Starting /dee2/code/volunteer_pipeline.sh SRR1174002
    current disk space = 1524708962304
    free memory = 1339054452 
SRR1174002 SRAfilesize
9e3168c5f22621716e940b238186453c  SRR1174002.sra
SRR1174002.sra file validated
SRR1174002 is single end
SRR1174002 is conventional basespace
SRR1174002 read1 length is 42 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR1174002_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	42
%GC	47
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	32.12475	33.0	33.0	33.0	31.0	33.0
2	32.405	33.0	32.0	34.0	30.0	34.0
3	32.04225	33.0	32.0	34.0	29.0	34.0
4	32.28925	33.0	32.0	34.0	30.0	34.0
5	32.2205	33.0	32.0	34.0	29.0	34.0
6	32.2205	33.0	32.0	34.0	29.0	34.0
7	32.22025	33.0	32.0	34.0	29.0	34.0
8	32.0425	33.0	32.0	34.0	29.0	34.0
9	31.8225	33.0	32.0	34.0	28.0	34.0
10	32.0535	33.0	32.0	34.0	29.0	34.0
11	31.6685	33.0	31.0	34.0	28.0	34.0
12	31.61425	33.0	31.0	34.0	27.0	34.0
13	31.43325	33.0	31.0	33.0	27.0	34.0
14	31.77025	33.0	32.0	34.0	28.0	34.0
15	31.8515	33.0	32.0	34.0	29.0	34.0
16	31.6745	33.0	32.0	34.0	28.0	34.0
17	31.6	33.0	31.0	34.0	28.0	34.0
18	31.553	33.0	31.0	33.0	27.0	34.0
19	31.40975	33.0	31.0	33.0	27.0	34.0
20	31.1045	33.0	31.0	33.0	26.0	34.0
21	31.0325	33.0	31.0	33.0	26.0	34.0
22	30.82975	33.0	30.0	33.0	26.0	34.0
23	31.22625	33.0	31.0	33.0	27.0	34.0
24	30.91975	33.0	31.0	33.0	26.0	34.0
25	31.1835	33.0	31.0	33.0	27.0	34.0
26	30.582	32.0	30.0	33.0	25.0	34.0
27	29.54725	32.0	29.0	33.0	22.0	34.0
28	30.44775	32.0	30.0	33.0	25.0	34.0
29	29.53375	32.0	28.0	33.0	23.0	33.0
30	30.15375	32.0	30.0	33.0	24.0	34.0
31	29.4295	32.0	28.0	33.0	23.0	33.0
32	29.7495	32.0	29.0	33.0	23.0	33.0
33	29.58425	32.0	29.0	33.0	22.0	34.0
34	29.6205	32.0	29.0	33.0	23.0	33.0
35	28.53225	31.0	27.0	33.0	21.0	33.0
36	28.45375	31.0	27.0	33.0	21.0	33.0
37	29.166	32.0	28.0	33.0	22.0	34.0
38	28.12175	31.0	27.0	33.0	19.0	33.0
39	28.11325	31.0	27.0	33.0	19.0	33.0
40	29.01975	32.0	28.0	33.0	21.0	34.0
41	28.225	31.0	28.0	33.0	19.0	33.0
42	26.13425	30.0	24.0	33.0	4.0	33.0
>>END_MODULE
>>Per tile sequence quality	pass
#Tile	Base	Mean
1	1	0.0
1	2	0.0
1	3	0.0
1	4	0.0
1	5	0.0
1	6	0.0
1	7	0.0
1	8	0.0
1	9	0.0
1	10	0.0
1	11	0.0
1	12	0.0
1	13	0.0
1	14	0.0
1	15	0.0
1	16	0.0
1	17	0.0
1	18	0.0
1	19	0.0
1	20	0.0
1	21	0.0
1	22	0.0
1	23	0.0
1	24	0.0
1	25	0.0
1	26	0.0
1	27	0.0
1	28	0.0
1	29	0.0
1	30	0.0
1	31	0.0
1	32	0.0
1	33	0.0
1	34	0.0
1	35	0.0
1	36	0.0
1	37	0.0
1	38	0.0
1	39	0.0
1	40	0.0
1	41	0.0
1	42	0.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
4	2.0
5	1.0
6	2.0
7	0.0
8	2.0
9	1.0
10	1.0
11	1.0
12	1.0
13	1.0
14	4.0
15	2.0
16	4.0
17	7.0
18	10.0
19	12.0
20	9.0
21	27.0
22	26.0
23	33.0
24	73.0
25	58.0
26	110.0
27	126.0
28	213.0
29	320.0
30	509.0
31	862.0
32	1180.0
33	403.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	33.26592517694641	29.87866531850354	20.222446916076844	16.632962588473205
2	36.05	24.224999999999998	22.875	16.85
3	31.864831038798496	25.131414267834796	17.69712140175219	25.306633291614517
4	35.0	31.55	19.625	13.825000000000001
5	30.14007003501751	27.388694347173587	23.88694347173587	18.584292146073036
6	27.474999999999998	30.025000000000002	27.075	15.425
7	29.475	27.375	27.750000000000004	15.4
8	26.23811905952976	25.41270635317659	32.566283141570786	15.78289144572286
9	24.099999999999998	31.275	28.95	15.675
10	35.71785892946473	28.489244622311155	20.560280140070038	15.232616308154077
11	25.15	24.05	29.025000000000002	21.775
12	21.980495123780948	22.73068267066767	29.782445611402853	25.506376594148538
13	26.138069034517258	23.761880940470235	20.635317658829415	29.464732366183092
14	21.630407601900476	41.98549637409352	23.355838959739934	13.028257064266066
15	26.60665166291573	36.6591647911978	21.005251312828207	15.728932233058265
16	26.775	24.525	33.975	14.725
17	25.431357839459867	24.8062015503876	35.38384596149037	14.378594648662165
18	37.943971985992995	22.886443221610804	21.5607803901951	17.608804402201102
19	34.300000000000004	24.099999999999998	23.925	17.675
20	24.412206103051524	30.965482741370685	29.139569784892444	15.482741370685343
21	22.775000000000002	24.5	26.650000000000002	26.075
22	24.7997997997998	29.52952952952953	21.696696696696698	23.973973973973976
23	30.597948461346007	27.395546659994995	26.26970227670753	15.736802601951464
24	23.386693346673336	29.389694847423716	20.985492746373186	26.23811905952976
25	20.155038759689923	41.18529632408102	22.655663915978995	16.004001000250064
26	16.55	11.774999999999999	47.725	23.95
27	14.757378689344671	13.981990995497748	21.1855927963982	50.07503751875938
28	11.058293720290218	15.761821366024517	50.23767825869402	22.942206654991242
29	22.22222222222222	10.735735735735735	17.14214214214214	49.8998998998999
30	48.225	8.924999999999999	29.299999999999997	13.55
31	19.009504752376188	14.507253626813407	47.57378689344672	18.90945472736368
32	14.307153576788394	39.94497248624312	22.161080540270135	23.58679339669835
33	13.900000000000002	14.224999999999998	51.4	20.474999999999998
34	43.735933983495876	11.177794448612154	25.10627656914228	19.979994998749685
35	10.741111667501253	10.465698547821733	28.592889334001004	50.20030045067602
36	14.107053526763384	14.607303651825912	20.335167583791897	50.95047523761881
37	39.40985246311578	10.127531882970743	34.25856464116029	16.204051012753187
38	10.40260065016254	10.802700675168792	54.363590897724436	24.431107776944234
39	11.852963240810203	12.42810702675669	29.00725181295324	46.71167791947987
40	11.377844461115279	14.50362590647662	57.96449112278069	16.15403850962741
41	15.944931163954942	19.44931163954944	49.912390488110134	14.693366708385483
42	8.979489744872437	19.984992496248125	27.863931965982992	43.17158579289645
>>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	0.0
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	2.5
26	5.0
27	20.0
28	35.0
29	35.0
30	34.5
31	34.0
32	37.0
33	40.0
34	40.0
35	59.5
36	79.0
37	118.0
38	157.0
39	215.5
40	274.0
41	274.0
42	355.0
43	436.0
44	507.5
45	579.0
46	594.0
47	609.0
48	609.0
49	630.0
50	651.0
51	614.0
52	577.0
53	577.0
54	428.5
55	280.0
56	201.0
57	122.0
58	93.0
59	64.0
60	64.0
61	45.0
62	26.0
63	18.5
64	11.0
65	12.0
66	13.0
67	13.0
68	7.5
69	2.0
70	2.0
71	2.0
72	2.0
73	1.5
74	1.0
75	1.5
76	2.0
77	1.0
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	0.5
100	1.0
>>END_MODULE
>>Per base N content	pass
#Base	N-Count
1	1.0999999999999999
2	0.0
3	0.125
4	0.0
5	0.05
6	0.0
7	0.0
8	0.05
9	0.0
10	0.05
11	0.0
12	0.025
13	0.05
14	0.025
15	0.025
16	0.0
17	0.025
18	0.05
19	0.0
20	0.05
21	0.0
22	0.1
23	0.075
24	0.05
25	0.025
26	0.0
27	0.05
28	0.075
29	0.1
30	0.0
31	0.05
32	0.05
33	0.0
34	0.025
35	0.15
36	0.05
37	0.025
38	0.025
39	0.025
40	0.025
41	0.125
42	0.05
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
42	4000.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	77.225
#Duplication Level	Percentage of deduplicated	Percentage of total
1	94.8203302039495	73.225
2	2.136613790870832	3.3000000000000003
3	1.0035610229847847	2.325
4	0.32372936225315635	1.0
5	0.4208481709291033	1.625
6	0.19423761735189382	0.8999999999999999
7	0.16186468112657817	0.8750000000000001
8	0.09711880867594691	0.6
9	0.03237293622531564	0.22499999999999998
>10	0.7445775331822596	10.375
>50	0.03237293622531564	1.925
>100	0.03237293622531564	3.6249999999999996
>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
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTATCTCGT	145	3.6249999999999996	No Hit
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCATCTCGTAT	77	1.925	No Hit
TAACGAACGAACGATTTGAACATCTCGTATGCCGTCTTCTGC	32	0.8	Illumina PCR Primer Index 7 (96% over 25bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTGATCTCGT	29	0.7250000000000001	No Hit
CGAACGAACGATTTGAACATCTCGTATGCCGTCTTCTGCTTG	28	0.7000000000000001	RNA PCR Primer, Index 19 (96% over 29bp)
TGCTTGGACTACATATGGTTGAGGGTTGTATCGTATGCCGTC	26	0.65	No Hit
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTATCTCGTAT	26	0.65	No Hit
AACGAACGAACGATTTGAACATCTCGTATGCCGTCTTCTGCT	23	0.575	RNA PCR Primer, Index 19 (96% over 27bp)
CTAACGAACGAACGATTTGAACATCTCGTATGCCGTCTTCTG	22	0.5499999999999999	RNA PCR Primer, Index 19 (96% over 25bp)
AACGAACGATTTGAACATCTCGTATGCCGTCTTCTGCTTGAA	21	0.525	RNA PCR Primer, Index 19 (96% over 29bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCCATCTCGTA	19	0.475	No Hit
ATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAAAAAAAAAAA	17	0.42500000000000004	Illumina Single End Adapter 1 (95% over 24bp)
ACGAACGATTTGAACATCTCGTATGCCGTCTTCTGCTTGAAA	17	0.42500000000000004	Illumina PCR Primer Index 7 (96% over 28bp)
GGGGATGTAGCTCAGAATCTCGTATGCCGTCTTCTGCTTGAA	15	0.375	RNA PCR Primer, Index 40 (100% over 30bp)
CGAACGATTTGAACATCTCGTATGCCGTCTTCTGCTTGAAAA	15	0.375	RNA PCR Primer, Index 19 (96% over 29bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACTGATCTCGTA	15	0.375	No Hit
ACGAACGAACGATTTGAACATCTCGTATGCCGTCTTCTGCTT	15	0.375	Illumina PCR Primer Index 7 (96% over 27bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCATCTCGTATG	14	0.35000000000000003	No Hit
GAACGAACGATTTGAACATCTCGTATGCCGTCTTCTGCTTGA	13	0.325	Illumina PCR Primer Index 7 (96% over 28bp)
AGGGCTATAGCTCAGTTCGGATCTCGTATGCCGTCTTCTGCT	13	0.325	TruSeq Adapter, Index 9 (96% over 26bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACATCTCGTATG	12	0.3	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATTGATCTCG	12	0.3	No Hit
TTTGGATTGAAGGGAGCTCTGATCTCGTATGCCGTCTTCTGC	11	0.27499999999999997	Illumina PCR Primer Index 9 (96% over 25bp)
TGACAGAAGAGAGTGAGCACATCTCGTATGCCGTCTTCTGCT	10	0.25	Illumina PCR Primer Index 9 (96% over 25bp)
GGGATTGTAGTTCAATTGGTCAGAGCACCGCCCTATCTCGTA	10	0.25	No Hit
TCCTAACGAACGAACGATTTGAACATCTCGTATGCCGTCTTC	9	0.22499999999999998	Illumina PCR Primer Index 7 (95% over 22bp)
GCCTTGATGGTGAAATGGTAGACACGCGAGACTCAATCTCGT	8	0.2	No Hit
GCGAGCGTAGTTCAATGGTAAAACATCTCCTTGCCAAGGAGA	8	0.2	No Hit
TCGCTTGGTGCAGATCGGGACATCTCGTATGCCGTCTTCTGC	8	0.2	Illumina PCR Primer Index 3 (95% over 24bp)
CCCCGAGATCTCGTATGCCGTCTTCTGCTTGAAAAAAAAAAA	7	0.17500000000000002	RNA PCR Primer, Index 17 (96% over 28bp)
CATCCTAACGAACGAACGATTTGAACATCTCGTATGCCGTCT	7	0.17500000000000002	No Hit
GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATATCTCGTA	7	0.17500000000000002	No Hit
GACACGACTCTCGGCAACGGATATCTATCTCGTATGCCGTCT	7	0.17500000000000002	No Hit
TCCGTCGTAGTCTAGGATCTCGTATGCCGTCTTCTGCTTGAA	7	0.17500000000000002	RNA PCR Primer, Index 22 (96% over 28bp)
AAGGAAGCTATAAGATCTCGTATGCCGTCTTCTGCTTGAAAA	6	0.15	RNA PCR Primer, Index 44 (96% over 31bp)
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTATCTCGTA	6	0.15	No Hit
CCTAACGAACGAACGATTTGAACATCTCGTATGCCGTCTTCT	6	0.15	RNA PCR Primer, Index 19 (95% over 24bp)
GCACCAGTGGTCTAGTGGTAGAATAGTACCATCTCGTATGCC	6	0.15	No Hit
ATCCTAACGAACGAACGATTTGAACATCTCGTATGCCGTCTT	6	0.15	RNA PCR Primer, Index 19 (95% over 22bp)
GTCAGGATAGCTCAGTTGGTAGAGCAGAGGACCATCTCGTAT	6	0.15	No Hit
GTCGTTGTAGTATAGTGGTATCTCGTATGCCGTCTTCTGCTT	5	0.125	RNA PCR Primer, Index 34 (96% over 27bp)
GGGGATGTAGCTCAAAATCTCGTATGCCGTCTTCTGCTTGAA	5	0.125	RNA PCR Primer, Index 40 (96% over 30bp)
GGGATTGTAGTTCAATATCTCGTATGCCGTCTTCTGCTTGAA	5	0.125	Illumina PCR Primer Index 6 (96% over 29bp)
AGGCATCCTAACGAACGAACGATTTGAACATCTCGTATGCCG	5	0.125	No Hit
ACGATTTGAACATCTCGTATGCCGTCTTCTGCTTGAAAAAAA	5	0.125	Illumina PCR Primer Index 7 (96% over 28bp)
GTCGTTGTAGTATAGTGGTAAGTATTCCCGCATCTCGTATGC	5	0.125	No Hit
AGGGCAAAGAACGCGAGTGAGATCTCGTATGCCGTCTTCTGC	5	0.125	TruSeq Adapter, Index 25 (96% over 25bp)
GAACGATTTGAACATCTCGTATGCCGTCTTCTGCTTGAAAAA	5	0.125	RNA PCR Primer, Index 19 (96% over 29bp)
GGGGACGTAGCTCATAATCTCGTATGCCGTCTTCTGCTTGAA	5	0.125	RNA PCR Primer, Index 40 (96% over 30bp)
CTGAGGCATCCTAACGAACGAACGATTTGAACATCTCGTATG	5	0.125	No Hit
GCATCCTAACGAACGAACGATTTGAACATCTCGTATGCCGTC	5	0.125	No Hit
TAATTCATGATCTGGATCTCGTATGCCGTCTTCTGCTTGAAA	5	0.125	RNA PCR Primer, Index 23 (96% over 28bp)
GGAGAGATGGCTGAGTGGACTAAAGCGGCGGATTGATCTCGT	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	0.0	0.0	0.0	0.0	0.0
11	0.0	0.0	0.0	0.0	0.0
12	0.0	0.0	0.0	0.0	0.0
13	0.0	0.0	0.0	0.0	0.0
14	0.0	0.0	0.0	0.0	0.0
15	0.0	0.0	0.0	0.0	0.0
16	0.0	0.0	0.0	0.0	0.0
17	0.0	0.0	0.0	0.0	0.0
18	0.0	0.0	0.0	0.0	0.0
19	0.0	0.0	0.0	0.0	0.0
20	0.0	0.0	0.0	0.0	0.0
21	0.0	0.0	0.0	0.0	0.0
22	0.0	0.0	0.0	0.0	0.0
23	0.0	0.0	0.0	0.0	0.0
24	0.0	0.0	0.0	0.0	0.0
25	0.0	0.0	0.0	0.0	0.0
26	0.0	0.0	0.0	0.0	0.0
27	0.0	0.0	0.0	0.0	0.0
28	0.0	0.0	0.0	0.0	0.0
29	0.0	0.0	0.0	0.0	0.0
30	0.0	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
AGCCAAG	45	1.7644197E-9	36.36709	10
TAGCTCA	20	0.0017729009	36.36709	8
TAGCCAA	45	1.7644197E-9	36.36709	9
TGTAGCC	40	2.847446E-8	36.36709	7
GCCAAGT	45	1.7644197E-9	36.36709	11
CCAAGTG	45	1.7644197E-9	36.36709	12
GTAGCCA	45	1.7644197E-9	36.36709	8
CAAGTGG	45	1.7644197E-9	36.36709	13
GGATCAA	50	1.2551027E-10	35.912502	18
GGATTAT	40	3.200512E-8	35.912502	31
ATTATCT	35	5.0466224E-7	35.912502	33
GCAGTGG	40	3.200512E-8	35.912502	26
TGGATTA	35	5.0466224E-7	35.912502	30
TGGATCA	50	1.2551027E-10	35.912502	17
GATCAAG	50	1.2551027E-10	35.912502	19
AGGCAGT	40	3.200512E-8	35.912502	24
GATTATC	35	5.0466224E-7	35.912502	32
ATCAAGG	50	1.2551027E-10	35.912502	20
GTGGATT	40	3.200512E-8	35.912502	29
GTGGATC	50	1.2551027E-10	35.912502	16
>>END_MODULE
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650434 spots for SRR1174002.sra
Written 650434 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
Read 650429 spots for SRR1174002.sra
Written 650429 spots for SRR1174002.sra
SRR ids: ['SRR1174002.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_sm358wi8
SRR1174002.sra spots: 13008585
blocks: [[1, 650429], [650430, 1300858], [1300859, 1951287], [1951288, 2601716], [2601717, 3252145], [3252146, 3902574], [3902575, 4553003], [4553004, 5203432], [5203433, 5853861], [5853862, 6504290], [6504291, 7154719], [7154720, 7805148], [7805149, 8455577], [8455578, 9106006], [9106007, 9756435], [9756436, 10406864], [10406865, 11057293], [11057294, 11707722], [11707723, 12358151], [12358152, 13008585]]
SRR1174002 file size 1815624
SRR1174002 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 SRR1174002 SRR1174002_1.fastq
Input file:	SRR1174002_1.fastq
trimmed:	SRR1174002-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
Mon Dec  9 14:12:31 2024 >> started

Mon Dec  9 14:13:03 2024 >> done (31.333s)
13008585 reads processed; of these:
   52034 ( 0.40%) short reads filtered out after trimming by size control
   23452 ( 0.18%) empty reads filtered out after trimming by size control
12933099 (99.42%) reads available; of these:
 1706069 (13.19%) trimmed reads available after processing
11227030 (86.81%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	    7648	  0.06%
 19	    8938	  0.07%
 20	    9645	  0.07%
 21	   10480	  0.08%
 22	   12728	  0.10%
 23	   18825	  0.15%
 24	   21047	  0.16%
 25	   19686	  0.15%
 26	   25361	  0.20%
 27	   37212	  0.29%
 28	   31434	  0.24%
 29	   40283	  0.31%
 30	   44150	  0.34%
 31	   45619	  0.35%
 32	   46490	  0.36%
 33	   40710	  0.31%
 34	   41815	  0.32%
 35	   44496	  0.34%
 36	   45804	  0.35%
 37	   64823	  0.50%
 38	   73586	  0.57%
 39	  105743	  0.82%
 40	  261245	  2.02%
 41	  648301	  5.01%
 42	11227030	 86.81%
12933099 reads passed initial QC


criterion=sequence-density
sequence-density=73.07
sequence-density-rank=1
fanout-score=31.89
fanout-score-rank=1
prefix-density=75.96
prefix-fanout=30.7
sequence=ATCTCGTATGCCGTCTTCTGCTTGAAAAAA


criterion=fanout-score
sequence-density=73.07
sequence-density-rank=1
fanout-score=31.89
fanout-score-rank=1
prefix-density=75.96
prefix-fanout=30.7
sequence=ATCTCGTATGCCGTCTTCTGCTTGAAAAAA
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 ATCTCGTATGCCGTCTTCTGCTTGAAAAAA -o SRR1174002 -
Input file:	STDIN
trimmed:	SRR1174002-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	ATCTCGTATGCCGTCTTCTGCTTGAAAAAA
-- 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
Mon Dec  9 14:14:38 2024 >> started

Mon Dec  9 14:15:26 2024 >> done (47.595s)
12583556 reads processed; of these:
 2101720 (16.70%) short reads filtered out after trimming by size control
  224391 ( 1.78%) empty reads filtered out after trimming by size control
10257445 (81.51%) reads available; of these:
 9638872 (93.97%) trimmed reads available after processing
  618573 ( 6.03%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  259877	  2.53%
 19	  302931	  2.95%
 20	  331631	  3.23%
 21	  674070	  6.57%
 22	  309714	  3.02%
 23	  798181	  7.78%
 24	 3995365	 38.95%
 25	  282269	  2.75%
 26	  157870	  1.54%
 27	  127168	  1.24%
 28	  107645	  1.05%
 29	  152225	  1.48%
 30	  179242	  1.75%
 31	  165193	  1.61%
 32	  221055	  2.16%
 33	  550727	  5.37%
 34	  307506	  3.00%
 35	  713838	  6.96%
 36	  111742	  1.09%
 37	   56401	  0.55%
 38	   28330	  0.28%
 39	   22270	  0.22%
 40	   12533	  0.12%
 41	   17570	  0.17%
 42	  372092	  3.63%


criterion=sequence-density
sequence-density=6.31
sequence-density-rank=1
fanout-score=1.00
fanout-score-rank=20
prefix-density=0.01
prefix-fanout=1.0
sequence=GGCGGATGTAGCCAAGTGGATCAAGGCAGTGGATT


criterion=fanout-score
sequence-density=0.15
sequence-density-rank=28
fanout-score=42.55
fanout-score-rank=1
prefix-density=6.20
prefix-fanout=1.0
sequence=GATCAAGGCAGGGGATT
                                 Started job on |	Dec 09 14:17:18
                             Started mapping on |	Dec 09 14:17:19
                                    Finished on |	Dec 09 14:19:35
       Mapping speed, Million of reads per hour |	280.77

                          Number of input reads |	10606988
                      Average input read length |	26
                                    UNIQUE READS:
                   Uniquely mapped reads number |	4112273
                        Uniquely mapped reads % |	38.77%
                          Average mapped length |	23.79
                       Number of splices: Total |	35127
            Number of splices: Annotated (sjdb) |	4406
                       Number of splices: GT/AG |	32265
                       Number of splices: GC/AG |	1231
                       Number of splices: AT/AC |	15
               Number of splices: Non-canonical |	1616
                      Mismatch rate per base, % |	0.21%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.21
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.02
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	4153057
             % of reads mapped to multiple loci |	39.15%
        Number of reads mapped to too many loci |	1526129
             % of reads mapped to too many loci |	14.39%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	5.57%
                     % of reads unmapped: other |	2.12%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	2341658	2341658	2341658
N_multimapping	4153057	4153057	4153057
N_noFeature	3420599	3695720	3828176
N_ambiguous	18162	8384	1246
UnstrandedReadsAssigned:673512 PositiveStrandReadsAssigned:408169 NegativeStrandReadsAssigned:282851
Dataset is classified unstranded
MeadianReadLen=24 20thPercentileLength=23 echo kmer=19
SRR1174002 Starting Kallisto single end mapping to ensembl reference transcriptome. kmer=19

[quant] fragment length distribution is truncated gaussian with mean = 100, sd = 20
[index] k-mer length: 19
[index] number of targets: 52,972
[index] number of k-mers: 65,492,969
[index] number of equivalence classes: 320,172
[quant] running in single-end mode
[quant] will process file 1: SRR1174002-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 10,606,988 reads, 3,250,979 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,164 rounds

  52973 SRR1174002.ke.tsv
  35125 SRR1174002.se.tsv
  88098 total
==> SRR1174002.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	3.61881	0.230066
PNS24243	293	194	0	0
KQK14069	1603	1504	25.8035	1.49648
KQK14071	474	375	0	0

==> SRR1174002.se.tsv <==
BRADI_1g14170v3	25
BRADI_1g53295v3	1
BRADI_1g59795v3	1
BRADI_1g07683v3	0
BRADI_1g00485v3	1
BRADI_1g20270v3	10
BRADI_1g74790v3	84
BRADI_1g09890v3	1
BRADI_1g77505v3	0
BRADI_1g48960v3	0
SRR1174002 completed mapping pipeline successfully
