%
 27	     37	  0.00%
 28	     48	  0.00%
 29	     45	  0.00%
 30	     51	  0.00%
 31	     35	  0.00%
 32	     42	  0.00%
 33	     41	  0.00%
 34	     57	  0.00%
 35	     78	  0.00%
 36	     56	  0.00%
 37	     67	  0.00%
 38	     57	  0.00%
 39	     67	  0.00%
 40	     73	  0.00%
 41	     81	  0.00%
 42	     83	  0.00%
 43	     82	  0.00%
 44	     56	  0.00%
 45	     99	  0.00%
 46	     85	  0.00%
 47	     76	  0.00%
 48	     66	  0.00%
 49	     58	  0.00%
 50	     73	  0.00%
 51	     72	  0.00%
 52	     60	  0.00%
 53	     60	  0.00%
 54	     80	  0.00%
 55	     55	  0.00%
 56	     61	  0.00%
 57	     42	  0.00%
 58	     50	  0.00%
 59	     69	  0.00%
 60	     63	  0.00%
 61	     74	  0.00%
 62	     74	  0.00%
 63	     87	  0.00%
 64	     77	  0.00%
 65	     93	  0.00%
 66	    104	  0.00%
 67	    121	  0.00%
 68	    196	  0.00%
 69	    230	  0.00%
 70	    311	  0.01%
 71	    312	  0.01%
 72	    537	  0.01%
 73	   1388	  0.03%
 74	   9195	  0.17%
 75	   6599	  0.12%
 76	   2201	  0.04%
 77	    666	  0.01%
 78	    863	  0.02%
 79	    806	  0.01%
 80	    927	  0.02%
 81	    879	  0.02%
 82	    991	  0.02%
 83	   1419	  0.03%
 84	   2042	  0.04%
 85	   2346	  0.04%
 86	   2516	  0.05%
 87	   2718	  0.05%
 88	   3031	  0.06%
 89	   3996	  0.07%
 90	   5549	  0.10%
 91	   8089	  0.15%
 92	  11014	  0.20%
 93	  19864	  0.37%
 94	  33590	  0.62%
 95	  75143	  1.40%
 96	  85712	  1.59%
 97	  94348	  1.76%
 98	 143645	  2.67%
 99	 167687	  3.12%
100	  77665	  1.44%
101	4606197	 85.69%
5375541 reads passed initial QC


criterion=sequence-density
sequence-density=97.49
sequence-density-rank=1
fanout-score=25.93
fanout-score-rank=2
prefix-density=97.31
prefix-fanout=25.9
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGCCAATATCTCGTATGCCGTCTTCTGCTTGAAAAA


criterion=fanout-score
sequence-density=0.01
sequence-density-rank=11
fanout-score=27.53
fanout-score-rank=1
prefix-density=0.30
prefix-fanout=1.0
sequence=CCATCGAGTAGACCTTGTTATTGTGAGAATT
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGCCAATATCTCGTATGCCGTCTTCTGCTTGAAAAA -o SRR6941567 -
Input file:	STDIN
trimmed:	SRR6941567-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGCCAATATCTCGTATGCCGTCTTCTGCTTGA
-- 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 11:35:31 2024 >> started

Fri Dec  6 11:35:38 2024 >> done (7.053s)
5265836 reads processed; of these:
  38450 ( 0.73%) short reads filtered out after trimming by size control
  35396 ( 0.67%) empty reads filtered out after trimming by size control
5191990 (98.60%) reads available; of these:
5150787 (99.21%) trimmed reads available after processing
  41203 ( 0.79%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  15151	  0.29%
 19	  32582	  0.63%
 20	  45033	  0.87%
 21	 176709	  3.40%
 22	 162721	  3.13%
 23	 133607	  2.57%
 24	 667101	 12.85%
 25	 158714	  3.06%
 26	 150977	  2.91%
 27	 142802	  2.75%
 28	 143498	  2.76%
 29	 377008	  7.26%
 30	 654529	 12.61%
 31	 438753	  8.45%
 32	 432457	  8.33%
 33	 409882	  7.89%
 34	 314934	  6.07%
 35	 284368	  5.48%
 36	 129175	  2.49%
 37	  75737	  1.46%
 38	  43952	  0.85%
 39	  31431	  0.61%
 40	  38063	  0.73%
 41	  37006	  0.71%
 42	  28016	  0.54%
 43	   7157	  0.14%
 44	   7520	  0.14%
 45	   4300	  0.08%
 46	   1688	  0.03%
 47	   1927	  0.04%
 48	    797	  0.02%
 49	    423	  0.01%
 50	    248	  0.00%
 51	    192	  0.00%
 52	    100	  0.00%
 53	     93	  0.00%
 54	     64	  0.00%
 55	     65	  0.00%
 56	     37	  0.00%
 57	     51	  0.00%
 58	     47	  0.00%
 59	     45	  0.00%
 60	     33	  0.00%
 61	     24	  0.00%
 62	     36	  0.00%
 63	     30	  0.00%
 64	     31	  0.00%
 65	     24	  0.00%
 66	     34	  0.00%
 67	     35	  0.00%
 68	     55	  0.00%
 69	     62	  0.00%
 70	     79	  0.00%
 71	     56	  0.00%
 72	     55	  0.00%
 73	     56	  0.00%
 74	     61	  0.00%
 75	     71	  0.00%
 76	    125	  0.00%
 77	    480	  0.01%
 78	    107	  0.00%
 79	    154	  0.00%
 80	    375	  0.01%
 81	    162	  0.00%
 82	    279	  0.01%
 83	    225	  0.00%
 84	    105	  0.00%
 85	    107	  0.00%
 86	    153	  0.00%
 87	    237	  0.00%
 88	    143	  0.00%
 89	    105	  0.00%
 90	    165	  0.00%
 91	    260	  0.01%
 92	    220	  0.00%
 93	    253	  0.00%
 94	    307	  0.01%
 95	    369	  0.01%
 96	    427	  0.01%
 97	    474	  0.01%
 98	    796	  0.02%
 99	    530	  0.01%
100	    609	  0.01%
101	  35121	  0.68%


criterion=sequence-density
sequence-density=7.21
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=19
prefix-density=0.00
prefix-fanout=1.0
sequence=GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTCAAGGCGG


criterion=fanout-score
sequence-density=0.01
sequence-density-rank=33
fanout-score=375.10
fanout-score-rank=1
prefix-density=3.11
prefix-fanout=1.0
sequence=GTAGCCAAGTGCGGAGAGGATAACTGCTGAAAGCATATAAGTAGTAAGCCCACCCCAAGATGAGTGCTCTCTC
                                 Started job on |	Dec 06 11:35:51
                             Started mapping on |	Dec 06 11:35:51
                                    Finished on |	Dec 06 11:36:05
       Mapping speed, Million of reads per hour |	1363.29

                          Number of input reads |	5301695
                      Average input read length |	31
                                    UNIQUE READS:
                   Uniquely mapped reads number |	741803
                        Uniquely mapped reads % |	13.99%
                          Average mapped length |	25.99
                       Number of splices: Total |	5539
            Number of splices: Annotated (sjdb) |	2855
                       Number of splices: GT/AG |	5246
                       Number of splices: GC/AG |	154
                       Number of splices: AT/AC |	3
               Number of splices: Non-canonical |	136
                      Mismatch rate per base, % |	0.14%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.68
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.08
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	3419375
             % of reads mapped to multiple loci |	64.50%
        Number of reads mapped to too many loci |	931707
             % of reads mapped to too many loci |	17.57%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	3.44%
                     % of reads unmapped: other |	0.50%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	1140517	1140517	1140517
N_multimapping	3419375	3419375	3419375
N_noFeature	510512	597153	652220
N_ambiguous	7364	4303	154
UnstrandedReadsAssigned:223927 PositiveStrandReadsAssigned:140347 NegativeStrandReadsAssigned:89429
Dataset is classified unstranded
MeadianReadLen=30 20thPercentileLength=24 echo kmer=19
SRR6941567 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: SRR6941567-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 5,301,695 reads, 2,489,875 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 915 rounds

  52973 SRR6941567.ke.tsv
  35125 SRR6941567.se.tsv
  88098 total
==> SRR6941567.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	0	0
PNS24249	1928	1829	2	0.249149
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	1	0.166069
PNS24243	293	194	0	0
KQK14069	1603	1504	25.3809	3.84505
KQK14071	474	375	1.69151	1.02775

==> SRR6941567.se.tsv <==
BRADI_1g14170v3	40
BRADI_1g53295v3	2
BRADI_1g59795v3	1
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	0
BRADI_1g74790v3	13
BRADI_1g09890v3	0
BRADI_1g77505v3	0
BRADI_1g48960v3	0
SRR6941567 completed mapping pipeline successfully
