Starting /dee2/code/volunteer_pipeline.sh SRR6892964
    current disk space = 1550669144064
    free memory = 1603353584 
SRR6892964 SRAfilesize
762fc61f465c9300faee97341b1d1644  SRR6892964.sra
SRR6892964.sra file validated
SRR6892964 is single end
SRR6892964 is conventional basespace
SRR6892964 read1 length is 50 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR6892964_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	50
%GC	52
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	32.4125	34.0	31.0	34.0	31.0	34.0
2	32.73925	34.0	31.0	34.0	31.0	34.0
3	32.85875	34.0	31.0	34.0	31.0	34.0
4	36.3285	37.0	37.0	37.0	35.0	37.0
5	36.25975	37.0	37.0	37.0	35.0	37.0
6	36.25775	37.0	37.0	37.0	35.0	37.0
7	36.19525	37.0	37.0	37.0	35.0	37.0
8	36.24875	37.0	37.0	37.0	35.0	37.0
9	38.10575	39.0	39.0	39.0	37.0	39.0
10	38.08475	39.0	39.0	39.0	37.0	39.0
11	38.021	39.0	39.0	39.0	35.0	39.0
12	38.078	39.0	39.0	39.0	35.0	39.0
13	37.97125	39.0	38.0	39.0	35.0	39.0
14	39.35275	41.0	39.0	41.0	36.0	41.0
15	39.50775	41.0	39.0	41.0	36.0	41.0
16	39.45525	41.0	39.0	41.0	36.0	41.0
17	39.50525	41.0	39.0	41.0	36.0	41.0
18	39.30025	41.0	39.0	41.0	36.0	41.0
19	39.46675	41.0	39.0	41.0	36.0	41.0
20	39.4105	41.0	39.0	41.0	36.0	41.0
21	39.24625	41.0	39.0	41.0	36.0	41.0
22	39.223	41.0	39.0	41.0	36.0	41.0
23	40.0965	41.0	40.0	41.0	39.0	41.0
24	39.50425	41.0	40.0	41.0	37.0	41.0
25	40.17375	41.0	40.0	41.0	39.0	41.0
26	39.88425	41.0	40.0	41.0	38.0	41.0
27	40.36825	41.0	40.0	41.0	39.0	41.0
28	39.547	41.0	40.0	41.0	37.0	41.0
29	39.01325	41.0	39.0	41.0	35.0	41.0
30	39.07325	41.0	39.0	41.0	36.0	41.0
31	39.0645	41.0	39.0	41.0	36.0	41.0
32	40.038	41.0	40.0	41.0	39.0	41.0
33	40.15425	41.0	40.0	41.0	40.0	41.0
34	35.1535	37.0	33.0	40.0	28.0	41.0
35	35.12175	37.0	34.0	39.0	30.0	39.0
36	37.15675	39.0	37.0	40.0	32.0	40.0
37	39.0375	40.0	39.0	41.0	37.0	41.0
38	38.7895	40.0	39.0	41.0	35.0	41.0
39	39.37875	40.0	39.0	41.0	37.0	41.0
40	39.212	41.0	40.0	41.0	36.0	41.0
41	39.74575	41.0	40.0	41.0	38.0	41.0
42	38.23325	40.0	38.0	41.0	34.0	41.0
43	38.779	40.0	38.0	41.0	36.0	41.0
44	39.0355	40.0	39.0	41.0	36.0	41.0
45	39.21825	41.0	40.0	41.0	36.0	41.0
46	39.3665	41.0	40.0	41.0	37.0	41.0
47	39.631	41.0	40.0	41.0	37.0	41.0
48	38.50575	41.0	38.0	41.0	35.0	41.0
49	37.281	40.0	37.0	41.0	33.0	41.0
50	36.407	39.0	36.0	40.0	31.0	41.0
>>END_MODULE
>>Per tile sequence quality	pass
#Tile	Base	Mean
1101	1	0.0
1101	2	0.0
1101	3	0.0
1101	4	0.0
1101	5	0.0
1101	6	0.0
1101	7	0.0
1101	8	0.0
1101	9	0.0
1101	10	0.0
1101	11	0.0
1101	12	0.0
1101	13	0.0
1101	14	0.0
1101	15	0.0
1101	16	0.0
1101	17	0.0
1101	18	0.0
1101	19	0.0
1101	20	0.0
1101	21	0.0
1101	22	0.0
1101	23	0.0
1101	24	0.0
1101	25	0.0
1101	26	0.0
1101	27	0.0
1101	28	0.0
1101	29	0.0
1101	30	0.0
1101	31	0.0
1101	32	0.0
1101	33	0.0
1101	34	0.0
1101	35	0.0
1101	36	0.0
1101	37	0.0
1101	38	0.0
1101	39	0.0
1101	40	0.0
1101	41	0.0
1101	42	0.0
1101	43	0.0
1101	44	0.0
1101	45	0.0
1101	46	0.0
1101	47	0.0
1101	48	0.0
1101	49	0.0
1101	50	0.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
12	1.0
13	1.0
14	2.0
15	2.0
16	0.0
17	1.0
18	2.0
19	2.0
20	4.0
21	2.0
22	3.0
23	1.0
24	6.0
25	8.0
26	10.0
27	13.0
28	16.0
29	15.0
30	19.0
31	28.0
32	33.0
33	49.0
34	78.0
35	140.0
36	230.0
37	368.0
38	665.0
39	2301.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	16.603678508440414	23.507180650037792	26.35424540186445	33.53489543965734
2	18.625	27.750000000000004	26.474999999999998	27.150000000000002
3	23.674999999999997	20.05	23.175	33.1
4	29.975	21.55	23.549999999999997	24.925
5	24.675	30.4	24.025	20.9
6	25.874999999999996	20.125	24.6	29.4
7	23.799999999999997	21.175	34.925	20.1
8	21.525	21.0	28.749999999999996	28.725
9	23.95	19.400000000000002	34.875	21.775
10	24.3	19.55	26.174999999999997	29.975
11	31.025000000000002	21.15	25.624999999999996	22.2
12	34.175	20.674999999999997	25.324999999999996	19.825
13	24.85	21.675	24.65	28.825
14	26.174999999999997	30.175	23.175	20.474999999999998
15	26.724999999999998	30.349999999999998	23.575	19.35
16	23.549999999999997	26.375	22.975	27.1
17	30.475	24.5	23.225	21.8
18	34.975	22.425	19.925	22.675
19	25.624999999999996	36.8	19.400000000000002	18.175
20	23.75	25.95	29.4	20.9
21	8.3	9.175	70.875	11.65
22	61.3	0.75	37.9	0.05
23	98.15	1.375	0.42500000000000004	0.05
24	37.8	61.25000000000001	0.8500000000000001	0.1
25	0.05	98.125	1.4500000000000002	0.375
26	0.075	37.85	61.550000000000004	0.525
27	0.15	0.0	98.6	1.25
28	0.44999999999999996	0.025	38.9	60.62499999999999
29	0.8750000000000001	0.0	60.3	38.824999999999996
30	1.825	0.0	37.925	60.25
31	61.7	0.05	0.375	37.875
32	99.3	0.05	0.44999999999999996	0.2
33	98.3	0.17500000000000002	1.0999999999999999	0.42500000000000004
34	40.175	0.2	58.8	0.8250000000000001
35	61.050000000000004	0.42500000000000004	36.875	1.6500000000000001
36	37.775	0.8250000000000001	0.075	61.324999999999996
37	0.475	1.8499999999999999	0.075	97.6
38	0.8250000000000001	61.35	0.0	37.824999999999996
39	2.0	97.82499999999999	0.05	0.125
40	61.175000000000004	38.525	0.15	0.15
41	97.175	2.15	0.15	0.525
42	37.574999999999996	61.175000000000004	0.5499999999999999	0.7000000000000001
43	0.15	96.975	0.7000000000000001	2.175
44	0.075	37.5	1.775	60.650000000000006
45	0.125	0.5	59.599999999999994	39.775
46	0.44999999999999996	0.7250000000000001	37.375	61.45
47	0.625	1.825	0.5499999999999999	97.0
48	1.775	59.4	0.8500000000000001	37.974999999999994
49	59.361648655441066	37.748177934154306	1.9351595878361396	0.9550138225684845
50	37.425000000000004	1.0	58.975	2.6
>>END_MODULE
>>Per sequence GC content	fail
#GC Content	Count
0	0.0
1	0.0
2	0.0
3	0.0
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
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	0.0
26	0.0
27	0.0
28	0.0
29	0.0
30	0.0
31	0.0
32	0.0
33	2.0
34	4.0
35	5.0
36	6.0
37	13.0
38	20.0
39	35.0
40	50.0
41	80.5
42	111.0
43	153.5
44	196.0
45	264.5
46	333.0
47	373.0
48	413.0
49	437.0
50	461.0
51	454.0
52	447.0
53	461.0
54	475.0
55	576.5
56	678.0
57	497.0
58	316.0
59	278.5
60	241.0
61	183.5
62	126.0
63	93.0
64	60.0
65	47.5
66	35.0
67	28.0
68	21.0
69	13.5
70	6.0
71	3.5
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	0.0
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	0.775
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	0.0
26	0.0
27	0.0
28	0.0
29	0.0
30	0.0
31	0.0
32	0.0
33	0.0
34	0.0
35	0.0
36	0.0
37	0.0
38	0.0
39	0.0
40	0.0
41	0.0
42	0.0
43	0.0
44	0.0
45	0.0
46	0.0
47	0.0
48	0.0
49	0.525
50	0.0
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
50	4000.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	84.775
#Duplication Level	Percentage of deduplicated	Percentage of total
1	98.37805956944854	83.39999999999999
2	0.7962253022707166	1.35
3	0.29489826010026543	0.75
4	0.0	0.0
5	0.08846947803007962	0.375
6	0.029489826010026542	0.15
7	0.058979652020053085	0.35000000000000003
8	0.0	0.0
9	0.0	0.0
>10	0.32438808611029196	6.175
>50	0.0	0.0
>100	0.029489826010026542	7.449999999999999
>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
CACGACTCTCGGCAACGGATTGGAATTCTCGGGTGCCAAGGAACTCCAGT	298	7.449999999999999	RNA PCR Primer, Index 1 (100% over 30bp)
TACCTGGTTGATCCTGCCAGTGGAATTCTCGGGTGCCAAGGAACTCCAGT	50	1.25	RNA PCR Primer, Index 1 (100% over 30bp)
CGACACGACTCTCGGCAACGGTGGAATTCTCGGGTGCCAAGGAACTCCAG	36	0.8999999999999999	RNA PCR Primer, Index 1 (100% over 29bp)
TCCCGCGCGCTGTGGACCTTTGGAATTCTCGGGTGCCAAGGAACTCCAGT	25	0.625	RNA PCR Primer, Index 1 (100% over 30bp)
GACACGACTCTCGGCAACGGATGGAATTCTCGGGTGCCAAGGAACTCCAG	25	0.625	RNA PCR Primer, Index 1 (100% over 29bp)
ACACGACTCTCGGCAACGGATGGAATTCTCGGGTGCCAAGGAACTCCAGT	24	0.6	RNA PCR Primer, Index 1 (100% over 30bp)
GACACGACTCTCGGCAACGGTGGAATTCTCGGGTGCCAAGGAACTCCAGT	18	0.44999999999999996	RNA PCR Primer, Index 1 (100% over 30bp)
TCCCGCGCGCTGTGGACCTTCTGGAATTCTCGGGTGCCAAGGAACTCCAG	17	0.42500000000000004	RNA PCR Primer, Index 1 (100% over 29bp)
TACCTGGTTGATCCTGCCAGTTGGAATTCTCGGGTGCCAAGGAACTCCAG	15	0.375	RNA PCR Primer, Index 1 (100% over 29bp)
ACGACTCTCGGCAACGGATATTGGAATTCTCGGGTGCCAAGGAACTCCAG	15	0.375	RNA PCR Primer, Index 1 (100% over 29bp)
CACGACTCTCGGCAACGGATTGGAATTCTCGGGGGCCAAGGAACTCCAGT	11	0.27499999999999997	RNA PCR Primer, Index 1 (96% over 30bp)
ACACGACTCTCGGCAACGGATTGGAATTCTCGGGTGCCAAGGAACTCCAG	11	0.27499999999999997	RNA PCR Primer, Index 1 (100% over 29bp)
TAAGTGGGAGCCTTTACGGGCTGGAATTCTCGGGTGCCAAGGAACTCCAG	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 29bp)
CGACACGACTCTCGGCAACGTGGAATTCTCGGGTGCCAAGGAACTCCAGT	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 30bp)
TTCACACAATTGGTCATCGCTGGAATTCTCGGGTGCCAAGGAACTCCAGT	6	0.15	RNA PCR Primer, Index 1 (100% over 30bp)
TTACGGTGCCCAACTGCGCGCTGGAATTCTCGGGTGCCAAGGAACTCCAG	5	0.125	RNA PCR Primer, Index 1 (100% over 29bp)
NACGACTCTCGGCAACGGATTGGAATTCTCGGGTGCCAAGGAACTCCAGT	5	0.125	RNA PCR Primer, Index 1 (100% over 30bp)
ACCGTGCCGCGATAGTAATTCTGGAATTCTCGGGTGCCAAGGAACTCCAG	5	0.125	RNA PCR Primer, Index 1 (100% over 29bp)
>>END_MODULE
>>Adapter Content	fail
#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	0.05	0.0	0.0	0.0
17	0.0	0.125	0.0	0.0	0.0
18	0.0	0.4	0.0	0.0	0.0
19	0.0	0.8	0.0	0.0	0.0
20	0.0	1.7	0.0	0.0	0.0
21	0.0	61.475	0.0	0.0	0.0
22	0.0	98.9	0.0	0.0	0.0
23	0.0	98.9	0.0	0.0	0.0
24	0.0	98.9	0.0	0.0	0.0
25	0.0	98.9	0.0	0.0	0.0
26	0.0	98.9	0.0	0.0	0.0
27	0.0	98.9	0.0	0.0	0.0
28	0.0	98.9	0.0	0.0	0.0
29	0.0	98.9	0.0	0.0	0.0
30	0.0	98.9	0.0	0.0	0.0
31	0.0	98.9	0.0	0.0	0.0
32	0.0	98.9	0.0	0.0	0.0
33	0.0	98.9	0.0	0.0	0.0
34	0.0	98.9	0.0	0.0	0.0
35	0.0	98.9	0.0	0.0	0.0
36	0.0	98.9	0.0	0.0	0.0
37	0.0	98.9	0.0	0.0	0.0
38	0.0	98.9	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	fail
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GGATTGG	40	5.315087E-9	44.000004	17
CGGATTG	40	5.315087E-9	44.000004	16
GATTGGA	40	5.315087E-9	44.000004	18
ACGGATT	45	1.506669E-8	39.111115	15
CTCCAGT	260	0.0	38.92308	44
ATTGGAA	55	1.9645086E-9	36.0	19
CACGACT	50	3.81915E-8	35.2	1
GACTGGA	25	0.002084305	35.2	18
ACTGGAA	50	3.81915E-8	35.2	19
GGCAACG	55	8.843199E-8	32.0	11
TCGGCAA	55	8.843199E-8	32.0	9
CTCTCGG	55	8.843199E-8	32.0	6
ACTCTCG	55	8.843199E-8	32.0	5
GCAACGG	55	8.843199E-8	32.0	12
TCTCGGC	55	8.843199E-8	32.0	7
CTGGAAT	110	0.0	32.0	20
CTCGGCA	55	8.843199E-8	32.0	8
CGGCAAC	55	8.843199E-8	32.0	10
AACGGAT	55	8.843199E-8	32.0	14
GACTCTC	55	8.843199E-8	32.0	4
>>END_MODULE
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550537 spots for SRR6892964.sra
Written 1550537 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
Read 1550530 spots for SRR6892964.sra
Written 1550530 spots for SRR6892964.sra
SRR ids: ['SRR6892964.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_o27qvhrp
SRR6892964.sra spots: 31010607
blocks: [[1, 1550530], [1550531, 3101060], [3101061, 4651590], [4651591, 6202120], [6202121, 7752650], [7752651, 9303180], [9303181, 10853710], [10853711, 12404240], [12404241, 13954770], [13954771, 15505300], [15505301, 17055830], [17055831, 18606360], [18606361, 20156890], [20156891, 21707420], [21707421, 23257950], [23257951, 24808480], [24808481, 26359010], [26359011, 27909540], [27909541, 29460070], [29460071, 31010607]]
SRR6892964 file size 5364019
SRR6892964 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 SRR6892964 SRR6892964_1.fastq
Input file:	SRR6892964_1.fastq
trimmed:	SRR6892964-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
Fri Dec  6 13:54:42 2024 >> started

Fri Dec  6 13:55:03 2024 >> done (20.393s)
31010607 reads processed; of these:
   12959 ( 0.04%) short reads filtered out after trimming by size control
      14 ( 0.00%) empty reads filtered out after trimming by size control
30997634 (99.96%) reads available; of these:
 1275316 ( 4.11%) trimmed reads available after processing
29722318 (95.89%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	   10430	  0.03%
 19	   12313	  0.04%
 20	   10244	  0.03%
 21	    3383	  0.01%
 22	    1877	  0.01%
 23	    6073	  0.02%
 24	    4099	  0.01%
 25	    5183	  0.02%
 26	    7101	  0.02%
 27	   29626	  0.10%
 28	    4330	  0.01%
 29	    1798	  0.01%
 30	    2226	  0.01%
 31	    3243	  0.01%
 32	    9848	  0.03%
 33	   50786	  0.16%
 34	   23327	  0.08%
 35	   26358	  0.09%
 36	   19130	  0.06%
 37	   28433	  0.09%
 38	   16389	  0.05%
 39	   15089	  0.05%
 40	   10152	  0.03%
 41	   39342	  0.13%
 42	   16873	  0.05%
 43	   77249	  0.25%
 44	   28068	  0.09%
 45	   13751	  0.04%
 46	   36451	  0.12%
 47	  409520	  1.32%
 48	  231789	  0.75%
 49	  120835	  0.39%
 50	29722318	 95.89%
30997634 reads passed initial QC


criterion=sequence-density
sequence-density=98.59
sequence-density-rank=1
fanout-score=31.97
fanout-score-rank=4
prefix-density=98.89
prefix-fanout=31.9
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACACAGTGATCTCGTATGC


criterion=fanout-score
sequence-density=1.91
sequence-density-rank=4
fanout-score=195.99
fanout-score-rank=1
prefix-density=98.84
prefix-fanout=3.8
sequence=GAATTCTCGGGGGCCAAGGAACT
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACACAGTGATCTCGTATGC -o SRR6892964 -
Input file:	STDIN
trimmed:	SRR6892964-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACACAGTGATCTCGTATGC
-- 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
Fri Dec  6 13:55:43 2024 >> started

Fri Dec  6 13:56:20 2024 >> done (37.156s)
30371419 reads processed; of these:
  143965 ( 0.47%) short reads filtered out after trimming by size control
    2765 ( 0.01%) empty reads filtered out after trimming by size control
30224689 (99.52%) reads available; of these:
30029767 (99.36%) trimmed reads available after processing
  194922 ( 0.64%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  144001	  0.48%
 19	  234000	  0.77%
 20	17968964	 59.45%
 21	11661140	 38.58%
 22	   38664	  0.13%
 23	    9462	  0.03%
 24	    2366	  0.01%
 25	    2058	  0.01%
 26	    1359	  0.00%
 27	    3092	  0.01%
 28	     620	  0.00%
 29	     820	  0.00%
 30	     792	  0.00%
 31	     373	  0.00%
 32	     618	  0.00%
 33	    1011	  0.00%
 34	    2955	  0.01%
 35	   11802	  0.04%
 36	   10746	  0.04%
 37	    4410	  0.01%
 38	    1637	  0.01%
 39	    1411	  0.00%
 40	     676	  0.00%
 41	    5946	  0.02%
 42	    4214	  0.01%
 43	    1585	  0.01%
 44	    1342	  0.00%
 45	    1117	  0.00%
 46	    1451	  0.00%
 47	    1352	  0.00%
 48	    1472	  0.00%
 49	    1358	  0.00%
 50	  101875	  0.34%


criterion=sequence-density
sequence-density=1.72
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=11
prefix-density=0.00
prefix-fanout=1.0
sequence=TACCTGGTTGATCCTGCCAGT


criterion=fanout-score
sequence-density=0.09
sequence-density-rank=6
fanout-score=79.54
fanout-score-rank=1
prefix-density=0.28
prefix-fanout=24.2
sequence=TGGAATTCTCGTATGCCGTCTTCTGCTTGAA
                                 Started job on |	Dec 06 13:56:40
                             Started mapping on |	Dec 06 13:56:40
                                    Finished on |	Dec 06 13:57:48
       Mapping speed, Million of reads per hour |	1633.28

                          Number of input reads |	30850904
                      Average input read length |	21
                                    UNIQUE READS:
                   Uniquely mapped reads number |	22073719
                        Uniquely mapped reads % |	71.55%
                          Average mapped length |	20.32
                       Number of splices: Total |	465905
            Number of splices: Annotated (sjdb) |	440423
                       Number of splices: GT/AG |	460729
                       Number of splices: GC/AG |	4950
                       Number of splices: AT/AC |	161
               Number of splices: Non-canonical |	65
                      Mismatch rate per base, % |	0.07%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.08
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.00
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	2330276
             % of reads mapped to multiple loci |	7.55%
        Number of reads mapped to too many loci |	5616606
             % of reads mapped to too many loci |	18.21%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	2.54%
                     % of reads unmapped: other |	0.16%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	6446909	6446909	6446909
N_multimapping	2330276	2330276	2330276
N_noFeature	1191997	1441787	21315444
N_ambiguous	529094	20551	2366
UnstrandedReadsAssigned:20352628 PositiveStrandReadsAssigned:20611381 NegativeStrandReadsAssigned:755909
Dataset is classified positive stranded
MeadianReadLen=20 20thPercentileLength=20 echo kmer=19
SRR6892964 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: SRR6892964-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 30,850,904 reads, 19,935,811 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,209 rounds

  52973 SRR6892964.ke.tsv
  35125 SRR6892964.se.tsv
  88098 total
==> SRR6892964.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	1.23612	0.0927664
PNS24249	1928	1829	52.0473	2.01811
PNS24246	1044	945	1.23612	0.0927664
PNS24248	1044	945	1.23612	0.0927664
PNS24244	1471	1372	658.368	34.031
PNS24243	293	194	3	1.09668
KQK14069	1603	1504	5669.74	267.348
KQK14071	474	375	23.7118	4.48429

==> SRR6892964.se.tsv <==
BRADI_1g14170v3	5602
BRADI_1g53295v3	18
BRADI_1g59795v3	43
BRADI_1g07683v3	0
BRADI_1g00485v3	14
BRADI_1g20270v3	287
BRADI_1g74790v3	522
BRADI_1g09890v3	11
BRADI_1g77505v3	132
BRADI_1g48960v3	1
SRR6892964 completed mapping pipeline successfully
