Starting /dee2/code/volunteer_pipeline.sh SRR8846508
    current disk space = 1506930139136
    free memory = 1364855392 
SRR8846508 SRAfilesize
06a0e5fe8e41b4cf633e583453d4e550  SRR8846508.sra
SRR8846508.sra file validated
SRR8846508 is single end
SRR8846508 is conventional basespace
SRR8846508 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR8846508_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	31.222	34.0	33.0	34.0	30.0	34.0
2	32.63425	34.0	33.0	34.0	28.0	34.0
3	32.982	34.0	33.0	34.0	32.0	34.0
4	33.162	34.0	33.0	34.0	32.0	34.0
5	33.24875	34.0	33.0	34.0	33.0	34.0
6	36.9775	38.0	37.0	38.0	36.0	38.0
7	37.30475	38.0	38.0	38.0	36.0	38.0
8	37.488	38.0	38.0	38.0	37.0	38.0
9	37.53525	38.0	38.0	38.0	37.0	38.0
10-11	37.56925	38.0	38.0	38.0	38.0	38.0
12-13	37.594	38.0	38.0	38.0	38.0	38.0
14-15	37.514250000000004	38.0	38.0	38.0	38.0	38.0
16-17	37.496624999999995	38.0	38.0	38.0	37.5	38.0
18-19	37.506375000000006	38.0	38.0	38.0	38.0	38.0
20-21	37.466125	38.0	38.0	38.0	38.0	38.0
22-23	37.494125	38.0	38.0	38.0	38.0	38.0
24-25	37.612	38.0	38.0	38.0	38.0	38.0
26-27	37.541	38.0	38.0	38.0	38.0	38.0
28-29	37.574	38.0	38.0	38.0	38.0	38.0
30-31	37.543875	38.0	38.0	38.0	38.0	38.0
32-33	37.497375000000005	38.0	38.0	38.0	38.0	38.0
34-35	37.383250000000004	38.0	38.0	38.0	37.5	38.0
36-37	37.210875	38.0	38.0	38.0	37.0	38.0
38-39	37.144	38.0	38.0	38.0	37.0	38.0
40-41	37.210125000000005	38.0	38.0	38.0	37.0	38.0
42-43	37.230875	38.0	38.0	38.0	37.0	38.0
44-45	37.277125	38.0	38.0	38.0	37.0	38.0
46-47	37.307625	38.0	38.0	38.0	37.0	38.0
48-49	37.27825	38.0	38.0	38.0	37.0	38.0
50-51	37.28475	38.0	38.0	38.0	37.0	38.0
52-53	37.357375	38.0	38.0	38.0	37.0	38.0
54-55	37.320750000000004	38.0	38.0	38.0	37.0	38.0
56-57	37.241	38.0	38.0	38.0	37.0	38.0
58-59	37.0675	38.0	38.0	38.0	36.5	38.0
60-61	37.142375	38.0	38.0	38.0	36.0	38.0
62-63	36.612	38.0	38.0	38.0	34.0	38.0
64-65	36.485375	38.0	38.0	38.0	33.5	38.0
66-67	36.356875	38.0	37.0	38.0	34.0	38.0
68-69	36.163	38.0	37.0	38.0	33.5	38.0
70-71	36.06175	38.0	37.0	38.0	33.0	38.0
72-73	36.05475	38.0	38.0	38.0	33.0	38.0
74-75	35.919124999999994	38.0	37.0	38.0	33.0	38.0
76-77	35.714124999999996	38.0	37.0	38.0	31.0	38.0
78-79	35.627625	38.0	37.0	38.0	31.0	38.0
80-81	35.726375000000004	38.0	37.0	38.0	32.0	38.0
82-83	35.381875	38.0	37.0	38.0	29.0	38.0
84-85	35.428375	38.0	37.0	38.0	29.5	38.0
86-87	35.448125	38.0	37.0	38.0	31.0	38.0
88-89	35.549875	38.0	37.0	38.0	32.0	38.0
90-91	35.345375000000004	38.0	37.0	38.0	31.0	38.0
92-93	34.928875	38.0	37.0	38.0	28.5	38.0
94-95	34.126875	38.0	36.5	38.0	21.0	38.0
96-97	32.08525	38.0	34.0	38.0	2.0	38.0
98-99	30.0185	38.0	28.5	38.0	2.0	38.0
100-101	27.372125	37.5	19.5	38.0	2.0	38.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
15	1.0
16	3.0
17	1.0
18	1.0
19	1.0
20	2.0
21	1.0
22	4.0
23	3.0
24	14.0
25	30.0
26	24.0
27	17.0
28	20.0
29	26.0
30	43.0
31	54.0
32	81.0
33	144.0
34	247.0
35	392.0
36	740.0
37	2151.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	33.28004263256062	22.968292033040235	22.56861177724487	21.183053557154278
2	26.075	29.125	17.8	27.0
3	25.775	20.625	19.0	34.599999999999994
4	25.7	35.449999999999996	15.75	23.1
5	26.575	24.925	23.075000000000003	25.424999999999997
6	27.175	25.05	26.55	21.224999999999998
7	36.275	28.299999999999997	17.349999999999998	18.075
8	20.65	23.625	34.0	21.725
9	23.974999999999998	34.225	22.775000000000002	19.025
10-11	29.4375	23.8125	26.387500000000003	20.3625
12-13	22.75	21.6625	22.75	32.8375
14-15	24.875	36.15	20.8	18.175
16-17	23.150000000000002	28.3375	29.5	19.0125
18-19	33.287499999999994	22.725	21.375	22.6125
20-21	23.400000000000002	27.762500000000003	26.700000000000003	22.1375
22-23	27.8375	30.0875	27.825	14.249999999999998
24-25	27.737499999999997	27.0625	26.025	19.175
26-27	28.549999999999997	27.737499999999997	23.7875	19.925
28-29	24.0	26.400000000000002	25.4375	24.1625
30-31	27.8875	20.424999999999997	31.8125	19.875
32-33	23.9125	18.5	34.6875	22.900000000000002
34-35	30.2375	14.975	31.162499999999998	23.625
36-37	35.2875	16.175	28.7375	19.8
38-39	35.55	18.375	26.400000000000002	19.675
40-41	30.2875	19.5875	24.675	25.45
42-43	30.887500000000003	22.4375	21.587500000000002	25.087500000000002
44-45	36.725	22.6125	14.774999999999999	25.887500000000003
46-47	32.237500000000004	28.175	16.1	23.4875
48-49	27.625	25.35	17.5375	29.4875
50-51	22.3	26.637499999999996	15.625	35.4375
52-53	23.5	30.099999999999998	12.8875	33.5125
54-55	20.7125	29.7375	15.475	34.075
56-57	18.5625	31.1	14.2625	36.075
58-59	13.7125	32.875	14.424999999999999	38.987500000000004
60-61	14.887500000000001	29.75	15.6	39.7625
62-63	14.000000000000002	30.925000000000004	20.7375	34.3375
64-65	13.6875	32.237500000000004	23.775	30.3
66-67	12.675	25.624999999999996	26.700000000000003	35.0
68-69	14.762500000000001	25.412499999999998	25.337500000000002	34.4875
70-71	17.4125	24.8625	28.962500000000002	28.762500000000003
72-73	20.9125	20.7375	31.9625	26.387500000000003
74-75	16.1375	18.15	33.7125	32.0
76-77	19.8	13.1625	36.8125	30.225
78-79	19.7125	9.950000000000001	37.7875	32.550000000000004
80-81	19.7125	11.2375	38.800000000000004	30.25
82-83	19.475	11.774999999999999	42.175000000000004	26.575
84-85	21.224999999999998	12.425	37.3	29.049999999999997
86-87	19.8625	19.1	34.849999999999994	26.187500000000004
88-89	15.987499999999999	31.5625	34.7125	17.7375
90-91	13.337499999999999	41.875	28.775000000000002	16.0125
92-93	12.837499999999999	52.1125	20.75	14.299999999999999
94-95	10.725	60.35	19.7	9.225
96-97	8.35	69.7625	14.875	7.012500000000001
98-99	6.625	78.85	10.1125	4.4125
100-101	3.8875	85.1625	6.775	4.175
>>END_MODULE
>>Per sequence GC content	pass
#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	3.0
33	6.0
34	9.5
35	13.0
36	10.5
37	6.5
38	12.5
39	35.5
40	65.5
41	131.5
42	195.5
43	216.0
44	282.5
45	337.5
46	369.0
47	392.0
48	367.0
49	313.0
50	296.5
51	270.0
52	171.5
53	109.0
54	96.0
55	130.0
56	96.0
57	25.0
58	14.0
59	5.0
60	6.0
61	7.5
62	3.5
63	1.0
64	0.5
65	1.0
66	1.0
67	0.5
68	0.0
69	0.0
70	0.0
71	0.0
72	0.0
73	0.0
74	0.0
75	0.0
76	0.0
77	0.0
78	0.0
79	0.0
80	0.0
81	0.0
82	0.0
83	0.0
84	0.0
85	0.0
86	0.0
87	0.0
88	0.0
89	0.0
90	0.0
91	0.0
92	0.0
93	0.0
94	0.0
95	0.0
96	0.0
97	0.0
98	0.0
99	0.0
100	0.0
>>END_MODULE
>>Per base N content	warn
#Base	N-Count
1	6.175
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	56.775
#Duplication Level	Percentage of deduplicated	Percentage of total
1	82.82694848084545	47.025
2	8.234258036107441	9.35
3	3.126376045794804	5.325
4	1.4971378247468077	3.4000000000000004
5	0.9687362395420519	2.75
6	0.7045354469396742	2.4
7	0.3522677234698371	1.4000000000000001
8	0.3522677234698371	1.6
9	0.22016732716864817	1.125
>10	1.4090708938793484	12.925
>50	0.26420079260237783	10.100000000000001
>100	0.044033465433729636	2.6
>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	104	2.6	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	93	2.325	No Hit
GACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	84	2.1	RNA PCR Primer, Index 1 (100% over 23bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	63	1.575	No Hit
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	59	1.4749999999999999	RNA PCR Primer, Index 1 (100% over 29bp)
GGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGA	54	1.35	RNA PCR Primer, Index 1 (100% over 22bp)
GACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAAC	51	1.275	RNA PCR Primer, Index 1 (100% over 24bp)
AGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGC	43	1.075	No Hit
GACACGACTCTCGGCAACGGATATCTGGAATTCTCGGGTGCCAAGGAACT	30	0.75	RNA PCR Primer, Index 1 (100% over 25bp)
AGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGG	26	0.65	Illumina Small RNA Adapter 2 (100% over 21bp)
CTCTGATGATGATCAAACTAATACTTTCGTTCTTCTGGAATTCTCGGGTG	22	0.5499999999999999	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	21	0.525	No Hit
GCACCAGTGGTCTAGTGGTAGAATAGTACCTGGAATTCTCGGGTGCCAAG	21	0.525	No Hit
CTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGTCTTC	21	0.525	RNA PCR Primer, Index 31 (100% over 50bp)
CTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	20	0.5	RNA PCR Primer, Index 1 (100% over 28bp)
CATCGAGTAGACCTTGTTATTGTGAGAATATGGAATTCTCGGGTGCCAAG	18	0.44999999999999996	No Hit
TCTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGTCTT	17	0.42500000000000004	RNA PCR Primer, Index 31 (100% over 50bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCTGGAATTCTCGGGTGCCAAGG	16	0.4	Illumina Small RNA Adapter 2 (100% over 21bp)
GAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAG	16	0.4	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCATGGAATTCTCGGGTG	16	0.4	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGG	15	0.375	Illumina Small RNA Adapter 2 (100% over 21bp)
TTCGGACCAGGCTTCATTCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	15	0.375	RNA PCR Primer, Index 1 (100% over 29bp)
GCCCACCCCAAGATGAGTGCTCTCTCTGGAATTCTCGGGTGCCAAGGAAC	15	0.375	RNA PCR Primer, Index 1 (100% over 24bp)
GCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCC	14	0.35000000000000003	No Hit
CACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAACT	13	0.325	RNA PCR Primer, Index 1 (100% over 25bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCTGGAATTCTCGGGTGC	13	0.325	No Hit
CACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGATGGAATTC	13	0.325	No Hit
GCACCAGTGGTCTAGTGGTAGAATAGTATGGAATTCTCGGGTGCCAAGGA	12	0.3	RNA PCR Primer, Index 1 (100% over 22bp)
CATCGAGTAGACCTTGTTATTGTGAGATGGAATTCTCGGGTGCCAAGGAA	12	0.3	RNA PCR Primer, Index 1 (100% over 23bp)
TGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAA	12	0.3	No Hit
ACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTGC	12	0.3	No Hit
GACACGACTCTCGGCAACGGATATCTCGGCTGGAATTCTCGGGTGCCAAG	11	0.27499999999999997	No Hit
TCCGTCGTAGTCTAGGTGGTTAGGATATGGAATTCTCGGGTGCCAAGGAA	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 23bp)
TTCTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGTCT	11	0.27499999999999997	RNA PCR Primer, Index 31 (100% over 50bp)
ACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCC	11	0.27499999999999997	No Hit
GCACCAGTAGTCTAGTGGTAGAATAGTACCTGGAATTCTCGGGTGCCAAG	10	0.25	No Hit
CGACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGA	10	0.25	RNA PCR Primer, Index 1 (100% over 22bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTGGAATTCTCGGGTGCCAAGG	10	0.25	Illumina Small RNA Adapter 2 (100% over 21bp)
CCAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGG	10	0.25	No Hit
CAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGG	9	0.22499999999999998	No Hit
TCGGATAACCGTAGTAATTCTAGAGCTAATACGTGGAATTCTCGGGTGCC	9	0.22499999999999998	No Hit
ATATATTTCAAGTTATTTCGGATCTTGGAATTCTCGGGTGCCAAGGAACT	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 25bp)
CAGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTG	9	0.22499999999999998	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTTGGAATTCTCGGGTGC	9	0.22499999999999998	No Hit
CGACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAA	8	0.2	RNA PCR Primer, Index 1 (100% over 23bp)
TCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTC	8	0.2	RNA PCR Primer, Index 1 (100% over 26bp)
GATAACCGTAGTAATTCTAGAGCTAATTGGAATTCTCGGGTGCCAAGGAA	8	0.2	RNA PCR Primer, Index 1 (100% over 23bp)
ATAACCGTAGTAATTCTAGAGCTAATTGGAATTCTCGGGTGCCAAGGAAC	8	0.2	RNA PCR Primer, Index 1 (100% over 24bp)
ATAACCGTAGTAATTCTAGAGCTAATGGAATTCTCGGGTGCCAAGGAACT	8	0.2	RNA PCR Primer, Index 1 (100% over 25bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTCAAGGCGTGGAATT	8	0.2	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGACTGGAATTCTCGGGTGCCA	8	0.2	No Hit
TACCTGGTTGATCCTGCCAGTAGTCATATGCTTGTGGAATTCTCGGGTGC	8	0.2	No Hit
TCCGTCGTAGTCTAGGTGGTTAGGATACTCTGGAATTCTCGGGTGCCAAG	7	0.17500000000000002	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTCAAGGGTGGAATTC	7	0.17500000000000002	No Hit
CCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTG	7	0.17500000000000002	No Hit
GATAACCGTAGTAATTCTAGAGCTAATGGAATTCTCGGGTGCCAAGGAAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 24bp)
CACGACTCTCGGCAACGGATATCTGGAATTCTCGGGTGCCAAGGAACTCC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 27bp)
TAACCGTAGTAATTCTAGAGCTAATATGGAATTCTCGGGTGCCAAGGAAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 24bp)
ATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAA	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 23bp)
ATTCTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGTC	7	0.17500000000000002	RNA PCR Primer, Index 31 (100% over 50bp)
CGGATAACCGTAGTAATTCTAGAGCTAATACGTGGAATTCTCGGGTGCCA	6	0.15	No Hit
CATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTGCC	6	0.15	No Hit
GACACGACTCTCGGCAACGGATATCTCGGCTCTCGTGGAATTCTCGGGTG	6	0.15	No Hit
GACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTG	6	0.15	No Hit
GACACGACTCTCGGCAACGTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	6	0.15	RNA PCR Primer, Index 1 (100% over 31bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCAAAATCTTGGAATTCT	6	0.15	No Hit
ACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAACT	6	0.15	RNA PCR Primer, Index 1 (100% over 25bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTTGGAATTCTCGGGTG	6	0.15	No Hit
AAGGGTGCTGAGAATACTTTGAATCTGACACTGGAATTCTCGGGTGCCAA	6	0.15	No Hit
CCAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTTGAATTCTCGG	6	0.15	No Hit
NGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	6	0.15	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAATGGAATTCTCGGGTG	6	0.15	No Hit
GACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTTGAATTCTCGGGTG	6	0.15	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTATGGAATTCTCGGGTGCCAA	6	0.15	No Hit
TAACCGTAGTAATTCTAGAGCTAATGGAATTCTCGGGTGCCAAGGAACTC	6	0.15	RNA PCR Primer, Index 1 (100% over 26bp)
TCGCTTGGTGCAGATCGGGACTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
GACACGACTCTCGGCAACGGATATGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
ACCGTAGTAATTCTAGAGCTAATGGAATTCTCGGGTGCCAAGGAACTCCA	5	0.125	RNA PCR Primer, Index 1 (100% over 28bp)
TAATTCATGATCTGGCATGTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	5	0.125	RNA PCR Primer, Index 1 (100% over 31bp)
CGACACGACTCTCGGCAACGGATGGAATTCTCGGGTGCCAAGGAACTCCA	5	0.125	RNA PCR Primer, Index 1 (100% over 28bp)
CAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTTGAATTCTCGGG	5	0.125	No Hit
AACCGTAGTAATTCTAGAGCTAATTGGAATTCTCGGGTGCCAAGGAACTC	5	0.125	RNA PCR Primer, Index 1 (100% over 26bp)
TCCAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCG	5	0.125	No Hit
TGCAAGTATGAACTAATTTGAACTGTGAAACTTGGAATTCTCGGGTGCCA	5	0.125	No Hit
CATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
ATGCAGTTACTAATTCATGATCTGGCTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
TGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAA	5	0.125	No Hit
CACGACTCTCGGCAACGGATATCTCGTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGATGGAATTCTCGGGTGCCAA	5	0.125	No Hit
NACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	5	0.125	RNA PCR Primer, Index 1 (100% over 23bp)
TCTCTGATGATGATCAAACTAATACTTTCGTTCTTCTGGAATTCTCGGGT	5	0.125	No Hit
GACACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGTGGAATTCTC	5	0.125	No Hit
CAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTC	5	0.125	RNA PCR Primer, Index 1 (100% over 26bp)
CGGATAACCGTAGTAATTCTAGAGCTAATACTGGAATTCTCGGGTGCCAA	5	0.125	No Hit
AGGGCTATAGCTCAGTTCGGTAGAGCAACTCGTTTACACCGAGATGGAAT	5	0.125	No Hit
AATTCTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGT	5	0.125	RNA PCR Primer, Index 31 (100% over 50bp)
CACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGC	5	0.125	No Hit
CAGGGTTCGTTTCCCTGGATGCGCACCATGGAATTCTCGGGTGCCAAGGA	5	0.125	RNA PCR Primer, Index 1 (100% over 22bp)
>>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	0.075	0.0	0.0	0.0
4	0.0	0.075	0.0	0.0	0.0
5	0.0	0.1	0.0	0.0	0.0
6	0.0	0.1	0.0	0.0	0.0
7	0.0	0.125	0.0	0.0	0.0
8	0.0	0.125	0.0	0.0	0.0
9	0.0	0.225	0.0	0.0	0.0
10-11	0.0	0.4125	0.0	0.0	0.0
12-13	0.0	0.4625	0.0	0.0	0.0
14-15	0.0	0.6375	0.0	0.0	0.0
16-17	0.0	1.4375	0.0	0.0	0.0
18-19	0.0	3.075	0.0	0.0	0.0
20-21	0.0	5.762499999999999	0.0	0.0	0.0
22-23	0.0	12.825	0.0	0.0	0.0
24-25	0.0	22.425	0.0	0.0	0.0
26-27	0.0	34.025000000000006	0.0	0.0	0.0
28-29	0.0	45.474999999999994	0.0	0.0	0.0
30-31	0.0	55.075	0.0	0.0	0.0
32-33	0.0	63.137499999999996	0.0	0.0	0.0
34-35	0.0	73.55000000000001	0.0	0.0	0.0
36-37	0.0	81.8875	0.0	0.0	0.0
38-39	0.0	86.4375	0.0	0.0	0.0
40-41	0.0	89.0625	0.0	0.0	0.0
42-43	0.0	91.425	0.0	0.0	0.0
44-45	0.0	93.05	0.0	0.0	0.0
46-47	0.0	93.7625	0.0	0.0	0.0
48-49	0.0	93.85	0.0	0.0	0.0
50-51	0.0	93.875	0.0	0.0	0.0
52-53	0.0	93.92500000000001	0.0	0.0	0.0
54-55	0.0	93.9625	0.0	0.0	0.0
56-57	0.0	93.975	0.0	0.0	0.0
58-59	0.0	93.975	0.0	0.0	0.0
60-61	0.0	93.975	0.0	0.0	0.0
62-63	0.0	93.975	0.0	0.0	0.0
64-65	0.0	93.9875	0.0	0.0	0.0
66-67	0.0	94.0	0.0	0.0	0.0
68-69	0.0	94.0	0.0	0.0	0.0
70-71	0.0	94.0125	0.0	0.0	0.0
72-73	0.0	94.025	0.0	0.0	0.0
74-75	0.0	94.0625	0.0	0.0	0.0
76-77	0.0	94.075	0.0	0.0	0.0
78-79	0.0	94.125	0.0	0.0	0.0
80-81	0.0	94.1875	0.0	0.0	0.0
82-83	0.0	94.2875	0.0	0.0	0.0
84-85	0.0	94.4875	0.0	0.0	0.0
86-87	0.0	94.5875	0.0	0.0	0.0
88-89	0.0	94.6125	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGGATTG	25	2.583074E-7	101.26667	1
CTCTGAT	15	4.7401295E-4	101.26666	1
CATCGAG	30	5.9571903E-9	101.26666	1
GGATTGT	25	3.8440157E-7	94.93751	2
GATTGTA	25	3.8440157E-7	94.93751	3
TAGTTCA	25	3.8440157E-7	94.93751	8
ATTGTAG	25	3.8440157E-7	94.93751	4
AGTTCAA	25	3.8440157E-7	94.93751	9
GTAGACC	30	9.502401E-9	94.9375	7
TTGTAGT	30	9.502401E-9	94.9375	5
AGTAGAC	30	9.502401E-9	94.9375	6
ATGATCA	15	6.1582687E-4	94.9375	9
GATGATC	15	6.1582687E-4	94.9375	8
GAGTAGA	30	9.502401E-9	94.9375	5
CGAGTAG	30	9.502401E-9	94.9375	4
AGACCTT	30	9.502401E-9	94.9375	9
ATCGAGT	30	9.502401E-9	94.9375	2
TCGAGTA	30	9.502401E-9	94.9375	3
TAGACCT	30	9.502401E-9	94.9375	8
TGTAGTT	30	1.1382763E-6	79.11458	6
>>END_MODULE
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842994 READS because READLEN < 1
Read 842994 spots for SRR8846508.sra
Written 842994 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
Rejected 842975 READS because READLEN < 1
Read 842975 spots for SRR8846508.sra
Written 842975 spots for SRR8846508.sra
SRR ids: ['SRR8846508.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_8oygw8wb
SRR8846508.sra spots: 16859519
blocks: [[1, 842975], [842976, 1685950], [1685951, 2528925], [2528926, 3371900], [3371901, 4214875], [4214876, 5057850], [5057851, 5900825], [5900826, 6743800], [6743801, 7586775], [7586776, 8429750], [8429751, 9272725], [9272726, 10115700], [10115701, 10958675], [10958676, 11801650], [11801651, 12644625], [12644626, 13487600], [13487601, 14330575], [14330576, 15173550], [15173551, 16016525], [16016526, 16859519]]
SRR8846508 file size 4045000
SRR8846508 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 SRR8846508 SRR8846508_1.fastq
Input file:	SRR8846508_1.fastq
trimmed:	SRR8846508-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
Mon Dec  9 03:45:54 2024 >> started

Mon Dec  9 03:46:34 2024 >> done (40.664s)
16859519 reads processed; of these:
     308 ( 0.00%) short reads filtered out after trimming by size control
      35 ( 0.00%) empty reads filtered out after trimming by size control
16859176 (100.00%) reads available; of these:
 3643433 (21.61%) trimmed reads available after processing
13215743 (78.39%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      49	  0.00%
 19	      43	  0.00%
 20	      42	  0.00%
 21	      44	  0.00%
 22	      43	  0.00%
 23	      52	  0.00%
 24	      82	  0.00%
 25	     106	  0.00%
 26	     135	  0.00%
 27	     180	  0.00%
 28	     265	  0.00%
 29	     296	  0.00%
 30	     290	  0.00%
 31	     335	  0.00%
 32	     292	  0.00%
 33	     244	  0.00%
 34	     280	  0.00%
 35	     224	  0.00%
 36	     230	  0.00%
 37	     200	  0.00%
 38	     148	  0.00%
 39	     186	  0.00%
 40	     182	  0.00%
 41	     186	  0.00%
 42	     188	  0.00%
 43	     221	  0.00%
 44	     227	  0.00%
 45	     289	  0.00%
 46	     244	  0.00%
 47	     236	  0.00%
 48	     257	  0.00%
 49	     283	  0.00%
 50	     241	  0.00%
 51	     282	  0.00%
 52	     279	  0.00%
 53	     308	  0.00%
 54	     323	  0.00%
 55	     361	  0.00%
 56	     409	  0.00%
 57	     461	  0.00%
 58	     518	  0.00%
 59	     614	  0.00%
 60	     679	  0.00%
 61	    1110	  0.01%
 62	    1501	  0.01%
 63	    1837	  0.01%
 64	    3180	  0.02%
 65	    4054	  0.02%
 66	   10453	  0.06%
 67	   48800	  0.29%
 68	   56273	  0.33%
 69	   39015	  0.23%
 70	   34089	  0.20%
 71	   38475	  0.23%
 72	   17175	  0.10%
 73	    5996	  0.04%
 74	    7298	  0.04%
 75	    5074	  0.03%
 76	    4532	  0.03%
 77	    4171	  0.02%
 78	    5476	  0.03%
 79	    5610	  0.03%
 80	    7304	  0.04%
 81	    9107	  0.05%
 82	   18189	  0.11%
 83	   16469	  0.10%
 84	   14107	  0.08%
 85	   15580	  0.09%
 86	   20059	  0.12%
 87	   23368	  0.14%
 88	   38353	  0.23%
 89	   54357	  0.32%
 90	   77079	  0.46%
 91	   82227	  0.49%
 92	  109572	  0.65%
 93	  174281	  1.03%
 94	  203620	  1.21%
 95	  375627	  2.23%
 96	  410936	  2.44%
 97	  407315	  2.42%
 98	  459457	  2.73%
 99	  502451	  2.98%
100	  319302	  1.89%
101	13215743	 78.39%
16859176 reads passed initial QC


criterion=sequence-density
sequence-density=94.28
sequence-density-rank=1
fanout-score=34.28
fanout-score-rank=1
prefix-density=94.64
prefix-fanout=34.1
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA


criterion=fanout-score
sequence-density=94.28
sequence-density-rank=1
fanout-score=34.28
fanout-score-rank=1
prefix-density=94.64
prefix-fanout=34.1
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA -o SRR8846508 -
Input file:	STDIN
trimmed:	SRR8846508-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCACGATATCTCGTATGCCGTCTTCTGCTTGA
-- 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
Mon Dec  9 03:49:08 2024 >> started

Mon Dec  9 03:50:26 2024 >> done (77.947s)
16504246 reads processed; of these:
  477752 ( 2.89%) short reads filtered out after trimming by size control
   10945 ( 0.07%) empty reads filtered out after trimming by size control
16015549 (97.04%) reads available; of these:
15464859 (96.56%) trimmed reads available after processing
  550690 ( 3.44%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  147126	  0.92%
 19	  269159	  1.68%
 20	  271604	  1.70%
 21	  829907	  5.18%
 22	  484606	  3.03%
 23	  604278	  3.77%
 24	 1344171	  8.39%
 25	  786130	  4.91%
 26	  845560	  5.28%
 27	 1004466	  6.27%
 28	  834347	  5.21%
 29	  716817	  4.48%
 30	  857588	  5.35%
 31	  576145	  3.60%
 32	  937725	  5.86%
 33	  873164	  5.45%
 34	  782791	  4.89%
 35	  693205	  4.33%
 36	  823946	  5.14%
 37	  321441	  2.01%
 38	  257647	  1.61%
 39	  218270	  1.36%
 40	  198332	  1.24%
 41	  192554	  1.20%
 42	  221054	  1.38%
 43	  106203	  0.66%
 44	   86515	  0.54%
 45	   40625	  0.25%
 46	   17723	  0.11%
 47	    9924	  0.06%
 48	    8066	  0.05%
 49	    4336	  0.03%
 50	    2975	  0.02%
 51	    2992	  0.02%
 52	    1906	  0.01%
 53	    1528	  0.01%
 54	    1869	  0.01%
 55	     788	  0.00%
 56	    1170	  0.01%
 57	     705	  0.00%
 58	     690	  0.00%
 59	     720	  0.00%
 60	     809	  0.01%
 61	    1231	  0.01%
 62	    1470	  0.01%
 63	    1764	  0.01%
 64	    3042	  0.02%
 65	    3812	  0.02%
 66	   10167	  0.06%
 67	   47611	  0.30%
 68	   54989	  0.34%
 69	   37892	  0.24%
 70	   33350	  0.21%
 71	   37304	  0.23%
 72	   15369	  0.10%
 73	    4723	  0.03%
 74	    3497	  0.02%
 75	    2635	  0.02%
 76	    4099	  0.03%
 77	    8498	  0.05%
 78	    3484	  0.02%
 79	    4253	  0.03%
 80	   13503	  0.08%
 81	   11179	  0.07%
 82	    8922	  0.06%
 83	   18949	  0.12%
 84	    5314	  0.03%
 85	    4536	  0.03%
 86	    3882	  0.02%
 87	    3336	  0.02%
 88	    2016	  0.01%
 89	    2903	  0.02%
 90	    2096	  0.01%
 91	    1942	  0.01%
 92	    2462	  0.02%
 93	    2928	  0.02%
 94	    2098	  0.01%
 95	    3131	  0.02%
 96	    3808	  0.02%
 97	    5143	  0.03%
 98	    6953	  0.04%
 99	    7349	  0.05%
100	    8754	  0.05%
101	  233578	  1.46%


criterion=sequence-density
sequence-density=4.36
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=12
prefix-density=0.00
prefix-fanout=1.0
sequence=CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAATTCAAGAGTTGTAAGGAGGGACTTA


criterion=fanout-score
sequence-density=0.01
sequence-density-rank=43
fanout-score=147.92
fanout-score-rank=1
prefix-density=0.77
prefix-fanout=1.0
sequence=TAGCCAAGTGCGGAGAGGATAACTGCTGAAAGCATATAAGTAGTAAGCCCACCCCAAGATGAGTGCTCTCTCCTCCGACTTCC
                                 Started job on |	Dec 09 03:52:19
                             Started mapping on |	Dec 09 03:52:20
                                    Finished on |	Dec 09 03:58:18
       Mapping speed, Million of reads per hour |	164.62

                          Number of input reads |	16370479
                      Average input read length |	33
                                    UNIQUE READS:
                   Uniquely mapped reads number |	2222622
                        Uniquely mapped reads % |	13.58%
                          Average mapped length |	29.25
                       Number of splices: Total |	32047
            Number of splices: Annotated (sjdb) |	20296
                       Number of splices: GT/AG |	29513
                       Number of splices: GC/AG |	1966
                       Number of splices: AT/AC |	22
               Number of splices: Non-canonical |	546
                      Mismatch rate per base, % |	0.16%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.41
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.11
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	6014834
             % of reads mapped to multiple loci |	36.74%
        Number of reads mapped to too many loci |	7065400
             % of reads mapped to too many loci |	43.16%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	6.09%
                     % of reads unmapped: other |	0.43%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	8133023	8133023	8133023
N_multimapping	6014834	6014834	6014834
N_noFeature	1162089	1292705	2075238
N_ambiguous	52675	35648	388
UnstrandedReadsAssigned:1007858 PositiveStrandReadsAssigned:894269 NegativeStrandReadsAssigned:146996
Dataset is classified positive stranded
MeadianReadLen=29 20thPercentileLength=24 echo kmer=19
SRR8846508 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: SRR8846508-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 16,370,479 reads, 2,636,423 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 985 rounds

  52973 SRR8846508.ke.tsv
  35125 SRR8846508.se.tsv
  88098 total
==> SRR8846508.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	0	0
PNS24249	1928	1829	0	0
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	3	1.0363
PNS24243	293	194	0	0
KQK14069	1603	1504	144.055	45.394
KQK14071	474	375	0	0

==> SRR8846508.se.tsv <==
BRADI_1g14170v3	198
BRADI_1g53295v3	3
BRADI_1g59795v3	6
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	26
BRADI_1g74790v3	15
BRADI_1g09890v3	1
BRADI_1g77505v3	5
BRADI_1g48960v3	0
SRR8846508 completed mapping pipeline successfully
