Starting /dee2/code/volunteer_pipeline.sh SRR6941544
    current disk space = 1551498694656
    free memory = 1599087132 
SRR6941544 SRAfilesize
a135d765708ed65532e290b04e4e6a62  SRR6941544.sra
SRR6941544.sra file validated
SRR6941544 is single end
SRR6941544 is conventional basespace
SRR6941544 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR6941544_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	fail
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	33.258	34.0	33.0	34.0	32.0	34.0
2	33.32275	34.0	33.0	34.0	33.0	34.0
3	33.06575	34.0	33.0	34.0	31.0	34.0
4	33.22375	34.0	33.0	34.0	32.0	34.0
5	33.201	34.0	33.0	34.0	33.0	34.0
6	37.00175	38.0	37.0	38.0	36.0	38.0
7	37.35675	38.0	38.0	38.0	37.0	38.0
8	37.4985	38.0	38.0	38.0	37.0	38.0
9	37.499	38.0	38.0	38.0	38.0	38.0
10-11	37.524249999999995	38.0	38.0	38.0	37.5	38.0
12-13	37.39175	38.0	38.0	38.0	37.0	38.0
14-15	37.45825	38.0	38.0	38.0	37.0	38.0
16-17	36.035624999999996	38.0	37.0	38.0	27.0	38.0
18-19	36.820499999999996	38.0	37.5	38.0	33.5	38.0
20-21	36.327375	38.0	38.0	38.0	31.5	38.0
22-23	37.342875	38.0	38.0	38.0	36.5	38.0
24-25	37.462875	38.0	38.0	38.0	37.0	38.0
26-27	37.4345	38.0	38.0	38.0	37.0	38.0
28-29	37.439	38.0	38.0	38.0	37.5	38.0
30-31	37.36425	38.0	38.0	38.0	37.5	38.0
32-33	37.2375	38.0	38.0	38.0	37.0	38.0
34-35	37.228375	38.0	38.0	38.0	37.0	38.0
36-37	37.1505	38.0	38.0	38.0	36.5	38.0
38-39	37.168	38.0	38.0	38.0	37.0	38.0
40-41	37.15	38.0	38.0	38.0	37.0	38.0
42-43	37.170500000000004	38.0	38.0	38.0	37.0	38.0
44-45	37.126625000000004	38.0	38.0	38.0	36.5	38.0
46-47	37.052625	38.0	38.0	38.0	36.5	38.0
48-49	37.21725	38.0	38.0	38.0	37.0	38.0
50-51	37.012625	38.0	38.0	38.0	36.0	38.0
52-53	37.11625	38.0	38.0	38.0	36.5	38.0
54-55	37.188625	38.0	38.0	38.0	37.0	38.0
56-57	37.02775	38.0	38.0	38.0	36.0	38.0
58-59	37.24575	38.0	38.0	38.0	37.0	38.0
60-61	37.116875	38.0	38.0	38.0	37.0	38.0
62-63	36.65775	38.0	38.0	38.0	35.0	38.0
64-65	36.414249999999996	38.0	37.5	38.0	33.5	38.0
66-67	36.008875	38.0	37.0	38.0	32.0	38.0
68-69	36.871125	38.0	38.0	38.0	36.0	38.0
70-71	36.67225	38.0	38.0	38.0	34.5	38.0
72-73	36.375625	38.0	37.5	38.0	34.0	38.0
74-75	35.904624999999996	38.0	37.0	38.0	31.0	38.0
76-77	36.156	38.0	37.5	38.0	33.5	38.0
78-79	36.461124999999996	38.0	38.0	38.0	34.5	38.0
80-81	36.71875	38.0	38.0	38.0	36.0	38.0
82-83	36.651250000000005	38.0	38.0	38.0	36.0	38.0
84-85	36.734375	38.0	38.0	38.0	36.0	38.0
86-87	36.475375	38.0	38.0	38.0	35.0	38.0
88-89	36.4295	38.0	38.0	38.0	34.0	38.0
90-91	36.3535	38.0	38.0	38.0	34.5	38.0
92-93	36.27325	38.0	38.0	38.0	34.5	38.0
94-95	35.743625	38.0	38.0	38.0	33.5	38.0
96-97	32.563625	38.0	35.0	38.0	8.0	38.0
98-99	28.836125	37.5	18.0	38.0	2.0	38.0
100-101	24.273	34.5	2.0	38.0	2.0	38.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
8	1.0
9	0.0
10	0.0
11	1.0
12	0.0
13	0.0
14	0.0
15	0.0
16	0.0
17	1.0
18	1.0
19	2.0
20	0.0
21	3.0
22	2.0
23	4.0
24	9.0
25	9.0
26	8.0
27	18.0
28	40.0
29	31.0
30	35.0
31	50.0
32	73.0
33	101.0
34	199.0
35	554.0
36	884.0
37	1974.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	33.975	30.275000000000002	17.0	18.75
2	28.75718929732433	26.65666416604151	21.605401350337583	22.980745186296573
3	32.475	19.950000000000003	23.875	23.7
4	25.825	32.175	17.349999999999998	24.65
5	38.6	21.25	23.75	16.400000000000002
6	23.575	27.925	25.4	23.1
7	38.175	23.275000000000002	22.2	16.35
8	21.25	18.45	41.65	18.65
9	21.425	39.85	21.5	17.224999999999998
10-11	36.25	24.575	19.3	19.875
12-13	19.287499999999998	16.525000000000002	27.3125	36.875
14-15	21.212500000000002	36.8875	23.425	18.475
16-17	25.087500000000002	18.1875	40.7875	15.937499999999998
18-19	38.7875	19.425	24.762500000000003	17.025000000000002
20-21	16.125	26.8125	34.1625	22.900000000000002
22-23	31.887500000000003	28.237499999999997	24.55	15.325
24-25	29.825000000000003	28.3875	25.8125	15.975
26-27	41.2875	24.625	19.9625	14.124999999999998
28-29	14.787500000000001	40.050000000000004	22.287499999999998	22.875
30-31	18.462500000000002	10.0	48.825	22.7125
32-33	28.537499999999998	8.7625	31.874999999999996	30.825000000000003
34-35	40.849999999999994	15.187500000000002	25.587500000000002	18.375
36-37	50.0125	16.7875	21.6	11.600000000000001
38-39	24.175	20.9375	34.8375	20.05
40-41	19.875	15.55	22.2125	42.3625
42-43	31.4875	33.6875	15.7625	19.0625
44-45	56.39999999999999	15.787499999999998	11.1875	16.625
46-47	26.474999999999998	32.6375	16.85	24.0375
48-49	17.837500000000002	22.0875	20.5625	39.5125
50-51	22.537499999999998	23.65	9.6125	44.2
52-53	30.2625	43.7125	6.9625	19.0625
54-55	17.1625	24.2375	21.9375	36.662499999999994
56-57	7.025	30.5125	20.7	41.7625
58-59	13.600000000000001	14.374999999999998	34.075	37.95
60-61	20.8125	23.9875	30.575000000000003	24.625
62-63	11.9625	30.2625	33.375	24.4
64-65	5.55	26.787499999999998	36.6	31.0625
66-67	13.275	10.375	38.737500000000004	37.6125
68-69	21.625	17.349999999999998	36.449999999999996	24.575
70-71	18.099999999999998	27.224999999999998	41.75	12.925
72-73	22.662499999999998	20.0	35.8	21.5375
74-75	13.1375	10.237499999999999	28.9125	47.712500000000006
76-77	21.762500000000003	8.4875	46.5125	23.2375
78-79	17.4625	7.7	44.125	30.7125
80-81	18.5	10.362499999999999	37.2875	33.85
82-83	29.612500000000004	5.2124999999999995	40.45	24.725
84-85	20.0625	8.649999999999999	36.0875	35.199999999999996
86-87	20.9875	18.862499999999997	40.112500000000004	20.0375
88-89	10.100000000000001	45.300000000000004	29.4125	15.187500000000002
90-91	8.7	49.075	25.6	16.625
92-93	14.5875	53.37499999999999	19.9375	12.1
94-95	9.175	65.55	18.875	6.4
96-97	8.8375	79.4125	9.4	2.35
98-99	3.25	91.0125	3.75	1.9875
100-101	1.3875	91.95	4.1625000000000005	2.5
>>END_MODULE
>>Per sequence GC content	fail
#GC Content	Count
0	0.0
1	0.0
2	0.0
3	0.0
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
10	0.0
11	0.0
12	0.0
13	0.0
14	0.0
15	0.0
16	0.0
17	0.0
18	0.0
19	0.0
20	0.0
21	0.0
22	0.0
23	0.0
24	0.0
25	0.0
26	0.0
27	0.0
28	0.0
29	0.0
30	0.0
31	0.0
32	1.0
33	1.5
34	3.5
35	6.0
36	4.0
37	3.5
38	6.5
39	18.0
40	47.0
41	102.5
42	215.5
43	536.5
44	645.0
45	446.0
46	373.0
47	296.5
48	202.5
49	246.5
50	307.5
51	231.0
52	123.0
53	60.0
54	38.0
55	25.5
56	11.5
57	23.5
58	21.0
59	2.0
60	0.5
61	0.5
62	0.0
63	0.5
64	0.5
65	0.0
66	0.0
67	0.0
68	0.0
69	0.0
70	0.0
71	0.0
72	0.0
73	0.0
74	0.0
75	0.0
76	0.0
77	0.0
78	0.0
79	0.0
80	0.0
81	0.0
82	0.0
83	0.0
84	0.0
85	0.0
86	0.0
87	0.0
88	0.0
89	0.0
90	0.0
91	0.0
92	0.0
93	0.0
94	0.0
95	0.0
96	0.0
97	0.0
98	0.0
99	0.0
100	0.0
>>END_MODULE
>>Per base N content	pass
#Base	N-Count
1	0.0
2	0.025
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	52.400000000000006
#Duplication Level	Percentage of deduplicated	Percentage of total
1	88.35877862595419	46.300000000000004
2	4.437022900763359	4.65
3	2.1946564885496183	3.45
4	1.1927480916030535	2.5
5	0.5248091603053435	1.375
6	0.33396946564885494	1.05
7	0.2862595419847328	1.05
8	0.4770992366412214	2.0
9	0.1431297709923664	0.675
>10	1.6698473282442747	20.025000000000002
>50	0.2862595419847328	11.4
>100	0.09541984732824427	5.525
>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
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	111	2.775	RNA PCR Primer, Index 1 (100% over 29bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTTGGAATTCTCGGGTGCC	110	2.75	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTTGGAATTCTCGGGTGCCAAG	100	2.5	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTTGGAATTCTCGGGTGC	91	2.275	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCC	85	2.125	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTGGAATTCTCGGGTGCCAA	62	1.55	No Hit
GAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAG	60	1.5	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTTGGAATTCTCGGGTGCCA	58	1.4500000000000002	No Hit
CTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	46	1.15	RNA PCR Primer, Index 1 (100% over 28bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTTGGAATTCTCGGGTG	44	1.0999999999999999	No Hit
ACCTGCTCTGATACCATGTTGTGATGGAATTCTCGGGTGCCAAGGAACTC	43	1.075	RNA PCR Primer, Index 1 (100% over 26bp)
ACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCCA	41	1.0250000000000001	RNA PCR Primer, Index 1 (100% over 28bp)
ATATTGGGTAGGTTGTGGTATTTCATTGCTTGGAATTCTCGGGTGCCAAG	37	0.9249999999999999	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTGGAATTCTCGGGTGCCAAGG	37	0.9249999999999999	Illumina Small RNA Adapter 2 (100% over 21bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCA	32	0.8	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTGGAATTCTCGGGTGCCAAGG	31	0.775	Illumina Small RNA Adapter 2 (100% over 21bp)
CGGTCGAGGGCACGCCTGCCTGGGCGTCACGCTGGAATTCTCGGGTGCCA	30	0.75	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTGGAATTCTCGGGTGCCA	30	0.75	No Hit
TCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTC	29	0.7250000000000001	RNA PCR Primer, Index 1 (100% over 26bp)
GAACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTC	29	0.7250000000000001	RNA PCR Primer, Index 1 (100% over 26bp)
TGAGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAA	26	0.65	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGG	25	0.625	Illumina Small RNA Adapter 2 (100% over 21bp)
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGTGGAATTCTCGGGTGCC	24	0.6	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCTGGAATTCTCGGGTGC	21	0.525	No Hit
TTCGGACCAGGCTTCATTCCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	21	0.525	RNA PCR Primer, Index 1 (100% over 29bp)
AACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCC	21	0.525	RNA PCR Primer, Index 1 (100% over 27bp)
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTTGGAATTCTCGGGTGC	21	0.525	No Hit
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTTGGAATTCTCGGGTGC	20	0.5	No Hit
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTGGAATTCTCGGGTGCCA	18	0.44999999999999996	No Hit
TCGCTTGGTGCAGATCGGGACTGGAATTCTCGGGTGCCAAGGAACTCCAG	17	0.42500000000000004	RNA PCR Primer, Index 1 (100% over 29bp)
TTGACAGAAGAGAGTGAGCACTGGAATTCTCGGGTGCCAAGGAACTCCAG	15	0.375	RNA PCR Primer, Index 1 (100% over 29bp)
AGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTCC	14	0.35000000000000003	RNA PCR Primer, Index 1 (100% over 27bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACCTGGAATTCTCGGGTGCC	14	0.35000000000000003	No Hit
CATCGAGTAGACCTTGTTATTGTGAGAATATGGAATTCTCGGGTGCCAAG	13	0.325	No Hit
ATATTGGGTAGGTTGTGGTATTTCATTGCTATGGAATTCTCGGGTGCCAA	13	0.325	No Hit
TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCTTGTAATCTCGTATGC	13	0.325	RNA PCR Primer, Index 12 (100% over 50bp)
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGGAATTCTCGGGTGCCAA	12	0.3	No Hit
GGTAGTTCGACCGCGGAATTTGGAATTCTCGGGTGCCAAGGAACTCCAGT	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 30bp)
TAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAG	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 29bp)
GTCGTTGTAGTATAGTGGTAAGTATTCCCGCCTTGGAATTCTCGGGTGCC	11	0.27499999999999997	No Hit
AGGCATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGG	11	0.27499999999999997	Illumina Small RNA Adapter 2 (100% over 21bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTATGGAATTCTCGGGTGCCAA	10	0.25	No Hit
ATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACT	10	0.25	RNA PCR Primer, Index 1 (100% over 25bp)
GAAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTGC	9	0.22499999999999998	No Hit
AGAAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTG	9	0.22499999999999998	No Hit
TGAAGCTGCCAGCATGATCTGATGGAATTCTCGGGTGCCAAGGAACTCCA	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 28bp)
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTGCTGGAATTCTCGGGT	8	0.2	No Hit
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTGCTAATCTGGAATTCT	8	0.2	No Hit
CGAACTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACT	8	0.2	RNA PCR Primer, Index 1 (100% over 25bp)
TAGAACTCCACATCCTTGGCCTGGAATTCTCGGGTGCCAAGGAACTCCAG	8	0.2	RNA PCR Primer, Index 1 (100% over 29bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCTGGAATTCTCGGGTGCCAAGG	8	0.2	Illumina Small RNA Adapter 2 (100% over 21bp)
CCCTATAGAACTCCACATCCTTGGAATTCTCGGGTGCCAAGGAACTCCAG	8	0.2	RNA PCR Primer, Index 1 (100% over 29bp)
TGTCGTGCCAATTCAACATAAACCCTGGAATTCTCGGGTGCCAAGGAACT	8	0.2	RNA PCR Primer, Index 1 (100% over 25bp)
AAGATACGGGTTCGATTCCCGCCGCTCGCCCCATGGAATTCTCGGGTGCC	8	0.2	No Hit
GCGTCTGTAGTCCAACGGTTAGGATAATTGCCTTGGAATTCTCGGGTGCC	8	0.2	No Hit
CAGCCCCACGTCGCACGGATTCGTTGGAATTCTCGGGTGCCAAGGAACTC	8	0.2	RNA PCR Primer, Index 1 (100% over 26bp)
TGTCGTGCCAATTCAACATAAACCCCTTGGAATTCTCGGGTGCCAAGGAA	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 23bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGTGGAATTCTCGGGTG	7	0.17500000000000002	No Hit
GGGTGTTTGGTCTAGTGGTATGATTCTCGCTTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
TGTCGTGCCAATTCAACATAAACCCCTGGAATTCTCGGGTGCCAAGGAAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 24bp)
CTTTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCCAG	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 29bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTCTTAATGGAATTCTCGGGTG	7	0.17500000000000002	No Hit
GGGATTGTAGTTCAATTGGACAGAGCACCGCCCTGGAATTCTCGGGTGCC	6	0.15	No Hit
TGACAGAAGAGAGTGAGCACTGGAATTCTCGGGTGCCAAGGAACTCCAGT	6	0.15	RNA PCR Primer, Index 1 (100% over 30bp)
GTCAGGATAGCTCAGTAGGTAGAGCAGAGGACTTGGAATTCTCGGGTGCC	6	0.15	No Hit
AATATTGGGTAGGTTGTGGTATTTCATTGCTTGGAATTCTCGGGTGCCAA	6	0.15	No Hit
CATCCTAACGAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAAC	6	0.15	RNA PCR Primer, Index 1 (100% over 24bp)
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGCCAAGGATGGAATTCTC	6	0.15	No Hit
GAACGAACGATTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGTCAC	6	0.15	RNA PCR Primer, Index 1 (100% over 33bp)
TTGTATCGCGCGCATGACTTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	5	0.125	RNA PCR Primer, Index 1 (100% over 31bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCAAAATCTTGGAATTCT	5	0.125	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGGAATTCTCGGGTGC	5	0.125	No Hit
GACACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAA	5	0.125	RNA PCR Primer, Index 1 (100% over 23bp)
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTGTGGAATTCTCGGGTG	5	0.125	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGTGGAATTCTCGGGTGCCAAG	5	0.125	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGTGAATCTGGAATTC	5	0.125	No Hit
CCCGCCTTGCACCAAGTGAATTGGAATTCTCGGGTGCCAAGGAACTCCAG	5	0.125	RNA PCR Primer, Index 1 (100% over 29bp)
ATGCAGTTACTAATTCATGATCTGGCTGGAATTCTCGGGTGCCAAGGAAC	5	0.125	RNA PCR Primer, Index 1 (100% over 24bp)
CATCGAGTAGACCTTGTTATTGTGAGAATTAATGGAATTCTCGGGTGCCA	5	0.125	No Hit
AAGCTGAAGCGGAAATGCAATTCTCGGGTGAGATGGAATTCTCGGGTGCC	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	0.475	0.0	0.0	0.0
2	0.0	0.475	0.0	0.0	0.0
3	0.0	0.475	0.0	0.0	0.0
4	0.0	0.475	0.0	0.0	0.0
5	0.0	0.475	0.0	0.0	0.0
6	0.0	0.475	0.0	0.0	0.0
7	0.0	0.475	0.0	0.0	0.0
8	0.0	0.475	0.0	0.0	0.0
9	0.0	0.475	0.0	0.0	0.0
10-11	0.0	0.5125	0.0	0.0	0.0
12-13	0.0	0.6	0.0	0.0	0.0
14-15	0.0	0.6625000000000001	0.0	0.0	0.0
16-17	0.0	0.8875	0.0	0.0	0.0
18-19	0.0	1.4875	0.0	0.0	0.0
20-21	0.0	2.9875	0.0	0.0	0.0
22-23	0.0	14.1625	0.0	0.0	0.0
24-25	0.0	31.1875	0.0	0.0	0.0
26-27	0.0	46.6375	0.0	0.0	0.0
28-29	0.0	49.6625	0.0	0.0	0.0
30-31	0.0	58.25	0.0	0.0	0.0
32-33	0.0	70.6875	0.0	0.0	0.0
34-35	0.0	86.8625	0.0	0.0	0.0
36-37	0.0	94.30000000000001	0.0	0.0	0.0
38-39	0.0	95.825	0.0	0.0	0.0
40-41	0.0	96.35	0.0	0.0	0.0
42-43	0.0	97.2625	0.0	0.0	0.0
44-45	0.0	97.6	0.0	0.0	0.0
46-47	0.0	97.65	0.0	0.0	0.0
48-49	0.0	97.65	0.0	0.0	0.0
50-51	0.0	97.65	0.0	0.0	0.0
52-53	0.0	97.65	0.0	0.0	0.0
54-55	0.0	97.65	0.0	0.0	0.0
56-57	0.0	97.65	0.0	0.0	0.0
58-59	0.0	97.65	0.0	0.0	0.0
60-61	0.0	97.65	0.0	0.0	0.0
62-63	0.0	97.65	0.0	0.0	0.0
64-65	0.0	97.65	0.0	0.0	0.0
66-67	0.0	97.65	0.0	0.0	0.0
68-69	0.0	97.65	0.0	0.0	0.0
70-71	0.0	97.65	0.0	0.0	0.0
72-73	0.0	97.65	0.0	0.0	0.0
74-75	0.0	97.65	0.0	0.0	0.0
76-77	0.0	97.65	0.0	0.0	0.0
78-79	0.0	97.65	0.0	0.0	0.0
80-81	0.0	97.65	0.0	0.0	0.0
82-83	0.0	97.65	0.0	0.0	0.0
84-85	0.0	97.675	0.0	0.0	0.0
86-87	0.0	97.675	0.0	0.0	0.0
88-89	0.0	97.675	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
TTGTAGT	40	5.456968E-12	95.00001	5
GGCTGTA	20	1.5392321E-5	95.00001	4
GTGGCTG	20	1.5392321E-5	95.00001	2
GGTGGCT	20	1.5392321E-5	95.00001	1
TGGCTGT	20	1.5392321E-5	95.00001	3
GGATGTA	15	6.142176E-4	95.0	4
GTAGACC	45	0.0	95.0	7
AGCTCAG	45	0.0	95.0	9
AGTAGAC	45	0.0	95.0	6
AGGATAG	45	0.0	95.0	4
TCAGGAT	45	0.0	95.0	2
GATGTAG	15	6.142176E-4	95.0	5
TAGCTCA	45	0.0	95.0	8
TAGCCAA	15	6.142176E-4	95.0	9
TAGTTTA	15	6.142176E-4	95.0	9
CGGATGT	15	6.142176E-4	95.0	3
GCGGATG	15	6.142176E-4	95.0	2
TAGTTCA	45	0.0	95.0	8
GGATAGC	45	0.0	95.0	5
ATAGCTC	45	0.0	95.0	7
>>END_MODULE
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304712 READS because READLEN < 1
Read 304712 spots for SRR6941544.sra
Written 304712 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
Rejected 304711 READS because READLEN < 1
Read 304711 spots for SRR6941544.sra
Written 304711 spots for SRR6941544.sra
SRR ids: ['SRR6941544.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_u4622x0j
SRR6941544.sra spots: 6094221
blocks: [[1, 304711], [304712, 609422], [609423, 914133], [914134, 1218844], [1218845, 1523555], [1523556, 1828266], [1828267, 2132977], [2132978, 2437688], [2437689, 2742399], [2742400, 3047110], [3047111, 3351821], [3351822, 3656532], [3656533, 3961243], [3961244, 4265954], [4265955, 4570665], [4570666, 4875376], [4875377, 5180087], [5180088, 5484798], [5484799, 5789509], [5789510, 6094221]]
SRR6941544 file size 1455920
SRR6941544 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 SRR6941544 SRR6941544_1.fastq
Input file:	SRR6941544_1.fastq
trimmed:	SRR6941544-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	AGATCGGAAGAGCACACGTCTGAACTCCAGTCAC
-- maximum error ratio allowed (-r):	0.100
-- maximum indel error ratio allowed (-d):	0.030
-- end quality threshold (-q):		10
-- minimum read length allowed after trimming (-l):	18
-- file format (-f):		Sanger/Illumina 1.8+ FASTQ 
-- minimum overlap length for adapter detection (-k):	inf
-- number of concurrent threads (-t):	20
Fri Dec  6 10:46:34 2024 >> started

Fri Dec  6 10:46:38 2024 >> done (3.598s)
6094221 reads processed; of these:
    107 ( 0.00%) short reads filtered out after trimming by size control
     17 ( 0.00%) empty reads filtered out after trimming by size control
6094097 (100.00%) reads available; of these:
1560776 (25.61%) trimmed reads available after processing
4533321 (74.39%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      7	  0.00%
 19	      8	  0.00%
 20	      8	  0.00%
 21	     11	  0.00%
 22	     21	  0.00%
 23	     11	  0.00%
 24	     14	  0.00%
 25	     25	  0.00%
 26	     34	  0.00%
 27	     54	  0.00%
 28	     63	  0.00%
 29	     71	  0.00%
 30	     73	  0.00%
 31	     61	  0.00%
 32	     44	  0.00%
 33	     54	  0.00%
 34	     60	  0.00%
 35	     39	  0.00%
 36	     33	  0.00%
 37	     26	  0.00%
 38	     14	  0.00%
 39	     23	  0.00%
 40	     18	  0.00%
 41	     18	  0.00%
 42	     24	  0.00%
 43	     28	  0.00%
 44	     20	  0.00%
 45	     42	  0.00%
 46	     44	  0.00%
 47	     43	  0.00%
 48	     29	  0.00%
 49	     31	  0.00%
 50	     25	  0.00%
 51	     30	  0.00%
 52	     25	  0.00%
 53	     23	  0.00%
 54	     17	  0.00%
 55	     22	  0.00%
 56	     31	  0.00%
 57	     38	  0.00%
 58	     13	  0.00%
 59	     27	  0.00%
 60	     38	  0.00%
 61	     32	  0.00%
 62	     45	  0.00%
 63	     53	  0.00%
 64	     65	  0.00%
 65	     69	  0.00%
 66	     71	  0.00%
 67	     89	  0.00%
 68	    160	  0.00%
 69	    161	  0.00%
 70	    241	  0.00%
 71	    233	  0.00%
 72	    381	  0.01%
 73	   1028	  0.02%
 74	   5840	  0.10%
 75	   4213	  0.07%
 76	   1300	  0.02%
 77	    470	  0.01%
 78	    572	  0.01%
 79	    572	  0.01%
 80	    692	  0.01%
 81	    687	  0.01%
 82	    876	  0.01%
 83	   1082	  0.02%
 84	   1626	  0.03%
 85	   1987	  0.03%
 86	   2481	  0.04%
 87	   3094	  0.05%
 88	   4284	  0.07%
 89	   6597	  0.11%
 90	  10504	  0.17%
 91	  15016	  0.25%
 92	  19076	  0.31%
 93	  36149	  0.59%
 94	  65693	  1.08%
 95	 218103	  3.58%
 96	 206534	  3.39%
 97	 183901	  3.02%
 98	 324458	  5.32%
 99	 341102	  5.60%
100	  99899	  1.64%
101	4533321	 74.39%
6094097 reads passed initial QC


criterion=sequence-density
sequence-density=97.83
sequence-density-rank=1
fanout-score=27.24
fanout-score-rank=2
prefix-density=97.91
prefix-fanout=27.2
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCTTGTAATCTCGTATGCCGTCTTCTGCTTGAAAAAA


criterion=fanout-score
sequence-density=1.77
sequence-density-rank=8
fanout-score=56.09
fanout-score-rank=1
prefix-density=98.50
prefix-fanout=1.0
sequence=CACCTTGTAATATCGTATGCCGT
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCTTGTAATCTCGTATGCCGTCTTCTGCTTGAAAAAA -o SRR6941544 -
Input file:	STDIN
trimmed:	SRR6941544-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCTTGTAATCTCGTATGCCGTCTTCTGCTTGA
-- maximum error ratio allowed (-r):	0.100
-- maximum indel error ratio allowed (-d):	0.030
-- minimum read length allowed after trimming (-l):	18
-- file format (-f):		Sanger/Illumina 1.8+ FASTQ 
-- minimum overlap length for adapter detection (-k):	3
-- number of concurrent threads (-t):	20
Fri Dec  6 10:47:01 2024 >> started

Fri Dec  6 10:47:10 2024 >> done (8.709s)
5969728 reads processed; of these:
  54962 ( 0.92%) short reads filtered out after trimming by size control
  20881 ( 0.35%) empty reads filtered out after trimming by size control
5893885 (98.73%) reads available; of these:
5856136 (99.36%) trimmed reads available after processing
  37749 ( 0.64%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  22299	  0.38%
 19	  54965	  0.93%
 20	  72624	  1.23%
 21	 534329	  9.07%
 22	 262702	  4.46%
 23	 195240	  3.31%
 24	1436231	 24.37%
 25	 168352	  2.86%
 26	 126635	  2.15%
 27	 100699	  1.71%
 28	  93118	  1.58%
 29	 259053	  4.40%
 30	 437737	  7.43%
 31	 314651	  5.34%
 32	 393048	  6.67%
 33	 551263	  9.35%
 34	 369346	  6.27%
 35	 195565	  3.32%
 36	  93796	  1.59%
 37	  44260	  0.75%
 38	  19868	  0.34%
 39	  13816	  0.23%
 40	  24032	  0.41%
 41	  30806	  0.52%
 42	  20732	  0.35%
 43	   4278	  0.07%
 44	   7192	  0.12%
 45	   2699	  0.05%
 46	    929	  0.02%
 47	    910	  0.02%
 48	    371	  0.01%
 49	    187	  0.00%
 50	    109	  0.00%
 51	    107	  0.00%
 52	     60	  0.00%
 53	     62	  0.00%
 54	     46	  0.00%
 55	     32	  0.00%
 56	     32	  0.00%
 57	     50	  0.00%
 58	     34	  0.00%
 59	     23	  0.00%
 60	     19	  0.00%
 61	     20	  0.00%
 62	     35	  0.00%
 63	     31	  0.00%
 64	     26	  0.00%
 65	     22	  0.00%
 66	     23	  0.00%
 67	     20	  0.00%
 68	     47	  0.00%
 69	     69	  0.00%
 70	    120	  0.00%
 71	     64	  0.00%
 72	     59	  0.00%
 73	     68	  0.00%
 74	     58	  0.00%
 75	     98	  0.00%
 76	    146	  0.00%
 77	    658	  0.01%
 78	    102	  0.00%
 79	    199	  0.00%
 80	    494	  0.01%
 81	    232	  0.00%
 82	    464	  0.01%
 83	    469	  0.01%
 84	    173	  0.00%
 85	    148	  0.00%
 86	    246	  0.00%
 87	    327	  0.01%
 88	    153	  0.00%
 89	    125	  0.00%
 90	    182	  0.00%
 91	    310	  0.01%
 92	    217	  0.00%
 93	    297	  0.01%
 94	    318	  0.01%
 95	    434	  0.01%
 96	    443	  0.01%
 97	    601	  0.01%
 98	    973	  0.02%
 99	    676	  0.01%
100	    677	  0.01%
101	  31754	  0.54%


criterion=sequence-density
sequence-density=8.79
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=10
prefix-density=0.00
prefix-fanout=1.0
sequence=CATCGAGTAGACCTTGTTATTGTGAGAATTCT


criterion=fanout-score
sequence-density=0.17
sequence-density-rank=25
fanout-score=53.09
fanout-score-rank=1
prefix-density=5.47
prefix-fanout=1.6
sequence=GTGAGAATTCTAAAAA
                                 Started job on |	Dec 06 10:47:32
                             Started mapping on |	Dec 06 10:47:32
                                    Finished on |	Dec 06 10:47:48
       Mapping speed, Million of reads per hour |	1354.11

                          Number of input reads |	6018254
                      Average input read length |	29
                                    UNIQUE READS:
                   Uniquely mapped reads number |	1570307
                        Uniquely mapped reads % |	26.09%
                          Average mapped length |	24.83
                       Number of splices: Total |	5609
            Number of splices: Annotated (sjdb) |	1982
                       Number of splices: GT/AG |	5389
                       Number of splices: GC/AG |	146
                       Number of splices: AT/AC |	0
               Number of splices: Non-canonical |	74
                      Mismatch rate per base, % |	0.11%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.51
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.07
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	3465659
             % of reads mapped to multiple loci |	57.59%
        Number of reads mapped to too many loci |	725018
             % of reads mapped to too many loci |	12.05%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	3.49%
                     % of reads unmapped: other |	0.79%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	982288	982288	982288
N_multimapping	3465659	3465659	3465659
N_noFeature	1166688	1317056	1415203
N_ambiguous	10793	5761	344
UnstrandedReadsAssigned:392826 PositiveStrandReadsAssigned:247490 NegativeStrandReadsAssigned:154760
Dataset is classified unstranded
MeadianReadLen=27 20thPercentileLength=24 echo kmer=19
SRR6941544 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: SRR6941544-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 6,018,254 reads, 2,815,021 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 976 rounds

  52973 SRR6941544.ke.tsv
  35125 SRR6941544.se.tsv
  88098 total
==> SRR6941544.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	1	0.151746
PNS24243	293	194	1	1.07318
KQK14069	1603	1504	44.5816	6.17135
KQK14071	474	375	9.50524	5.27721

==> SRR6941544.se.tsv <==
BRADI_1g14170v3	91
BRADI_1g53295v3	1
BRADI_1g59795v3	2
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	0
BRADI_1g74790v3	16
BRADI_1g09890v3	0
BRADI_1g77505v3	1
BRADI_1g48960v3	1
SRR6941544 completed mapping pipeline successfully
