Starting /dee2/code/volunteer_pipeline.sh ERR6133421
    current disk space = 1546902716416
    free memory = 1421013044 
ERR6133421 SRAfilesize
ef57c0bdc92115a74109fc3af96cf35f  ERR6133421.sra
ERR6133421.sra file validated
ERR6133421 is single end
ERR6133421 is conventional basespace
ERR6133421 read1 length is 70-93 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	ERR6133421_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	44
>>END_MODULE
>>Per base sequence quality	fail
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	29.9335	33.0	27.0	33.0	15.0	37.0
2	33.7265	37.0	33.0	37.0	27.0	37.0
3	33.75725	37.0	33.0	37.0	27.0	37.0
4	33.95325	37.0	33.0	37.0	27.0	37.0
5	34.0265	37.0	33.0	37.0	27.0	37.0
6	34.1885	37.0	33.0	37.0	27.0	37.0
7	35.3105	37.0	33.0	40.0	27.0	40.0
8	35.07875	37.0	33.0	40.0	27.0	40.0
9	35.4185	37.0	33.0	40.0	33.0	40.0
10-11	35.3725	37.0	33.0	40.0	30.0	40.0
12-13	35.15725	37.0	33.0	38.5	27.0	40.0
14-15	35.181	37.0	33.0	37.0	27.0	40.0
16-17	34.890625	37.0	33.0	37.0	27.0	40.0
18-19	34.681	37.0	33.0	37.0	27.0	40.0
20-21	34.09425	37.0	33.0	37.0	27.0	40.0
22-23	33.968125	37.0	33.0	37.0	24.5	40.0
24-25	33.397999999999996	37.0	33.0	37.0	22.0	40.0
26-27	33.258875	37.0	33.0	37.0	22.0	40.0
28-29	32.8615	37.0	33.0	37.0	22.0	40.0
30-31	32.8485	37.0	33.0	37.0	22.0	40.0
32-33	32.388125	35.0	33.0	37.0	22.0	40.0
34-35	31.57125	33.0	27.0	37.0	18.5	40.0
36-37	31.179625	33.0	27.0	37.0	15.0	40.0
38-39	31.378999999999998	33.0	27.0	37.0	22.0	40.0
40-41	31.532874999999997	33.0	27.0	37.0	22.0	40.0
42-43	31.07525	33.0	27.0	37.0	15.0	40.0
44-45	30.838124999999998	33.0	27.0	37.0	15.0	40.0
46-47	30.33275	33.0	27.0	37.0	15.0	37.0
48-49	29.9155	33.0	27.0	37.0	15.0	37.0
50-51	29.569125	33.0	27.0	37.0	15.0	37.0
52-53	29.385875	33.0	27.0	37.0	15.0	37.0
54-55	29.25025	33.0	27.0	37.0	15.0	37.0
56-57	28.614625	33.0	27.0	35.0	15.0	37.0
58-59	28.4375	33.0	27.0	33.0	15.0	37.0
60-61	28.119500000000002	33.0	27.0	33.0	15.0	37.0
62-63	27.836875	33.0	22.0	33.0	15.0	37.0
64-65	27.3375	33.0	22.0	33.0	10.5	37.0
66-67	26.874375	33.0	22.0	33.0	10.5	37.0
68-69	26.411125	27.0	22.0	33.0	10.5	35.0
70-71	28.12970163316583	33.0	27.0	33.0	15.0	37.0
72-73	28.53911117551594	33.0	27.0	33.0	15.0	37.0
74-75	28.568913460300834	33.0	27.0	33.0	15.0	37.0
76-77	28.234239548602204	33.0	27.0	33.0	15.0	37.0
78-79	27.512508571399298	33.0	27.0	33.0	10.5	37.0
80-81	26.971760237223926	33.0	24.5	33.0	6.0	37.0
82-83	26.109012235149606	33.0	22.0	33.0	4.0	37.0
84-85	25.505819822310137	33.0	22.0	33.0	2.0	37.0
86-87	24.44701374207188	27.0	15.0	33.0	2.0	37.0
88-89	23.86139006342495	30.0	15.0	33.0	2.0	35.0
90-91	22.57729915433404	27.0	2.0	33.0	2.0	35.0
92-93	21.219344608879492	27.0	2.0	33.0	2.0	33.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
20	80.0
21	100.0
22	145.0
23	152.0
24	195.0
25	209.0
26	231.0
27	241.0
28	248.0
29	266.0
30	263.0
31	265.0
32	258.0
33	262.0
34	299.0
35	316.0
36	258.0
37	184.0
38	27.0
39	1.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	70.75	7.35	7.199999999999999	14.7
2	52.925	23.724999999999998	14.549999999999999	8.799999999999999
3	32.35	36.775000000000006	17.125	13.750000000000002
4	27.925	29.725	21.099999999999998	21.25
5	25.874999999999996	25.275	29.45	19.400000000000002
6	17.150000000000002	36.3	28.7	17.849999999999998
7	34.849999999999994	27.025	20.674999999999997	17.45
8	23.95	26.075	28.349999999999998	21.625
9	22.3	33.1	26.224999999999998	18.375
10-11	22.3625	27.3	31.25	19.0875
12-13	21.6625	29.4	28.875	20.0625
14-15	19.900000000000002	31.1875	29.3375	19.575
16-17	23.724999999999998	29.062500000000004	24.587500000000002	22.625
18-19	24.5	24.637500000000003	31.3	19.5625
20-21	25.25	25.074999999999996	29.9	19.775000000000002
22-23	28.775000000000002	22.95	28.975	19.3
24-25	22.6875	25.974999999999998	29.525000000000002	21.8125
26-27	25.8	23.8875	29.25	21.0625
28-29	22.475	28.875	29.925	18.725
30-31	28.349999999999998	26.7625	26.2875	18.6
32-33	25.4625	24.2875	28.537499999999998	21.712500000000002
34-35	21.512500000000003	32.9625	26.3125	19.2125
36-37	25.362499999999997	26.400000000000002	25.025	23.2125
38-39	29.212500000000002	24.7	26.950000000000003	19.1375
40-41	24.087500000000002	24.2875	31.65	19.975
42-43	26.6	28.825	25.5625	19.0125
44-45	23.7625	25.5125	30.7125	20.0125
46-47	25.4375	25.775	26.325	22.4625
48-49	24.5625	25.0	28.0875	22.35
50-51	20.962500000000002	28.675	28.1875	22.175
52-53	23.125	27.3375	25.724999999999998	23.8125
54-55	21.55	26.7625	30.2625	21.425
56-57	26.474999999999998	27.725	26.687499999999996	19.112499999999997
58-59	22.3625	28.575	29.3875	19.675
60-61	28.6125	26.375	26.450000000000003	18.5625
62-63	20.849999999999998	27.750000000000004	31.4625	19.9375
64-65	20.5875	33.6	27.5875	18.224999999999998
66-67	24.587500000000002	29.599999999999998	26.700000000000003	19.112499999999997
68-69	21.2875	27.150000000000002	28.6375	22.925
70-71	22.24310776942356	28.345864661654137	26.829573934837093	22.581453634085214
72-73	25.463956571140006	25.640701931574295	29.768968564575182	19.126372932710517
74-75	25.616577676074243	28.14645308924485	27.536231884057973	18.700737350622934
76-77	21.743025339134885	25.223957000255954	27.732275403122603	25.300742257486565
78-79	25.14831054939386	27.98555584214599	28.3982460665463	18.467887541913854
80-81	21.350649350649352	33.42857142857143	27.844155844155843	17.376623376623375
82-83	23.36949418376683	26.140373807345448	26.36256698470788	24.127565024179844
84-85	21.755171959414945	25.74779285808407	31.82237448939254	20.674660693108446
86-87	19.70137420718816	30.88002114164905	27.048097251585624	22.370507399577168
88-89	20.031712473572938	27.906976744186046	30.377906976744185	21.68340380549683
90-91	24.947145877378436	29.92864693446089	25.34355179704017	19.780655391120508
92-93	20.65274841437632	30.64217758985201	27.048097251585624	21.656976744186046
>>END_MODULE
>>Per sequence GC content	warn
#GC Content	Count
0	0.0
1	0.0
2	0.0
3	0.0
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
10	0.0
11	0.0
12	0.0
13	0.0
14	0.0
15	0.5
16	0.5
17	2.0
18	3.5
19	2.5
20	3.5
21	6.5
22	6.5
23	5.0
24	7.0
25	12.0
26	11.0
27	13.0
28	18.5
29	17.5
30	28.0
31	43.5
32	58.5
33	75.5
34	77.0
35	85.0
36	118.5
37	176.0
38	220.0
39	210.5
40	208.0
41	220.0
42	224.0
43	232.5
44	214.0
45	178.5
46	156.5
47	145.0
48	126.0
49	123.0
50	125.5
51	128.0
52	131.5
53	137.0
54	201.0
55	187.0
56	105.0
57	85.0
58	62.5
59	33.0
60	23.5
61	23.5
62	17.5
63	11.0
64	8.0
65	8.0
66	10.0
67	8.0
68	6.0
69	8.0
70	11.0
71	11.0
72	7.0
73	1.5
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	0.0
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
>>END_MODULE
>>Sequence Length Distribution	warn
#Length	Count
70	20.0
71	12.0
72	15.0
73	16.0
74	8.0
75	14.0
76	16.0
77	16.0
78	12.0
79	14.0
80	14.0
81	10.0
82	15.0
83	13.0
84	21.0
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	3784.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	73.97500000000001
#Duplication Level	Percentage of deduplicated	Percentage of total
1	92.05812774586009	68.10000000000001
2	3.8188577222034468	5.65
3	1.2842176410949644	2.85
4	0.9800608313619465	2.9000000000000004
5	0.33795201081446435	1.25
6	0.37174721189591076	1.6500000000000001
7	0.16897600540723218	0.8750000000000001
8	0.13518080432578572	0.8
9	0.16897600540723218	1.125
>10	0.6421088205474822	9.975000000000001
>50	0.0	0.0
>100	0.03379520108144643	4.825
>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	193	4.825	No Hit
GGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAA	49	1.225	No Hit
GGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTC	33	0.8250000000000001	No Hit
CAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTG	30	0.75	No Hit
CAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGATAT	29	0.7250000000000001	No Hit
GGGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAA	29	0.7250000000000001	No Hit
CAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCT	28	0.7000000000000001	No Hit
GGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGG	27	0.675	No Hit
CAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTC	23	0.575	No Hit
TACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTT	20	0.5	No Hit
GGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAA	16	0.4	No Hit
GGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGT	16	0.4	No Hit
TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGA	16	0.4	No Hit
GTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCT	15	0.375	No Hit
GGAAAAGAAAGCAAAAGCGATTCCCGTAGTAGCGGCGAGCGAAATGGGAG	14	0.35000000000000003	No Hit
GGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAA	13	0.325	No Hit
GCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCT	11	0.27499999999999997	No Hit
GGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCTAAATGGATTC	10	0.25	No Hit
GGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGCCGC	10	0.25	No Hit
GTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAG	10	0.25	No Hit
CAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTT	9	0.22499999999999998	No Hit
GGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTG	9	0.22499999999999998	No Hit
GTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTT	9	0.22499999999999998	No Hit
GTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAA	9	0.22499999999999998	No Hit
GGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAA	9	0.22499999999999998	No Hit
GGGTTGTTTGGGAATGCAGCCCAAATCGGGCGGTAGACTCCGTCCAAGGC	8	0.2	No Hit
GGGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGG	8	0.2	No Hit
AGTCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAA	8	0.2	No Hit
GTATTAGTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCT	8	0.2	No Hit
GGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAAC	7	0.17500000000000002	No Hit
GGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCT	7	0.17500000000000002	No Hit
GGGGTTGTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTG	7	0.17500000000000002	No Hit
GTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCC	7	0.17500000000000002	No Hit
GGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTA	7	0.17500000000000002	No Hit
GGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTGTACAAGCTCGTAA	6	0.15	No Hit
GCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATC	6	0.15	No Hit
GGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTG	6	0.15	No Hit
GGTTGTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAG	6	0.15	No Hit
GATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAAT	6	0.15	No Hit
GAGGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAAT	6	0.15	No Hit
TCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGATATCAT	6	0.15	No Hit
GTCAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAAT	6	0.15	No Hit
CACGAACGTAATGCTCACAACTTCCCTCTAGATCTAGCTGCTCTTGAAGT	6	0.15	No Hit
AACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTGA	6	0.15	No Hit
GGGTGAGAGCCCCGTCCGGCCCGGACCCTGTCGCCCCACGAGGCGCCGTC	6	0.15	No Hit
CAGCTAATCGAGTGGCTTTAGAAGCCTGTGTACAAGCTCGTAACGAAGGG	5	0.125	No Hit
TATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATA	5	0.125	No Hit
CACCCTAGATGGCTAAAGTCCAGTAGCCGAAAGCATCACTAGCTTACGCT	5	0.125	No Hit
GGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAAA	5	0.125	No Hit
CTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGT	5	0.125	No Hit
GCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTGTACAAGCTCGTAACGA	5	0.125	No Hit
GGAGTTGAAAATAAGCATAGATCCGGAGATTCCCAAATAGGTCAACCTTT	5	0.125	No Hit
GGGTTGTGGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGA	5	0.125	No Hit
GGAGTATCCTTGATATATAAATATATAGATAAATAGATTTAAATGGAAAA	5	0.125	No Hit
GAAGGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGC	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	0.0	0.0	0.0	0.0	0.0
12-13	0.0	0.0	0.0	0.0	0.0
14-15	0.0	0.0	0.0	0.0	0.0
16-17	0.0	0.0	0.0	0.0	0.0
18-19	0.0	0.0	0.0	0.0	0.0
20-21	0.0	0.0	0.0	0.0	0.0
22-23	0.0	0.0	0.0	0.0	0.0
24-25	0.0	0.0	0.0	0.0	0.0
26-27	0.0	0.0	0.0	0.0	0.0
28-29	0.0	0.0	0.0	0.0	0.0
30-31	0.0	0.0	0.0	0.0	0.0
32-33	0.0	0.0	0.0	0.0	0.0
34-35	0.0	0.0	0.0	0.0	0.0
36-37	0.0	0.0	0.0	0.0	0.0
38-39	0.0	0.0	0.0	0.0	0.0
40-41	0.05	0.0	0.0	0.0	0.0
42-43	0.05	0.0	0.0	0.0	0.0
44-45	0.05	0.0	0.0	0.0	0.0
46-47	0.05	0.0	0.0	0.0	0.0
48-49	0.05	0.0	0.0	0.0	0.0
50-51	0.05	0.0	0.0	0.0	0.0
52-53	0.05	0.0	0.0	0.0	0.0
54-55	0.05	0.0	0.0	0.0	0.0
56-57	0.05	0.0	0.0	0.0	0.0
58-59	0.05	0.0	0.0	0.0	0.0
60-61	0.05	0.0	0.0	0.0	0.0
62-63	0.05	0.0	0.0	0.0	0.0
64-65	0.05	0.0	0.0	0.0	0.0
66-67	0.05	0.0	0.0	0.0	0.0
68-69	0.05	0.0	0.0	0.0	0.0
70-71	0.05	0.0	0.0	0.0	0.0
72-73	0.05	0.0	0.0	0.0	0.0
74-75	0.075	0.0	0.0	0.0	0.0
76-77	0.075	0.0	0.0	0.0	0.0
78-79	0.075	0.0	0.0	0.0	0.0
80-81	0.075	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGAGAGC	40	1.135331E-5	53.710938	2
AGAGCAA	40	1.135331E-5	53.710938	4
GAGAGCA	40	1.135331E-5	53.710938	3
AGCAATA	40	1.135331E-5	53.710938	6
GCAATAC	45	2.280516E-5	47.743057	7
GGGAGAG	45	2.280516E-5	47.743057	1
CAATACA	45	2.280516E-5	47.743057	8
TGCCGCA	25	4.6680747E-5	42.968754	44-45
GAGCAAT	50	4.25181E-5	42.968754	5
AATACAA	55	7.463215E-5	39.062504	9
CATCACT	30	8.575485E-5	38.710587	82-83
ATCACTA	30	8.575485E-5	38.710587	84-85
CACTAGC	30	8.575485E-5	38.710587	86-87
TCACTAG	30	8.575485E-5	38.710587	84-85
ACTAGCT	30	8.575485E-5	38.710587	86-87
GCATCAC	30	8.575485E-5	38.710587	82-83
CCGAAAG	30	1.0060981E-4	37.691887	76-77
TCCAGTA	30	1.2683614E-4	36.26055	68-69
GATGGCT	30	1.3674125E-4	35.80729	56-57
GAGTGCC	30	1.3674125E-4	35.80729	42-43
>>END_MODULE
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81969 READS because READLEN < 1
Read 81969 spots for ERR6133421.sra
Written 81969 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
Rejected 81965 READS because READLEN < 1
Read 81965 spots for ERR6133421.sra
Written 81965 spots for ERR6133421.sra
SRR ids: ['ERR6133421.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_avlme0kv
ERR6133421.sra spots: 1639304
blocks: [[1, 81965], [81966, 163930], [163931, 245895], [245896, 327860], [327861, 409825], [409826, 491790], [491791, 573755], [573756, 655720], [655721, 737685], [737686, 819650], [819651, 901615], [901616, 983580], [983581, 1065545], [1065546, 1147510], [1147511, 1229475], [1229476, 1311440], [1311441, 1393405], [1393406, 1475370], [1475371, 1557335], [1557336, 1639304]]
ERR6133421 file size 359799
ERR6133421 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 ERR6133421 ERR6133421_1.fastq
Input file:	ERR6133421_1.fastq
trimmed:	ERR6133421-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 04:52:07 2024 >> started

Sat Dec  7 04:52:12 2024 >> done (5.035s)
1639304 reads processed; of these:
     32 ( 0.00%) short reads filtered out after trimming by size control
      0 ( 0.00%) empty reads filtered out after trimming by size control
1639272 (100.00%) reads available; of these:
 422946 (25.80%) trimmed reads available after processing
1216326 (74.20%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	      9	  0.00%
 19	     20	  0.00%
 20	      5	  0.00%
 21	      1	  0.00%
 22	      6	  0.00%
 23	      2	  0.00%
 24	      2	  0.00%
 25	      1	  0.00%
 26	      1	  0.00%
 27	      3	  0.00%
 28	      4	  0.00%
 29	      5	  0.00%
 30	      1	  0.00%
 31	      7	  0.00%
 32	     11	  0.00%
 33	      3	  0.00%
 34	      0	  0.00%
 35	      1	  0.00%
 36	      3	  0.00%
 37	      2	  0.00%
 38	     16	  0.00%
 39	     22	  0.00%
 40	     25	  0.00%
 41	      8	  0.00%
 42	     14	  0.00%
 43	     21	  0.00%
 44	     22	  0.00%
 45	     31	  0.00%
 46	     45	  0.00%
 47	     62	  0.00%
 48	     94	  0.01%
 49	    116	  0.01%
 50	    184	  0.01%
 51	    233	  0.01%
 52	    288	  0.02%
 53	    440	  0.03%
 54	    639	  0.04%
 55	    913	  0.06%
 56	   1149	  0.07%
 57	   1767	  0.11%
 58	   1268	  0.08%
 59	   1539	  0.09%
 60	   1856	  0.11%
 61	   2118	  0.13%
 62	   2288	  0.14%
 63	   2355	  0.14%
 64	   2782	  0.17%
 65	   2897	  0.18%
 66	   2970	  0.18%
 67	   3048	  0.19%
 68	   2848	  0.17%
 69	   2789	  0.17%
 70	   9286	  0.57%
 71	   9610	  0.59%
 72	  11313	  0.69%
 73	  11943	  0.73%
 74	  12383	  0.76%
 75	  13704	  0.84%
 76	  14240	  0.87%
 77	  16047	  0.98%
 78	  16851	  1.03%
 79	  17946	  1.09%
 80	  19102	  1.17%
 81	  21928	  1.34%
 82	  23674	  1.44%
 83	  23890	  1.46%
 84	  26795	  1.63%
 85	  21527	  1.31%
 86	  22002	  1.34%
 87	  24710	  1.51%
 88	  29545	  1.80%
 89	  31458	  1.92%
 90	  33068	  2.02%
 91	  36146	  2.21%
 92	  31035	  1.89%
 93	1126135	 68.70%
1639272 reads passed initial QC


criterion=sequence-density
sequence-density=2.75
sequence-density-rank=1
fanout-score=2.07
fanout-score-rank=23
prefix-density=2.82
prefix-fanout=2.0
sequence=CAAGGCTAAATAC


criterion=fanout-score
sequence-density=0.01
sequence-density-rank=30
fanout-score=12.80
fanout-score-rank=1
prefix-density=0.04
prefix-fanout=2.5
sequence=GAAGAAATTAGAGTGCTCAAAGCAAGCCATCGCTCTGGATACATTAGCATGGGATAACATCATAGGATTCCGGTCCTATTGTGTTGGCCTTCGGGATCGGAGTAATGATTAATAGGGACAGTCGGGGGCATTCGTATTTCATAGTCAGAGGTGAAATTCTTGGATTTATGAAAGACGAACAACTGCGAAAGCATTTGCCAAGGATGTTTTCATTAATCAAGAACGAAAGTTGGGGGCTCGAAGACGATCAGATACCGT
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:
    0 (0.00%) aligned 0 times
    0 (0.00%) aligned exactly 1 time
    1 (100.00%) aligned >1 times
100.00% overall alignment rate
Potential adapter found in reference sequence. Continuing without clipping.
                                 Started job on |	Dec 07 04:53:48
                             Started mapping on |	Dec 07 04:53:49
                                    Finished on |	Dec 07 04:54:35
       Mapping speed, Million of reads per hour |	128.29

                          Number of input reads |	1639272
                      Average input read length |	89
                                    UNIQUE READS:
                   Uniquely mapped reads number |	702384
                        Uniquely mapped reads % |	42.85%
                          Average mapped length |	88.78
                       Number of splices: Total |	27042
            Number of splices: Annotated (sjdb) |	21133
                       Number of splices: GT/AG |	25553
                       Number of splices: GC/AG |	577
                       Number of splices: AT/AC |	36
               Number of splices: Non-canonical |	876
                      Mismatch rate per base, % |	0.81%
                         Deletion rate per base |	0.04%
                        Deletion average length |	1.73
                        Insertion rate per base |	0.02%
                       Insertion average length |	1.42
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	826063
             % of reads mapped to multiple loci |	50.39%
        Number of reads mapped to too many loci |	48376
             % of reads mapped to too many loci |	2.95%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	3.29%
                     % of reads unmapped: other |	0.52%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	110825	110825	110825
N_multimapping	826063	826063	826063
N_noFeature	65087	72191	671196
N_ambiguous	28843	4717	177
UnstrandedReadsAssigned:608454 PositiveStrandReadsAssigned:625476 NegativeStrandReadsAssigned:31011
Dataset is classified positive stranded
MeadianReadLen=93 20thPercentileLength=85 echo kmer=81
ERR6133421 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: ERR6133421-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 1,639,272 reads, 1,112,378 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 902 rounds

  52973 ERR6133421.ke.tsv
  35125 ERR6133421.se.tsv
  88098 total
==> ERR6133421.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	22	18.8136
PNS24243	293	194	0	0
KQK14069	1603	1504	6	4.68066
KQK14071	474	375	0	0

==> ERR6133421.se.tsv <==
BRADI_1g14170v3	6
BRADI_1g53295v3	4
BRADI_1g59795v3	5
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	6
BRADI_1g74790v3	3
BRADI_1g09890v3	0
BRADI_1g77505v3	12
BRADI_1g48960v3	0
ERR6133421 completed mapping pipeline successfully
