Starting /dee2/code/volunteer_pipeline.sh SRR7472592
    current disk space = 3088090419200
    free memory = 1438721536 
SRR7472592 SRAfilesize
6cf0e0eae9836432bb3c112756f9b8e6  SRR7472592.sra
SRR7472592.sra file validated
SRR7472592 is single end
SRR7472592 is conventional basespace
SRR7472592 read1 length is 51 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR7472592_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	51
%GC	52
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	30.91475	32.0	32.0	32.0	27.0	32.0
2	31.31175	32.0	32.0	32.0	32.0	32.0
3	31.20725	32.0	32.0	32.0	32.0	32.0
4	31.424	32.0	32.0	32.0	32.0	32.0
5	31.16475	32.0	32.0	32.0	32.0	32.0
6	35.20125	37.0	37.0	37.0	32.0	37.0
7	35.614	37.0	37.0	37.0	32.0	37.0
8	35.15325	37.0	37.0	37.0	32.0	37.0
9	35.194	37.0	37.0	37.0	32.0	37.0
10	35.52525	37.0	37.0	37.0	32.0	37.0
11	35.3725	37.0	37.0	37.0	32.0	37.0
12	35.4945	37.0	37.0	37.0	32.0	37.0
13	35.41225	37.0	37.0	37.0	32.0	37.0
14	35.28225	37.0	37.0	37.0	32.0	37.0
15	35.4755	37.0	37.0	37.0	32.0	37.0
16	35.48825	37.0	37.0	37.0	32.0	37.0
17	35.51825	37.0	37.0	37.0	32.0	37.0
18	35.3345	37.0	37.0	37.0	32.0	37.0
19	35.03875	37.0	37.0	37.0	32.0	37.0
20	34.88475	37.0	37.0	37.0	32.0	37.0
21	34.9375	37.0	37.0	37.0	32.0	37.0
22	34.9235	37.0	37.0	37.0	27.0	37.0
23	35.23675	37.0	37.0	37.0	32.0	37.0
24	35.119	37.0	37.0	37.0	32.0	37.0
25	35.23575	37.0	37.0	37.0	32.0	37.0
26	35.673	37.0	37.0	37.0	32.0	37.0
27	35.64475	37.0	37.0	37.0	32.0	37.0
28	35.51475	37.0	37.0	37.0	32.0	37.0
29	35.6765	37.0	37.0	37.0	32.0	37.0
30	35.27975	37.0	37.0	37.0	32.0	37.0
31	35.45025	37.0	37.0	37.0	32.0	37.0
32	35.40125	37.0	37.0	37.0	32.0	37.0
33	35.346	37.0	37.0	37.0	32.0	37.0
34	35.55825	37.0	37.0	37.0	32.0	37.0
35	35.56475	37.0	37.0	37.0	37.0	37.0
36	35.86375	37.0	37.0	37.0	37.0	37.0
37	35.7425	37.0	37.0	37.0	37.0	37.0
38	35.588	37.0	37.0	37.0	32.0	37.0
39	35.55975	37.0	37.0	37.0	32.0	37.0
40	35.309	37.0	37.0	37.0	32.0	37.0
41	35.423	37.0	37.0	37.0	32.0	37.0
42	35.48475	37.0	37.0	37.0	32.0	37.0
43	35.32375	37.0	37.0	37.0	32.0	37.0
44	35.44525	37.0	37.0	37.0	32.0	37.0
45	35.54125	37.0	37.0	37.0	32.0	37.0
46	35.29625	37.0	37.0	37.0	32.0	37.0
47	35.003	37.0	37.0	37.0	32.0	37.0
48	35.474	37.0	37.0	37.0	32.0	37.0
49	35.0	37.0	37.0	37.0	32.0	37.0
50	35.196	37.0	37.0	37.0	32.0	37.0
51	34.72175	37.0	37.0	37.0	27.0	37.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
17	1.0
18	1.0
19	4.0
20	1.0
21	4.0
22	6.0
23	8.0
24	15.0
25	21.0
26	35.0
27	31.0
28	46.0
29	50.0
30	62.0
31	83.0
32	120.0
33	190.0
34	418.0
35	1198.0
36	1706.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	19.925	30.5	28.549999999999997	21.025
2	25.324999999999996	24.675	22.95	27.05
3	28.849999999999998	27.575	21.875	21.7
4	31.85	26.474999999999998	19.7	21.975
5	26.950000000000003	34.8	18.4	19.85
6	27.921092564491655	25.67020738492666	17.071320182094084	29.337379868487606
7	27.900000000000002	25.4	21.9	24.8
8	26.650000000000002	30.375000000000004	19.8	23.175
9	31.025000000000002	28.375	19.425	21.175
10	35.8	24.4	18.575	21.224999999999998
11	31.624999999999996	23.075000000000003	22.0	23.3
12	28.875	23.150000000000002	25.074999999999996	22.900000000000002
13	24.95	22.8	27.55	24.7
14	23.125	29.325000000000003	22.475	25.074999999999996
15	28.799999999999997	33.85	19.475	17.875
16	25.874999999999996	26.325	25.074999999999996	22.725
17	22.650000000000002	27.400000000000002	30.599999999999998	19.35
18	26.450000000000003	23.599999999999998	22.45	27.500000000000004
19	25.0	22.775000000000002	28.825	23.400000000000002
20	26.55	27.224999999999998	22.0	24.224999999999998
21	26.75	28.349999999999998	20.075000000000003	24.825
22	23.075000000000003	26.075	32.0	18.85
23	34.525	24.7	22.45	18.325
24	34.300000000000004	23.175	26.3	16.225
25	25.387693846923458	29.63981990995498	31.89094547273637	13.081540770385192
26	33.074999999999996	30.65	23.7	12.575
27	29.897423067300476	24.293219914936202	31.22341756317238	14.585939454590942
28	18.998748435544428	32.46558197747184	32.340425531914896	16.195244055068837
29	19.914936202151615	25.569176882662	29.321991493620214	25.193895421566175
30	19.46459844883663	15.861896422316738	48.08606454841131	16.587440580435324
31	24.44333249937453	13.284963722792096	34.475856892669505	27.795846885163872
32	33.97548161120841	12.284213159869903	24.718538904178132	29.02176632474356
33	35.90192644483363	13.88541406054541	33.950462847135356	16.262196647485613
34	39.27945959469602	13.460095071303476	23.19239429572179	24.06805103827871
35	41.20590442832124	11.533650237678259	32.624468351263445	14.635976982737054
36	48.3112334250688	12.709532149111835	23.19239429572179	15.786840130097573
37	38.1285964473355	13.835376532399298	19.53965474105579	28.49637227920941
38	25.869402051538653	13.93545158869152	30.172629472104077	30.022516887665752
39	32.89967475606705	24.7935951963973	19.11433575181386	23.19239429572179
40	26.5015015015015	27.87787787787788	15.515515515515515	30.105105105105107
41	37.61261261261261	18.993993993993993	14.68968968968969	28.703703703703702
42	38.63863863863864	27.927927927927925	12.962962962962962	20.47047047047047
43	30.197648236177134	39.27945959469602	12.48436327245434	18.038528896672503
44	39.554665999499626	32.99974981235927	9.457092819614711	17.988491368526393
45	36.05203902927195	23.19239429572179	9.807355516637479	30.94821115836878
46	23.34250688016012	31.17338003502627	21.766324743557668	23.71778834125594
47	20.715536652489366	33.47510632974731	12.509382036527395	33.29997498123593
48	18.11358518889167	25.04378283712785	10.80810607955967	46.03452589442082
49	19.41456092069052	31.998999249437077	18.8141105829372	29.772329246935204
50	28.149261207112446	25.544703230653642	10.693713999499122	35.612321562734785
51	17.325	28.199999999999996	20.150000000000002	34.325
>>END_MODULE
>>Per sequence GC content	warn
#GC Content	Count
0	0.0
1	0.5
2	1.0
3	0.5
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
10	0.0
11	0.5
12	1.0
13	0.5
14	0.0
15	0.0
16	0.0
17	0.0
18	0.0
19	0.5
20	1.0
21	1.5
22	2.0
23	1.5
24	1.0
25	1.5
26	1.5
27	1.0
28	1.0
29	1.0
30	3.5
31	6.0
32	6.5
33	7.0
34	8.5
35	10.0
36	15.5
37	21.0
38	28.5
39	36.0
40	60.0
41	84.0
42	154.0
43	224.0
44	217.0
45	210.0
46	260.5
47	311.0
48	336.0
49	361.0
50	467.0
51	573.0
52	568.0
53	563.0
54	524.0
55	485.0
56	526.5
57	568.0
58	379.0
59	190.0
60	153.0
61	116.0
62	114.0
63	112.0
64	85.0
65	58.0
66	42.5
67	27.0
68	22.5
69	18.0
70	12.0
71	6.0
72	4.5
73	3.0
74	1.5
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	0.5
90	1.0
91	0.5
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	0.0
3	0.0
4	0.0
5	0.0
6	1.15
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	0.05
26	0.0
27	0.075
28	0.125
29	0.075
30	0.075
31	0.075
32	0.075
33	0.075
34	0.075
35	0.075
36	0.075
37	0.075
38	0.075
39	0.075
40	0.1
41	0.1
42	0.1
43	0.075
44	0.075
45	0.075
46	0.075
47	0.075
48	0.075
49	0.075
50	0.17500000000000002
51	0.0
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
51	4000.0
>>END_MODULE
>>Sequence Duplication Levels	warn
#Total Deduplicated Percentage	67.9
#Duplication Level	Percentage of deduplicated	Percentage of total
1	91.08983799705449	61.85000000000001
2	4.9337260677466865	6.7
3	1.1045655375552283	2.25
4	0.5522827687776142	1.5
5	0.3681885125184094	1.25
6	0.40500736377025043	1.6500000000000001
7	0.29455081001472755	1.4000000000000001
8	0.22091310751104565	1.2
9	0.11045655375552282	0.675
>10	0.7731958762886598	11.425
>50	0.11045655375552282	4.8500000000000005
>100	0.036818851251840944	5.25
>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
TCGGACCAGGCTTCATTCCCCTGGAATTCTCGGGTGCCAAGGAACTCCAGT	210	5.25	RNA PCR Primer, Index 1 (100% over 30bp)
TCTCGGACCAGGCTTCATTCCTGGAATTCTCGGGTGCCAAGGAACTCCAGT	75	1.875	RNA PCR Primer, Index 1 (100% over 30bp)
CTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCA	65	1.625	RNA PCR Primer, Index 1 (100% over 28bp)
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGGA	54	1.35	RNA PCR Primer, Index 1 (100% over 22bp)
AGTTACTAATTCATGATCTGGCTGGAATTCTCGGGTGCCAAGGAACTCCAG	50	1.25	RNA PCR Primer, Index 1 (100% over 29bp)
CCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACTCC	37	0.9249999999999999	RNA PCR Primer, Index 1 (100% over 27bp)
ATCCGGTTAGGATCGATCTAAACCAGCCCTGGAATTCTCGGGTGCCAAGGA	37	0.9249999999999999	RNA PCR Primer, Index 1 (100% over 22bp)
CGATTGGGGGAGTAAGAATAGTATTTAATTGCTGGAATTCTCGGGTGCCAA	36	0.8999999999999999	No Hit
TCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACTC	30	0.75	RNA PCR Primer, Index 1 (100% over 26bp)
TAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAG	29	0.7250000000000001	RNA PCR Primer, Index 1 (100% over 29bp)
ATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACT	28	0.7000000000000001	RNA PCR Primer, Index 1 (100% over 25bp)
GCATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAA	24	0.6	RNA PCR Primer, Index 1 (100% over 23bp)
AGGCATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGG	20	0.5	Illumina Small RNA Adapter 2 (100% over 21bp)
AACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGT	19	0.475	RNA PCR Primer, Index 1 (100% over 30bp)
ACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	18	0.44999999999999996	RNA PCR Primer, Index 1 (100% over 31bp)
TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAGGCGATCTCGTATGCC	15	0.375	RNA PCR Primer, Index 33 (100% over 51bp)
CGATTGGGGGAGTAAGAATAGTATTTAATTGCTTGGAATTCTCGGGTGCCA	15	0.375	No Hit
CGATTGGGGGAGTAAGAATAGTATTTAATTGCTACTGGAATTCTCGGGTGC	15	0.375	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGGAATTCTCGGGTGCCA	13	0.325	No Hit
CATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAAC	13	0.325	RNA PCR Primer, Index 1 (100% over 24bp)
TTTGGATTGAAGGGAGCTCTTGGAATTCTCGGGTGCCAAGGAACTCCAGTC	13	0.325	RNA PCR Primer, Index 1 (100% over 31bp)
TGAGGCATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAA	13	0.325	No Hit
ATCCGGTTAGGATCGATCTAAACCAGCCTGGAATTCTCGGGTGCCAAGGAA	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 23bp)
AACGACTCTCGGCAACGGATATCTCGGCTTGGAATTCTCGGGTGCCAAGGA	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 22bp)
TCAGCCCCATGTCGCTCCGATTCGTTGGAATTCTCGGGTGCCAAGGAACTC	10	0.25	RNA PCR Primer, Index 1 (100% over 26bp)
GGTCGAGGGCACGTCTGCCTGGGTGTCACGCTGGAATTCTCGGGTGCCAAG	9	0.22499999999999998	No Hit
CAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGTCA	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 32bp)
TAAACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAAC	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 24bp)
TAAACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGAAGAACGT	8	0.2	No Hit
CAGCTGAGGCATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTG	8	0.2	No Hit
GCGGATGTAGCCAAGTGGATCAAGGCAGTGGAATTCTCGGGTGCCAAGGAA	8	0.2	RNA PCR Primer, Index 1 (100% over 23bp)
GAGGCATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAG	8	0.2	No Hit
CAGCCCCATGTCGCTCCGATTCGTTGGAATTCTCGGGTGCCAAGGAACTCC	8	0.2	RNA PCR Primer, Index 1 (100% over 27bp)
GCGACCCCAGGTCAGGCGGGACTTGGAATTCTCGGGTGCCAAGGAACTCCA	8	0.2	RNA PCR Primer, Index 1 (100% over 28bp)
AGCTGAGGCATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGC	7	0.17500000000000002	No Hit
ACTGAGATTCAGCCCCATGTCGCTCCGATTCGTTGGAATTCTCGGGTGCCA	7	0.17500000000000002	No Hit
GATTGGGGGAGTAAGAATAGTATTTAATTGCTGGAATTCTCGGGTGCCAAG	7	0.17500000000000002	No Hit
GTCGTTGTAGTATAGTGGTAAGTATTCCCGCCTGGAATTCTCGGGTGCCAA	7	0.17500000000000002	No Hit
AGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGAACTCCAGTCAC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 33bp)
TCTCATGGAGAGTTCGATCCTGGCTTGGAATTCTCGGGTGCCAAGGAACTC	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 26bp)
CGATTGGGGGAGTAAGAATAGTATTTAATTGTGGAATTCTCGGGTGCCAAG	7	0.17500000000000002	No Hit
GTCGTTGTAGTATAGTGGTGAGTATTCCCGCCTTGGAATTCTCGGGTGCCA	7	0.17500000000000002	No Hit
GGCATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCCAAGGA	6	0.15	RNA PCR Primer, Index 1 (100% over 22bp)
GGGGATGTAGCTCAGATGGTAGATGGAATTCTCGGGTGCCAAGGAACTCCA	6	0.15	RNA PCR Primer, Index 1 (100% over 28bp)
ATTCAGCCCCATGTCGCTCCGATTCGTTGGAATTCTCGGGTGCCAAGGAAC	6	0.15	RNA PCR Primer, Index 1 (100% over 24bp)
AGTTACTAATTCATGATCTGGCCTGGAATTCTCGGGTGCCAAGGAACTCCA	6	0.15	RNA PCR Primer, Index 1 (100% over 28bp)
GTCGTTGTAGTATAGTGGTAAGTATTCCCGCCTTGGAATTCTCGGGTGCCA	6	0.15	No Hit
CGATTGGGGGAGTAAGAATAGTATTTAATTGCTATGGAATTCTCGGGTGCC	6	0.15	No Hit
AACGACTCTCGGCAACGGATATCTCGGCTCTCGCATCGATGAAGAACGTAG	6	0.15	No Hit
GATTGGGGGAGTAAGAATAGTATTTAATTGCTTGGAATTCTCGGGTGCCAA	6	0.15	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCTGGAATTCTCGGGTGCCAA	6	0.15	No Hit
AGTTACTAATTCATGATCTGGCATGGAATTCTCGGGTGCCAAGGAACTCCA	6	0.15	RNA PCR Primer, Index 1 (100% over 28bp)
GGTGCGGCTGGATCACCTCCTTGGAATTCTCGGGTGCCAAGGAACTCCAGT	6	0.15	RNA PCR Primer, Index 1 (100% over 30bp)
CTGAGATTCAGCCCCATGTCGCTCCGATTCGTTGGAATTCTCGGGTGCCAA	5	0.125	No Hit
GGTGGCTGTAGTTTAGTGGTGAGAATTCCACGTTTGGAATTCTCGGGTGCC	5	0.125	No Hit
GCTGAGGCATCCTAACAGACCGGTAGACTTGAACTGGAATTCTCGGGTGCC	5	0.125	No Hit
CGGAAAAATAGCTCGACGCCAGGATTGGAATTCTCGGGTGCCAAGGAACTC	5	0.125	RNA PCR Primer, Index 1 (100% over 26bp)
AACGACTCTCGGCAACGGATATCTCTGGAATTCTCGGGTGCCAAGGAACTC	5	0.125	RNA PCR Primer, Index 1 (100% over 26bp)
TAAACGACTCTCGGCAACGGATATCTCGGCTTGGAATTCTCGGGTGCCAAG	5	0.125	No Hit
GAGATTCAGCCCCATGTCGCTCCGATTCGTTGGAATTCTCGGGTGCCAAGG	5	0.125	Illumina Small RNA Adapter 2 (100% over 21bp)
CCACCCCAAGATGAGTGCTCTCCTTGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
ATGAGCTCAACGAGAACAGAAATCTCGTGTGGAATTCTCGGGTGCCAAGGA	5	0.125	RNA PCR Primer, Index 1 (100% over 22bp)
AGTTACTAATTCATGATCTGGCATTGGAATTCTCGGGTGCCAAGGAACTCC	5	0.125	RNA PCR Primer, Index 1 (100% over 27bp)
>>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	0.425	0.0	0.0	0.0
2	0.0	0.425	0.0	0.0	0.0
3	0.0	0.425	0.0	0.0	0.0
4	0.0	0.425	0.0	0.0	0.0
5	0.0	0.425	0.0	0.0	0.0
6	0.0	0.425	0.0	0.0	0.0
7	0.0	0.425	0.0	0.0	0.0
8	0.0	0.45	0.0	0.0	0.0
9	0.0	0.475	0.0	0.0	0.0
10	0.0	0.475	0.0	0.0	0.0
11	0.0	0.525	0.0	0.0	0.0
12	0.0	0.575	0.0	0.0	0.0
13	0.0	0.625	0.0	0.0	0.0
14	0.0	0.7	0.0	0.0	0.0
15	0.0	0.875	0.0	0.0	0.0
16	0.0	1.1	0.0	0.0	0.0
17	0.0	1.775	0.0	0.0	0.0
18	0.0	2.575	0.0	0.0	0.0
19	0.0	3.9	0.0	0.0	0.0
20	0.0	5.6	0.0	0.0	0.0
21	0.0	8.975	0.0	0.0	0.0
22	0.0	22.45	0.0	0.0	0.0
23	0.0	28.75	0.0	0.0	0.0
24	0.0	34.15	0.0	0.0	0.0
25	0.0	47.225	0.0	0.0	0.0
26	0.0	52.375	0.0	0.0	0.0
27	0.0	56.825	0.0	0.0	0.0
28	0.0	60.375	0.0	0.0	0.0
29	0.0	64.375	0.0	0.0	0.0
30	0.0	69.95	0.0	0.0	0.0
31	0.0	73.4	0.0	0.0	0.0
32	0.0	76.975	0.0	0.0	0.0
33	0.0	81.625	0.0	0.0	0.0
34	0.0	85.175	0.0	0.0	0.0
35	0.0	87.325	0.0	0.0	0.0
36	0.0	89.325	0.0	0.0	0.0
37	0.0	90.525	0.0	0.0	0.0
38	0.0	91.25	0.0	0.0	0.0
39	0.0	91.8	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
TTCCCCT	20	6.222983E-4	45.0	16
CCCCTGG	20	6.222983E-4	45.0	18
ATTCCCC	25	3.236105E-5	45.0	15
TCCCCTG	20	6.222983E-4	45.0	17
CTTCATT	35	4.8309703E-6	38.571426	11
GGACCAG	35	4.8309703E-6	38.571426	3
CGGACCA	35	4.8309703E-6	38.571426	2
TCGGACC	35	4.8309703E-6	38.571426	1
AGGCTTC	35	4.8309703E-6	38.571426	8
CCCTGGA	35	4.8309703E-6	38.571426	19
GGCTTCA	35	4.8309703E-6	38.571426	9
CAGGCTT	35	4.8309703E-6	38.571426	7
GCTTCAT	35	4.8309703E-6	38.571426	10
GACCAGG	35	4.8309703E-6	38.571426	4
TTCATTC	30	9.4943156E-5	37.499996	12
CATTCCC	30	9.4943156E-5	37.499996	14
TCATTCC	30	9.4943156E-5	37.499996	13
CCAGGCT	40	1.2085775E-5	33.75	6
ACCAGGC	45	2.707939E-5	30.000002	5
CTCCAGT	100	5.3034273E-7	20.25	45
>>END_MODULE
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012038 READS because READLEN < 1
Read 1012038 spots for SRR7472592.sra
Written 1012038 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
Rejected 1012032 READS because READLEN < 1
Read 1012032 spots for SRR7472592.sra
Written 1012032 spots for SRR7472592.sra
SRR ids: ['SRR7472592.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_9rx0ngfu
SRR7472592.sra spots: 20240646
blocks: [[1, 1012032], [1012033, 2024064], [2024065, 3036096], [3036097, 4048128], [4048129, 5060160], [5060161, 6072192], [6072193, 7084224], [7084225, 8096256], [8096257, 9108288], [9108289, 10120320], [10120321, 11132352], [11132353, 12144384], [12144385, 13156416], [13156417, 14168448], [14168449, 15180480], [15180481, 16192512], [16192513, 17204544], [17204545, 18216576], [18216577, 19228608], [19228609, 20240646]]
SRR7472592 file size 2864172
SRR7472592 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 SRR7472592 SRR7472592_1.fastq
Input file:	SRR7472592_1.fastq
trimmed:	SRR7472592-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
Thu Feb 13 18:22:35 2025 >> started

Thu Feb 13 18:22:43 2025 >> done (8.057s)
20240646 reads processed; of these:
       0 ( 0.00%) short reads filtered out after trimming by size control
       0 ( 0.00%) empty reads filtered out after trimming by size control
20240646 (100.00%) reads available; of these:
  307018 ( 1.52%) trimmed reads available after processing
19933628 (98.48%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 36	       1	  0.00%
 37	       0	  0.00%
 38	       1	  0.00%
 39	       1	  0.00%
 40	       5	  0.00%
 41	      10	  0.00%
 42	      22	  0.00%
 43	      51	  0.00%
 44	     145	  0.00%
 45	     374	  0.00%
 46	    1204	  0.01%
 47	    3796	  0.02%
 48	   11411	  0.06%
 49	   40832	  0.20%
 50	  249165	  1.23%
 51	19933628	 98.48%
20240646 reads passed initial QC


criterion=sequence-density
sequence-density=93.02
sequence-density-rank=1
fanout-score=27.02
fanout-score-rank=2
prefix-density=94.06
prefix-fanout=26.7
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAGGCGATCTCGTATGCC


criterion=fanout-score
sequence-density=1.43
sequence-density-rank=2
fanout-score=28.29
fanout-score-rank=1
prefix-density=1.42
prefix-fanout=28.3
sequence=GACTGGAATTCT
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAGGCGATCTCGTATGCC -o SRR7472592 -
Input file:	STDIN
trimmed:	SRR7472592-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAGGCGATCTCGTATGCC
-- 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
Thu Feb 13 18:23:12 2025 >> started

Thu Feb 13 18:23:26 2025 >> done (13.610s)
19809994 reads processed; of these:
  480802 ( 2.43%) short reads filtered out after trimming by size control
   57153 ( 0.29%) empty reads filtered out after trimming by size control
19272039 (97.28%) reads available; of these:
18825744 (97.68%) trimmed reads available after processing
  446295 ( 2.32%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  300279	  1.56%
 19	  381188	  1.98%
 20	  631115	  3.27%
 21	 2739965	 14.22%
 22	 1422941	  7.38%
 23	 1281290	  6.65%
 24	 2742811	 14.23%
 25	 1079992	  5.60%
 26	  794642	  4.12%
 27	  768061	  3.99%
 28	  803036	  4.17%
 29	 1212703	  6.29%
 30	  710109	  3.68%
 31	  728576	  3.78%
 32	  930233	  4.83%
 33	  704965	  3.66%
 34	  453514	  2.35%
 35	  378581	  1.96%
 36	  249253	  1.29%
 37	  159413	  0.83%
 38	  115601	  0.60%
 39	   81389	  0.42%
 40	   51633	  0.27%
 41	   29406	  0.15%
 42	   29386	  0.15%
 43	   15889	  0.08%
 44	   10360	  0.05%
 45	    7544	  0.04%
 46	    5565	  0.03%
 47	    5594	  0.03%
 48	    9445	  0.05%
 49	   15107	  0.08%
 50	   39852	  0.21%
 51	  382601	  1.99%


criterion=sequence-density
sequence-density=2.21
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=17
prefix-density=0.00
prefix-fanout=1.0
sequence=TCTCGGACCAGGCTTCATTCCCCTGGAATTCT


criterion=fanout-score
sequence-density=0.05
sequence-density-rank=21
fanout-score=59.27
fanout-score-rank=1
prefix-density=3.06
prefix-fanout=1.0
sequence=TCCTAACAGACAGGTAGACTTGA
                                 Started job on |	Feb 13 18:23:44
                             Started mapping on |	Feb 13 18:23:44
                                    Finished on |	Feb 13 18:24:25
       Mapping speed, Million of reads per hour |	1729.99

                          Number of input reads |	19702691
                      Average input read length |	27
                                    UNIQUE READS:
                   Uniquely mapped reads number |	6289951
                        Uniquely mapped reads % |	31.92%
                          Average mapped length |	26.18
                       Number of splices: Total |	79436
            Number of splices: Annotated (sjdb) |	32484
                       Number of splices: GT/AG |	77754
                       Number of splices: GC/AG |	945
                       Number of splices: AT/AC |	76
               Number of splices: Non-canonical |	661
                      Mismatch rate per base, % |	0.41%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.18
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.05
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	3467363
             % of reads mapped to multiple loci |	17.60%
        Number of reads mapped to too many loci |	8813212
             % of reads mapped to too many loci |	44.73%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	4.44%
                     % of reads unmapped: other |	1.31%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	9945377	9945377	9945377
N_multimapping	3467363	3467363	3467363
N_noFeature	2776028	2899039	4982340
N_ambiguous	1188578	2998	1010
UnstrandedReadsAssigned:2325345 PositiveStrandReadsAssigned:3387914 NegativeStrandReadsAssigned:1306601
Dataset is classified unstranded
MeadianReadLen=25 20thPercentileLength=21 echo kmer=19
SRR7472592 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: 52,400
[index] number of k-mers: 59,590,899
[index] number of equivalence classes: 293,668
[quant] running in single-end mode
[quant] will process file 1: SRR7472592-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 19,702,691 reads, 10,526,910 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,187 rounds

  52401 SRR7472592.ke.tsv
  34699 SRR7472592.se.tsv
  87100 total
==> SRR7472592.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
Potri.005G200100.1.v4.1	2018	1919	29.7137	1.10202
Potri.005G024800.1.v4.1	1035	936	7.03149	0.534662
Potri.004G059700.1.v4.1	961	862	0	0
Potri.007G009000.2.v4.1	1416	1317	0	0
Potri.003G141000.2.v4.1	2943	2844	23.1993	0.580567
Potri.016G087400.1.v4.1	270	171	3	1.24863
Potri.015G069301.1.v4.1	564	465	4	0.61223
Potri.010G195200.1.v4.1	1773	1674	0	0
Potri.012G127500.1.v4.1	977	878	20	1.62123

==> SRR7472592.se.tsv <==
Potri.001G166300.v4.1	2
Potri.001G448400.v4.1	5
Potri.001G233950.v4.1	0
Potri.001G122700.v4.1	10
Potri.001G212900.v4.1	0
Potri.001G182400.v4.1	5
Potri.001G256600.v4.1	0
Potri.001G040500.v4.1	3
Potri.001G416900.v4.1	4
Potri.001G452600.v4.1	1
SRR7472592 completed mapping pipeline successfully
