Starting /dee2/code/volunteer_pipeline.sh ERR6133525
    current disk space = 1544442867712
    free memory = 1435679636 
ERR6133525 SRAfilesize
a05787606a7bd66b07b744db3820f5dd  ERR6133525.sra
ERR6133525.sra file validated
ERR6133525 is single end
ERR6133525 is conventional basespace
ERR6133525 read1 length is 70-93 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	ERR6133525_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	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	36.56025	37.0	37.0	37.0	37.0	37.0
2	36.778	37.0	37.0	37.0	37.0	37.0
3	36.569	37.0	37.0	37.0	37.0	37.0
4	36.01725	37.0	37.0	37.0	33.0	37.0
5	36.173	37.0	37.0	37.0	33.0	37.0
6	36.27625	37.0	37.0	37.0	33.0	37.0
7	38.40275	40.0	37.0	40.0	37.0	40.0
8	38.4955	40.0	37.0	40.0	37.0	40.0
9	38.51825	40.0	37.0	40.0	37.0	40.0
10-11	38.47924999999999	40.0	37.0	40.0	37.0	40.0
12-13	38.373000000000005	40.0	37.0	40.0	37.0	40.0
14-15	38.343875	40.0	37.0	40.0	37.0	40.0
16-17	38.288625	40.0	37.0	40.0	37.0	40.0
18-19	38.22525	40.0	37.0	40.0	37.0	40.0
20-21	38.182625	40.0	37.0	40.0	37.0	40.0
22-23	38.379374999999996	40.0	37.0	40.0	37.0	40.0
24-25	38.23825	40.0	37.0	40.0	37.0	40.0
26-27	38.215125	40.0	37.0	40.0	37.0	40.0
28-29	38.201875	40.0	37.0	40.0	37.0	40.0
30-31	38.24225	40.0	37.0	40.0	37.0	40.0
32-33	38.289125	40.0	37.0	40.0	37.0	40.0
34-35	38.15	40.0	37.0	40.0	37.0	40.0
36-37	38.0875	40.0	37.0	40.0	37.0	40.0
38-39	37.952625	38.5	37.0	40.0	37.0	40.0
40-41	37.71725	37.0	37.0	40.0	35.0	40.0
42-43	37.69	37.0	37.0	40.0	37.0	40.0
44-45	37.401250000000005	37.0	37.0	40.0	35.0	40.0
46-47	37.31575	37.0	37.0	40.0	33.0	40.0
48-49	37.174875	37.0	37.0	40.0	33.0	40.0
50-51	37.028625	37.0	37.0	38.5	33.0	40.0
52-53	36.712875	37.0	37.0	37.0	33.0	40.0
54-55	36.678375	37.0	37.0	37.0	33.0	40.0
56-57	36.490125000000006	37.0	37.0	37.0	33.0	40.0
58-59	35.98675	37.0	37.0	37.0	33.0	38.5
60-61	36.171375	37.0	37.0	37.0	33.0	37.0
62-63	36.087500000000006	37.0	37.0	37.0	33.0	37.0
64-65	35.914249999999996	37.0	37.0	37.0	33.0	37.0
66-67	35.886375	37.0	37.0	37.0	33.0	37.0
68-69	34.955375000000004	35.0	35.0	37.0	33.0	37.0
70-71	35.18279658092848	37.0	33.0	37.0	33.0	37.0
72-73	35.62681280345644	37.0	33.0	37.0	33.0	37.0
74-75	35.600208769745805	37.0	35.0	37.0	33.0	37.0
76-77	35.572883400621066	37.0	33.0	37.0	33.0	37.0
78-79	35.47704399711935	37.0	33.0	37.0	33.0	37.0
80-81	35.292144669010725	37.0	33.0	37.0	33.0	37.0
82-83	35.262658942009594	37.0	33.0	37.0	33.0	37.0
84-85	35.03817143404659	37.0	33.0	37.0	33.0	37.0
86-87	35.09344692005243	37.0	33.0	37.0	33.0	37.0
88-89	35.057273918741814	37.0	33.0	37.0	33.0	37.0
90-91	34.9735255570118	37.0	33.0	37.0	33.0	37.0
92-93	34.95845347313237	37.0	33.0	37.0	33.0	37.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
20	2.0
21	0.0
22	1.0
23	11.0
24	4.0
25	7.0
26	12.0
27	8.0
28	14.0
29	18.0
30	24.0
31	34.0
32	54.0
33	58.0
34	94.0
35	294.0
36	975.0
37	1445.0
38	919.0
39	26.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	80.85	4.575	7.775	6.800000000000001
2	64.5	19.925	9.65	5.925
3	33.475	35.475	16.225	14.825
4	29.625	29.375	19.0	22.0
5	28.749999999999996	25.8	29.099999999999998	16.35
6	18.099999999999998	39.375	25.25	17.275
7	37.5	27.0	20.125	15.375
8	29.599999999999998	29.349999999999998	22.325	18.725
9	24.85	31.374999999999996	25.8	17.974999999999998
10-11	23.175	29.762499999999996	28.012500000000003	19.05
12-13	24.5625	28.025	26.5625	20.849999999999998
14-15	21.55	35.075	25.9625	17.4125
16-17	25.05	30.562499999999996	24.45	19.9375
18-19	23.925	27.175	29.0875	19.8125
20-21	25.9407425928241	25.17814726840855	29.753719214901864	19.127390923865484
22-23	29.475	22.125	28.9875	19.412499999999998
24-25	23.4375	27.0125	28.6375	20.9125
26-27	26.2875	24.5375	30.012499999999996	19.162499999999998
28-29	23.962500000000002	28.025	28.775000000000002	19.2375
30-31	29.0875	25.025	26.887499999999996	19.0
32-33	24.962500000000002	26.7125	28.0875	20.2375
34-35	22.3875	32.2875	25.124999999999996	20.200000000000003
36-37	25.6	25.674999999999997	26.237500000000004	22.4875
38-39	30.025000000000002	23.400000000000002	28.7375	17.837500000000002
40-41	23.80595148787197	24.85621405351338	30.532633158289574	20.80520130032508
42-43	26.19404851212803	30.820205051262818	25.893973493373345	17.09177294323581
44-45	23.3	27.2625	31.1875	18.25
46-47	25.95	24.5625	27.625	21.8625
48-49	24.45	24.2	29.612500000000004	21.7375
50-51	21.065133141642704	27.903487935992	28.216027003375423	22.815351918989872
52-53	24.430252942649634	25.45704983721513	25.59479088404708	24.517906336088156
54-55	24.553069133641706	24.915614451806476	31.378922365295665	19.15239404925616
56-57	26.3	27.187499999999996	27.212500000000002	19.3
58-59	23.0625	25.874999999999996	31.912499999999998	19.15
60-61	26.950000000000003	26.875	28.249999999999996	17.925
62-63	20.925	29.299999999999997	31.5	18.275
64-65	21.625	32.237500000000004	28.549999999999997	17.5875
66-67	23.4875	31.662499999999998	27.2625	17.5875
68-69	21.425	26.650000000000002	28.9	23.025000000000002
70-71	21.9536631183469	29.079524107701943	27.91484032561052	21.05197244834064
72-73	26.544766708701133	25.535939470365697	29.936948297604037	17.98234552332913
74-75	25.06977924384674	28.72367419436691	28.051256026389243	18.155290535397107
76-77	20.93467464663186	24.411053100725837	27.67095377562715	26.983318477015157
78-79	26.375735858715128	26.798054773483493	28.871256718710008	17.954952649091375
80-81	21.449723187846015	34.23458220677224	27.732715334105833	16.58297927127591
82-83	23.45614945511157	26.141670991177996	28.165542293720808	22.23663725998962
84-85	21.56965336821452	24.931327665140614	33.34205362982342	20.156965336821454
86-87	20.0	28.75491480996068	28.401048492791613	22.84403669724771
88-89	19.29226736566186	29.580602883355176	29.921363040629096	21.205766710353867
90-91	25.897771952817823	28.872870249017033	28.36173001310616	16.86762778505898
92-93	21.022280471821755	30.432503276539975	29.1218872870249	19.42332896461337
>>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	1.0
16	2.0
17	14.0
18	18.0
19	5.5
20	0.5
21	2.0
22	4.0
23	4.0
24	5.0
25	6.5
26	10.0
27	16.0
28	27.0
29	34.0
30	27.5
31	27.5
32	35.5
33	52.5
34	67.0
35	75.0
36	104.5
37	146.0
38	195.5
39	206.5
40	208.0
41	220.0
42	222.5
43	233.0
44	218.0
45	186.5
46	189.0
47	187.0
48	169.0
49	169.0
50	205.0
51	195.0
52	139.5
53	131.5
54	188.0
55	154.5
56	53.5
57	43.5
58	36.5
59	24.0
60	13.5
61	10.5
62	11.5
63	11.0
64	10.0
65	8.0
66	6.0
67	7.0
68	8.0
69	4.5
70	2.5
71	3.0
72	2.0
73	1.5
74	1.0
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	0.0125
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	0.025
42-43	0.025
44-45	0.0
46-47	0.0
48-49	0.0
50-51	0.0125
52-53	0.17500000000000002
54-55	0.0125
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	15.0
71	12.0
72	16.0
73	12.0
74	8.0
75	5.0
76	11.0
77	8.0
78	12.0
79	10.0
80	15.0
81	12.0
82	20.0
83	14.0
84	15.0
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	3815.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	73.02499999999999
#Duplication Level	Percentage of deduplicated	Percentage of total
1	92.2629236562821	67.375
2	4.3478260869565215	6.35
3	1.1982197877439233	2.625
4	0.6162273194111606	1.7999999999999998
5	0.20540910647038688	0.75
6	0.3081136597055803	1.35
7	0.17117425539198905	0.8750000000000001
8	0.13693940431359122	0.8
9	0.06846970215679561	0.44999999999999996
>10	0.5819924683327627	8.275
>50	0.034234851078397806	1.425
>100	0.06846970215679561	7.925
>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	207	5.175	No Hit
TACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTT	110	2.75	No Hit
GGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAA	57	1.425	No Hit
GGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTC	50	1.25	No Hit
GGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCTTGG	48	1.2	No Hit
GGAGTATCCTTGATATATAAATATATAGATAAATAGATTTAAATGGAAAA	27	0.675	No Hit
GGGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGG	21	0.525	No Hit
GGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGT	21	0.525	No Hit
GTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAA	20	0.5	No Hit
GGCCTGTAGTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCG	20	0.5	No Hit
GGGAGTATTATGAAAGGAGATTAATCATAGATTATCAAAAACCCTAGAAA	19	0.475	No Hit
GGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTG	15	0.375	No Hit
GGGGATGGAGCGACAGAAGTATGGAAATAGGATAAGGTAGCGGCGAGACG	15	0.375	No Hit
GGAGTCCTGAACTAGCCGCAGCTTGTGAAGTATGGAAGGCGATCAAATTC	12	0.3	No Hit
GGGCTGATATCATCAACCGTGCTAATCTTGGTATGGAAGTAATGCACGAA	12	0.3	No Hit
GGAGGAACTTTAGGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAA	11	0.27499999999999997	No Hit
GGGCGCGATCTTGCTCGTGAAGGTAATGAAATTATCCGAGCAGCTTGCAA	10	0.25	No Hit
GATACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGC	10	0.25	No Hit
GAAGGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGC	10	0.25	No Hit
TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGA	10	0.25	No Hit
CAAGGTCGCGTTATTAATACTTGGGCTGATATCATCAACCGTGCTAATCT	9	0.22499999999999998	No Hit
CAACCTAAATGGATTCAATTTCAACCAATCTGTAGTTGATAGTCAAGGTC	9	0.22499999999999998	No Hit
GGTGGGGCAATGGGCATTCCGTTGAGTTTGTATGGTGGGTGCTGTTTTGC	8	0.2	No Hit
GGATGATTCTGTATTACAATTTGGTGGAGGAACTTTAGGACATCCTTGGG	8	0.2	No Hit
GGACATCCTTGGGGAAATGCACCTGGTGCAGCAGCTAATCGAGTGGCTTT	8	0.2	No Hit
CGAGGAAGGGCGTAGCAAGCGACGAAATGCTTCGGGGAGTTGAAAATAAG	8	0.2	No Hit
GGAGTTGAAAATAAGCATAGATCCGGAGATTCCCAAATAGGTCAACCTTT	7	0.17500000000000002	No Hit
GGGAGTATCCTTGATATATAAATATATAGATAAATAGATTTAAATGGAAA	7	0.17500000000000002	No Hit
GGGACGCATGCAACGACCATCTACATATAGCTACTCGATCTACCGCTACC	7	0.17500000000000002	No Hit
GGATTCTTCTTTTTTGTGGGCCATTTGTGGCATGCAGGAAGAGCCCGAGC	7	0.17500000000000002	No Hit
CAACCAATCTGTAGTTGATAGTCAAGGTCGCGTTATTAATACTTGGGCTG	7	0.17500000000000002	No Hit
GAAGGAACAAACGAGGATAAGATAAAATTTCTTTAAATTTATTTTGCCCA	6	0.15	No Hit
GGTGCAGCAGCTAATCGAGTGGCTTTAGAAGCCTGTGTACAAGCTCGTAA	6	0.15	No Hit
GTACTATGGCGTTCAACCTAAATGGATTCAATTTCAACCAATCTGTAGTT	6	0.15	No Hit
GGGATGGAGCGACAGAAGTATGGAAATAGGATAAGGTAGCGGCGAGACGA	6	0.15	No Hit
ACACGTCTGAACTCCAGTCACACCGGCATCTCGTATGCCGTCTTCTGCTT	6	0.15	Illumina PCR Primer Index 3 (96% over 27bp)
GGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAATACTCCT	6	0.15	No Hit
CTGAGCCGTGCTCTCTTCTGTGTACATCTTCATGTCATTTTAGCGATTCT	6	0.15	No Hit
GGTAATGAAATTATCCGAGCAGCTTGCAAATGGAGTCCTGAACTAGCCGC	6	0.15	No Hit
TTCACAAGTCTGGTTCAGGGTGTCCTCCGGTGGAGTTGTCGCGTGTCTGA	6	0.15	No Hit
GGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATACTATCGATTAATAG	5	0.125	No Hit
GAAGTATGGAAGGCGATCAAATTCGAGTTCGCGCCGGTAGATACTATCGA	5	0.125	No Hit
GACACCATGCTTCCTGGAGAGATGTAGGTGCTTCAACATGAAGACTTTCC	5	0.125	No Hit
GTAGGAATCTGGTTCACTGCTTTAGGTATTAGTACTATGGCGTTCAACCT	5	0.125	No Hit
GATATCTATCTGAACTGAGAACTGAGTCAGTATATACCAGTCTGTATCAC	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	0.0	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	0.037500000000000006	0.0	0.0	0.0	0.0
38-39	0.05	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	0.075	0.0	0.0	0.0	0.0
52-53	0.1	0.0	0.0	0.0	0.0
54-55	0.1	0.0	0.0	0.0	0.0
56-57	0.1	0.0	0.0	0.0	0.0
58-59	0.1	0.0	0.0	0.0	0.0
60-61	0.1	0.0	0.0	0.0	0.0
62-63	0.1	0.0	0.0	0.0	0.0
64-65	0.1	0.0	0.0	0.0	0.0
66-67	0.1	0.0	0.0	0.0	0.0
68-69	0.1	0.0	0.0	0.0	0.0
70-71	0.1	0.0	0.0	0.0	0.0
72-73	0.125	0.0	0.0	0.0	0.0
74-75	0.125	0.0	0.0	0.0	0.0
76-77	0.125	0.0	0.0	0.0	0.0
78-79	0.125	0.0	0.0	0.0	0.0
80-81	0.125	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGGATGA	20	2.4532965E-5	86.4875	1
GGATGAT	15	8.920271E-4	86.487495	2
ATGATTC	15	8.920271E-4	86.487495	4
TTCTGTA	15	8.920271E-4	86.487495	8
TGATTCT	15	8.920271E-4	86.487495	5
ATTCTGT	15	8.920271E-4	86.487495	7
GGAGAGC	20	0.0027946017	64.86562	2
GATGATT	20	0.0027946017	64.86562	3
GCAATAC	20	0.0027946017	64.86562	7
GGGAGAG	20	0.0027946017	64.86562	1
CAATACA	20	0.0027946017	64.86562	8
GAGCAAT	20	0.0027946017	64.86562	5
TCTGTAT	20	0.0027946017	64.86562	9
AGAGCAA	20	0.0027946017	64.86562	4
AATACAA	20	0.0027946017	64.86562	9
AGCAATA	20	0.0027946017	64.86562	6
GATTCTG	25	0.006763133	51.8925	6
GAGAGCA	25	0.006763133	51.8925	3
>>END_MODULE
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32119 READS because READLEN < 1
Read 32119 spots for ERR6133525.sra
Written 32119 spots for ERR6133525.sra
Rejected 32122 READS because READLEN < 1
Read 32122 spots for ERR6133525.sra
Written 32122 spots for ERR6133525.sra
SRR ids: ['ERR6133525.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_i0q3egrp
ERR6133525.sra spots: 642383
blocks: [[1, 32119], [32120, 64238], [64239, 96357], [96358, 128476], [128477, 160595], [160596, 192714], [192715, 224833], [224834, 256952], [256953, 289071], [289072, 321190], [321191, 353309], [353310, 385428], [385429, 417547], [417548, 449666], [449667, 481785], [481786, 513904], [513905, 546023], [546024, 578142], [578143, 610261], [610262, 642383]]
ERR6133525 file size 140620
ERR6133525 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 ERR6133525 ERR6133525_1.fastq
Input file:	ERR6133525_1.fastq
trimmed:	ERR6133525-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 07:55:14 2024 >> started

Sat Dec  7 07:55:15 2024 >> done (0.512s)
642383 reads processed; of these:
   217 ( 0.03%) short reads filtered out after trimming by size control
    16 ( 0.00%) empty reads filtered out after trimming by size control
642150 (99.96%) reads available; of these:
  3533 ( 0.55%) trimmed reads available after processing
638617 (99.45%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	    42	  0.01%
 19	    44	  0.01%
 20	    15	  0.00%
 21	    16	  0.00%
 22	    13	  0.00%
 23	     8	  0.00%
 24	     5	  0.00%
 25	     8	  0.00%
 26	     9	  0.00%
 27	    10	  0.00%
 28	    21	  0.00%
 29	    21	  0.00%
 30	    13	  0.00%
 31	    14	  0.00%
 32	    19	  0.00%
 33	    12	  0.00%
 34	    11	  0.00%
 35	   110	  0.02%
 36	    87	  0.01%
 37	     8	  0.00%
 38	    23	  0.00%
 39	    45	  0.01%
 40	    57	  0.01%
 41	    24	  0.00%
 42	     7	  0.00%
 43	     7	  0.00%
 44	    14	  0.00%
 45	    10	  0.00%
 46	     7	  0.00%
 47	     3	  0.00%
 48	     2	  0.00%
 49	     7	  0.00%
 50	     6	  0.00%
 51	    17	  0.00%
 52	    11	  0.00%
 53	     6	  0.00%
 54	     3	  0.00%
 55	     2	  0.00%
 56	     9	  0.00%
 57	     5	  0.00%
 58	     3	  0.00%
 59	     2	  0.00%
 60	     7	  0.00%
 61	     7	  0.00%
 62	     1	  0.00%
 63	     1	  0.00%
 64	     1	  0.00%
 65	     0	  0.00%
 66	     2	  0.00%
 67	     3	  0.00%
 68	     1	  0.00%
 69	     9	  0.00%
 70	  2226	  0.35%
 71	  1965	  0.31%
 72	  2083	  0.32%
 73	  1931	  0.30%
 74	  1975	  0.31%
 75	  1849	  0.29%
 76	  1579	  0.25%
 77	  1706	  0.27%
 78	  1957	  0.30%
 79	  2150	  0.33%
 80	  1841	  0.29%
 81	  2073	  0.32%
 82	  2379	  0.37%
 83	  2379	  0.37%
 84	  1907	  0.30%
 85	     6	  0.00%
 86	    16	  0.00%
 87	    30	  0.00%
 88	    64	  0.01%
 89	    99	  0.02%
 90	   172	  0.03%
 91	   446	  0.07%
 92	  1769	  0.28%
 93	608760	 94.80%
642150 reads passed initial QC


criterion=sequence-density
sequence-density=6.83
sequence-density-rank=1
fanout-score=1.44
fanout-score-rank=22
prefix-density=0.26
prefix-fanout=1.4
sequence=GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCACCCTAGATGGCTAAAGTCCAGTAGCCGAAAGCATCACTAGCTTACGCTCTGACCCGAGTAGCATGGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAAT


criterion=fanout-score
sequence-density=0.12
sequence-density-rank=15
fanout-score=33.97
fanout-score-rank=1
prefix-density=4.09
prefix-fanout=1.0
sequence=GGAGATTCCCAGATAG
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 GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCACCCTAGATGGCTAAAGTCCAGTAGCCGAAAGCATCACTAGCTTACGCTCTGACCCGAGTAGCATGGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAAT -o ERR6133525 -
Input file:	STDIN
trimmed:	ERR6133525-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 07:55:19 2024 >> started

Sat Dec  7 07:55:20 2024 >> done (0.681s)
458679 reads processed; of these:
  1236 ( 0.27%) short reads filtered out after trimming by size control
 30499 ( 6.65%) empty reads filtered out after trimming by size control
426944 (93.08%) reads available; of these:
  6074 ( 1.42%) trimmed reads available after processing
420870 (98.58%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	    30	  0.01%
 19	    33	  0.01%
 20	    10	  0.00%
 21	    10	  0.00%
 22	    15	  0.00%
 23	     6	  0.00%
 24	     5	  0.00%
 25	     9	  0.00%
 26	     7	  0.00%
 27	    10	  0.00%
 28	    16	  0.00%
 29	    13	  0.00%
 30	    11	  0.00%
 31	   151	  0.04%
 32	    18	  0.00%
 33	     9	  0.00%
 34	    10	  0.00%
 35	    76	  0.02%
 36	    64	  0.01%
 37	    24	  0.01%
 38	    16	  0.00%
 39	    33	  0.01%
 40	    40	  0.01%
 41	    19	  0.00%
 42	     7	  0.00%
 43	     2	  0.00%
 44	    14	  0.00%
 45	    12	  0.00%
 46	     7	  0.00%
 47	     3	  0.00%
 48	     2	  0.00%
 49	    10	  0.00%
 50	     4	  0.00%
 51	    15	  0.00%
 52	    10	  0.00%
 53	     7	  0.00%
 54	     3	  0.00%
 55	     2	  0.00%
 56	     7	  0.00%
 57	     4	  0.00%
 58	     3	  0.00%
 59	     2	  0.00%
 60	     4	  0.00%
 61	     5	  0.00%
 62	     1	  0.00%
 63	     1	  0.00%
 64	     0	  0.00%
 65	     0	  0.00%
 66	     3	  0.00%
 67	    31	  0.01%
 68	    17	  0.00%
 69	    48	  0.01%
 70	  1591	  0.37%
 71	  1388	  0.33%
 72	  1502	  0.35%
 73	  1333	  0.31%
 74	  1376	  0.32%
 75	  1336	  0.31%
 76	  1142	  0.27%
 77	  1552	  0.36%
 78	  1468	  0.34%
 79	  1805	  0.42%
 80	  1301	  0.30%
 81	  1591	  0.37%
 82	  1522	  0.36%
 83	  1706	  0.40%
 84	  1306	  0.31%
 85	     9	  0.00%
 86	    57	  0.01%
 87	   101	  0.02%
 88	   276	  0.06%
 89	   952	  0.22%
 90	  3694	  0.87%
 91	   317	  0.07%
 92	  1153	  0.27%
 93	397607	 93.13%


criterion=sequence-density
sequence-density=2.05
sequence-density-rank=1
fanout-score=1.99
fanout-score-rank=22
prefix-density=0.11
prefix-fanout=2.0
sequence=GGGAGAGCAATACAAGCGTTGTGCTGCTAGGCGAAGCGGTTGAGTGCCGCACCCTAGATGGCTAAAGTCCAGTAGCCGAAAGCATCACTAGCTTACGCTCTGACCCGAGTAGCATGGGGCACGTGGAATCCCGTGTGAATCAGCAAGGACCACCTTGCAAGGCTAAAT


criterion=fanout-score
sequence-density=0.13
sequence-density-rank=15
fanout-score=34.01
fanout-score-rank=1
prefix-density=4.31
prefix-fanout=1.0
sequence=GGAGATTCCCAGATAG
                                 Started job on |	Dec 07 07:55:35
                             Started mapping on |	Dec 07 07:55:35
                                    Finished on |	Dec 07 07:55:39
       Mapping speed, Million of reads per hour |	549.37

                          Number of input reads |	610415
                      Average input read length |	92
                                    UNIQUE READS:
                   Uniquely mapped reads number |	398475
                        Uniquely mapped reads % |	65.28%
                          Average mapped length |	91.72
                       Number of splices: Total |	22915
            Number of splices: Annotated (sjdb) |	19228
                       Number of splices: GT/AG |	22258
                       Number of splices: GC/AG |	366
                       Number of splices: AT/AC |	12
               Number of splices: Non-canonical |	279
                      Mismatch rate per base, % |	0.22%
                         Deletion rate per base |	0.02%
                        Deletion average length |	1.52
                        Insertion rate per base |	0.01%
                       Insertion average length |	1.55
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	192700
             % of reads mapped to multiple loci |	31.57%
        Number of reads mapped to too many loci |	3365
             % of reads mapped to too many loci |	0.55%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	2.57%
                     % of reads unmapped: other |	0.03%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	19240	19240	19240
N_multimapping	192700	192700	192700
N_noFeature	28650	32681	381368
N_ambiguous	15019	1905	79
UnstrandedReadsAssigned:354806 PositiveStrandReadsAssigned:363889 NegativeStrandReadsAssigned:17028
Dataset is classified positive stranded
MeadianReadLen=93 20thPercentileLength=93 echo kmer=89
ERR6133525 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: ERR6133525-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 610,415 reads, 484,537 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 819 rounds

  52973 ERR6133525.ke.tsv
  35125 ERR6133525.se.tsv
  88098 total
==> ERR6133525.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	5	10.0026
PNS24243	293	194	0	0
KQK14069	1603	1504	32	58.3983
KQK14071	474	375	0	0

==> ERR6133525.se.tsv <==
BRADI_1g14170v3	32
BRADI_1g53295v3	4
BRADI_1g59795v3	3
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	4
BRADI_1g74790v3	1
BRADI_1g09890v3	0
BRADI_1g77505v3	9
BRADI_1g48960v3	0
ERR6133525 completed mapping pipeline successfully
