Starting /dee2/code/volunteer_pipeline.sh SRR8846549
    current disk space = 1528877613056
    free memory = 1607803048 
SRR8846549 SRAfilesize
f093e5197a9335fdd024630011073ac3  SRR8846549.sra
SRR8846549.sra file validated
SRR8846549 is single end
SRR8846549 is conventional basespace
SRR8846549 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR8846549_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	47
>>END_MODULE
>>Per base sequence quality	fail
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	30.425	33.0	33.0	34.0	25.0	34.0
2	32.72775	34.0	33.0	34.0	28.0	34.0
3	32.861	34.0	33.0	34.0	31.0	34.0
4	33.024	34.0	33.0	34.0	32.0	34.0
5	32.87975	34.0	33.0	34.0	32.0	34.0
6	36.563	38.0	37.0	38.0	34.0	38.0
7	37.09225	38.0	38.0	38.0	36.0	38.0
8	37.29925	38.0	38.0	38.0	36.0	38.0
9	37.3115	38.0	38.0	38.0	37.0	38.0
10-11	37.420500000000004	38.0	38.0	38.0	37.0	38.0
12-13	37.449375	38.0	38.0	38.0	37.0	38.0
14-15	37.391999999999996	38.0	38.0	38.0	37.0	38.0
16-17	37.345749999999995	38.0	38.0	38.0	37.0	38.0
18-19	37.358875	38.0	38.0	38.0	37.0	38.0
20-21	37.407125	38.0	38.0	38.0	37.0	38.0
22-23	37.418	38.0	38.0	38.0	37.0	38.0
24-25	37.485375000000005	38.0	38.0	38.0	37.0	38.0
26-27	37.4735	38.0	38.0	38.0	37.5	38.0
28-29	37.380875	38.0	38.0	38.0	37.0	38.0
30-31	37.380250000000004	38.0	38.0	38.0	37.0	38.0
32-33	37.3225	38.0	38.0	38.0	37.0	38.0
34-35	37.12975	38.0	38.0	38.0	36.5	38.0
36-37	37.079625	38.0	38.0	38.0	36.0	38.0
38-39	36.993625	38.0	38.0	38.0	36.0	38.0
40-41	36.9685	38.0	38.0	38.0	36.0	38.0
42-43	36.908625	38.0	38.0	38.0	35.5	38.0
44-45	37.0145	38.0	38.0	38.0	36.0	38.0
46-47	37.089625	38.0	38.0	38.0	36.0	38.0
48-49	37.19525	38.0	38.0	38.0	36.5	38.0
50-51	37.208375000000004	38.0	38.0	38.0	37.0	38.0
52-53	37.247	38.0	38.0	38.0	37.0	38.0
54-55	37.082125000000005	38.0	38.0	38.0	36.0	38.0
56-57	37.016000000000005	38.0	38.0	38.0	36.0	38.0
58-59	36.783125	38.0	38.0	38.0	35.0	38.0
60-61	36.73125	38.0	38.0	38.0	35.0	38.0
62-63	36.413250000000005	38.0	38.0	38.0	33.5	38.0
64-65	36.245875	38.0	37.5	38.0	32.5	38.0
66-67	36.0405	38.0	37.0	38.0	31.0	38.0
68-69	36.025625	38.0	37.0	38.0	31.0	38.0
70-71	36.235125	38.0	37.0	38.0	33.0	38.0
72-73	36.1955	38.0	37.5	38.0	32.0	38.0
74-75	35.8805	38.0	37.0	38.0	30.5	38.0
76-77	35.692875	38.0	37.0	38.0	30.0	38.0
78-79	35.387875	38.0	36.5	38.0	28.0	38.0
80-81	35.373375	38.0	36.5	38.0	28.5	38.0
82-83	35.3965	38.0	37.0	38.0	29.0	38.0
84-85	35.273250000000004	38.0	36.5	38.0	28.5	38.0
86-87	35.5655	38.0	37.0	38.0	30.0	38.0
88-89	35.4445	38.0	37.0	38.0	30.0	38.0
90-91	35.326	38.0	37.0	38.0	30.0	38.0
92-93	35.137	38.0	37.0	38.0	30.0	38.0
94-95	34.113875	38.0	36.0	38.0	25.0	38.0
96-97	32.13175	38.0	34.0	38.0	8.0	38.0
98-99	29.43825	38.0	28.0	38.0	2.0	38.0
100-101	26.156125	36.5	2.0	38.0	2.0	38.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
7	1.0
8	0.0
9	0.0
10	0.0
11	0.0
12	0.0
13	0.0
14	2.0
15	0.0
16	2.0
17	1.0
18	0.0
19	0.0
20	0.0
21	0.0
22	2.0
23	6.0
24	11.0
25	17.0
26	26.0
27	21.0
28	30.0
29	30.0
30	56.0
31	72.0
32	94.0
33	148.0
34	267.0
35	502.0
36	876.0
37	1836.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	34.25218340611353	23.71724890829694	22.59825327510917	19.432314410480352
2	24.15	28.525	18.175	29.15
3	27.775	18.9	19.275000000000002	34.050000000000004
4	27.275	33.975	15.55	23.200000000000003
5	25.3	25.3	24.175	25.224999999999998
6	25.924999999999997	23.474999999999998	24.925	25.674999999999997
7	35.325	28.225	17.75	18.7
8	17.325	20.925	37.05	24.7
9	23.575	34.575	24.075	17.775
10-11	30.2625	22.175	26.5	21.0625
12-13	23.6125	19.2625	23.9	33.225
14-15	24.25	35.4125	21.1625	19.175
16-17	24.1375	26.974999999999998	30.775000000000002	18.1125
18-19	35.6375	21.275	21.6	21.4875
20-21	23.1125	26.674999999999997	28.1375	22.075
22-23	28.287499999999998	29.062500000000004	27.250000000000004	15.4
24-25	28.287499999999998	25.374999999999996	26.4125	19.925
26-27	31.275	25.5125	24.15	19.0625
28-29	23.7	27.9125	26.0625	22.325
30-31	25.7875	20.4875	34.0125	19.7125
32-33	23.974999999999998	17.125	35.475	23.425
34-35	33.3625	13.65	29.349999999999998	23.6375
36-37	36.4625	16.85	26.8	19.8875
38-39	36.85	16.9625	27.0625	19.125
40-41	29.312500000000004	18.35	23.7125	28.625
42-43	31.874999999999996	25.074999999999996	18.987499999999997	24.0625
44-45	39.1625	23.4125	13.8125	23.6125
46-47	31.574999999999996	31.025000000000002	15.3375	22.0625
48-49	26.200000000000003	25.6125	16.900000000000002	31.2875
50-51	21.65	26.9125	15.437500000000002	36.0
52-53	26.474999999999998	28.95	13.6625	30.912499999999998
54-55	23.2875	29.3375	15.775	31.6
56-57	25.9625	25.2625	18.087500000000002	30.6875
58-59	28.1625	26.2125	14.575	31.05
60-61	23.875	27.5625	19.162499999999998	29.4
62-63	27.224999999999998	21.1125	21.125	30.5375
64-65	22.125	28.0875	23.1125	26.674999999999997
66-67	22.8	19.3	26.787499999999998	31.112499999999997
68-69	23.2125	19.8875	27.3125	29.5875
70-71	24.9875	20.1375	28.8375	26.0375
72-73	25.4625	17.549999999999997	31.374999999999996	25.6125
74-75	18.675	14.149999999999999	30.275000000000002	36.9
76-77	24.6125	10.15	36.15	29.0875
78-79	19.6375	9.825000000000001	37.9375	32.6
80-81	20.0	9.049999999999999	38.425	32.525
82-83	20.3125	9.0125	43.3625	27.3125
84-85	20.5875	11.1	38.574999999999996	29.7375
86-87	21.3125	18.1125	35.3	25.275
88-89	14.2375	34.375	34.7625	16.625
90-91	14.8625	45.1875	25.324999999999996	14.625
92-93	10.7375	55.2	20.225	13.8375
94-95	10.7875	62.9	18.1875	8.125
96-97	7.0874999999999995	73.375	13.3125	6.225
98-99	5.5	80.375	9.85	4.275
100-101	4.025	85.6	6.1375	4.237500000000001
>>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	0.5
33	1.5
34	1.5
35	2.0
36	3.5
37	5.5
38	7.5
39	13.0
40	42.0
41	72.0
42	113.0
43	156.0
44	212.5
45	321.0
46	339.0
47	350.5
48	388.5
49	377.0
50	346.5
51	310.0
52	261.0
53	174.0
54	123.0
55	93.5
56	113.0
57	94.0
58	33.5
59	19.5
60	7.5
61	5.5
62	5.5
63	4.5
64	1.5
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	8.4
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	58.375
#Duplication Level	Percentage of deduplicated	Percentage of total
1	85.18201284796574	49.725
2	6.980728051391863	8.15
3	2.4839400428265526	4.35
4	1.4132762312633833	3.3000000000000003
5	0.5995717344753747	1.7500000000000002
6	0.47109207708779444	1.6500000000000001
7	0.556745182012848	2.275
8	0.17130620985010706	0.8
9	0.5139186295503212	2.7
>10	1.4561027837259102	16.45
>50	0.1284796573875803	5.675
>100	0.042826552462526764	3.175
>500	0.0	0.0
>1k	0.0	0.0
>5k	0.0	0.0
>10k+	0.0	0.0
>>END_MODULE
>>Overrepresented sequences	fail
#Sequence	Count	Percentage	Possible Source
GACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	127	3.175	RNA PCR Primer, Index 1 (100% over 23bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	80	2.0	No Hit
TCCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGT	74	1.8499999999999999	No Hit
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	73	1.825	RNA PCR Primer, Index 1 (100% over 29bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	49	1.225	No Hit
TCCGTCGTAGTCTAGGTGGTTAGGATATGGAATTCTCGGGTGCCAAGGAA	47	1.175	RNA PCR Primer, Index 1 (100% over 23bp)
GCCCACCCCAAGATGAGTGCTCTCTCTGGAATTCTCGGGTGCCAAGGAAC	42	1.05	RNA PCR Primer, Index 1 (100% over 24bp)
GGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGA	39	0.975	RNA PCR Primer, Index 1 (100% over 22bp)
CACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAACT	30	0.75	RNA PCR Primer, Index 1 (100% over 25bp)
AGCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGC	24	0.6	No Hit
GACACGACTCTCGGCAACGGATATCTGGAATTCTCGGGTGCCAAGGAACT	23	0.575	RNA PCR Primer, Index 1 (100% over 25bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	21	0.525	No Hit
GCACCAGTGGTCTAGTGGTAGAATAGTACCTGGAATTCTCGGGTGCCAAG	21	0.525	No Hit
ACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCC	21	0.525	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCTGGAATTCTCGGGTGCCAAGG	20	0.5	Illumina Small RNA Adapter 2 (100% over 21bp)
GACACGACTCTCGGCAACGGATATCTTGGAATTCTCGGGTGCCAAGGAAC	20	0.5	RNA PCR Primer, Index 1 (100% over 24bp)
GCCTTGATGGTGAAATGGTAGACATGGAATTCTCGGGTGCCAAGGAACTC	20	0.5	RNA PCR Primer, Index 1 (100% over 26bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCTGGAATTCTCGGGTGC	18	0.44999999999999996	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATATGGAATTCTCGGGTGCCAAG	18	0.44999999999999996	No Hit
CACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGATGGAATTC	18	0.44999999999999996	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTGGAATTCTCGGGTGCCAAGG	17	0.42500000000000004	Illumina Small RNA Adapter 2 (100% over 21bp)
NACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	17	0.42500000000000004	RNA PCR Primer, Index 1 (100% over 23bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTGGAATTCTCGGGTGCCA	15	0.375	No Hit
TTCGGACCAGGCTTCATTCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	14	0.35000000000000003	RNA PCR Primer, Index 1 (100% over 29bp)
AGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTCC	14	0.35000000000000003	RNA PCR Primer, Index 1 (100% over 27bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTTGGAATTCTCGGGTG	14	0.35000000000000003	No Hit
ACCTGCTCTGATACCATGTTGTGATGGAATTCTCGGGTGCCAAGGAACTC	13	0.325	RNA PCR Primer, Index 1 (100% over 26bp)
CTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	13	0.325	RNA PCR Primer, Index 1 (100% over 28bp)
GAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAG	13	0.325	No Hit
CTCTGATGATGATCAAACTAATACTTTCGTTCTTCTGGAATTCTCGGGTG	12	0.3	No Hit
ATGCAGTTACTAATTCATGATCTGGCTGGAATTCTCGGGTGCCAAGGAAC	12	0.3	RNA PCR Primer, Index 1 (100% over 24bp)
TGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAA	12	0.3	No Hit
TCCACAGGCTTTCTTGAACTGTGGAATTCTCGGGTGCCAAGGAACTCCAG	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 29bp)
AATTCTCGGGTGCCAAGGAACTCCAGTCACGGTAGCATCTCGTATGCCGT	10	0.25	RNA PCR Primer, Index 24 (100% over 50bp)
ATATATTTCAAGTTATTTCGGATCTTGGAATTCTCGGGTGCCAAGGAACT	10	0.25	RNA PCR Primer, Index 1 (100% over 25bp)
TCTCGGACCAGGCTTCATTCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	10	0.25	RNA PCR Primer, Index 1 (100% over 29bp)
CAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTC	10	0.25	RNA PCR Primer, Index 1 (100% over 26bp)
CAGGGTTCGTTTCCCTGGATGCGCACCATGGAATTCTCGGGTGCCAAGGA	10	0.25	RNA PCR Primer, Index 1 (100% over 22bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTTGGAATTCTCGGGTGCC	9	0.22499999999999998	No Hit
GACATAGCAAGGATTGACAGACTGAGAGCTCTTTCTGGAATTCTCGGGTG	9	0.22499999999999998	No Hit
GCACCAGTAGTCTAGTGGTAGAATAGTACCTGGAATTCTCGGGTGCCAAG	9	0.22499999999999998	No Hit
TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGGTAGCATCTCGTATGC	9	0.22499999999999998	RNA PCR Primer, Index 24 (100% over 50bp)
ACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAAC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 24bp)
GCGACCCCAGGTCAGGCGGGACTTGGAATTCTCGGGTGCCAAGGAACTCC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 27bp)
TCTCGGGTGCCAAGGAACTCCAGTCACGGTAGCATCTCGTATGCCGTCTT	9	0.22499999999999998	RNA PCR Primer, Index 24 (100% over 50bp)
CATCGAGTAGACCTTGTTATTGTGAGATGGAATTCTCGGGTGCCAAGGAA	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 23bp)
AGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGG	9	0.22499999999999998	Illumina Small RNA Adapter 2 (100% over 21bp)
GACACGACTCTCGGCAACGGATATCTCGTGGAATTCTCGGGTGCCAAGGA	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 22bp)
TACCTGGTTGATCCTGCCAGTAGTCATATGCTTGTGGAATTCTCGGGTGC	9	0.22499999999999998	No Hit
AGGGCTATAGCTCAGTTCGGTAGAGCAACTCGTTTACACCGAGATGGAAT	9	0.22499999999999998	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTCAAGGGTGGAATTC	8	0.2	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCAAAATCTTGGAATTCT	8	0.2	No Hit
CGACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGA	8	0.2	RNA PCR Primer, Index 1 (100% over 22bp)
NGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	8	0.2	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGCCAAGGAGTGGAATTCT	7	0.17500000000000002	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGACTTGGAATTCTCGGGTGCC	7	0.17500000000000002	No Hit
GAAGTCCTCGTGTTGCATTCCTTGGAATTCTCGGGTGCCAAGGAACTCCA	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 28bp)
TGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
CACGACTCTCGGCAACGGATATCTCGTGGAATTCTCGGGTGCCAAGGAAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 24bp)
AAGGGTGCTGAGAATACTTTGAATCTGACACTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
GCCTTGATGGTGAAATGGTAGACACGCGAGATGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTTGGAATTCTCGGGTGCCA	7	0.17500000000000002	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
CCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACT	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 25bp)
TCCGTCGTAGTCTAGGTGGTTAGGATTGGAATTCTCGGGTGCCAAGGAAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 24bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTTGGAATTCTCGGGTGC	7	0.17500000000000002	No Hit
CACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGC	7	0.17500000000000002	No Hit
GCACCAGTGGTCTAGTGGTAGAATAGTATGGAATTCTCGGGTGCCAAGGA	6	0.15	RNA PCR Primer, Index 1 (100% over 22bp)
CATCGAGTAGACCTTGTTATTGTGAGAATAAATGGAATTCTCGGGTGCCA	6	0.15	No Hit
TCCGTCGTAGTCTAGGTGGTTAGGATACTCTGGAATTCTCGGGTGCCAAG	6	0.15	No Hit
TTTGTTTTTATGTTATTTTGTGAAGGTGGAATTCTCGGGTGCCAAGGAAC	6	0.15	RNA PCR Primer, Index 1 (100% over 24bp)
ATCAGCTGACACGAGCAAATCTGAACCTGGAATTCTCGGGTGCCAAGGAA	6	0.15	RNA PCR Primer, Index 1 (100% over 23bp)
ATTCTCGGGTGCCAAGGAACTCCAGTCACGGTAGCATCTCGTATGCCGTC	6	0.15	RNA PCR Primer, Index 24 (100% over 50bp)
AGTTACTAATTCATGATCTGGCTGGAATTCTCGGGTGCCAAGGAACTCCA	6	0.15	RNA PCR Primer, Index 1 (100% over 28bp)
TAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTAATGGAATTCTCGGGTGCCA	6	0.15	No Hit
GCGTCTGTAGTCCAACGGTTAGGATAATTGCCTGGAATTCTCGGGTGCCA	6	0.15	No Hit
TCGCTTGGTGCAGATCGGGACTGGAATTCTCGGGTGCCAAGGAACTCCAG	6	0.15	RNA PCR Primer, Index 1 (100% over 29bp)
GACACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCTGGAATTCTCG	5	0.125	No Hit
GTCGTTGTAGTATAGTGGTAAGTATTCCCGCCTGGAATTCTCGGGTGCCA	5	0.125	No Hit
TAATTCATGATCTGGCATGTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	5	0.125	RNA PCR Primer, Index 1 (100% over 31bp)
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTTGGAATTCTCGGGTGC	5	0.125	No Hit
GGGGATATGGCGAAATCGGTAGACGCTACGGACTTTGGAATTCTCGGGTG	5	0.125	No Hit
NCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	5	0.125	RNA PCR Primer, Index 1 (100% over 29bp)
CATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
CTTAGCGGATACTATGATAGCACCTGGAATTCTCGGGTGCCAAGGAACTC	5	0.125	RNA PCR Primer, Index 1 (100% over 26bp)
GCTGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCC	5	0.125	No Hit
TGCCACGATCCACTGAGATCCAGCCCCACGTCGCACGGATTCGTTGGAAT	5	0.125	No Hit
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTGCTAATCCTGGAATTC	5	0.125	No Hit
TTGACAGAAGAGAGTGAGCACTGGAATTCTCGGGTGCCAAGGAACTCCAG	5	0.125	RNA PCR Primer, Index 1 (100% over 29bp)
GGGGATATAGCTCAGTTGGTAGATGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTATGGAATTCTCGGGTGCCAA	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	0.225	0.0	0.0	0.0
2	0.0	0.225	0.0	0.0	0.0
3	0.0	0.225	0.0	0.0	0.0
4	0.0	0.225	0.0	0.0	0.0
5	0.0	0.225	0.0	0.0	0.0
6	0.0	0.225	0.0	0.0	0.0
7	0.0	0.275	0.0	0.0	0.0
8	0.0	0.35	0.0	0.0	0.0
9	0.0	0.45	0.0	0.0	0.0
10-11	0.0	0.525	0.0	0.0	0.0
12-13	0.0	0.65	0.0	0.0	0.0
14-15	0.0	0.9125000000000001	0.0	0.0	0.0
16-17	0.0	1.6	0.0	0.0	0.0
18-19	0.0	2.625	0.0	0.0	0.0
20-21	0.0	4.8375	0.0	0.0	0.0
22-23	0.0	13.0	0.0	0.0	0.0
24-25	0.0	24.0375	0.0	0.0	0.0
26-27	0.0	37.0625	0.0	0.0	0.0
28-29	0.0	50.1	0.0	0.0	0.0
30-31	0.0	58.125	0.0	0.0	0.0
32-33	0.0	67.275	0.0	0.0	0.0
34-35	0.0	77.3	0.0	0.0	0.0
36-37	0.0	84.5625	0.0	0.0	0.0
38-39	0.0	89.05000000000001	0.0	0.0	0.0
40-41	0.0	91.15	0.0	0.0	0.0
42-43	0.0	93.7875	0.0	0.0	0.0
44-45	0.0	95.5625	0.0	0.0	0.0
46-47	0.0	96.225	0.0	0.0	0.0
48-49	0.0	96.375	0.0	0.0	0.0
50-51	0.0	96.425	0.0	0.0	0.0
52-53	0.0	96.5	0.0	0.0	0.0
54-55	0.0	96.525	0.0	0.0	0.0
56-57	0.0	96.525	0.0	0.0	0.0
58-59	0.0	96.525	0.0	0.0	0.0
60-61	0.0	96.525	0.0	0.0	0.0
62-63	0.0	96.525	0.0	0.0	0.0
64-65	0.0	96.525	0.0	0.0	0.0
66-67	0.0	96.525	0.0	0.0	0.0
68-69	0.0	96.525	0.0	0.0	0.0
70-71	0.0	96.525	0.0	0.0	0.0
72-73	0.0	96.525	0.0	0.0	0.0
74-75	0.0	96.525	0.0	0.0	0.0
76-77	0.0	96.525	0.0	0.0	0.0
78-79	0.0	96.525	0.0	0.0	0.0
80-81	0.0	96.525	0.0	0.0	0.0
82-83	0.0	96.5375	0.0	0.0	0.0
84-85	0.0	96.55	0.0	0.0	0.0
86-87	0.0	96.55	0.0	0.0	0.0
88-89	0.0	96.55	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GACACGA	25	2.1896449E-7	104.0137	1
ACACGAC	25	3.8500548E-7	94.912506	2
TTGTAGT	15	6.164719E-4	94.9125	5
TAGTTCA	15	6.164719E-4	94.9125	8
AGTTCAA	15	6.164719E-4	94.9125	9
GTAGTTC	15	6.164719E-4	94.9125	7
CTCTCGG	30	1.1400607E-6	79.09375	8
ACTCTCG	30	1.1400607E-6	79.09375	7
CACGACT	30	1.1400607E-6	79.09375	3
ACGACTC	30	1.1400607E-6	79.09375	4
GACTCTC	30	1.1400607E-6	79.09375	6
CGACTCT	30	1.1400607E-6	79.09375	5
TCTCGGC	40	6.299526E-6	59.320312	9
AAAAACA	20	5.094958E-4	47.456253	94-95
GATATCT	30	7.616909E-5	39.546875	20-21
GGCAACG	30	7.616909E-5	39.546875	12-13
CGGATAT	30	7.616909E-5	39.546875	18-19
GCAACGG	30	7.616909E-5	39.546875	14-15
GGATATC	30	7.616909E-5	39.546875	18-19
CTCGGCA	30	7.616909E-5	39.546875	10-11
>>END_MODULE
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
Rejected 1144652 READS because READLEN < 1
Read 1144652 spots for SRR8846549.sra
Written 1144652 spots for SRR8846549.sra
SRR ids: ['SRR8846549.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_342hjxby
SRR8846549.sra spots: 22893040
blocks: [[1, 1144652], [1144653, 2289304], [2289305, 3433956], [3433957, 4578608], [4578609, 5723260], [5723261, 6867912], [6867913, 8012564], [8012565, 9157216], [9157217, 10301868], [10301869, 11446520], [11446521, 12591172], [12591173, 13735824], [13735825, 14880476], [14880477, 16025128], [16025129, 17169780], [17169781, 18314432], [18314433, 19459084], [19459085, 20603736], [20603737, 21748388], [21748389, 22893040]]
SRR8846549 file size 5500351
SRR8846549 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 SRR8846549 SRR8846549_1.fastq
Input file:	SRR8846549_1.fastq
trimmed:	SRR8846549-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 10:00:11 2024 >> started

Mon Dec  9 10:00:22 2024 >> done (10.756s)
22893040 reads processed; of these:
     623 ( 0.00%) short reads filtered out after trimming by size control
      77 ( 0.00%) empty reads filtered out after trimming by size control
22892340 (100.00%) reads available; of these:
 4885180 (21.34%) trimmed reads available after processing
18007160 (78.66%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      74	  0.00%
 19	      63	  0.00%
 20	      69	  0.00%
 21	      75	  0.00%
 22	      88	  0.00%
 23	      90	  0.00%
 24	     133	  0.00%
 25	     171	  0.00%
 26	     232	  0.00%
 27	     339	  0.00%
 28	     418	  0.00%
 29	     490	  0.00%
 30	     442	  0.00%
 31	     403	  0.00%
 32	     374	  0.00%
 33	     334	  0.00%
 34	     343	  0.00%
 35	     269	  0.00%
 36	     265	  0.00%
 37	     259	  0.00%
 38	     256	  0.00%
 39	     250	  0.00%
 40	     264	  0.00%
 41	     303	  0.00%
 42	     394	  0.00%
 43	     365	  0.00%
 44	     419	  0.00%
 45	     420	  0.00%
 46	     404	  0.00%
 47	     411	  0.00%
 48	     352	  0.00%
 49	     274	  0.00%
 50	     334	  0.00%
 51	     328	  0.00%
 52	     312	  0.00%
 53	     356	  0.00%
 54	     362	  0.00%
 55	     416	  0.00%
 56	     462	  0.00%
 57	     511	  0.00%
 58	     484	  0.00%
 59	     609	  0.00%
 60	     796	  0.00%
 61	     868	  0.00%
 62	    1064	  0.00%
 63	    1291	  0.01%
 64	    1810	  0.01%
 65	    2018	  0.01%
 66	    4599	  0.02%
 67	   16663	  0.07%
 68	   20391	  0.09%
 69	   16834	  0.07%
 70	   18958	  0.08%
 71	   30045	  0.13%
 72	   14619	  0.06%
 73	    6975	  0.03%
 74	   20908	  0.09%
 75	   10294	  0.04%
 76	    5311	  0.02%
 77	    4234	  0.02%
 78	    5056	  0.02%
 79	    5802	  0.03%
 80	    7637	  0.03%
 81	   10414	  0.05%
 82	   15857	  0.07%
 83	   15908	  0.07%
 84	   15360	  0.07%
 85	   15942	  0.07%
 86	   20174	  0.09%
 87	   28906	  0.13%
 88	   41107	  0.18%
 89	   54942	  0.24%
 90	   84267	  0.37%
 91	   95170	  0.42%
 92	  120787	  0.53%
 93	  192456	  0.84%
 94	  237032	  1.04%
 95	  514084	  2.25%
 96	  622603	  2.72%
 97	  581515	  2.54%
 98	  836532	  3.65%
 99	  732119	  3.20%
100	  440615	  1.92%
101	18007160	 78.66%
22892340 reads passed initial QC


criterion=sequence-density
sequence-density=96.39
sequence-density-rank=1
fanout-score=35.77
fanout-score-rank=1
prefix-density=96.78
prefix-fanout=35.6
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGGTAGCATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA


criterion=fanout-score
sequence-density=96.39
sequence-density-rank=1
fanout-score=35.77
fanout-score-rank=1
prefix-density=96.78
prefix-fanout=35.6
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGGTAGCATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGGTAGCATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAA -o SRR8846549 -
Input file:	STDIN
trimmed:	SRR8846549-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACGGTAGCATCTCGTATGCCGTCTTCTGCTTGA
-- 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 10:01:00 2024 >> started

Mon Dec  9 10:01:20 2024 >> done (19.771s)
22420333 reads processed; of these:
  463459 ( 2.07%) short reads filtered out after trimming by size control
   46597 ( 0.21%) empty reads filtered out after trimming by size control
21910277 (97.73%) reads available; of these:
21615923 (98.66%) trimmed reads available after processing
  294354 ( 1.34%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  145483	  0.66%
 19	  274871	  1.25%
 20	  283264	  1.29%
 21	 1242585	  5.67%
 22	  642836	  2.93%
 23	  837751	  3.82%
 24	 2670202	 12.19%
 25	  958032	  4.37%
 26	 1147948	  5.24%
 27	 1688534	  7.71%
 28	 1083225	  4.94%
 29	  834979	  3.81%
 30	 1088402	  4.97%
 31	  830070	  3.79%
 32	 1353552	  6.18%
 33	 1184511	  5.41%
 34	  943786	  4.31%
 35	  834420	  3.81%
 36	  988552	  4.51%
 37	  447368	  2.04%
 38	  348991	  1.59%
 39	  310402	  1.42%
 40	  311421	  1.42%
 41	  308782	  1.41%
 42	  350303	  1.60%
 43	  165903	  0.76%
 44	  181701	  0.83%
 45	   60889	  0.28%
 46	   42971	  0.20%
 47	   19090	  0.09%
 48	   11063	  0.05%
 49	    6713	  0.03%
 50	    4189	  0.02%
 51	    3580	  0.02%
 52	    2088	  0.01%
 53	    1395	  0.01%
 54	    1316	  0.01%
 55	     620	  0.00%
 56	     835	  0.00%
 57	     379	  0.00%
 58	     366	  0.00%
 59	     387	  0.00%
 60	     435	  0.00%
 61	     513	  0.00%
 62	     608	  0.00%
 63	     845	  0.00%
 64	    1279	  0.01%
 65	    1443	  0.01%
 66	    3841	  0.02%
 67	   15595	  0.07%
 68	   19028	  0.09%
 69	   15414	  0.07%
 70	   17292	  0.08%
 71	   27790	  0.13%
 72	   11601	  0.05%
 73	    2315	  0.01%
 74	    1296	  0.01%
 75	     890	  0.00%
 76	    1078	  0.00%
 77	    1441	  0.01%
 78	    1119	  0.01%
 79	    1037	  0.00%
 80	    1995	  0.01%
 81	    1532	  0.01%
 82	    1363	  0.01%
 83	    2123	  0.01%
 84	    1075	  0.00%
 85	     878	  0.00%
 86	     856	  0.00%
 87	     968	  0.00%
 88	     660	  0.00%
 89	     809	  0.00%
 90	     767	  0.00%
 91	     784	  0.00%
 92	     959	  0.00%
 93	    1128	  0.01%
 94	    1160	  0.01%
 95	    1434	  0.01%
 96	    2000	  0.01%
 97	    2709	  0.01%
 98	    4263	  0.02%
 99	    3713	  0.02%
100	    4670	  0.02%
101	  135816	  0.62%


criterion=sequence-density
sequence-density=6.20
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=13
prefix-density=0.00
prefix-fanout=1.0
sequence=GGGATTGTAGTTCAATTGGTCAGAGCACCGCCC


criterion=fanout-score
sequence-density=0.30
sequence-density-rank=16
fanout-score=10.01
fanout-score-rank=1
prefix-density=2.97
prefix-fanout=1.0
sequence=ATTGTGAGAATAAAAA
                                 Started job on |	Dec 09 10:01:38
                             Started mapping on |	Dec 09 10:01:38
                                    Finished on |	Dec 09 10:02:29
       Mapping speed, Million of reads per hour |	1579.93

                          Number of input reads |	22382284
                      Average input read length |	31
                                    UNIQUE READS:
                   Uniquely mapped reads number |	3652224
                        Uniquely mapped reads % |	16.32%
                          Average mapped length |	26.88
                       Number of splices: Total |	45728
            Number of splices: Annotated (sjdb) |	29277
                       Number of splices: GT/AG |	42490
                       Number of splices: GC/AG |	2380
                       Number of splices: AT/AC |	30
               Number of splices: Non-canonical |	828
                      Mismatch rate per base, % |	0.16%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.38
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.02
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	8378383
             % of reads mapped to multiple loci |	37.43%
        Number of reads mapped to too many loci |	9191189
             % of reads mapped to too many loci |	41.06%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	4.63%
                     % of reads unmapped: other |	0.56%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	10351677	10351677	10351677
N_multimapping	8378383	8378383	8378383
N_noFeature	2157504	2453205	3335067
N_ambiguous	58699	36689	763
UnstrandedReadsAssigned:1436021 PositiveStrandReadsAssigned:1162330 NegativeStrandReadsAssigned:316394
Dataset is classified unstranded
MeadianReadLen=28 20thPercentileLength=24 echo kmer=19
SRR8846549 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: SRR8846549-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 22,382,284 reads, 6,654,032 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,149 rounds

  52973 SRR8846549.ke.tsv
  35125 SRR8846549.se.tsv
  88098 total
==> SRR8846549.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	0	0
PNS24249	1928	1829	2.52842	0.196555
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	6.931	0.718275
PNS24243	293	194	0	0
KQK14069	1603	1504	390.201	36.8883
KQK14071	474	375	2.34081	0.887529

==> SRR8846549.se.tsv <==
BRADI_1g14170v3	411
BRADI_1g53295v3	6
BRADI_1g59795v3	1
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	45
BRADI_1g74790v3	48
BRADI_1g09890v3	0
BRADI_1g77505v3	3
BRADI_1g48960v3	0
SRR8846549 completed mapping pipeline successfully
