Starting /dee2/code/volunteer_pipeline.sh ERR6133485
    current disk space = 1544809775104
    free memory = 1600136568 
ERR6133485 SRAfilesize
42163321a00f194396ac8167a1d97de7  ERR6133485.sra
ERR6133485.sra file validated
ERR6133485 is single end
ERR6133485 is conventional basespace
ERR6133485 read1 length is 70-93 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	ERR6133485_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	70-93
%GC	45
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	35.0735	37.0	33.0	37.0	33.0	37.0
2	36.27125	37.0	37.0	37.0	33.0	37.0
3	35.6635	37.0	37.0	37.0	33.0	37.0
4	35.22675	37.0	37.0	37.0	33.0	37.0
5	35.33875	37.0	37.0	37.0	33.0	37.0
6	35.4915	37.0	37.0	37.0	33.0	37.0
7	37.30275	37.0	37.0	40.0	33.0	40.0
8	37.287	37.0	37.0	40.0	33.0	40.0
9	37.365	37.0	37.0	40.0	33.0	40.0
10-11	37.349625	37.0	37.0	40.0	33.0	40.0
12-13	37.254875	37.0	37.0	40.0	33.0	40.0
14-15	37.246875	37.0	37.0	40.0	33.0	40.0
16-17	37.054125	37.0	37.0	40.0	33.0	40.0
18-19	36.813874999999996	37.0	37.0	40.0	33.0	40.0
20-21	36.531375	37.0	37.0	40.0	33.0	40.0
22-23	36.504125	37.0	37.0	40.0	33.0	40.0
24-25	36.308	37.0	37.0	40.0	33.0	40.0
26-27	36.6865	37.0	37.0	40.0	33.0	40.0
28-29	36.85375	37.0	37.0	40.0	33.0	40.0
30-31	36.68875	37.0	37.0	40.0	33.0	40.0
32-33	36.547375	37.0	37.0	40.0	33.0	40.0
34-35	36.419	37.0	37.0	40.0	33.0	40.0
36-37	36.340375	37.0	37.0	40.0	33.0	40.0
38-39	36.266875	37.0	37.0	40.0	33.0	40.0
40-41	35.906625	37.0	35.0	40.0	33.0	40.0
42-43	35.933499999999995	37.0	35.0	40.0	33.0	40.0
44-45	35.89275000000001	37.0	35.0	40.0	33.0	40.0
46-47	35.855625	37.0	33.0	40.0	33.0	40.0
48-49	35.867999999999995	37.0	33.0	37.0	33.0	40.0
50-51	35.72775	37.0	33.0	37.0	33.0	40.0
52-53	35.445625	37.0	33.0	37.0	33.0	40.0
54-55	35.277375	37.0	33.0	37.0	33.0	40.0
56-57	34.995625000000004	37.0	33.0	37.0	33.0	40.0
58-59	33.850875	37.0	33.0	37.0	27.0	37.0
60-61	34.527249999999995	37.0	33.0	37.0	27.0	37.0
62-63	34.546125	37.0	33.0	37.0	30.0	37.0
64-65	34.408	37.0	33.0	37.0	27.0	37.0
66-67	34.3165	37.0	33.0	37.0	30.0	37.0
68-69	33.461625	35.0	33.0	37.0	27.0	37.0
70-71	33.62506573980876	35.0	33.0	37.0	27.0	37.0
72-73	34.051170924535	37.0	33.0	37.0	27.0	37.0
74-75	34.02723293077121	37.0	33.0	37.0	27.0	37.0
76-77	33.76083367395516	37.0	33.0	37.0	27.0	37.0
78-79	33.54315523368973	37.0	33.0	37.0	27.0	37.0
80-81	33.51089977728221	37.0	33.0	37.0	27.0	37.0
82-83	33.28838141839524	35.0	33.0	37.0	27.0	37.0
84-85	33.15057174894274	33.0	33.0	37.0	27.0	37.0
86-87	33.32295988934993	33.0	33.0	37.0	27.0	37.0
88-89	33.397510373443986	33.0	33.0	37.0	27.0	37.0
90-91	33.224619640387274	33.0	33.0	37.0	27.0	37.0
92-93	33.03582295988935	33.0	33.0	37.0	27.0	37.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
20	7.0
21	11.0
22	12.0
23	19.0
24	23.0
25	37.0
26	39.0
27	56.0
28	48.0
29	70.0
30	115.0
31	127.0
32	156.0
33	198.0
34	278.0
35	477.0
36	812.0
37	924.0
38	557.0
39	34.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	75.125	6.950000000000001	9.475	8.450000000000001
2	57.62500000000001	23.175	11.95	7.249999999999999
3	31.8	33.300000000000004	16.775000000000002	18.125
4	28.249999999999996	29.925	18.475	23.35
5	29.125	23.7	29.075	18.099999999999998
6	17.95	40.225	24.5	17.325
7	39.85	27.675	18.0	14.475
8	29.625	27.400000000000002	22.05	20.925
9	22.825	31.15	25.95	20.075000000000003
10-11	22.237499999999997	30.275000000000002	28.525	18.9625
12-13	23.8625	27.800000000000004	25.4625	22.875
14-15	21.8	34.362500000000004	26.400000000000002	17.4375
16-17	25.650000000000002	30.412499999999998	22.6125	21.325
18-19	25.203150393799223	26.140767595949495	28.066008251031377	20.5900737592199
20-21	27.938969484742373	25.312656328164078	28.501750875437722	18.246623311655828
22-23	31.624999999999996	21.512500000000003	27.325	19.537499999999998
24-25	23.6875	27.5625	27.462500000000002	21.2875
26-27	29.6625	23.45	26.6125	20.275000000000002
28-29	24.587500000000002	28.537499999999998	27.325	19.55
30-31	30.4625	24.725	25.900000000000002	18.912499999999998
32-33	26.487500000000004	27.0125	25.3	21.2
34-35	23.025000000000002	32.75	24.6	19.625
36-37	27.28182045511378	25.95648912228057	23.63090772693173	23.13078269567392
38-39	31.874999999999996	23.8875	26.2625	17.974999999999998
40-41	23.418354588647162	24.731182795698924	29.744936234058517	22.1055263815954
42-43	27.3375	32.0125	23.5125	17.1375
44-45	22.1875	29.6625	30.025000000000002	18.125
46-47	27.212500000000002	24.825	25.7625	22.2
48-49	24.7875	25.1875	26.937499999999996	23.0875
50-51	21.4875	27.925	26.700000000000003	23.8875
52-53	26.01626016260163	24.102564102564102	24.690431519699814	25.19074421513446
54-55	26.0625	25.4375	28.8625	19.6375
56-57	27.1375	29.4875	25.25	18.125
58-59	21.525	27.900000000000002	31.2375	19.3375
60-61	30.099999999999998	27.1375	25.2375	17.525
62-63	20.2875	31.887500000000003	28.475	19.35
64-65	21.075	34.1625	27.425	17.3375
66-67	24.337500000000002	33.862500000000004	24.212500000000002	17.5875
68-69	21.912499999999998	26.087500000000002	28.1	23.9
70-71	22.134436919989966	29.408076247805365	25.909204915976925	22.54828191622774
72-73	27.60853008377761	26.68189895912668	27.900482355927902	17.809088601167808
74-75	24.064789818742767	29.10399794318036	28.35840082272786	18.472811415349017
76-77	21.60718937223235	24.602761135712427	24.811148736650168	28.97890075540505
78-79	28.82159315339039	26.899275839368002	26.214614878209346	18.064516129032256
80-81	22.685370741482966	36.00534402137608	24.141616566466265	17.167668670674683
82-83	23.087357569180682	27.807921866521973	27.794357026587086	21.310363537710256
84-85	20.96418732782369	25.6198347107438	33.388429752066116	20.02754820936639
86-87	19.723374827109268	29.05947441217151	25.988934993084374	25.228215767634854
88-89	17.7731673582296	33.11203319502074	28.561549100968186	20.553250345781464
90-91	25.089903181189488	31.507607192254493	25.76763485477178	17.634854771784234
92-93	21.82572614107884	30.843706777316736	27.39972337482711	19.930843706777317
>>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	0.5
10	0.5
11	0.0
12	0.0
13	0.0
14	0.0
15	0.5
16	1.5
17	8.5
18	10.0
19	3.0
20	0.5
21	0.0
22	3.0
23	9.0
24	9.5
25	11.5
26	14.5
27	16.0
28	22.0
29	24.5
30	29.0
31	40.5
32	39.0
33	42.5
34	67.0
35	94.0
36	129.0
37	147.5
38	178.5
39	185.5
40	177.5
41	189.0
42	202.0
43	222.0
44	188.0
45	168.0
46	175.0
47	166.0
48	149.5
49	145.5
50	214.0
51	221.0
52	147.0
53	133.5
54	222.5
55	190.5
56	68.5
57	59.5
58	44.0
59	29.5
60	25.5
61	21.0
62	22.5
63	18.0
64	19.0
65	17.5
66	13.5
67	14.0
68	10.5
69	9.0
70	6.5
71	4.0
72	2.5
73	2.0
74	2.5
75	4.0
76	3.5
77	1.0
78	0.5
79	0.0
80	0.0
81	0.0
82	0.5
83	0.5
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	0.0
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	0.0125
20-21	0.05
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	0.025
38-39	0.0
40-41	0.025
42-43	0.0
44-45	0.0
46-47	0.0
48-49	0.0
50-51	0.0
52-53	0.0625
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
>>END_MODULE
>>Sequence Length Distribution	warn
#Length	Count
70	26.0
71	18.0
72	34.0
73	22.0
74	21.0
75	27.0
76	26.0
77	19.0
78	19.0
79	30.0
80	31.0
81	25.0
82	32.0
83	25.0
84	30.0
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	3615.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	70.6
#Duplication Level	Percentage of deduplicated	Percentage of total
1	91.39518413597733	64.525
2	4.674220963172805	6.6000000000000005
3	1.3810198300283285	2.9250000000000003
4	0.6728045325779036	1.9
5	0.3186968838526912	1.125
6	0.17705382436260625	0.75
7	0.17705382436260625	0.8750000000000001
8	0.17705382436260625	1.0
9	0.10623229461756376	0.675
>10	0.84985835694051	9.8
>50	0.0	0.0
>100	0.0708215297450425	9.825000000000001
>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
GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGC	247	6.175	No Hit
TACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTT	146	3.65	No Hit
GGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGG	38	0.95	No Hit
GGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAA	32	0.8	No Hit
GGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAA	29	0.7250000000000001	No Hit
GAAGGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGC	28	0.7000000000000001	No Hit
GGAGTCCTGAACTAGCCGCAGCTTGTGAAGTATGGAAGGCGATCAAATTC	20	0.5	No Hit
GGGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGG	18	0.44999999999999996	No Hit
GTATTTAGCCTTGCAAGGTGGTCCTTGCTGATTCACACGGGATTCCACGT	17	0.42500000000000004	No Hit
GGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGT	17	0.42500000000000004	No Hit
GGGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAA	16	0.4	No Hit
GGAGTATCCTTGATATATAAATATATAGATAAATAGATTTAAATGGAAAA	16	0.4	No Hit
GGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGCCGC	14	0.35000000000000003	No Hit
GGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTG	13	0.325	No Hit
GGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAAA	13	0.325	No Hit
GGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTC	12	0.3	No Hit
GGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGGG	12	0.3	No Hit
GTCCTGAACTAGCCGCAGCTTGTGAAGTATGGAAGGCGATCAAATTCGAG	12	0.3	No Hit
GGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCT	11	0.27499999999999997	No Hit
CGAGGAAGGGCGTAGCAAGCGACGAAATGCTTCGGGGAGTTGAAAATAAG	11	0.27499999999999997	No Hit
GTACAAGCTCGTAACGAAGGGCGCGATCTTGCTCGTGAAGGTAATGAAAT	11	0.27499999999999997	No Hit
TCTCATGGAGAGTTCGATCCTGGCTCAGGATGAACGCTGGCGGCATGCTT	11	0.27499999999999997	No Hit
TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGA	11	0.27499999999999997	No Hit
GTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAA	10	0.25	No Hit
GTATGGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATACTATCGATTA	10	0.25	No Hit
GGGGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTG	10	0.25	No Hit
GGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTT	9	0.22499999999999998	No Hit
CAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTC	9	0.22499999999999998	No Hit
GGAGGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAA	9	0.22499999999999998	No Hit
GTAACGAAGGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCA	8	0.2	No Hit
GGCCTGTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCG	8	0.2	No Hit
GGAGTTGAAAATAAGCATAGATCCGGAGATTCCCAAATAGGTCAACCTTT	8	0.2	No Hit
GCAGCTTGCAAATGGAGTCCTGAACTAGCCGCAGCTTGTGAAGTATGGAA	8	0.2	No Hit
GAAGTATGGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATACTATCGA	8	0.2	No Hit
GGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTGTACAAGCTCGTAA	7	0.17500000000000002	No Hit
CACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTTCGGGGAGT	7	0.17500000000000002	No Hit
GGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATACTATCGATTAATAG	7	0.17500000000000002	No Hit
AACAGTAAAGCTTCATAGGGTCTTTCTGTCCAGGTGCAGGTAGTCCGCAT	7	0.17500000000000002	No Hit
GATACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGC	7	0.17500000000000002	No Hit
GGGGGTCGCAGTGACCAGGCCCGGGCGACTGTTTACCAAAAACACAGGTC	6	0.15	No Hit
CAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCT	6	0.15	No Hit
GGGAGTATTATGAAAGGAGATTAATCATAGATTATCAAAAACCCTAGAAA	6	0.15	No Hit
GGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCA	6	0.15	No Hit
GCTTGTGAAGTATGGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATAC	6	0.15	No Hit
GGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCG	5	0.125	No Hit
GCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCT	5	0.125	No Hit
GGATACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATG	5	0.125	No Hit
GGTGGAGGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGC	5	0.125	No Hit
GGTTTCAGTATATTGAAATAGAAAGATAAAATAGAAGAGAGAGGATAGGC	5	0.125	No Hit
GGGCCGGGTATCTCTCTGCATGTACGTATGCCTGTAATGTACGTAGCTAC	5	0.125	No Hit
AGTATGGCATCGGTTACATACTTCAGTGCCGTAGCGCCTGGTATGAGCCT	5	0.125	No Hit
CAACATAGGTCATCGAAAAGATCTCGGACGACTCACCAAAGCACGAAAGC	5	0.125	No Hit
GGAAAAGAAAGCAAAAGCGATTCCCGTAGTAGCGGCGAGCGAAATGGGAG	5	0.125	No Hit
>>END_MODULE
>>Adapter Content	pass
#Position	Illumina Universal Adapter	Illumina Small RNA 3' Adapter	Illumina Small RNA 5' Adapter	Nextera Transposase Sequence	SOLID Small RNA Adapter
1	0.0	0.0	0.0	0.0	0.0
2	0.0	0.0	0.0	0.0	0.0
3	0.0	0.0	0.0	0.0	0.0
4	0.0	0.0	0.0	0.0	0.0
5	0.0	0.0	0.0	0.0	0.0
6	0.0	0.0	0.0	0.0	0.0
7	0.0	0.0	0.0	0.0	0.0
8	0.0	0.0	0.0	0.0	0.0
9	0.0	0.0	0.0	0.0	0.0
10-11	0.025	0.0	0.0	0.0	0.0
12-13	0.025	0.0	0.0	0.0	0.0
14-15	0.075	0.0	0.0	0.0	0.0
16-17	0.075	0.0	0.0	0.0	0.0
18-19	0.075	0.0	0.0	0.0	0.0
20-21	0.075	0.0	0.0	0.0	0.0
22-23	0.075	0.0	0.0	0.0	0.0
24-25	0.075	0.0	0.0	0.0	0.0
26-27	0.075	0.0	0.0	0.0	0.0
28-29	0.11249999999999999	0.0	0.0	0.0	0.0
30-31	0.175	0.0	0.0	0.0	0.0
32-33	0.175	0.0	0.0	0.0	0.0
34-35	0.2	0.0	0.0	0.0	0.0
36-37	0.21250000000000002	0.0	0.0	0.0	0.0
38-39	0.225	0.0	0.0	0.0	0.0
40-41	0.25	0.0	0.0	0.0	0.0
42-43	0.25	0.0	0.0	0.0	0.0
44-45	0.25	0.0	0.0	0.0	0.0
46-47	0.275	0.0	0.0	0.0	0.0
48-49	0.275	0.0	0.0	0.0	0.0
50-51	0.275	0.0	0.0	0.0	0.0
52-53	0.275	0.0	0.0	0.0	0.0
54-55	0.275	0.0	0.0	0.0	0.0
56-57	0.3	0.0	0.0	0.0	0.0
58-59	0.3	0.0	0.0	0.0	0.0
60-61	0.3	0.0	0.0	0.0	0.0
62-63	0.3	0.0	0.0	0.0	0.0
64-65	0.3	0.0	0.0	0.0	0.0
66-67	0.3	0.0	0.0	0.0	0.0
68-69	0.3	0.0	0.0	0.0	0.0
70-71	0.325	0.0	0.0	0.0	0.0
72-73	0.4	0.0	0.0	0.0	0.0
74-75	0.4125	0.0	0.0	0.0	0.0
76-77	0.425	0.0	0.0	0.0	0.0
78-79	0.425	0.0	0.0	0.0	0.0
80-81	0.4375	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGCACCC	15	9.4021007E-4	85.35	7
AGGCACC	15	9.4021007E-4	85.35	6
GCACCCA	15	9.4021007E-4	85.35	8
TACCTAG	15	9.4021007E-4	85.35	1
ACCTAGG	15	9.4021007E-4	85.35	2
CCTAGGC	15	9.4021007E-4	85.35	3
TAGGCAC	15	9.4021007E-4	85.35	5
CTAGGCA	20	0.0029452087	64.0125	4
CACCCAG	20	0.0029452087	64.0125	9
>>END_MODULE
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22371 READS because READLEN < 1
Read 22371 spots for ERR6133485.sra
Written 22371 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
Rejected 22357 READS because READLEN < 1
Read 22357 spots for ERR6133485.sra
Written 22357 spots for ERR6133485.sra
SRR ids: ['ERR6133485.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_5ooul8aa
ERR6133485.sra spots: 447154
blocks: [[1, 22357], [22358, 44714], [44715, 67071], [67072, 89428], [89429, 111785], [111786, 134142], [134143, 156499], [156500, 178856], [178857, 201213], [201214, 223570], [223571, 245927], [245928, 268284], [268285, 290641], [290642, 312998], [312999, 335355], [335356, 357712], [357713, 380069], [380070, 402426], [402427, 424783], [424784, 447154]]
ERR6133485 file size 96936
ERR6133485 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 ERR6133485 ERR6133485_1.fastq
Input file:	ERR6133485_1.fastq
trimmed:	ERR6133485-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
Sat Dec  7 07:02:28 2024 >> started

Sat Dec  7 07:02:28 2024 >> done (0.351s)
447154 reads processed; of these:
   239 ( 0.05%) short reads filtered out after trimming by size control
    49 ( 0.01%) empty reads filtered out after trimming by size control
446866 (99.94%) reads available; of these:
  9291 ( 2.08%) trimmed reads available after processing
437575 (97.92%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	    34	  0.01%
 19	    49	  0.01%
 20	    28	  0.01%
 21	    13	  0.00%
 22	    33	  0.01%
 23	    16	  0.00%
 24	     9	  0.00%
 25	    16	  0.00%
 26	    11	  0.00%
 27	    24	  0.01%
 28	   172	  0.04%
 29	    70	  0.02%
 30	    23	  0.01%
 31	    37	  0.01%
 32	    39	  0.01%
 33	    47	  0.01%
 34	    42	  0.01%
 35	   222	  0.05%
 36	   434	  0.10%
 37	    20	  0.00%
 38	    29	  0.01%
 39	    92	  0.02%
 40	    40	  0.01%
 41	    37	  0.01%
 42	    15	  0.00%
 43	    17	  0.00%
 44	    10	  0.00%
 45	    17	  0.00%
 46	    16	  0.00%
 47	    16	  0.00%
 48	     7	  0.00%
 49	     7	  0.00%
 50	    14	  0.00%
 51	    33	  0.01%
 52	     9	  0.00%
 53	     9	  0.00%
 54	     5	  0.00%
 55	    11	  0.00%
 56	    15	  0.00%
 57	    11	  0.00%
 58	    12	  0.00%
 59	     8	  0.00%
 60	    14	  0.00%
 61	     6	  0.00%
 62	     0	  0.00%
 63	     1	  0.00%
 64	     0	  0.00%
 65	     3	  0.00%
 66	     3	  0.00%
 67	     1	  0.00%
 68	     8	  0.00%
 69	    32	  0.01%
 70	  3486	  0.78%
 71	  3106	  0.70%
 72	  3590	  0.80%
 73	  3039	  0.68%
 74	  3025	  0.68%
 75	  3261	  0.73%
 76	  2638	  0.59%
 77	  2766	  0.62%
 78	  3260	  0.73%
 79	  3617	  0.81%
 80	  3127	  0.70%
 81	  3385	  0.76%
 82	  4014	  0.90%
 83	  4125	  0.92%
 84	  3076	  0.69%
 85	    17	  0.00%
 86	    37	  0.01%
 87	    56	  0.01%
 88	    83	  0.02%
 89	   190	  0.04%
 90	   337	  0.08%
 91	   968	  0.22%
 92	  4932	  1.10%
 93	388894	 87.03%
446866 reads passed initial QC


criterion=sequence-density
sequence-density=6.91
sequence-density-rank=1
fanout-score=1.42
fanout-score-rank=18
prefix-density=0.32
prefix-fanout=1.4
sequence=GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCACCCTAGATGGCTAAAGTCCAGTAGCCGAAAGCATCACTAGCTTACGCTCTGACCCGAGTAGCATGGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCTGGGTGACCGATAGCGAAGTAGTACCGTGAGGGAAA


criterion=fanout-score
sequence-density=0.10
sequence-density-rank=21
fanout-score=63.77
fanout-score-rank=1
prefix-density=6.29
prefix-fanout=1.0
sequence=AAGCATAGATCGGAAGAGCACACGTCTGAACTCCAGTCACGCACCCATCTCGTATGCCG
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 GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCACCCTAGATGGCTAAAGTCCAGTAGCCGAAAGCATCACTAGCTTACGCTCTGACCCGAGTAGCATGGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCTGGGTGACCGATAGCGAAGTAGTACCGTGAGGGAAA -o ERR6133485 -
Input file:	STDIN
trimmed:	ERR6133485-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCACCCTAGATGGCTA
-- 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
Sat Dec  7 07:02:30 2024 >> started

Sat Dec  7 07:02:31 2024 >> done (0.400s)
319190 reads processed; of these:
  1028 ( 0.32%) short reads filtered out after trimming by size control
 21362 ( 6.69%) empty reads filtered out after trimming by size control
296800 (92.99%) reads available; of these:
  4715 ( 1.59%) trimmed reads available after processing
292085 (98.41%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	    28	  0.01%
 19	    36	  0.01%
 20	    21	  0.01%
 21	    10	  0.00%
 22	    23	  0.01%
 23	    11	  0.00%
 24	     8	  0.00%
 25	    13	  0.00%
 26	    11	  0.00%
 27	    14	  0.00%
 28	   128	  0.04%
 29	    51	  0.02%
 30	    16	  0.01%
 31	   115	  0.04%
 32	    41	  0.01%
 33	    38	  0.01%
 34	    32	  0.01%
 35	   169	  0.06%
 36	   320	  0.11%
 37	    34	  0.01%
 38	    21	  0.01%
 39	    66	  0.02%
 40	    28	  0.01%
 41	    27	  0.01%
 42	    17	  0.01%
 43	    15	  0.01%
 44	    15	  0.01%
 45	    17	  0.01%
 46	    16	  0.01%
 47	    12	  0.00%
 48	     6	  0.00%
 49	     9	  0.00%
 50	    13	  0.00%
 51	    25	  0.01%
 52	    16	  0.01%
 53	    11	  0.00%
 54	     2	  0.00%
 55	     5	  0.00%
 56	    10	  0.00%
 57	     8	  0.00%
 58	     9	  0.00%
 59	     8	  0.00%
 60	    10	  0.00%
 61	     5	  0.00%
 62	     0	  0.00%
 63	     1	  0.00%
 64	     0	  0.00%
 65	     2	  0.00%
 66	     5	  0.00%
 67	    44	  0.01%
 68	    63	  0.02%
 69	    75	  0.03%
 70	  2535	  0.85%
 71	  2198	  0.74%
 72	  2535	  0.85%
 73	  2185	  0.74%
 74	  2151	  0.72%
 75	  2312	  0.78%
 76	  1888	  0.64%
 77	  2318	  0.78%
 78	  2388	  0.80%
 79	  2961	  1.00%
 80	  2204	  0.74%
 81	  2491	  0.84%
 82	  2505	  0.84%
 83	  2873	  0.97%
 84	  2043	  0.69%
 85	    26	  0.01%
 86	    97	  0.03%
 87	   101	  0.03%
 88	   190	  0.06%
 89	   639	  0.22%
 90	  2354	  0.79%
 91	   658	  0.22%
 92	  3248	  1.09%
 93	252220	 84.98%


criterion=sequence-density
sequence-density=2.06
sequence-density-rank=1
fanout-score=1.97
fanout-score-rank=18
prefix-density=0.14
prefix-fanout=2.0
sequence=GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCACCCTAGATGGCTAAAGTCCAGTAGCCGAAAGCATCACTAGCTTACGCTCTGACCCGAGTAGCATGGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCTGGGTGACCGATAGCGAAGTAGTACCGTGAGGGAAA


criterion=fanout-score
sequence-density=0.10
sequence-density-rank=22
fanout-score=63.77
fanout-score-rank=1
prefix-density=6.63
prefix-fanout=1.0
sequence=AAGCATAGATCGGAAGAGCACACGTCTGAACTCCAGTCACGCACCCATCTCGTATGCCG
                                 Started job on |	Dec 07 07:02:42
                             Started mapping on |	Dec 07 07:02:42
                                    Finished on |	Dec 07 07:02:46
       Mapping speed, Million of reads per hour |	382.03

                          Number of input reads |	424476
                      Average input read length |	90
                                    UNIQUE READS:
                   Uniquely mapped reads number |	225229
                        Uniquely mapped reads % |	53.06%
                          Average mapped length |	90.11
                       Number of splices: Total |	7220
            Number of splices: Annotated (sjdb) |	5635
                       Number of splices: GT/AG |	6758
                       Number of splices: GC/AG |	148
                       Number of splices: AT/AC |	3
               Number of splices: Non-canonical |	311
                      Mismatch rate per base, % |	0.50%
                         Deletion rate per base |	0.04%
                        Deletion average length |	1.79
                        Insertion rate per base |	0.02%
                       Insertion average length |	1.92
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	165889
             % of reads mapped to multiple loci |	39.08%
        Number of reads mapped to too many loci |	4106
             % of reads mapped to too many loci |	0.97%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	6.82%
                     % of reads unmapped: other |	0.07%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	33358	33358	33358
N_multimapping	165889	165889	165889
N_noFeature	17119	20025	214683
N_ambiguous	8702	1053	41
UnstrandedReadsAssigned:199408 PositiveStrandReadsAssigned:204151 NegativeStrandReadsAssigned:10505
Dataset is classified positive stranded
MeadianReadLen=93 20thPercentileLength=93 echo kmer=89
ERR6133485 Starting Kallisto single end mapping to ensembl reference transcriptome. kmer=31

[quant] fragment length distribution is truncated gaussian with mean = 100, sd = 20
[index] k-mer length: 31
[index] number of targets: 52,972
[index] number of k-mers: 66,720,672
[index] number of equivalence classes: 111,837
[quant] running in single-end mode
[quant] will process file 1: ERR6133485-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 424,476 reads, 299,052 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 756 rounds

  52973 ERR6133485.ke.tsv
  35125 ERR6133485.se.tsv
  88098 total
==> ERR6133485.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	9	30.8644
PNS24243	293	194	0	0
KQK14069	1603	1504	6	18.7704
KQK14071	474	375	0	0

==> ERR6133485.se.tsv <==
BRADI_1g14170v3	6
BRADI_1g53295v3	2
BRADI_1g59795v3	1
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	3
BRADI_1g74790v3	4
BRADI_1g09890v3	0
BRADI_1g77505v3	5
BRADI_1g48960v3	0
ERR6133485 completed mapping pipeline successfully
