Starting /dee2/code/volunteer_pipeline.sh SRR8846483
    current disk space = 1505283002368
    free memory = 1379981396 
SRR8846483 SRAfilesize
517e78cee8511a787c1bc50d931f067c  SRR8846483.sra
SRR8846483.sra file validated
SRR8846483 is single end
SRR8846483 is conventional basespace
SRR8846483 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR8846483_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	45
>>END_MODULE
>>Per base sequence quality	warn
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	30.701	34.0	33.0	34.0	27.0	34.0
2	32.6275	34.0	33.0	34.0	28.0	34.0
3	32.99375	34.0	33.0	34.0	32.0	34.0
4	33.222	34.0	33.0	34.0	32.0	34.0
5	33.27075	34.0	33.0	34.0	33.0	34.0
6	37.007	38.0	37.0	38.0	36.0	38.0
7	37.3545	38.0	38.0	38.0	36.0	38.0
8	37.449	38.0	38.0	38.0	37.0	38.0
9	37.513	38.0	38.0	38.0	37.0	38.0
10-11	37.592375000000004	38.0	38.0	38.0	38.0	38.0
12-13	37.636624999999995	38.0	38.0	38.0	38.0	38.0
14-15	37.569375	38.0	38.0	38.0	38.0	38.0
16-17	37.494375000000005	38.0	38.0	38.0	37.5	38.0
18-19	37.48325	38.0	38.0	38.0	38.0	38.0
20-21	37.523375	38.0	38.0	38.0	38.0	38.0
22-23	37.590625	38.0	38.0	38.0	38.0	38.0
24-25	37.6265	38.0	38.0	38.0	38.0	38.0
26-27	37.5845	38.0	38.0	38.0	38.0	38.0
28-29	37.565875000000005	38.0	38.0	38.0	38.0	38.0
30-31	37.5	38.0	38.0	38.0	38.0	38.0
32-33	37.455625	38.0	38.0	38.0	37.0	38.0
34-35	37.287125	38.0	38.0	38.0	37.0	38.0
36-37	37.1725	38.0	38.0	38.0	37.0	38.0
38-39	37.01675	38.0	38.0	38.0	36.0	38.0
40-41	37.1055	38.0	38.0	38.0	37.0	38.0
42-43	37.114875	38.0	38.0	38.0	36.5	38.0
44-45	37.201625	38.0	38.0	38.0	37.0	38.0
46-47	37.134875	38.0	38.0	38.0	36.5	38.0
48-49	37.214124999999996	38.0	38.0	38.0	36.5	38.0
50-51	37.2505	38.0	38.0	38.0	37.0	38.0
52-53	37.376875	38.0	38.0	38.0	37.0	38.0
54-55	37.332625	38.0	38.0	38.0	37.0	38.0
56-57	37.16125	38.0	38.0	38.0	36.5	38.0
58-59	37.121375	38.0	38.0	38.0	36.5	38.0
60-61	37.070750000000004	38.0	38.0	38.0	36.5	38.0
62-63	36.445625	38.0	38.0	38.0	34.0	38.0
64-65	36.03575	38.0	37.5	38.0	31.0	38.0
66-67	35.877875	38.0	37.0	38.0	30.5	38.0
68-69	36.010125	38.0	37.0	38.0	32.0	38.0
70-71	35.734625	38.0	37.0	38.0	30.0	38.0
72-73	35.69825	38.0	37.0	38.0	31.0	38.0
74-75	35.4995	38.0	37.0	38.0	29.5	38.0
76-77	35.25925	38.0	37.0	38.0	28.5	38.0
78-79	35.24725	38.0	37.0	38.0	28.5	38.0
80-81	35.544875000000005	38.0	37.0	38.0	30.0	38.0
82-83	35.1	38.0	37.0	38.0	28.0	38.0
84-85	35.392125	38.0	37.0	38.0	29.0	38.0
86-87	35.384625	38.0	37.0	38.0	30.0	38.0
88-89	35.472375	38.0	37.0	38.0	31.0	38.0
90-91	35.3815	38.0	37.0	38.0	32.0	38.0
92-93	35.30025	38.0	38.0	38.0	31.0	38.0
94-95	34.716499999999996	38.0	37.5	38.0	29.0	38.0
96-97	32.882999999999996	38.0	35.0	38.0	8.5	38.0
98-99	30.376625	38.0	29.5	38.0	2.0	38.0
100-101	26.753875	37.5	8.5	38.0	2.0	38.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
12	1.0
13	0.0
14	1.0
15	1.0
16	0.0
17	1.0
18	1.0
19	0.0
20	1.0
21	3.0
22	3.0
23	6.0
24	16.0
25	35.0
26	30.0
27	24.0
28	19.0
29	29.0
30	49.0
31	60.0
32	88.0
33	121.0
34	181.0
35	380.0
36	880.0
37	2070.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	26.85838307107976	28.567552902875747	22.544763971785134	22.02930005425936
2	23.35	31.424999999999997	17.974999999999998	27.250000000000004
3	23.925	20.25	21.175	34.65
4	28.025	30.25	18.075	23.65
5	30.5	25.45	18.875	25.174999999999997
6	24.325	27.6	25.074999999999996	23.0
7	37.4	23.375	19.2	20.025000000000002
8	22.425	23.7	32.275	21.6
9	25.2	32.25	22.675	19.875
10-11	29.125	26.224999999999998	23.6375	21.0125
12-13	22.725	22.4375	21.1625	33.675
14-15	22.825	35.425000000000004	23.799999999999997	17.95
16-17	24.224999999999998	28.762500000000003	26.887499999999996	20.125
18-19	28.449999999999996	25.087500000000002	21.987499999999997	24.474999999999998
20-21	21.3125	28.487499999999997	27.425	22.775000000000002
22-23	27.900000000000002	27.675	29.45	14.975
24-25	26.75	24.55	27.6625	21.0375
26-27	34.3125	27.3	21.925	16.4625
28-29	21.15	31.6875	26.575	20.5875
30-31	23.7875	20.549999999999997	37.875	17.7875
32-33	23.125	20.1875	34.725	21.9625
34-35	29.475	16.7125	29.925	23.8875
36-37	38.7	13.0125	30.587500000000002	17.7
38-39	36.05	17.9	26.237500000000004	19.8125
40-41	28.95	19.3375	22.5125	29.2
42-43	30.349999999999998	26.5125	22.675	20.4625
44-45	39.324999999999996	19.725	15.6	25.35
46-47	30.15	32.0625	13.3875	24.4
48-49	28.3875	23.6375	19.1875	28.787499999999998
50-51	23.2625	23.375	15.625	37.737500000000004
52-53	22.900000000000002	33.2375	12.4125	31.45
54-55	18.987499999999997	27.462500000000002	17.875	35.675000000000004
56-57	18.075	35.4125	11.4875	35.025
58-59	9.049999999999999	36.65	15.312500000000002	38.987500000000004
60-61	7.324999999999999	37.487500000000004	15.5	39.6875
62-63	8.0375	38.2125	20.625	33.125
64-65	7.675	37.55	24.3	30.475
66-67	6.275	29.525000000000002	27.950000000000003	36.25
68-69	11.3125	31.4375	24.0625	33.1875
70-71	10.875	31.974999999999998	29.925	27.224999999999998
72-73	18.0625	23.5	30.7875	27.650000000000002
74-75	13.5875	21.212500000000002	29.525000000000002	35.675000000000004
76-77	19.325	15.9125	38.987500000000004	25.775
78-79	16.412499999999998	10.15	38.2	35.2375
80-81	18.675	11.25	37.737500000000004	32.337500000000006
82-83	21.65	10.6	43.65	24.099999999999998
84-85	19.2375	9.7375	38.5625	32.4625
86-87	22.4625	16.125	36.9	24.5125
88-89	15.625	34.0125	33.037499999999994	17.325
90-91	12.7	42.15	28.050000000000004	17.1
92-93	12.375	52.5625	21.8125	13.25
94-95	10.424999999999999	62.612500000000004	17.837500000000002	9.125
96-97	7.449999999999999	70.2625	15.712499999999999	6.575
98-99	6.65	79.5125	10.025	3.8125
100-101	3.5749999999999997	87.41250000000001	5.325	3.6875
>>END_MODULE
>>Per sequence GC content	warn
#GC Content	Count
0	0.0
1	0.0
2	0.0
3	0.0
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
10	0.0
11	0.0
12	0.0
13	0.0
14	0.0
15	0.0
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	1.0
31	3.0
32	5.0
33	11.0
34	17.5
35	18.0
36	13.5
37	16.0
38	50.0
39	72.5
40	114.0
41	188.5
42	242.0
43	337.0
44	381.0
45	421.5
46	403.5
47	324.5
48	303.5
49	243.5
50	181.0
51	124.5
52	87.0
53	94.0
54	163.0
55	124.0
56	23.0
57	14.5
58	9.0
59	4.5
60	4.0
61	1.5
62	2.0
63	1.5
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	warn
#Base	N-Count
1	7.85
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	56.474999999999994
#Duplication Level	Percentage of deduplicated	Percentage of total
1	83.88667552014165	47.375
2	7.791057990261177	8.799999999999999
3	3.054448871181939	5.175
4	0.9738822487826472	2.1999999999999997
5	0.8853474988933155	2.5
6	0.7082779991146525	2.4
7	0.35413899955732625	1.4000000000000001
8	0.3098716246126605	1.4000000000000001
9	0.17706949977866313	0.8999999999999999
>10	1.6378928729526339	16.175
>50	0.17706949977866313	8.05
>100	0.04426737494466578	3.6249999999999996
>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
TCCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGT	145	3.6249999999999996	No Hit
GGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGA	87	2.175	RNA PCR Primer, Index 1 (100% over 22bp)
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	81	2.025	RNA PCR Primer, Index 1 (100% over 29bp)
AGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGC	78	1.95	No Hit
GACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	76	1.9	RNA PCR Primer, Index 1 (100% over 23bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	36	0.8999999999999999	No Hit
CTCTGATGATGATCAAACTAATACTTTCGTTCTTCTGGAATTCTCGGGTG	35	0.8750000000000001	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTGGAATTCTCGGGTGCCAAGG	28	0.7000000000000001	Illumina Small RNA Adapter 2 (100% over 21bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	27	0.675	No Hit
CACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGATGGAATTC	27	0.675	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATATGGAATTCTCGGGTGCCAAG	26	0.65	No Hit
ATATATTTCAAGTTATTTCGGATCTTGGAATTCTCGGGTGCCAAGGAACT	25	0.625	RNA PCR Primer, Index 1 (100% over 25bp)
AAGGGTGCTGAGAATACTTTGAATCTGACACTGGAATTCTCGGGTGCCAA	25	0.625	No Hit
GACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAAC	23	0.575	RNA PCR Primer, Index 1 (100% over 24bp)
TCTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTCTT	23	0.575	RNA PCR Primer, Index 29 (100% over 50bp)
GACACGACTCTCGGCAACGGATATCTGGAATTCTCGGGTGCCAAGGAACT	22	0.5499999999999999	RNA PCR Primer, Index 1 (100% over 25bp)
CTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTCTTC	22	0.5499999999999999	RNA PCR Primer, Index 29 (100% over 50bp)
AGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGG	19	0.475	Illumina Small RNA Adapter 2 (100% over 21bp)
GCCCACCCCAAGATGAGTGCTCTCTCTGGAATTCTCGGGTGCCAAGGAAC	18	0.44999999999999996	RNA PCR Primer, Index 1 (100% over 24bp)
AATTCTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGT	18	0.44999999999999996	RNA PCR Primer, Index 29 (100% over 50bp)
TGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAA	16	0.4	No Hit
GCACCAGTGGTCTAGTGGTAGAATAGTACCTGGAATTCTCGGGTGCCAAG	15	0.375	No Hit
CCAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGG	15	0.375	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCATGGAATTCTCGGGTG	15	0.375	No Hit
NGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGA	14	0.35000000000000003	RNA PCR Primer, Index 1 (100% over 22bp)
TCCTGTGGATGAGAAGGCATTTATATTCTGATGATATGGAATTCTCGGGT	14	0.35000000000000003	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCTGGAATTCTCGGGTGCCAAGG	14	0.35000000000000003	Illumina Small RNA Adapter 2 (100% over 21bp)
ATTCTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTC	14	0.35000000000000003	RNA PCR Primer, Index 29 (100% over 50bp)
GAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAG	14	0.35000000000000003	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	13	0.325	No Hit
CTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	13	0.325	RNA PCR Primer, Index 1 (100% over 28bp)
CATCGAGTAGACCTTGTTATTGTGAGAATAAATGGAATTCTCGGGTGCCA	12	0.3	No Hit
AAGGGTGCTGAGAATACTTTGAATCTGACATGGAATTCTCGGGTGCCAAG	12	0.3	No Hit
TATTCTGGTGTCCTAGGCGTAGAGGATGGAATTCTCGGGTGCCAAGGAAC	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 24bp)
ACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTGC	11	0.27499999999999997	No Hit
CACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAACT	10	0.25	RNA PCR Primer, Index 1 (100% over 25bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCTGGAATTCTCGGGTGC	10	0.25	No Hit
TCCGTCGTAGTCTAGGTGGTTAGGATACTCTGGAATTCTCGGGTGCCAAG	10	0.25	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGG	10	0.25	Illumina Small RNA Adapter 2 (100% over 21bp)
CATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTGCC	10	0.25	No Hit
ATATATTTCAAGTTATTTCGGATCTGGAATTCTCGGGTGCCAAGGAACTC	10	0.25	RNA PCR Primer, Index 1 (100% over 26bp)
TTCTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTCT	10	0.25	RNA PCR Primer, Index 29 (100% over 50bp)
NCCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGT	9	0.22499999999999998	No Hit
CAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGG	9	0.22499999999999998	No Hit
CAGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTG	9	0.22499999999999998	No Hit
TACCTGGTTGATCCTGCCAGTAGTCATATGCTTGTGGAATTCTCGGGTGC	9	0.22499999999999998	No Hit
TCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTC	8	0.2	RNA PCR Primer, Index 1 (100% over 26bp)
CATCGAGTAGACCTTGTTATTGTGAGAATGGAATTCTCGGGTGCCAAGGA	8	0.2	RNA PCR Primer, Index 1 (100% over 22bp)
TCCGTCGTAGTCTAGGTGGTTAGGATATGGAATTCTCGGGTGCCAAGGAA	8	0.2	RNA PCR Primer, Index 1 (100% over 23bp)
ATAACCGTAGTAATTCTAGAGCTAATGGAATTCTCGGGTGCCAAGGAACT	8	0.2	RNA PCR Primer, Index 1 (100% over 25bp)
CCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTG	8	0.2	No Hit
ACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCC	8	0.2	No Hit
CAGGGTTCGTTTCCCTGGATGCGCACCATGGAATTCTCGGGTGCCAAGGA	8	0.2	RNA PCR Primer, Index 1 (100% over 22bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTTGGAATTCTCGGGTGCC	7	0.17500000000000002	No Hit
TTCGGACCAGGCTTCATTCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 29bp)
TCTCGGACCAGGCTTCATTCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 29bp)
GGGGATGTAGCTCAGATGGTAGATGGAATTCTCGGGTGCCAAGGAACTCC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 27bp)
TGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
CACGACTCTCGGCAACGGATATCTGGAATTCTCGGGTGCCAAGGAACTCC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 27bp)
GCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCC	7	0.17500000000000002	No Hit
CGGATAACCGTAGTAATTCTAGAGCTAATACTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
CGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGATGGAATTCTC	6	0.15	No Hit
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTGCTAATCTGGAATTCT	6	0.15	No Hit
GACACGACTCTCGGCAACGGATATCTCGGCTGGAATTCTCGGGTGCCAAG	6	0.15	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCAAAATCTTGGAATTCT	6	0.15	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATAAAAATGGAATTCTCGGGTGC	6	0.15	No Hit
ATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTGCCA	6	0.15	No Hit
CATCGAGTAGACCTTGTTATTGTGAGATGGAATTCTCGGGTGCCAAGGAA	6	0.15	RNA PCR Primer, Index 1 (100% over 23bp)
NCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGTGAATCTGGAATTC	6	0.15	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGACTTGGAATTCTCGGGTGCC	6	0.15	No Hit
CACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGTGGAATTCTCGG	6	0.15	No Hit
GACACGACTCTCGGCAACGGATATCTCGTGGAATTCTCGGGTGCCAAGGA	6	0.15	RNA PCR Primer, Index 1 (100% over 22bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGTGGAATTCTCGGGT	6	0.15	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAATGGAATTCTCGGGTG	6	0.15	No Hit
ATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAA	6	0.15	RNA PCR Primer, Index 1 (100% over 23bp)
CTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCA	6	0.15	No Hit
GATAACCGTAGTAATTCTAGAGCTAATTGGAATTCTCGGGTGCCAAGGAA	5	0.125	RNA PCR Primer, Index 1 (100% over 23bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAAATGGAATTCTCGGGT	5	0.125	No Hit
GACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTG	5	0.125	No Hit
ACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
TGTATGCAGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCT	5	0.125	No Hit
TCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTCTTCT	5	0.125	RNA PCR Primer, Index 29 (100% over 50bp)
GAAGTCCTCGTGTTGCATTCCTTGGAATTCTCGGGTGCCAAGGAACTCCA	5	0.125	RNA PCR Primer, Index 1 (100% over 28bp)
CACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGGAATTCTCG	5	0.125	No Hit
ACACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGATGGAATT	5	0.125	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTTGGAATTCTCGGGTG	5	0.125	No Hit
ACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTTGAATTCTCGGGTGC	5	0.125	No Hit
CACGACTCTCGGCAACGGATATCTCGTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
NCCTTGATGGTGAAATGGTAGACACGCGAGACTCATGGAATTCTCGGGTG	5	0.125	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTGGAATTCTCGGGTGCCAAGG	5	0.125	Illumina Small RNA Adapter 2 (100% over 21bp)
ACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	5	0.125	RNA PCR Primer, Index 1 (100% over 31bp)
AACCGTAGTAATTCTAGAGCTAATGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
GGGGATATAGCTCAGTTGGTAGATGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
AGCTGAGGCATCCTAACGAACGAACGATTTGAATGGAATTCTCGGGTGCC	5	0.125	No Hit
NACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	5	0.125	RNA PCR Primer, Index 1 (100% over 23bp)
CTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCA	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	0.025	0.0	0.0	0.0
2	0.0	0.05	0.0	0.0	0.0
3	0.0	0.05	0.0	0.0	0.0
4	0.0	0.05	0.0	0.0	0.0
5	0.0	0.05	0.0	0.0	0.0
6	0.0	0.05	0.0	0.0	0.0
7	0.0	0.1	0.0	0.0	0.0
8	0.0	0.125	0.0	0.0	0.0
9	0.0	0.175	0.0	0.0	0.0
10-11	0.0	0.2125	0.0	0.0	0.0
12-13	0.0	0.3125	0.0	0.0	0.0
14-15	0.0	0.5125	0.0	0.0	0.0
16-17	0.0	1.0875	0.0	0.0	0.0
18-19	0.0	1.775	0.0	0.0	0.0
20-21	0.0	3.5375	0.0	0.0	0.0
22-23	0.0	10.4875	0.0	0.0	0.0
24-25	0.0	22.2625	0.0	0.0	0.0
26-27	0.0	35.8625	0.0	0.0	0.0
28-29	0.0	45.8	0.0	0.0	0.0
30-31	0.0	55.7875	0.0	0.0	0.0
32-33	0.0	64.36250000000001	0.0	0.0	0.0
34-35	0.0	73.225	0.0	0.0	0.0
36-37	0.0	83.025	0.0	0.0	0.0
38-39	0.0	88.3375	0.0	0.0	0.0
40-41	0.0	90.5625	0.0	0.0	0.0
42-43	0.0	93.23750000000001	0.0	0.0	0.0
44-45	0.0	94.575	0.0	0.0	0.0
46-47	0.0	94.9375	0.0	0.0	0.0
48-49	0.0	94.975	0.0	0.0	0.0
50-51	0.0	94.975	0.0	0.0	0.0
52-53	0.0	94.975	0.0	0.0	0.0
54-55	0.0	94.975	0.0	0.0	0.0
56-57	0.0	94.975	0.0	0.0	0.0
58-59	0.0	94.975	0.0	0.0	0.0
60-61	0.0	94.975	0.0	0.0	0.0
62-63	0.0	94.975	0.0	0.0	0.0
64-65	0.0	94.975	0.0	0.0	0.0
66-67	0.0	94.975	0.0	0.0	0.0
68-69	0.0	94.975	0.0	0.0	0.0
70-71	0.0	94.975	0.0	0.0	0.0
72-73	0.0	94.975	0.0	0.0	0.0
74-75	0.0	94.975	0.0	0.0	0.0
76-77	0.0	94.9875	0.0	0.0	0.0
78-79	0.0	95.0	0.0	0.0	0.0
80-81	0.0	95.0	0.0	0.0	0.0
82-83	0.0	95.0125	0.0	0.0	0.0
84-85	0.0	95.025	0.0	0.0	0.0
86-87	0.0	95.025	0.0	0.0	0.0
88-89	0.0	95.025	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGGATTG	20	9.691041E-6	104.013695	1
GTAGACC	20	1.5462934E-5	94.912506	7
AGCTCAG	20	1.5462934E-5	94.912506	9
AGTAGAC	20	1.5462934E-5	94.912506	6
TAGCTCA	20	1.5462934E-5	94.912506	8
GGATTGT	20	1.5462934E-5	94.912506	2
GATTGTA	20	1.5462934E-5	94.912506	3
TAGTTCA	25	3.8500548E-7	94.912506	8
GAGTAGA	20	1.5462934E-5	94.912506	5
ATTGTAG	20	1.5462934E-5	94.912506	4
TGTAGTT	20	1.5462934E-5	94.912506	6
CGAGTAG	20	1.5462934E-5	94.912506	4
AGACCTT	20	1.5462934E-5	94.912506	9
TCGAGTA	20	1.5462934E-5	94.912506	3
AGTTCAA	25	3.8500548E-7	94.912506	9
GTAGTTC	25	3.8500548E-7	94.912506	7
TAGACCT	20	1.5462934E-5	94.912506	8
GTCGTAG	15	6.164719E-4	94.9125	4
CGTAGTC	15	6.164719E-4	94.9125	6
CCGTCGT	15	6.164719E-4	94.9125	2
>>END_MODULE
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901640 READS because READLEN < 1
Read 901640 spots for SRR8846483.sra
Written 901640 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
Rejected 901629 READS because READLEN < 1
Read 901629 spots for SRR8846483.sra
Written 901629 spots for SRR8846483.sra
SRR ids: ['SRR8846483.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_318g52_d
SRR8846483.sra spots: 18032591
blocks: [[1, 901629], [901630, 1803258], [1803259, 2704887], [2704888, 3606516], [3606517, 4508145], [4508146, 5409774], [5409775, 6311403], [6311404, 7213032], [7213033, 8114661], [8114662, 9016290], [9016291, 9917919], [9917920, 10819548], [10819549, 11721177], [11721178, 12622806], [12622807, 13524435], [13524436, 14426064], [14426065, 15327693], [15327694, 16229322], [16229323, 17130951], [17130952, 18032591]]
SRR8846483 file size 4327957
SRR8846483 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 SRR8846483 SRR8846483_1.fastq
Input file:	SRR8846483_1.fastq
trimmed:	SRR8846483-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
Sun Dec  8 17:22:32 2024 >> started

Sun Dec  8 17:23:19 2024 >> done (47.177s)
18032591 reads processed; of these:
     291 ( 0.00%) short reads filtered out after trimming by size control
      50 ( 0.00%) empty reads filtered out after trimming by size control
18032250 (100.00%) reads available; of these:
 3844902 (21.32%) trimmed reads available after processing
14187348 (78.68%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      38	  0.00%
 19	      31	  0.00%
 20	      38	  0.00%
 21	      40	  0.00%
 22	      39	  0.00%
 23	      40	  0.00%
 24	      58	  0.00%
 25	      60	  0.00%
 26	      93	  0.00%
 27	     117	  0.00%
 28	     144	  0.00%
 29	     164	  0.00%
 30	     164	  0.00%
 31	     154	  0.00%
 32	     184	  0.00%
 33	     250	  0.00%
 34	     241	  0.00%
 35	     229	  0.00%
 36	     278	  0.00%
 37	     266	  0.00%
 38	     243	  0.00%
 39	     309	  0.00%
 40	     298	  0.00%
 41	     322	  0.00%
 42	     318	  0.00%
 43	     323	  0.00%
 44	     289	  0.00%
 45	     231	  0.00%
 46	     190	  0.00%
 47	     210	  0.00%
 48	     263	  0.00%
 49	     289	  0.00%
 50	     337	  0.00%
 51	     350	  0.00%
 52	     304	  0.00%
 53	     338	  0.00%
 54	     266	  0.00%
 55	     207	  0.00%
 56	     309	  0.00%
 57	     289	  0.00%
 58	     350	  0.00%
 59	     395	  0.00%
 60	     557	  0.00%
 61	     903	  0.01%
 62	    1591	  0.01%
 63	    1844	  0.01%
 64	    3589	  0.02%
 65	    4711	  0.03%
 66	   13100	  0.07%
 67	   68059	  0.38%
 68	   75958	  0.42%
 69	   47696	  0.26%
 70	   37523	  0.21%
 71	   43330	  0.24%
 72	   19445	  0.11%
 73	    6711	  0.04%
 74	    6558	  0.04%
 75	    4981	  0.03%
 76	    4576	  0.03%
 77	    4027	  0.02%
 78	    4834	  0.03%
 79	    5051	  0.03%
 80	    5725	  0.03%
 81	    6401	  0.04%
 82	   10180	  0.06%
 83	   10491	  0.06%
 84	   10344	  0.06%
 85	   11835	  0.07%
 86	   13331	  0.07%
 87	   15751	  0.09%
 88	   24901	  0.14%
 89	   35927	  0.20%
 90	   58770	  0.33%
 91	   58129	  0.32%
 92	   73622	  0.41%
 93	  116145	  0.64%
 94	  153963	  0.85%
 95	  346725	  1.92%
 96	  399988	  2.22%
 97	  418613	  2.32%
 98	  629307	  3.49%
 99	  717321	  3.98%
100	  363331	  2.01%
101	14187348	 78.68%
18032250 reads passed initial QC


criterion=sequence-density
sequence-density=94.11
sequence-density-rank=1
fanout-score=33.51
fanout-score-rank=1
prefix-density=94.49
prefix-fanout=33.4
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA


criterion=fanout-score
sequence-density=94.11
sequence-density-rank=1
fanout-score=33.51
fanout-score-rank=1
prefix-density=94.49
prefix-fanout=33.4
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA -o SRR8846483 -
Input file:	STDIN
trimmed:	SRR8846483-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAACTAATCTCGTATGCCGTCTTCTGCTTGA
-- 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
Sun Dec  8 17:26:25 2024 >> started

Sun Dec  8 17:27:50 2024 >> done (84.859s)
17652624 reads processed; of these:
  305703 ( 1.73%) short reads filtered out after trimming by size control
    8179 ( 0.05%) empty reads filtered out after trimming by size control
17338742 (98.22%) reads available; of these:
16741306 (96.55%) trimmed reads available after processing
  597436 ( 3.45%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	   93689	  0.54%
 19	  161189	  0.93%
 20	  207256	  1.20%
 21	  822474	  4.74%
 22	  430252	  2.48%
 23	  660781	  3.81%
 24	 2354824	 13.58%
 25	  852947	  4.92%
 26	  814280	  4.70%
 27	  894989	  5.16%
 28	  950905	  5.48%
 29	  825363	  4.76%
 30	 1021468	  5.89%
 31	  660161	  3.81%
 32	  630504	  3.64%
 33	  827673	  4.77%
 34	  888010	  5.12%
 35	  785787	  4.53%
 36	 1036294	  5.98%
 37	  384519	  2.22%
 38	  305407	  1.76%
 39	  241385	  1.39%
 40	  206459	  1.19%
 41	  235862	  1.36%
 42	  228394	  1.32%
 43	   72259	  0.42%
 44	   69466	  0.40%
 45	   30531	  0.18%
 46	   15663	  0.09%
 47	    7717	  0.04%
 48	    6151	  0.04%
 49	    3273	  0.02%
 50	    2308	  0.01%
 51	    2078	  0.01%
 52	    1042	  0.01%
 53	     776	  0.00%
 54	     977	  0.01%
 55	     336	  0.00%
 56	     632	  0.00%
 57	     294	  0.00%
 58	     330	  0.00%
 59	     357	  0.00%
 60	     483	  0.00%
 61	     865	  0.00%
 62	    1435	  0.01%
 63	    1694	  0.01%
 64	    3327	  0.02%
 65	    4436	  0.03%
 66	   12685	  0.07%
 67	   66343	  0.38%
 68	   74033	  0.43%
 69	   46377	  0.27%
 70	   36271	  0.21%
 71	   41890	  0.24%
 72	   17595	  0.10%
 73	    4883	  0.03%
 74	    3541	  0.02%
 75	    2672	  0.02%
 76	    2893	  0.02%
 77	    3572	  0.02%
 78	    2901	  0.02%
 79	    2895	  0.02%
 80	    4242	  0.02%
 81	    3239	  0.02%
 82	    2773	  0.02%
 83	    3108	  0.02%
 84	    1842	  0.01%
 85	    1795	  0.01%
 86	    1651	  0.01%
 87	    1542	  0.01%
 88	    1315	  0.01%
 89	    1378	  0.01%
 90	    1216	  0.01%
 91	    1248	  0.01%
 92	    1295	  0.01%
 93	    1611	  0.01%
 94	    1799	  0.01%
 95	    2379	  0.01%
 96	    3637	  0.02%
 97	    4967	  0.03%
 98	    7003	  0.04%
 99	    8211	  0.05%
100	   10037	  0.06%
101	  206601	  1.19%


criterion=sequence-density
sequence-density=6.07
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=11
prefix-density=0.00
prefix-fanout=1.0
sequence=CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAA


criterion=fanout-score
sequence-density=0.26
sequence-density-rank=16
fanout-score=21.13
fanout-score-rank=1
prefix-density=5.54
prefix-fanout=1.0
sequence=TTGTGAGAATTAAAAA
                                 Started job on |	Dec 08 17:30:19
                             Started mapping on |	Dec 08 17:30:20
                                    Finished on |	Dec 08 17:39:28
       Mapping speed, Million of reads per hour |	116.40

                          Number of input reads |	17718368
                      Average input read length |	32
                                    UNIQUE READS:
                   Uniquely mapped reads number |	3332376
                        Uniquely mapped reads % |	18.81%
                          Average mapped length |	26.71
                       Number of splices: Total |	30149
            Number of splices: Annotated (sjdb) |	17461
                       Number of splices: GT/AG |	27934
                       Number of splices: GC/AG |	1540
                       Number of splices: AT/AC |	21
               Number of splices: Non-canonical |	654
                      Mismatch rate per base, % |	0.13%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.36
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.02
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	5895247
             % of reads mapped to multiple loci |	33.27%
        Number of reads mapped to too many loci |	7237136
             % of reads mapped to too many loci |	40.85%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	6.39%
                     % of reads unmapped: other |	0.69%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	8490745	8490745	8490745
N_multimapping	5895247	5895247	5895247
N_noFeature	2077633	2275256	3118898
N_ambiguous	57038	40622	747
UnstrandedReadsAssigned:1197705 PositiveStrandReadsAssigned:1016498 NegativeStrandReadsAssigned:212731
Dataset is classified unstranded
MeadianReadLen=29 20thPercentileLength=24 echo kmer=19
SRR8846483 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: SRR8846483-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 17,718,368 reads, 5,276,998 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,098 rounds

  52973 SRR8846483.ke.tsv
  35125 SRR8846483.se.tsv
  88098 total
==> SRR8846483.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	2.43551	0.552872
PNS24247	1044	945	0	0
PNS24249	1928	1829	0	0
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	2.56449	0.355145
PNS24243	293	194	0	0
KQK14069	1603	1504	141.726	17.9045
KQK14071	474	375	0	0

==> SRR8846483.se.tsv <==
BRADI_1g14170v3	262
BRADI_1g53295v3	0
BRADI_1g59795v3	18
BRADI_1g07683v3	0
BRADI_1g00485v3	2
BRADI_1g20270v3	44
BRADI_1g74790v3	39
BRADI_1g09890v3	0
BRADI_1g77505v3	1
BRADI_1g48960v3	0
SRR8846483 completed mapping pipeline successfully
