Starting /dee2/code/volunteer_pipeline.sh SRR8846494
    current disk space = 1501070024704
    free memory = 1385000264 
SRR8846494 SRAfilesize
0764a8ac8fbd5e48c5c3f5ff6386cd71  SRR8846494.sra
SRR8846494.sra file validated
SRR8846494 is single end
SRR8846494 is conventional basespace
SRR8846494 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR8846494_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	31.274	34.0	33.0	34.0	31.0	34.0
2	32.901	34.0	33.0	34.0	31.0	34.0
3	32.9675	34.0	33.0	34.0	32.0	34.0
4	33.06	34.0	33.0	34.0	32.0	34.0
5	33.0445	34.0	33.0	34.0	32.0	34.0
6	36.58075	38.0	37.0	38.0	34.0	38.0
7	37.02975	38.0	38.0	38.0	35.0	38.0
8	37.29175	38.0	38.0	38.0	36.0	38.0
9	37.25875	38.0	38.0	38.0	36.0	38.0
10-11	37.3275	38.0	38.0	38.0	37.0	38.0
12-13	37.422625	38.0	38.0	38.0	37.0	38.0
14-15	37.361125	38.0	38.0	38.0	37.0	38.0
16-17	37.309625	38.0	38.0	38.0	37.0	38.0
18-19	37.354124999999996	38.0	38.0	38.0	37.0	38.0
20-21	37.332375	38.0	38.0	38.0	37.0	38.0
22-23	37.30975	38.0	38.0	38.0	37.0	38.0
24-25	37.31625	38.0	38.0	38.0	37.0	38.0
26-27	37.316125	38.0	38.0	38.0	37.0	38.0
28-29	37.275625000000005	38.0	38.0	38.0	37.0	38.0
30-31	37.289	38.0	38.0	38.0	37.0	38.0
32-33	37.141875	38.0	38.0	38.0	36.0	38.0
34-35	36.937125	38.0	38.0	38.0	35.5	38.0
36-37	36.7125	38.0	38.0	38.0	34.5	38.0
38-39	36.650625	38.0	38.0	38.0	34.5	38.0
40-41	36.969375	38.0	38.0	38.0	35.5	38.0
42-43	37.025000000000006	38.0	38.0	38.0	36.0	38.0
44-45	36.893375	38.0	38.0	38.0	35.5	38.0
46-47	36.857375000000005	38.0	38.0	38.0	35.0	38.0
48-49	36.9955	38.0	38.0	38.0	36.0	38.0
50-51	37.053875000000005	38.0	38.0	38.0	36.0	38.0
52-53	37.14125	38.0	38.0	38.0	36.0	38.0
54-55	36.943375	38.0	38.0	38.0	36.0	38.0
56-57	36.867000000000004	38.0	38.0	38.0	35.0	38.0
58-59	36.849875	38.0	38.0	38.0	35.5	38.0
60-61	36.783874999999995	38.0	38.0	38.0	35.0	38.0
62-63	36.334875	38.0	37.5	38.0	33.5	38.0
64-65	36.094375	38.0	37.0	38.0	31.5	38.0
66-67	35.8255	38.0	37.0	38.0	30.0	38.0
68-69	35.810625	38.0	37.0	38.0	29.0	38.0
70-71	35.4965	38.0	37.0	38.0	29.0	38.0
72-73	35.2605	38.0	36.5	38.0	29.0	38.0
74-75	34.70225	38.0	36.0	38.0	26.0	38.0
76-77	34.86775	38.0	36.0	38.0	27.5	38.0
78-79	34.86	38.0	36.0	38.0	27.5	38.0
80-81	34.47925	38.0	35.5	38.0	26.0	38.0
82-83	34.644125	38.0	36.0	38.0	27.0	38.0
84-85	34.6005	38.0	35.5	38.0	27.0	38.0
86-87	34.728875	38.0	36.0	38.0	27.0	38.0
88-89	34.831500000000005	38.0	36.0	38.0	27.5	38.0
90-91	34.29600000000001	38.0	35.5	38.0	26.0	38.0
92-93	34.183499999999995	38.0	35.5	38.0	25.5	38.0
94-95	33.638625000000005	38.0	35.0	38.0	19.5	38.0
96-97	31.99825	38.0	34.0	38.0	8.0	38.0
98-99	29.721625	38.0	28.5	38.0	2.0	38.0
100-101	26.916	36.5	8.5	38.0	2.0	38.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
16	1.0
17	1.0
18	0.0
19	0.0
20	4.0
21	1.0
22	4.0
23	8.0
24	17.0
25	37.0
26	26.0
27	21.0
28	32.0
29	32.0
30	57.0
31	81.0
32	137.0
33	169.0
34	258.0
35	520.0
36	993.0
37	1601.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	35.4753053637812	25.27881040892193	20.738183749336166	18.5077004779607
2	28.1	26.325	16.2	29.375
3	29.299999999999997	17.525	19.2	33.975
4	25.8	35.425000000000004	17.7	21.075
5	26.224999999999998	25.124999999999996	26.35	22.3
6	23.486743371685844	24.137068534267133	27.763881940970485	24.61230615307654
7	36.675000000000004	24.375	17.974999999999998	20.974999999999998
8	20.625	19.725	38.725	20.925
9	23.849999999999998	36.95	19.875	19.325
10-11	30.9	23.1	26.075	19.925
12-13	21.8	21.675	24.0375	32.487500000000004
14-15	22.0625	41.6375	19.4375	16.8625
16-17	24.1875	25.412499999999998	32.35	18.05
18-19	34.7125	22.650000000000002	20.7875	21.85
20-21	20.7125	28.5625	27.0875	23.6375
22-23	28.549999999999997	29.275000000000002	27.5125	14.662500000000001
24-25	27.987499999999997	26.6125	25.7375	19.662499999999998
26-27	31.125000000000004	28.462500000000002	21.5375	18.875
28-29	22.3875	27.437499999999996	25.174999999999997	25.0
30-31	27.0	19.4625	33.6625	19.875
32-33	23.1125	18.35	34.2625	24.275
34-35	32.6	16.0625	29.375	21.9625
36-37	36.0875	18.325	26.575	19.0125
38-39	33.300000000000004	18.7625	28.775000000000002	19.162499999999998
40-41	28.762500000000003	17.349999999999998	24.875	29.012500000000003
42-43	30.825000000000003	24.125	21.1625	23.8875
44-45	41.3	20.7875	13.737499999999999	24.175
46-47	31.275	29.212500000000002	16.425	23.0875
48-49	26.400000000000002	24.125	17.875	31.6
50-51	21.6125	27.575	15.3375	35.475
52-53	26.575	31.6	12.1875	29.6375
54-55	20.474999999999998	32.525	16.375	30.625000000000004
56-57	19.5125	30.6875	16.9125	32.887499999999996
58-59	15.925	33.8375	16.037499999999998	34.2
60-61	14.075	34.862500000000004	18.55	32.5125
62-63	14.299999999999999	37.9375	19.8625	27.900000000000002
64-65	11.3125	37.3625	23.724999999999998	27.6
66-67	12.1625	32.574999999999996	25.75	29.512500000000003
68-69	16.6875	29.512500000000003	25.887500000000003	27.9125
70-71	15.187500000000002	32.025	28.1	24.6875
72-73	18.475	26.5875	29.775000000000002	25.162499999999998
74-75	14.662500000000001	21.2625	30.0	34.075
76-77	20.45	13.975000000000001	37.4125	28.1625
78-79	17.95	12.025	38.2125	31.8125
80-81	19.275000000000002	12.875	37.487500000000004	30.362499999999997
82-83	20.7625	10.25	40.75	28.237499999999997
84-85	21.1125	11.262500000000001	37.6	30.025000000000002
86-87	20.225	18.0625	36.525	25.1875
88-89	14.4875	32.775	34.575	18.1625
90-91	13.9875	41.5	28.275	16.2375
92-93	12.4	51.5875	21.1625	14.85
94-95	10.9875	60.5625	20.2125	8.2375
96-97	7.6625	72.52499999999999	13.700000000000001	6.1125
98-99	5.6625000000000005	81.4375	8.6375	4.2625
100-101	3.5749999999999997	86.7875	5.6625000000000005	3.975
>>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	0.5
31	2.0
32	6.5
33	7.0
34	9.5
35	13.0
36	17.5
37	23.0
38	41.0
39	64.0
40	121.5
41	186.5
42	227.0
43	307.0
44	326.0
45	366.5
46	392.5
47	312.0
48	290.0
49	351.5
50	317.0
51	165.0
52	83.0
53	83.0
54	131.5
55	99.5
56	26.5
57	13.0
58	6.5
59	4.5
60	2.0
61	1.5
62	1.0
63	0.5
64	0.0
65	0.5
66	0.5
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	5.8500000000000005
2	0.0
3	0.0
4	0.0
5	0.0
6	0.05
7	0.0
8	0.0
9	0.0
10-11	0.0
12-13	0.0
14-15	0.0
16-17	0.0
18-19	0.0
20-21	0.0
22-23	0.0
24-25	0.0
26-27	0.0
28-29	0.0
30-31	0.0
32-33	0.0
34-35	0.0
36-37	0.0
38-39	0.0
40-41	0.0
42-43	0.0
44-45	0.0
46-47	0.0
48-49	0.0
50-51	0.0
52-53	0.0
54-55	0.0
56-57	0.0
58-59	0.0
60-61	0.0
62-63	0.0
64-65	0.0
66-67	0.0
68-69	0.0
70-71	0.0
72-73	0.0
74-75	0.0
76-77	0.0
78-79	0.0
80-81	0.0
82-83	0.0
84-85	0.0
86-87	0.0
88-89	0.0
90-91	0.0
92-93	0.0
94-95	0.0
96-97	0.0
98-99	0.0
100-101	0.0
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
101	4000.0
>>END_MODULE
>>Sequence Duplication Levels	warn
#Total Deduplicated Percentage	53.574999999999996
#Duplication Level	Percentage of deduplicated	Percentage of total
1	85.30097993467102	45.7
2	6.299580027998133	6.75
3	2.519832011199253	4.05
4	1.6332244517032197	3.5000000000000004
5	0.6066262249183387	1.625
6	0.5599626691553896	1.7999999999999998
7	0.23331777881474566	0.8750000000000001
8	0.4199720018665422	1.7999999999999998
9	0.18665422305179655	0.8999999999999999
>10	1.959869342043864	18.35
>50	0.18665422305179655	8.375
>100	0.09332711152589827	6.275
>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
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	148	3.6999999999999997	No Hit
GGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGA	103	2.5749999999999997	RNA PCR Primer, Index 1 (100% over 22bp)
TCCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGT	91	2.275	No Hit
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	88	2.1999999999999997	RNA PCR Primer, Index 1 (100% over 29bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	86	2.15	No Hit
AGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGC	70	1.7500000000000002	No Hit
GCCCACCCCAAGATGAGTGCTCTCTCTGGAATTCTCGGGTGCCAAGGAAC	40	1.0	RNA PCR Primer, Index 1 (100% over 24bp)
GACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	39	0.975	RNA PCR Primer, Index 1 (100% over 23bp)
GACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAAC	35	0.8750000000000001	RNA PCR Primer, Index 1 (100% over 24bp)
CACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGATGGAATTC	30	0.75	No Hit
CTCTGATGATGATCAAACTAATACTTTCGTTCTTCTGGAATTCTCGGGTG	28	0.7000000000000001	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATATGGAATTCTCGGGTGCCAAG	28	0.7000000000000001	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	27	0.675	No Hit
AGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGG	27	0.675	Illumina Small RNA Adapter 2 (100% over 21bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCTGGAATTCTCGGGTGCCAAGG	26	0.65	Illumina Small RNA Adapter 2 (100% over 21bp)
TCTCGGGTGCCAAGGAACTCCAGTCACAGTCAAATCTCGTATGCCGTCTT	25	0.625	RNA PCR Primer, Index 13 (100% over 50bp)
GAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAG	23	0.575	No Hit
CACGACTCTCGGCAACGGATATCTCGTGGAATTCTCGGGTGCCAAGGAAC	20	0.5	RNA PCR Primer, Index 1 (100% over 24bp)
TGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAA	19	0.475	No Hit
CTCGGGTGCCAAGGAACTCCAGTCACAGTCAAATCTCGTATGCCGTCTTC	18	0.44999999999999996	RNA PCR Primer, Index 13 (100% over 50bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGACTGGAATTCTCGGGTGCCA	17	0.42500000000000004	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCAAAATCTTGGAATTCT	16	0.4	No Hit
TCCGTCGTAGTCTAGGTGGTTAGGATATGGAATTCTCGGGTGCCAAGGAA	16	0.4	RNA PCR Primer, Index 1 (100% over 23bp)
AATTCTCGGGTGCCAAGGAACTCCAGTCACAGTCAAATCTCGTATGCCGT	15	0.375	RNA PCR Primer, Index 13 (100% over 50bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTGGAATTCTCGGGTGCCA	14	0.35000000000000003	No Hit
CATCGAGTAGACCTTGTTATTGTGAGATGGAATTCTCGGGTGCCAAGGAA	14	0.35000000000000003	RNA PCR Primer, Index 1 (100% over 23bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGACTTGGAATTCTCGGGTGCC	14	0.35000000000000003	No Hit
GGGGATATAGCTCAGTTGGTAGATGGAATTCTCGGGTGCCAAGGAACTCC	14	0.35000000000000003	RNA PCR Primer, Index 1 (100% over 27bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCAAAATCTGGAATTCTC	14	0.35000000000000003	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCTGGAATTCTCGGGTGC	13	0.325	No Hit
TCCTGTGGATGAGAAGGCATTTATATTCTGATGATATGGAATTCTCGGGT	13	0.325	No Hit
GACACGACTCTCGGCAACGGATATCTGGAATTCTCGGGTGCCAAGGAACT	13	0.325	RNA PCR Primer, Index 1 (100% over 25bp)
TTCTCGGGTGCCAAGGAACTCCAGTCACAGTCAAATCTCGTATGCCGTCT	13	0.325	RNA PCR Primer, Index 13 (100% over 50bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCATGGAATTCTCGGGTG	13	0.325	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTTGGAATTCTCGGGTGC	13	0.325	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGG	12	0.3	Illumina Small RNA Adapter 2 (100% over 21bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTTGGAATTCTCGGGTGCC	11	0.27499999999999997	No Hit
TAATTCATGATCTGGCATGTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 31bp)
GCACCAGTGGTCTAGTGGTAGAATAGTACCTGGAATTCTCGGGTGCCAAG	11	0.27499999999999997	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTGGAATTCTCGGGTGCCAAGG	11	0.27499999999999997	Illumina Small RNA Adapter 2 (100% over 21bp)
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTTGGAATTCTCGGGTGCCA	11	0.27499999999999997	No Hit
NGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGA	10	0.25	RNA PCR Primer, Index 1 (100% over 22bp)
GCGACCCCAGGTCAGGCGGGACTACCCGCTGATGGAATTCTCGGGTGCCA	10	0.25	No Hit
ATATATTTCAAGTTATTTCGGATCTTGGAATTCTCGGGTGCCAAGGAACT	10	0.25	RNA PCR Primer, Index 1 (100% over 25bp)
ATATATTTCAAGTTATTTCGGATCTGGAATTCTCGGGTGCCAAGGAACTC	10	0.25	RNA PCR Primer, Index 1 (100% over 26bp)
GCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCC	10	0.25	No Hit
GACACGACTCTCGGCAACGGATATCTCGTGGAATTCTCGGGTGCCAAGGA	10	0.25	RNA PCR Primer, Index 1 (100% over 22bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGATGGAATTCTCGGGTGCCAA	10	0.25	No Hit
CTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 28bp)
TCTCGGACCAGGCTTCATTCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 29bp)
ATGCAGTTACTAATTCATGATCTGGCTGGAATTCTCGGGTGCCAAGGAAC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 24bp)
CGGATAACCGTAGTAATTCTAGAGCTAATACTGGAATTCTCGGGTGCCAA	9	0.22499999999999998	No Hit
TCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTC	8	0.2	RNA PCR Primer, Index 1 (100% over 26bp)
CAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGG	8	0.2	No Hit
GCACCAGTAGTCTAGTGGTAGAATAGTACCTGGAATTCTCGGGTGCCAAG	8	0.2	No Hit
ATAACCGTAGTAATTCTAGAGCTAATGGAATTCTCGGGTGCCAAGGAACT	8	0.2	RNA PCR Primer, Index 1 (100% over 25bp)
CAGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTG	8	0.2	No Hit
CACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGGAATTCTCG	8	0.2	No Hit
ACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGATGGAATTCT	8	0.2	No Hit
GCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAA	8	0.2	RNA PCR Primer, Index 1 (100% over 23bp)
CAGGGTTCGTTTCCCTGGATGCGCACCATGGAATTCTCGGGTGCCAAGGA	8	0.2	RNA PCR Primer, Index 1 (100% over 22bp)
NCCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGT	7	0.17500000000000002	No Hit
AGAAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTG	7	0.17500000000000002	No Hit
ATTCTCGGGTGCCAAGGAACTCCAGTCACAGTCAAATCTCGTATGCCGTC	7	0.17500000000000002	RNA PCR Primer, Index 13 (100% over 50bp)
CCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTG	7	0.17500000000000002	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGTGGAATTCTCGGGTGCC	7	0.17500000000000002	No Hit
CACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAACT	6	0.15	RNA PCR Primer, Index 1 (100% over 25bp)
NGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	6	0.15	No Hit
GCACCAGTGGTCTAGTGGTAGAATAGTATGGAATTCTCGGGTGCCAAGGA	6	0.15	RNA PCR Primer, Index 1 (100% over 22bp)
TCCGTCGTAGTCTAGGTGGTTAGGATACTCTGGAATTCTCGGGTGCCAAG	6	0.15	No Hit
TTCGGACCAGGCTTCATTCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
AGTTACTAATTCATGATCTGGCTGGAATTCTCGGGTGCCAAGGAACTCCA	6	0.15	RNA PCR Primer, Index 1 (100% over 28bp)
GACACGACTCTCGGCAACGTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	6	0.15	RNA PCR Primer, Index 1 (100% over 31bp)
TCCACAGGCTTTCTTGAACTGTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
ACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAACT	6	0.15	RNA PCR Primer, Index 1 (100% over 25bp)
ACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTGC	6	0.15	No Hit
ACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCC	6	0.15	No Hit
ATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAA	6	0.15	RNA PCR Primer, Index 1 (100% over 23bp)
CATCGAGTAGACCTTGTTATTGTGAGAATAAATGGAATTCTCGGGTGCCA	5	0.125	No Hit
CACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCTGGAATTCTCGGG	5	0.125	No Hit
TATTCTGGTGTCCTAGGCGTAGAGGAACCTGGAATTCTCGGGTGCCAAGG	5	0.125	Illumina Small RNA Adapter 2 (100% over 21bp)
GGGGATGTAGCTCAGATGGTAGATGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
GAAGTCCTCGTGTTGCATTCCTTGGAATTCTCGGGTGCCAAGGAACTCCA	5	0.125	RNA PCR Primer, Index 1 (100% over 28bp)
TGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAA	5	0.125	No Hit
CCAGACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGG	5	0.125	No Hit
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTGCTAATCCTGGAATTC	5	0.125	No Hit
AGCTGAGGCATCCTAACGAACGAACGATTTGAATGGAATTCTCGGGTGCC	5	0.125	No Hit
TACCTGGTTGATCCTGCCAGTAGTCATATGCTTGTGGAATTCTCGGGTGC	5	0.125	No Hit
TGCAGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGG	5	0.125	No Hit
CCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACT	5	0.125	RNA PCR Primer, Index 1 (100% over 25bp)
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	0.05	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	0.075	0.0	0.0	0.0
7	0.0	0.1	0.0	0.0	0.0
8	0.0	0.1	0.0	0.0	0.0
9	0.0	0.15	0.0	0.0	0.0
10-11	0.0	0.2375	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	1.35	0.0	0.0	0.0
18-19	0.0	2.375	0.0	0.0	0.0
20-21	0.0	4.4875	0.0	0.0	0.0
22-23	0.0	11.825	0.0	0.0	0.0
24-25	0.0	22.225	0.0	0.0	0.0
26-27	0.0	34.275	0.0	0.0	0.0
28-29	0.0	44.425	0.0	0.0	0.0
30-31	0.0	53.8125	0.0	0.0	0.0
32-33	0.0	63.375	0.0	0.0	0.0
34-35	0.0	75.525	0.0	0.0	0.0
36-37	0.0	83.375	0.0	0.0	0.0
38-39	0.0	87.4875	0.0	0.0	0.0
40-41	0.0	89.8625	0.0	0.0	0.0
42-43	0.0	92.48750000000001	0.0	0.0	0.0
44-45	0.0	93.76249999999999	0.0	0.0	0.0
46-47	0.0	94.15	0.0	0.0	0.0
48-49	0.0	94.2625	0.0	0.0	0.0
50-51	0.0	94.275	0.0	0.0	0.0
52-53	0.0	94.2875	0.0	0.0	0.0
54-55	0.0	94.3125	0.0	0.0	0.0
56-57	0.0	94.325	0.0	0.0	0.0
58-59	0.0	94.325	0.0	0.0	0.0
60-61	0.0	94.325	0.0	0.0	0.0
62-63	0.0	94.325	0.0	0.0	0.0
64-65	0.0	94.325	0.0	0.0	0.0
66-67	0.0	94.325	0.0	0.0	0.0
68-69	0.0	94.325	0.0	0.0	0.0
70-71	0.0	94.325	0.0	0.0	0.0
72-73	0.0	94.325	0.0	0.0	0.0
74-75	0.0	94.325	0.0	0.0	0.0
76-77	0.0	94.3375	0.0	0.0	0.0
78-79	0.0	94.35	0.0	0.0	0.0
80-81	0.0	94.35	0.0	0.0	0.0
82-83	0.0125	94.35	0.0	0.0	0.0
84-85	0.025	94.375	0.0	0.0	0.0
86-87	0.025	94.375	0.0	0.0	0.0
88-89	0.025	94.375	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGGATTG	35	1.364242E-10	101.26667	1
TCGGACC	15	4.7401295E-4	101.26666	1
GTAGACC	20	1.5442722E-5	94.9375	7
TTGTAGT	35	2.3283064E-10	94.9375	5
AGTAGAC	20	1.5442722E-5	94.9375	6
GGACCAG	20	1.5442722E-5	94.9375	3
GGATTGT	35	2.3283064E-10	94.9375	2
CGGACCA	20	1.5442722E-5	94.9375	2
GATTGTA	35	2.3283064E-10	94.9375	3
GAGTAGA	20	1.5442722E-5	94.9375	5
ATTGTAG	35	2.3283064E-10	94.9375	4
AGGCTTC	20	1.5442722E-5	94.9375	8
TGTAGTT	35	2.3283064E-10	94.9375	6
GGCTTCA	20	1.5442722E-5	94.9375	9
CGAGTAG	20	1.5442722E-5	94.9375	4
CAGGCTT	20	1.5442722E-5	94.9375	7
AGACCTT	20	1.5442722E-5	94.9375	9
TCGAGTA	20	1.5442722E-5	94.9375	3
GACCAGG	20	1.5442722E-5	94.9375	4
TAGACCT	20	1.5442722E-5	94.9375	8
>>END_MODULE
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765745 READS because READLEN < 1
Read 765745 spots for SRR8846494.sra
Written 765745 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
Rejected 765726 READS because READLEN < 1
Read 765726 spots for SRR8846494.sra
Written 765726 spots for SRR8846494.sra
SRR ids: ['SRR8846494.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_hu8tq88f
SRR8846494.sra spots: 15314539
blocks: [[1, 765726], [765727, 1531452], [1531453, 2297178], [2297179, 3062904], [3062905, 3828630], [3828631, 4594356], [4594357, 5360082], [5360083, 6125808], [6125809, 6891534], [6891535, 7657260], [7657261, 8422986], [8422987, 9188712], [9188713, 9954438], [9954439, 10720164], [10720165, 11485890], [11485891, 12251616], [12251617, 13017342], [13017343, 13783068], [13783069, 14548794], [14548795, 15314539]]
SRR8846494 file size 3672333
SRR8846494 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 SRR8846494 SRR8846494_1.fastq
Input file:	SRR8846494_1.fastq
trimmed:	SRR8846494-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 22:00:32 2024 >> started

Sun Dec  8 22:01:11 2024 >> done (39.407s)
15314539 reads processed; of these:
     240 ( 0.00%) short reads filtered out after trimming by size control
      43 ( 0.00%) empty reads filtered out after trimming by size control
15314256 (100.00%) reads available; of these:
 3225863 (21.06%) trimmed reads available after processing
12088393 (78.94%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      45	  0.00%
 19	      26	  0.00%
 20	      29	  0.00%
 21	      37	  0.00%
 22	      42	  0.00%
 23	      48	  0.00%
 24	      70	  0.00%
 25	      83	  0.00%
 26	      98	  0.00%
 27	     176	  0.00%
 28	     241	  0.00%
 29	     228	  0.00%
 30	     200	  0.00%
 31	     164	  0.00%
 32	     200	  0.00%
 33	     119	  0.00%
 34	     129	  0.00%
 35	      92	  0.00%
 36	     116	  0.00%
 37	      86	  0.00%
 38	     116	  0.00%
 39	     144	  0.00%
 40	     124	  0.00%
 41	     143	  0.00%
 42	     121	  0.00%
 43	     134	  0.00%
 44	     133	  0.00%
 45	     156	  0.00%
 46	     124	  0.00%
 47	     123	  0.00%
 48	     117	  0.00%
 49	     127	  0.00%
 50	     115	  0.00%
 51	     135	  0.00%
 52	     108	  0.00%
 53	     133	  0.00%
 54	     139	  0.00%
 55	     133	  0.00%
 56	     189	  0.00%
 57	     160	  0.00%
 58	     247	  0.00%
 59	     313	  0.00%
 60	     449	  0.00%
 61	     814	  0.01%
 62	    1184	  0.01%
 63	    1316	  0.01%
 64	    1933	  0.01%
 65	    3209	  0.02%
 66	    8437	  0.06%
 67	   44202	  0.29%
 68	   50439	  0.33%
 69	   36746	  0.24%
 70	   29601	  0.19%
 71	   32371	  0.21%
 72	   16652	  0.11%
 73	    6197	  0.04%
 74	    6099	  0.04%
 75	    4070	  0.03%
 76	    3307	  0.02%
 77	    3543	  0.02%
 78	    3751	  0.02%
 79	    4236	  0.03%
 80	    4910	  0.03%
 81	    5775	  0.04%
 82	    7808	  0.05%
 83	    7654	  0.05%
 84	    8133	  0.05%
 85	    9088	  0.06%
 86	   10111	  0.07%
 87	   13779	  0.09%
 88	   26126	  0.17%
 89	   39126	  0.26%
 90	   50663	  0.33%
 91	   56006	  0.37%
 92	   70056	  0.46%
 93	  106648	  0.70%
 94	  148877	  0.97%
 95	  284290	  1.86%
 96	  374863	  2.45%
 97	  378456	  2.47%
 98	  529682	  3.46%
 99	  539668	  3.52%
100	  290125	  1.89%
101	12088393	 78.94%
15314256 reads passed initial QC


criterion=sequence-density
sequence-density=94.51
sequence-density-rank=1
fanout-score=31.24
fanout-score-rank=2
prefix-density=94.96
prefix-fanout=31.1
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACAGTCAAATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA


criterion=fanout-score
sequence-density=1.52
sequence-density-rank=4
fanout-score=65.38
fanout-score-rank=1
prefix-density=98.51
prefix-fanout=1.0
sequence=CACAGTCAAATATCGTATGCCGT
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACAGTCAAATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA -o SRR8846494 -
Input file:	STDIN
trimmed:	SRR8846494-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACAGTCAAATCTCGTATGCCGTCTTCTGCTTGA
-- 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 22:03:51 2024 >> started

Sun Dec  8 22:05:03 2024 >> done (72.255s)
14991851 reads processed; of these:
  306620 ( 2.05%) short reads filtered out after trimming by size control
    9166 ( 0.06%) empty reads filtered out after trimming by size control
14676065 (97.89%) reads available; of these:
14195722 (96.73%) trimmed reads available after processing
  480343 ( 3.27%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	   97947	  0.67%
 19	  190770	  1.30%
 20	  198347	  1.35%
 21	  807729	  5.50%
 22	  448605	  3.06%
 23	  568749	  3.88%
 24	 1773470	 12.08%
 25	  615411	  4.19%
 26	  822077	  5.60%
 27	  675760	  4.60%
 28	  847604	  5.78%
 29	  672426	  4.58%
 30	  677422	  4.62%
 31	  485547	  3.31%
 32	 1090071	  7.43%
 33	  863308	  5.88%
 34	  737557	  5.03%
 35	  580226	  3.95%
 36	  647736	  4.41%
 37	  230332	  1.57%
 38	  185608	  1.26%
 39	  176719	  1.20%
 40	  172249	  1.17%
 41	  231801	  1.58%
 42	  205964	  1.40%
 43	   69963	  0.48%
 44	   61473	  0.42%
 45	   25988	  0.18%
 46	   12342	  0.08%
 47	    5674	  0.04%
 48	    4833	  0.03%
 49	    2870	  0.02%
 50	    1758	  0.01%
 51	    1599	  0.01%
 52	     842	  0.01%
 53	     641	  0.00%
 54	     792	  0.01%
 55	     236	  0.00%
 56	     327	  0.00%
 57	     181	  0.00%
 58	     228	  0.00%
 59	     280	  0.00%
 60	     411	  0.00%
 61	     758	  0.01%
 62	    1073	  0.01%
 63	    1181	  0.01%
 64	    1773	  0.01%
 65	    2988	  0.02%
 66	    8077	  0.06%
 67	   43071	  0.29%
 68	   49194	  0.34%
 69	   35720	  0.24%
 70	   28623	  0.20%
 71	   31240	  0.21%
 72	   15015	  0.10%
 73	    4677	  0.03%
 74	    2957	  0.02%
 75	    1917	  0.01%
 76	    1867	  0.01%
 77	    2725	  0.02%
 78	    2029	  0.01%
 79	    2084	  0.01%
 80	    2545	  0.02%
 81	    1977	  0.01%
 82	    1688	  0.01%
 83	    1864	  0.01%
 84	    1327	  0.01%
 85	    1268	  0.01%
 86	    1038	  0.01%
 87	     878	  0.01%
 88	     843	  0.01%
 89	     864	  0.01%
 90	     796	  0.01%
 91	     847	  0.01%
 92	     954	  0.01%
 93	    1103	  0.01%
 94	    1533	  0.01%
 95	    2310	  0.02%
 96	    2936	  0.02%
 97	    3805	  0.03%
 98	    6160	  0.04%
 99	    6980	  0.05%
100	    8955	  0.06%
101	  194552	  1.33%


criterion=sequence-density
sequence-density=3.72
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=7
prefix-density=0.00
prefix-fanout=1.0
sequence=CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAATTCAAGA


criterion=fanout-score
sequence-density=0.03
sequence-density-rank=26
fanout-score=13.11
fanout-score-rank=1
prefix-density=0.31
prefix-fanout=1.1
sequence=GGCGGATTGCTCGAGCTGCTCACGCGGCGAGAGCGGGTCGCCGCGTGCCGGCCGGGGGACGGACCGGGAGTCGCCCCTTCGGGGGCTTTCCCCGAGCGCTGAACAGTCGACTCAGAACTGGTACGGACAAGGGGAATCCGACTGTTTAATTAAAACAAAGCATTGCG
                                 Started job on |	Dec 08 22:07:19
                             Started mapping on |	Dec 08 22:07:19
                                    Finished on |	Dec 08 22:13:49
       Mapping speed, Million of reads per hour |	138.45

                          Number of input reads |	14998470
                      Average input read length |	32
                                    UNIQUE READS:
                   Uniquely mapped reads number |	2537674
                        Uniquely mapped reads % |	16.92%
                          Average mapped length |	26.61
                       Number of splices: Total |	29245
            Number of splices: Annotated (sjdb) |	15835
                       Number of splices: GT/AG |	26462
                       Number of splices: GC/AG |	2179
                       Number of splices: AT/AC |	4
               Number of splices: Non-canonical |	600
                      Mismatch rate per base, % |	0.13%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.34
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.02
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	6625414
             % of reads mapped to multiple loci |	44.17%
        Number of reads mapped to too many loci |	4824331
             % of reads mapped to too many loci |	32.17%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	6.16%
                     % of reads unmapped: other |	0.58%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	5835382	5835382	5835382
N_multimapping	6625414	6625414	6625414
N_noFeature	1583620	1769768	2337839
N_ambiguous	40278	26154	588
UnstrandedReadsAssigned:913776 PositiveStrandReadsAssigned:741752 NegativeStrandReadsAssigned:199247
Dataset is classified unstranded
MeadianReadLen=29 20thPercentileLength=24 echo kmer=19
SRR8846494 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: SRR8846494-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 14,998,470 reads, 4,087,616 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,087 rounds

  52973 SRR8846494.ke.tsv
  35125 SRR8846494.se.tsv
  88098 total
==> SRR8846494.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	0	0
PNS24249	1928	1829	0	0
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	0	0
PNS24243	293	194	0	0
KQK14069	1603	1504	73.3424	10.8999
KQK14071	474	375	0	0

==> SRR8846494.se.tsv <==
BRADI_1g14170v3	70
BRADI_1g53295v3	1
BRADI_1g59795v3	3
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	27
BRADI_1g74790v3	35
BRADI_1g09890v3	0
BRADI_1g77505v3	4
BRADI_1g48960v3	0
SRR8846494 completed mapping pipeline successfully
