Starting /dee2/code/volunteer_pipeline.sh SRR1033815
    current disk space = 1548447850496
    free memory = 1598455864 
SRR1033815 SRAfilesize
b073afaf5655fe9bdff765adb302e622  SRR1033815.sra
SRR1033815.sra file validated
SRR1033815 is single end
SRR1033815 is conventional basespace
SRR1033815 read1 length is 46 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR1033815_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	46
%GC	48
>>END_MODULE
>>Per base sequence quality	fail
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	32.29075	33.0	33.0	33.0	32.0	33.0
2	31.60775	33.0	31.0	33.0	28.0	34.0
3	30.62275	32.0	30.0	33.0	26.0	33.0
4	29.79025	31.0	29.0	33.0	24.0	33.0
5	30.79025	32.0	30.0	33.0	26.0	33.0
6	30.705	32.0	30.0	33.0	26.0	33.0
7	30.86925	32.0	30.0	33.0	27.0	33.0
8	30.378	32.0	30.0	33.0	25.0	33.0
9	29.42025	31.0	28.0	33.0	23.0	33.0
10	29.68675	32.0	29.0	33.0	23.0	33.0
11	30.30975	32.0	30.0	33.0	25.0	33.0
12	29.55325	31.0	28.0	33.0	24.0	33.0
13	27.86925	30.0	25.0	32.0	20.0	33.0
14	25.98225	28.0	22.0	31.0	17.0	32.0
15	25.59625	28.0	21.0	31.0	16.0	32.0
16	25.787	28.0	22.0	31.0	17.0	33.0
17	25.3635	28.0	21.0	31.0	15.0	33.0
18	29.0975	31.0	28.0	33.0	22.0	33.0
19	27.88075	30.0	26.0	32.0	19.0	33.0
20	27.39425	30.0	25.0	32.0	20.0	33.0
21	28.76725	31.0	28.0	32.0	22.0	33.0
22	28.54075	31.0	27.0	32.0	21.0	33.0
23	28.38725	31.0	27.0	33.0	21.0	33.0
24	27.87775	30.0	26.0	32.0	20.0	33.0
25	27.03675	30.0	24.0	32.0	19.0	33.0
26	27.9145	30.0	26.0	32.0	20.0	33.0
27	27.2945	30.0	26.0	32.0	19.0	33.0
28	26.00625	28.0	23.0	31.0	17.0	33.0
29	25.384	28.0	22.0	31.0	16.0	32.0
30	25.5645	28.0	23.0	31.0	16.0	33.0
31	26.06025	29.0	24.0	32.0	15.0	33.0
32	24.64125	27.0	21.0	31.0	14.0	32.0
33	25.38525	28.0	22.0	31.0	14.0	33.0
34	26.38325	29.0	25.0	32.0	14.0	33.0
35	25.012	28.0	22.0	31.0	12.0	33.0
36	25.1655	28.0	22.0	31.0	10.0	33.0
37	25.25775	28.0	23.0	31.0	10.0	33.0
38	24.1165	27.0	20.0	31.0	7.0	33.0
39	23.23225	26.0	19.0	30.0	4.0	32.0
40	24.58375	28.0	22.0	31.0	4.0	33.0
41	23.31425	27.0	19.0	31.0	4.0	33.0
42	20.5225	23.0	15.0	28.0	4.0	31.0
43	21.18325	24.0	15.0	29.0	4.0	32.0
44	20.9845	25.0	13.0	29.0	4.0	32.0
45	18.53375	23.0	4.0	28.0	4.0	31.0
46	17.27725	21.0	4.0	28.0	4.0	31.0
>>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
1	43	0.0
1	44	0.0
1	45	0.0
1	46	0.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
4	16.0
5	6.0
6	3.0
7	3.0
8	4.0
9	8.0
10	8.0
11	10.0
12	17.0
13	25.0
14	32.0
15	37.0
16	29.0
17	35.0
18	48.0
19	57.0
20	61.0
21	86.0
22	101.0
23	178.0
24	219.0
25	302.0
26	373.0
27	452.0
28	533.0
29	546.0
30	419.0
31	308.0
32	79.0
33	5.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	18.914185639229423	25.519139354515886	44.283212409306984	11.283462596947711
2	38.72904678508882	22.39179384538404	16.46234676007005	22.416812609457093
3	38.704028021015766	33.12484363272454	13.009757317988491	15.161371028271203
4	23.705926481620406	26.6816704176044	13.253313328332084	36.35908977244311
5	19.204801200300075	37.934483620905226	23.605901475368842	19.254813703425857
6	36.25906476619154	21.330332583145786	27.031757939484873	15.378844711177795
7	35.23380845211303	33.758439609902474	16.129032258064516	14.87871967991998
8	29.2	35.3	16.150000000000002	19.35
9	36.51825912956478	22.411205602801402	28.36418209104552	12.706353176588294
10	36.88688688688689	31.78178178178178	13.313313313313312	18.01801801801802
11	34.733683420855215	22.305576394098527	17.90447611902976	25.056264066016503
12	26.43821910955478	42.94647323661831	16.08304152076038	14.532266133066532
13	49.56217162872154	22.491868901676256	12.43432574430823	15.511633725293972
14	24.661992989484226	34.852278417626444	27.190786179268905	13.294942413620431
15	35.88397099274819	22.43060765191298	27.806951737934483	13.87846961740435
16	25.86293146573287	36.19309654827414	13.006503251625812	24.937468734367183
17	46.4232116058029	25.337668834417208	15.682841420710355	12.556278139069535
18	40.88522130532633	17.854463615903978	11.45286321580395	29.80745186296574
19	35.708927231807955	32.05801450362591	15.053763440860216	17.179294823705927
20	19.23461730865433	32.14107053526764	19.05952976488244	29.5647823911956
21	18.75	20.375	30.95	29.925
22	16.504126031507877	13.12828207051763	38.38459614903726	31.98299574893723
23	30.857714428607153	18.554638659664917	17.479369842460617	33.10827706926732
24	31.41570785392696	13.556778389194598	41.145572786393195	13.881940970485243
25	9.45	22.925	55.50000000000001	12.125
26	12.437437437437438	26.176176176176174	31.23123123123123	30.155155155155157
27	47.85	8.1	35.199999999999996	8.85
28	29.5647823911956	10.25512756378189	34.61730865432716	25.56278139069535
29	11.836836836836836	29.47947947947948	14.364364364364365	44.31931931931932
30	28.760951188986233	5.857321652065081	33.81727158948686	31.564455569461824
31	51.49085442245052	4.234527687296417	26.409421197694815	17.865196692558253
32	10.693713999499122	2.404207362885049	31.02930127723516	55.87277736038067
33	11.4063675106543	2.1057909250438707	29.9824517422913	56.505389822010535
34	28.64661654135338	1.7543859649122806	53.659147869674186	15.939849624060152
35	5.989974937343359	1.7543859649122806	60.576441102756895	31.67919799498747
36	5.870546914199699	1.8815855494229805	39.262418464626194	52.985449071751134
37	20.55722891566265	1.6566265060240966	64.28212851405623	13.50401606425703
38	23.965906242165957	1.7297568312860365	43.77036851341188	30.533968413136126
39	7.64986205166792	2.2322548281916226	39.22748934035616	50.890393779784304
40	11.113898645258406	3.411941796287005	74.91219267436026	10.56196688409433
41	46.94082246740221	6.44433299899699	35.45636910732197	11.158475426278837
42	28.180677540777914	26.3237139272271	17.84190715181932	27.65370138017566
43	8.477552044143465	49.78680712315024	37.32129420617005	4.4143466265362425
44	9.28016052169551	55.50539252570855	31.95385001254076	3.260596940055179
45	27.156469408224677	63.66599799398195	7.647943831494483	1.5295887662988967
46	25.363773206221772	63.37180130456598	9.784244856999498	1.4801806322127444
>>END_MODULE
>>Per sequence GC content	fail
#GC Content	Count
0	56.0
1	30.0
2	4.0
3	3.0
4	2.0
5	1.0
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	0.5
26	1.0
27	2.5
28	4.0
29	2.5
30	1.0
31	1.0
32	2.0
33	3.0
34	7.0
35	11.0
36	11.0
37	11.0
38	25.0
39	39.0
40	91.5
41	144.0
42	185.5
43	227.0
44	227.0
45	591.0
46	955.0
47	712.5
48	470.0
49	477.0
50	484.0
51	686.5
52	889.0
53	622.5
54	356.0
55	255.5
56	155.0
57	155.0
58	123.5
59	92.0
60	74.0
61	56.0
62	40.0
63	24.0
64	17.0
65	10.0
66	6.0
67	2.0
68	1.0
69	0.0
70	0.0
71	0.5
72	1.0
73	0.5
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	0.5
93	1.0
94	1.0
95	0.5
96	0.0
97	0.0
98	0.0
99	1.0
100	2.0
>>END_MODULE
>>Per base N content	pass
#Base	N-Count
1	0.075
2	0.075
3	0.075
4	0.025
5	0.025
6	0.025
7	0.025
8	0.0
9	0.05
10	0.1
11	0.025
12	0.05
13	0.075
14	0.15
15	0.025
16	0.05
17	0.05
18	0.025
19	0.025
20	0.05
21	0.0
22	0.025
23	0.025
24	0.05
25	0.0
26	0.1
27	0.0
28	0.05
29	0.1
30	0.125
31	0.22499999999999998
32	0.17500000000000002
33	0.27499999999999997
34	0.25
35	0.25
36	0.35000000000000003
37	0.4
38	0.27499999999999997
39	0.325
40	0.35000000000000003
41	0.3
42	0.375
43	0.325
44	0.325
45	0.3
46	0.35000000000000003
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
46	4000.0
>>END_MODULE
>>Sequence Duplication Levels	warn
#Total Deduplicated Percentage	61.4
#Duplication Level	Percentage of deduplicated	Percentage of total
1	93.32247557003257	57.3
2	3.3794788273615635	4.15
3	1.0993485342019544	2.025
4	0.7328990228013029	1.7999999999999998
5	0.32573289902280134	1.0
6	0.20358306188925082	0.75
7	0.04071661237785017	0.17500000000000002
8	0.24429967426710095	1.2
9	0.04071661237785017	0.22499999999999998
>10	0.4478827361563518	4.875
>50	0.04071661237785017	1.825
>100	0.08143322475570033	11.75
>500	0.04071661237785017	12.925
>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
TGACAGAAGAGAGTGAGCACTCGTATGCCGTCTTCTGCTTGAAAAA	517	12.925	TruSeq Adapter, Index 19 (95% over 24bp)
TCGCTTGGTGCAGATCGGGACTCGTATGCCGTCTTCTGCTTGAAAA	355	8.875	TruSeq Adapter, Index 15 (95% over 24bp)
TTGACAGAAGAGAGTGAGCACTCGTATGCCGTCTTCTGCTTGAAAA	115	2.875	TruSeq Adapter, Index 13 (95% over 24bp)
TGGAAGGGGCATGCAGAGGAGTCGTATGCCGTCTTCTGCTTGAAAA	73	1.825	Illumina Single End Adapter 2 (95% over 22bp)
AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	48	1.2	No Hit
CACGACTCTCGGCAACGGATATCTTCGTATGCCGTCTTCTGCTTGG	25	0.625	Illumina Single End Adapter 1 (95% over 22bp)
GACACGACTCTCGGCAACGGATATCTTCGTATGCCGTCTTCTGCTT	18	0.44999999999999996	Illumina Single End Adapter 1 (95% over 21bp)
AGAATCTTGATGATGCTGCATTCGTATGCCGTCTTCTGCTTGAAAA	17	0.42500000000000004	Illumina Single End Adapter 2 (95% over 22bp)
GACACGACTCTCGGCAACGGATATTCGTATGCCGTCTTCTGCTTGG	15	0.375	Illumina Single End Adapter 1 (95% over 22bp)
AGTTCTACAGTCCGACGATCTCGTATGCCGTCTTCTGCTTGAAAAA	13	0.325	Illumina PCR Primer Index 1 (96% over 28bp)
GGGGATGTAGCTCAGATGGTATCGTATGCCGTCTTCTGCTTGAAAA	13	0.325	TruSeq Adapter, Index 14 (95% over 24bp)
GACACGACTCTCGGCAACGGATATCTCGTATGCCGTCTTCTGCTTT	13	0.325	RNA PCR Primer, Index 25 (96% over 29bp)
CACGACTCTCGGCAACGGATATCTCGTATGCCGTCTTCTGCTTGAA	12	0.3	Illumina PCR Primer Index 6 (96% over 27bp)
AGGTCCCGGCGACGGAACCATCGTATGCCGTCTTCTGCTTGAAAAA	11	0.27499999999999997	Illumina Single End Adapter 1 (95% over 22bp)
GGGGATGTAGCTCAGATGGTTCGTATGCCGTCTTCTGCTTGAAAAA	10	0.25	Illumina Single End Adapter 2 (95% over 23bp)
TGACAGAAGAGAGTGAGCACTCGTATGCCGTCTTCTGCTTGAAAAC	9	0.22499999999999998	TruSeq Adapter, Index 19 (95% over 24bp)
CTGACAGAAGAGAGTGAGCACTCGTATGCCGTCTTCTGCTTGAAAA	8	0.2	TruSeq Adapter, Index 13 (95% over 24bp)
AACGAACGAACGATTTGAACTCGTATGCCGTCTTCTGCTTGAAAAA	8	0.2	Illumina Single End Adapter 2 (96% over 25bp)
CACGACTCTCGGCAACGGATATCTCTCGTATGCCGTCTTCTGCTTT	8	0.2	Illumina PCR Primer Index 6 (96% over 25bp)
GACACGACTCTCGGCAACGGATATCGTATGCCGTCTTCTGCTTGAA	8	0.2	Illumina PCR Primer Index 5 (96% over 25bp)
CACGACTCTCGGCAACGGATATCTTCGTATGCCGTCTTCTGCTTGT	8	0.2	Illumina Single End Adapter 1 (95% over 22bp)
TCGCTTGGTGCAGATCTGGACTCGTATGCCGTCTTCTGCTTGAAAA	8	0.2	TruSeq Adapter, Index 15 (95% over 24bp)
CACGACTCTCGGCAACGGATATCTCGTCGTATGCCGTCTTCTGCTT	7	0.17500000000000002	Illumina Single End Adapter 1 (95% over 21bp)
CTAACGAACGAACGATTTGAACTCGTATGCCGTCTTCTGCTTGAAA	6	0.15	Illumina Single End Adapter 2 (96% over 25bp)
GACTCTCGGCAACGGATATCTTCGTATGCCGTCTTCTGCTTGAAAA	6	0.15	Illumina Single End Adapter 1 (95% over 22bp)
CAGGTCCCGGCGACGGAACCATCGTATGCCGTCTTCTGCTTGAAAA	6	0.15	Illumina Single End Adapter 1 (95% over 22bp)
GGGGATGTAGCTCAGATGGTAGTCGTATGCCGTCTTCTGCTTGAAA	6	0.15	Illumina Single End Adapter 2 (95% over 22bp)
GACACGACTCTCGGCAACGGATTCGTATGCCGTCTTCTGCTTGAAA	6	0.15	Illumina Single End Adapter 2 (95% over 22bp)
TTCTACAGTCCGACGATCTCGTATGCCGTCTTCTGCTTGAAAAAAA	5	0.125	RNA PCR Primer, Index 47 (96% over 29bp)
GCGTCTGTAGTCCAACGGTTTCGTATGCCGTCTTCTGCTTGAAAAA	5	0.125	TruSeq Adapter, Index 14 (95% over 24bp)
GGTGAACCTGCGGAAGGATCATTGTCGTATGCCGTCTTCTGCTTGG	5	0.125	TruSeq Adapter, Index 20 (95% over 24bp)
TGAAGCTGCCAGCATGATCTGATCGTATGCCGTCTTCTGCTTGAAA	5	0.125	Illumina Single End Adapter 1 (95% over 23bp)
CACGACTCTCGGCAACGGATATTCGTATGCCGTCTTCTGCTTGAAA	5	0.125	Illumina Single End Adapter 1 (95% over 22bp)
GTTCGAGACCTGTATGGGCCACCATCGTATGCCGTCTTCTGCTTGG	5	0.125	Illumina Single End Adapter 2 (95% over 22bp)
TCGTGACCTGTATGGGCCACCATCGTATGCCGTCTTCTGCTTGAAA	5	0.125	Illumina Single End Adapter 2 (95% over 22bp)
CCACGTCGCACGGATTCGTTCGTATGCCGTCTTCTGCTTGAAAAAA	5	0.125	Illumina Single End Adapter 2 (95% over 23bp)
>>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
31	0.0	0.0	0.0	0.0	0.0
32	0.0	0.0	0.0	0.0	0.0
33	0.0	0.0	0.0	0.0	0.0
34	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
CGCTTGG	55	1.8189894E-12	40.379745	2
TCGCTTG	55	1.8189894E-12	40.379745	1
GCTTGGT	55	1.8189894E-12	40.379745	3
ATCGGGA	50	4.0017767E-11	39.875004	14
CGGGACT	50	4.0017767E-11	39.875004	16
GGGACTC	50	4.0017767E-11	39.875004	17
CAGATCG	50	4.0017767E-11	39.875004	11
TCGGGAC	50	4.0017767E-11	39.875004	15
GTGCAGA	55	1.8189894E-12	39.875	8
CTTGGTG	55	1.8189894E-12	39.875	4
GCAGATC	55	1.8189894E-12	39.875	10
TTGGTGC	55	1.8189894E-12	39.875	5
TGGTGCA	55	1.8189894E-12	39.875	6
TGCAGAT	55	1.8189894E-12	39.875	9
GGTGCAG	55	1.8189894E-12	39.875	7
TGCTTGG	80	0.0	37.382812	40
GGACTCG	60	5.456968E-12	36.552082	18
GACTCGT	60	5.456968E-12	36.552082	19
GATCGGG	55	1.1277734E-10	36.25	13
AGATCGG	55	1.1277734E-10	36.25	12
>>END_MODULE
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647706 spots for SRR1033815.sra
Written 647706 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
Read 647697 spots for SRR1033815.sra
Written 647697 spots for SRR1033815.sra
SRR ids: ['SRR1033815.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_a2wwwiq0
SRR1033815.sra spots: 12953949
blocks: [[1, 647697], [647698, 1295394], [1295395, 1943091], [1943092, 2590788], [2590789, 3238485], [3238486, 3886182], [3886183, 4533879], [4533880, 5181576], [5181577, 5829273], [5829274, 6476970], [6476971, 7124667], [7124668, 7772364], [7772365, 8420061], [8420062, 9067758], [9067759, 9715455], [9715456, 10363152], [10363153, 11010849], [11010850, 11658546], [11658547, 12306243], [12306244, 12953949]]
SRR1033815 file size 1934521
SRR1033815 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 SRR1033815 SRR1033815_1.fastq
Input file:	SRR1033815_1.fastq
trimmed:	SRR1033815-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 01:09:03 2024 >> started

Sat Dec  7 01:09:12 2024 >> done (8.397s)
12953949 reads processed; of these:
  107649 ( 0.83%) short reads filtered out after trimming by size control
   25134 ( 0.19%) empty reads filtered out after trimming by size control
12821166 (98.97%) reads available; of these:
 5516798 (43.03%) trimmed reads available after processing
 7304368 (56.97%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	   27704	  0.22%
 19	   40091	  0.31%
 20	   52052	  0.41%
 21	   52153	  0.41%
 22	   46269	  0.36%
 23	   41657	  0.32%
 24	   54780	  0.43%
 25	   42666	  0.33%
 26	   50834	  0.40%
 27	   49554	  0.39%
 28	   37813	  0.29%
 29	   36433	  0.28%
 30	   46504	  0.36%
 31	   66823	  0.52%
 32	   45640	  0.36%
 33	   59034	  0.46%
 34	   56870	  0.44%
 35	   59931	  0.47%
 36	   93245	  0.73%
 37	  170635	  1.33%
 38	  219150	  1.71%
 39	  202103	  1.58%
 40	  378204	  2.95%
 41	  426026	  3.32%
 42	  452654	  3.53%
 43	  676070	  5.27%
 44	 1264932	  9.87%
 45	  766971	  5.98%
 46	 7304368	 56.97%
12821166 reads passed initial QC


criterion=sequence-density
sequence-density=89.07
sequence-density-rank=1
fanout-score=21.33
fanout-score-rank=4
prefix-density=91.13
prefix-fanout=20.9
sequence=TCGTATGCCGTCTTCTGCTTGAAAAACAA


criterion=fanout-score
sequence-density=1.53
sequence-density-rank=7
fanout-score=56.94
fanout-score-rank=1
prefix-density=85.88
prefix-fanout=1.0
sequence=TGCCGTCTTCTTCTTGAAAAA
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 TCGTATGCCGTCTTCTGCTTGAAAAACAA -o SRR1033815 -
Input file:	STDIN
trimmed:	SRR1033815-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TCGTATGCCGTCTTCTGCTTGAAAAACAA
-- 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 01:09:27 2024 >> started

Sat Dec  7 01:09:42 2024 >> done (14.998s)
12536251 reads processed; of these:
   45208 ( 0.36%) short reads filtered out after trimming by size control
    7277 ( 0.06%) empty reads filtered out after trimming by size control
12483766 (99.58%) reads available; of these:
12083210 (96.79%) trimmed reads available after processing
  400556 ( 3.21%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  232962	  1.87%
 19	  469753	  3.76%
 20	 2128651	 17.05%
 21	 2830911	 22.68%
 22	  819273	  6.56%
 23	 1176170	  9.42%
 24	 3689067	 29.55%
 25	  630507	  5.05%
 26	  385129	  3.09%
 27	   65593	  0.53%
 28	    7588	  0.06%
 29	    2369	  0.02%
 30	    1017	  0.01%
 31	    1086	  0.01%
 32	     533	  0.00%
 33	     613	  0.00%
 34	     378	  0.00%
 35	     438	  0.00%
 36	     575	  0.00%
 37	     800	  0.01%
 38	     892	  0.01%
 39	     682	  0.01%
 40	     799	  0.01%
 41	     806	  0.01%
 42	     645	  0.01%
 43	     823	  0.01%
 44	    1156	  0.01%
 45	     878	  0.01%
 46	   33672	  0.27%


criterion=sequence-density
sequence-density=9.01
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=9
prefix-density=0.00
prefix-fanout=1.0
sequence=TCGCTTGGTGCAGATCGGGACTCGT


criterion=fanout-score
sequence-density=0.15
sequence-density-rank=14
fanout-score=6.54
fanout-score-rank=1
prefix-density=0.31
prefix-fanout=3.2
sequence=ATAGCTCAGTTGG
                                 Started job on |	Dec 07 01:09:58
                             Started mapping on |	Dec 07 01:09:58
                                    Finished on |	Dec 07 01:10:40
       Mapping speed, Million of reads per hour |	1094.46

                          Number of input reads |	12768681
                      Average input read length |	22
                                    UNIQUE READS:
                   Uniquely mapped reads number |	4607784
                        Uniquely mapped reads % |	36.09%
                          Average mapped length |	22.42
                       Number of splices: Total |	70024
            Number of splices: Annotated (sjdb) |	8500
                       Number of splices: GT/AG |	69049
                       Number of splices: GC/AG |	783
                       Number of splices: AT/AC |	6
               Number of splices: Non-canonical |	186
                      Mismatch rate per base, % |	0.31%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.08
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.01
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	4204219
             % of reads mapped to multiple loci |	32.93%
        Number of reads mapped to too many loci |	3420566
             % of reads mapped to too many loci |	26.79%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	3.09%
                     % of reads unmapped: other |	1.11%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	3956678	3956678	3956678
N_multimapping	4204219	4204219	4204219
N_noFeature	2682713	2860030	4420376
N_ambiguous	14869	3889	1343
UnstrandedReadsAssigned:1910202 PositiveStrandReadsAssigned:1743865 NegativeStrandReadsAssigned:186065
Dataset is classified positive stranded
MeadianReadLen=22 20thPercentileLength=20 echo kmer=19
SRR1033815 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: SRR1033815-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 12,768,681 reads, 4,163,800 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 989 rounds

  52973 SRR1033815.ke.tsv
  35125 SRR1033815.se.tsv
  88098 total
==> SRR1033815.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	0	0
PNS24249	1928	1829	2.22839	0.0428434
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	3.77161	0.096667
PNS24243	293	194	0	0
KQK14069	1603	1504	70.4096	1.64623
KQK14071	474	375	22.1466	2.07674

==> SRR1033815.se.tsv <==
BRADI_1g14170v3	99
BRADI_1g53295v3	1
BRADI_1g59795v3	0
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	7
BRADI_1g74790v3	17
BRADI_1g09890v3	1
BRADI_1g77505v3	0
BRADI_1g48960v3	0
SRR1033815 completed mapping pipeline successfully
