Starting /dee2/code/volunteer_pipeline.sh SRR11216162
    current disk space = 1526762520576
    free memory = 1532449592 
SRR11216162 SRAfilesize
5c91999feca3ef2190d208060a429b35  SRR11216162.sra
SRR11216162.sra file validated
SRR11216162 is single end
SRR11216162 is conventional basespace
SRR11216162 read1 length is 101 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR11216162_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	101
%GC	50
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	32.3405	33.0	33.0	33.0	33.0	33.0
2	32.453	33.0	33.0	33.0	33.0	33.0
3	32.499	33.0	33.0	33.0	33.0	33.0
4	32.478	33.0	33.0	33.0	33.0	33.0
5	32.52925	33.0	33.0	33.0	33.0	33.0
6	35.61825	37.0	37.0	37.0	37.0	37.0
7	36.21875	37.0	37.0	37.0	37.0	37.0
8	36.2665	37.0	37.0	37.0	37.0	37.0
9	36.38375	37.0	37.0	37.0	37.0	37.0
10-11	36.417625	37.0	37.0	37.0	37.0	37.0
12-13	36.484125	37.0	37.0	37.0	37.0	37.0
14-15	36.438125	37.0	37.0	37.0	37.0	37.0
16-17	36.416375	37.0	37.0	37.0	37.0	37.0
18-19	36.434124999999995	37.0	37.0	37.0	37.0	37.0
20-21	36.461875000000006	37.0	37.0	37.0	37.0	37.0
22-23	36.394000000000005	37.0	37.0	37.0	37.0	37.0
24-25	36.427375	37.0	37.0	37.0	37.0	37.0
26-27	36.39725	37.0	37.0	37.0	37.0	37.0
28-29	36.400875	37.0	37.0	37.0	37.0	37.0
30-31	36.314125	37.0	37.0	37.0	37.0	37.0
32-33	36.3215	37.0	37.0	37.0	37.0	37.0
34-35	36.327875	37.0	37.0	37.0	37.0	37.0
36-37	36.334500000000006	37.0	37.0	37.0	37.0	37.0
38-39	36.3575	37.0	37.0	37.0	37.0	37.0
40-41	36.32275	37.0	37.0	37.0	37.0	37.0
42-43	36.35425	37.0	37.0	37.0	37.0	37.0
44-45	36.24675	37.0	37.0	37.0	37.0	37.0
46-47	36.335625	37.0	37.0	37.0	37.0	37.0
48-49	36.361000000000004	37.0	37.0	37.0	37.0	37.0
50-51	36.389125	37.0	37.0	37.0	37.0	37.0
52-53	36.389125	37.0	37.0	37.0	37.0	37.0
54-55	36.313625	37.0	37.0	37.0	37.0	37.0
56-57	36.336625	37.0	37.0	37.0	37.0	37.0
58-59	36.279125	37.0	37.0	37.0	37.0	37.0
60-61	36.30925	37.0	37.0	37.0	37.0	37.0
62-63	36.26649999999999	37.0	37.0	37.0	37.0	37.0
64-65	36.2785	37.0	37.0	37.0	37.0	37.0
66-67	36.259125	37.0	37.0	37.0	37.0	37.0
68-69	36.262625	37.0	37.0	37.0	37.0	37.0
70-71	36.256625	37.0	37.0	37.0	37.0	37.0
72-73	36.182249999999996	37.0	37.0	37.0	37.0	37.0
74-75	36.198875	37.0	37.0	37.0	37.0	37.0
76-77	36.1745	37.0	37.0	37.0	37.0	37.0
78-79	36.152	37.0	37.0	37.0	37.0	37.0
80-81	36.034375	37.0	37.0	37.0	37.0	37.0
82-83	36.131125	37.0	37.0	37.0	37.0	37.0
84-85	36.119625	37.0	37.0	37.0	37.0	37.0
86-87	36.038125	37.0	37.0	37.0	37.0	37.0
88-89	35.986125	37.0	37.0	37.0	37.0	37.0
90-91	35.917625	37.0	37.0	37.0	37.0	37.0
92-93	35.871125000000006	37.0	37.0	37.0	37.0	37.0
94-95	35.839375000000004	37.0	37.0	37.0	37.0	37.0
96-97	35.826499999999996	37.0	37.0	37.0	37.0	37.0
98-99	35.725750000000005	37.0	37.0	37.0	37.0	37.0
100-101	33.971375	37.0	35.0	37.0	27.5	37.0
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
2	9.0
3	0.0
4	0.0
5	0.0
6	0.0
7	0.0
8	0.0
9	0.0
10	2.0
11	0.0
12	2.0
13	1.0
14	0.0
15	0.0
16	1.0
17	0.0
18	0.0
19	1.0
20	2.0
21	1.0
22	5.0
23	6.0
24	8.0
25	7.0
26	7.0
27	8.0
28	23.0
29	14.0
30	43.0
31	40.0
32	50.0
33	86.0
34	115.0
35	230.0
36	3339.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	38.909821652851036	8.389851796031147	6.932931424265259	45.76739512685255
2	24.175	11.95	35.825	28.050000000000004
3	23.400000000000002	16.225	22.175	38.2
4	28.075	24.525	19.625	27.775
5	28.125	28.675	23.025000000000002	20.175
6	23.695596843980656	31.6110969712395	23.237465003817764	21.455841180962075
7	19.2	22.650000000000002	39.875	18.275
8	21.099999999999998	21.75	31.374999999999996	25.775
9	19.725	20.875	34.300000000000004	25.1
10-11	24.4	28.275	23.45	23.875
12-13	23.6875	21.825	28.025	26.4625
14-15	24.325	24.025	26.924999999999997	24.725
16-17	24.0375	24.9375	25.825	25.2
18-19	24.125	24.625	24.65	26.6
20-21	24.3	24.474999999999998	25.624999999999996	25.6
22-23	23.525	24.4125	25.7375	26.325
24-25	24.474999999999998	24.625	24.55	26.35
26-27	23.6625	24.25	25.8125	26.275
28-29	24.6625	24.525	24.5125	26.3
30-31	24.2	24.462500000000002	24.9875	26.35
32-33	23.4125	23.9	25.650000000000002	27.037499999999998
34-35	25.2625	23.849999999999998	24.55	26.337500000000002
36-37	24.712500000000002	24.65	24.725	25.912499999999998
38-39	24.4375	24.349999999999998	25.337500000000002	25.874999999999996
40-41	25.174999999999997	24.2	24.6	26.025
42-43	24.4875	24.474999999999998	25.3	25.7375
44-45	24.825	23.825	25.587500000000002	25.7625
46-47	24.975	24.175	25.1875	25.662499999999998
48-49	23.799999999999997	24.15	25.025	27.025
50-51	24.1875	24.125	25.174999999999997	26.5125
52-53	24.087500000000002	24.462500000000002	24.762500000000003	26.687499999999996
54-55	24.349999999999998	24.2625	24.775	26.6125
56-57	23.925	23.8875	25.5625	26.625
58-59	23.775	24.5	25.525	26.200000000000003
60-61	24.212500000000002	24.1125	25.1	26.575
62-63	25.5625	24.075	23.974999999999998	26.387500000000003
64-65	24.675	24.2	25.1	26.025
66-67	25.15	23.8125	24.575	26.4625
68-69	24.375	23.5875	24.8	27.237499999999997
70-71	25.662499999999998	24.575	24.637500000000003	25.124999999999996
72-73	24.95	23.825	24.6875	26.5375
74-75	24.125	24.837500000000002	24.075	26.9625
76-77	24.425	24.85	24.575	26.150000000000002
78-79	24.425	23.525	24.962500000000002	27.0875
80-81	24.0375	24.75	25.7375	25.474999999999998
82-83	25.137500000000003	24.0625	23.599999999999998	27.200000000000003
84-85	24.9875	23.9	24.325	26.787499999999998
86-87	24.7	24.3125	24.762500000000003	26.224999999999998
88-89	25.268817204301076	24.256064016004	24.081020255063766	26.39409852463116
90-91	25.406351587896975	24.10602650662666	23.755938984746187	26.731682920730183
92-93	24.543635908977244	24.718679669917478	25.35633908477119	25.381345336334082
94-95	24.74059257407176	25.378172271533945	23.51543942992874	26.365795724465556
96-97	26.0375	24.712500000000002	22.662499999999998	26.5875
98-99	25.05939727397774	24.84681755658372	24.571714392897338	25.5220707765412
100-101	26.415801975246904	25.065633204150515	24.14051756469559	24.37804725590699
>>END_MODULE
>>Per sequence GC content	fail
#GC Content	Count
0	1.0
1	0.5
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	0.5
27	1.5
28	2.0
29	3.0
30	5.0
31	3.5
32	6.5
33	10.5
34	14.5
35	22.0
36	33.5
37	49.0
38	64.5
39	84.0
40	97.0
41	111.5
42	135.0
43	157.5
44	165.5
45	168.0
46	183.5
47	181.5
48	163.5
49	165.5
50	164.5
51	150.5
52	149.5
53	134.5
54	117.5
55	121.0
56	136.5
57	137.5
58	124.5
59	112.5
60	105.5
61	99.5
62	90.5
63	86.5
64	75.5
65	72.0
66	72.0
67	64.5
68	49.0
69	34.0
70	27.5
71	19.0
72	10.0
73	5.5
74	3.5
75	4.5
76	2.5
77	0.5
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	0.475
2	0.0
3	0.0
4	0.0
5	0.0
6	1.775
7	0.0
8	0.0
9	0.0
10-11	0.0
12-13	0.0
14-15	0.0
16-17	0.0
18-19	0.0
20-21	0.0
22-23	0.0
24-25	0.0
26-27	0.0
28-29	0.0
30-31	0.0
32-33	0.0
34-35	0.0
36-37	0.0
38-39	0.0
40-41	0.0
42-43	0.0
44-45	0.0
46-47	0.0
48-49	0.0
50-51	0.0
52-53	0.0
54-55	0.0
56-57	0.0
58-59	0.0
60-61	0.0
62-63	0.0
64-65	0.0
66-67	0.0
68-69	0.0
70-71	0.0
72-73	0.0
74-75	0.0
76-77	0.0
78-79	0.0
80-81	0.0
82-83	0.0
84-85	0.0
86-87	0.0
88-89	0.025
90-91	0.025
92-93	0.025
94-95	0.0125
96-97	0.0
98-99	0.0375
100-101	0.0125
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
101	4000.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	97.75
#Duplication Level	Percentage of deduplicated	Percentage of total
1	97.8772378516624	95.675
2	1.9948849104859334	3.9
3	0.10230179028132991	0.3
4	0.0	0.0
5	0.025575447570332477	0.125
6	0.0	0.0
7	0.0	0.0
8	0.0	0.0
9	0.0	0.0
>10	0.0	0.0
>50	0.0	0.0
>100	0.0	0.0
>500	0.0	0.0
>1k	0.0	0.0
>5k	0.0	0.0
>10k+	0.0	0.0
>>END_MODULE
>>Overrepresented sequences	warn
#Sequence	Count	Percentage	Possible Source
GTCGAACTTGCCGGAGACGAAGTCGTAGTGGCCGCCCACGAGCTTGAGGG	5	0.125	No Hit
>>END_MODULE
>>Adapter Content	pass
#Position	Illumina Universal Adapter	Illumina Small RNA 3' Adapter	Illumina Small RNA 5' Adapter	Nextera Transposase Sequence	SOLID Small RNA Adapter
1	0.0	0.0	0.0	0.0	0.0
2	0.0	0.0	0.0	0.0	0.0
3	0.0	0.0	0.0	0.0	0.0
4	0.0	0.0	0.0	0.0	0.0
5	0.0	0.0	0.0	0.0	0.0
6	0.0	0.0	0.0	0.0	0.0
7	0.0	0.0	0.0	0.0	0.0
8	0.0	0.0	0.0	0.0	0.0
9	0.0	0.0	0.0	0.0	0.0
10-11	0.0	0.0	0.0	0.0	0.0
12-13	0.0	0.0	0.0	0.0	0.0
14-15	0.0	0.0	0.0	0.0	0.0
16-17	0.0	0.0	0.0	0.0	0.0
18-19	0.0	0.0	0.0	0.0	0.0
20-21	0.0	0.0	0.0	0.0	0.0
22-23	0.0	0.0	0.0	0.0	0.0
24-25	0.0	0.0	0.0	0.0	0.0
26-27	0.0	0.0	0.0	0.0	0.0
28-29	0.0	0.0	0.0	0.0	0.0
30-31	0.0	0.0	0.0	0.0	0.0
32-33	0.0	0.0	0.0	0.0	0.0
34-35	0.0	0.0	0.0	0.0	0.0
36-37	0.0	0.0	0.0	0.0	0.0
38-39	0.0125	0.0	0.0	0.0	0.0
40-41	0.025	0.0	0.0	0.0	0.0
42-43	0.025	0.0	0.0	0.0	0.0
44-45	0.025	0.0	0.0	0.0	0.0
46-47	0.025	0.0	0.0	0.0	0.0
48-49	0.025	0.0	0.0	0.0	0.0
50-51	0.025	0.0	0.0	0.0	0.0
52-53	0.037500000000000006	0.0	0.0	0.0	0.0
54-55	0.05	0.0	0.0	0.0	0.0
56-57	0.05	0.0	0.0	0.0	0.0
58-59	0.075	0.0	0.0	0.0	0.0
60-61	0.1	0.0	0.0	0.0	0.0
62-63	0.125	0.0	0.0	0.0	0.0
64-65	0.15	0.0	0.0	0.0	0.0
66-67	0.2	0.0	0.0	0.0	0.0
68-69	0.2375	0.0	0.0	0.0	0.0
70-71	0.275	0.0	0.0	0.0	0.0
72-73	0.3125	0.0	0.0	0.0	0.0
74-75	0.325	0.0	0.0	0.0	0.0
76-77	0.4	0.0	0.0	0.0	0.0
78-79	0.5125	0.0	0.0	0.0	0.0
80-81	0.7375	0.0	0.0	0.0	0.0
82-83	0.95	0.0	0.0	0.0	0.0
84-85	1.3	0.0	0.0	0.0	0.0
86-87	1.775	0.0	0.0	0.0	0.0
88-89	2.275	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	pass
>>END_MODULE
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609892 READS because READLEN < 1
Read 1609892 spots for SRR11216162.sra
Written 1609892 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
Rejected 1609878 READS because READLEN < 1
Read 1609878 spots for SRR11216162.sra
Written 1609878 spots for SRR11216162.sra
SRR ids: ['SRR11216162.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_zfweu0_3
SRR11216162.sra spots: 32197574
blocks: [[1, 1609878], [1609879, 3219756], [3219757, 4829634], [4829635, 6439512], [6439513, 8049390], [8049391, 9659268], [9659269, 11269146], [11269147, 12879024], [12879025, 14488902], [14488903, 16098780], [16098781, 17708658], [17708659, 19318536], [19318537, 20928414], [20928415, 22538292], [22538293, 24148170], [24148171, 25758048], [25758049, 27367926], [27367927, 28977804], [28977805, 30587682], [30587683, 32197574]]
SRR11216162 file size 7776149
SRR11216162 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 SRR11216162 SRR11216162_1.fastq
Input file:	SRR11216162_1.fastq
trimmed:	SRR11216162-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
Tue Dec 10 08:31:26 2024 >> started

Tue Dec 10 08:31:42 2024 >> done (15.834s)
32197574 reads processed; of these:
   12949 ( 0.04%) short reads filtered out after trimming by size control
   37503 ( 0.12%) empty reads filtered out after trimming by size control
32147122 (99.84%) reads available; of these:
 3248502 (10.11%) trimmed reads available after processing
28898620 (89.89%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	     567	  0.00%
 19	     566	  0.00%
 20	     619	  0.00%
 21	     690	  0.00%
 22	     711	  0.00%
 23	     850	  0.00%
 24	    1034	  0.00%
 25	    1168	  0.00%
 26	    1079	  0.00%
 27	     996	  0.00%
 28	     959	  0.00%
 29	     937	  0.00%
 30	     964	  0.00%
 31	     972	  0.00%
 32	     973	  0.00%
 33	     972	  0.00%
 34	     966	  0.00%
 35	     941	  0.00%
 36	    1019	  0.00%
 37	    1109	  0.00%
 38	    1184	  0.00%
 39	    1213	  0.00%
 40	    1224	  0.00%
 41	    1361	  0.00%
 42	    1355	  0.00%
 43	    1401	  0.00%
 44	    1551	  0.00%
 45	    1679	  0.01%
 46	    1734	  0.01%
 47	    1866	  0.01%
 48	    1941	  0.01%
 49	    2173	  0.01%
 50	    2395	  0.01%
 51	    2811	  0.01%
 52	    2759	  0.01%
 53	    3009	  0.01%
 54	    3139	  0.01%
 55	    3315	  0.01%
 56	    3647	  0.01%
 57	    3917	  0.01%
 58	    4335	  0.01%
 59	    4748	  0.01%
 60	    5276	  0.02%
 61	    5929	  0.02%
 62	    6571	  0.02%
 63	    7311	  0.02%
 64	    8122	  0.03%
 65	    8894	  0.03%
 66	    9701	  0.03%
 67	   10887	  0.03%
 68	   12052	  0.04%
 69	   13261	  0.04%
 70	    2639	  0.01%
 71	    3063	  0.01%
 72	    3191	  0.01%
 73	    4825	  0.02%
 74	    3642	  0.01%
 75	    3845	  0.01%
 76	    4279	  0.01%
 77	    4168	  0.01%
 78	    4485	  0.01%
 79	    5538	  0.02%
 80	    5496	  0.02%
 81	    5773	  0.02%
 82	    6383	  0.02%
 83	    8124	  0.03%
 84	    8115	  0.03%
 85	    8992	  0.03%
 86	   11277	  0.04%
 87	   11113	  0.03%
 88	   11520	  0.04%
 89	   13978	  0.04%
 90	   15412	  0.05%
 91	   17726	  0.06%
 92	   20786	  0.06%
 93	   25768	  0.08%
 94	   33223	  0.10%
 95	   42773	  0.13%
 96	   58216	  0.18%
 97	   88152	  0.27%
 98	  145551	  0.45%
 99	  475129	  1.48%
100	 2036467	  6.33%
101	28898620	 89.89%
32147122 reads passed initial QC


criterion=sequence-density
sequence-density=2.20
sequence-density-rank=1
fanout-score=59.60
fanout-score-rank=1
prefix-density=3.02
prefix-fanout=43.5
sequence=AGATCGGAAGAGCACACGTCTGAACTCCAGT


criterion=fanout-score
sequence-density=2.20
sequence-density-rank=1
fanout-score=59.60
fanout-score-rank=1
prefix-density=3.02
prefix-fanout=43.5
sequence=AGATCGGAAGAGCACACGTCTGAACTCCAGT
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 AGATCGGAAGAGCACACGTCTGAACTCCAGT -o SRR11216162 -
Input file:	STDIN
trimmed:	SRR11216162-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	AGATCGGAAGAGCACACGTCTGAACTCCAGT
-- 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
Tue Dec 10 08:32:44 2024 >> started

Tue Dec 10 08:32:58 2024 >> done (13.430s)
10715707 reads processed; of these:
       5 ( 0.00%) short reads filtered out after trimming by size control
       5 ( 0.00%) empty reads filtered out after trimming by size control
10715697 (100.00%) reads available; of these:
  854210 ( 7.97%) trimmed reads available after processing
 9861487 (92.03%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	     190	  0.00%
 19	     199	  0.00%
 20	     228	  0.00%
 21	     240	  0.00%
 22	     232	  0.00%
 23	     281	  0.00%
 24	     335	  0.00%
 25	     408	  0.00%
 26	     332	  0.00%
 27	     316	  0.00%
 28	     290	  0.00%
 29	     287	  0.00%
 30	     327	  0.00%
 31	     298	  0.00%
 32	     354	  0.00%
 33	     320	  0.00%
 34	     338	  0.00%
 35	     316	  0.00%
 36	     327	  0.00%
 37	     365	  0.00%
 38	     400	  0.00%
 39	     393	  0.00%
 40	     422	  0.00%
 41	     453	  0.00%
 42	     458	  0.00%
 43	     482	  0.00%
 44	     560	  0.01%
 45	     582	  0.01%
 46	     574	  0.01%
 47	     658	  0.01%
 48	     659	  0.01%
 49	     726	  0.01%
 50	     756	  0.01%
 51	     942	  0.01%
 52	     923	  0.01%
 53	    1040	  0.01%
 54	    1030	  0.01%
 55	    1107	  0.01%
 56	    1195	  0.01%
 57	    1301	  0.01%
 58	    1387	  0.01%
 59	    1680	  0.02%
 60	    1749	  0.02%
 61	    1993	  0.02%
 62	    2259	  0.02%
 63	    2422	  0.02%
 64	    2727	  0.03%
 65	    2968	  0.03%
 66	    3274	  0.03%
 67	    3628	  0.03%
 68	    3971	  0.04%
 69	    4465	  0.04%
 70	    5047	  0.05%
 71	    5893	  0.05%
 72	    6447	  0.06%
 73	    7593	  0.07%
 74	    7936	  0.07%
 75	    8786	  0.08%
 76	    9723	  0.09%
 77	   10695	  0.10%
 78	   11403	  0.11%
 79	   13331	  0.12%
 80	   14593	  0.14%
 81	   15995	  0.15%
 82	   17923	  0.17%
 83	   20121	  0.19%
 84	   21767	  0.20%
 85	   23574	  0.22%
 86	   25958	  0.24%
 87	   27336	  0.26%
 88	   30186	  0.28%
 89	   32749	  0.31%
 90	   35097	  0.33%
 91	   39079	  0.36%
 92	   42038	  0.39%
 93	   46325	  0.43%
 94	   52173	  0.49%
 95	   60444	  0.56%
 96	   77439	  0.72%
 97	  115975	  1.08%
 98	  252539	  2.36%
 99	  147254	  1.37%
100	  636686	  5.94%
101	 8840425	 82.50%


criterion=sequence-density
sequence-density=0.68
sequence-density-rank=1
fanout-score=6.28
fanout-score-rank=4
prefix-density=1.04
prefix-fanout=4.1
sequence=AGGTTCTCGAGGGGACCCTTGCCGGTGACAATGGCCTGGACGAAGAACCCAAACATGGA


criterion=fanout-score
sequence-density=0.01
sequence-density-rank=31
fanout-score=18.80
fanout-score-rank=1
prefix-density=0.04
prefix-fanout=2.8
sequence=GGATTGACTAATGGTACACACGATTCACGATTCTTCCGTCATTCATTCACTCGTGCACCTCATGCTTAATTACATTGCGCGGGGTTCACTCCACCATGGTACAAATCAACACATAACTAGACAAAGGTACAAGTTGATCTACGGCGTACAAGTACACATGCATGCATATATCGATCGTCCGATGGATGGACCGATATATACTACAGCTAGCTGCTAATTCTCATTTAGCTCCCGGGGGCGAAGTTGGTAGCAAAGGCCCATGCATTGTTGTTGACTGGGTCGGCGACGTGGTCGAAGAGGTTCTCGACGGGTCCCTTGCCCGTGACGATGGC
                                 Started job on |	Dec 10 08:33:27
                             Started mapping on |	Dec 10 08:33:27
                                    Finished on |	Dec 10 08:33:56
       Mapping speed, Million of reads per hour |	3990.68

                          Number of input reads |	32147112
                      Average input read length |	100
                                    UNIQUE READS:
                   Uniquely mapped reads number |	30445809
                        Uniquely mapped reads % |	94.71%
                          Average mapped length |	99.71
                       Number of splices: Total |	9794818
            Number of splices: Annotated (sjdb) |	9275132
                       Number of splices: GT/AG |	9656525
                       Number of splices: GC/AG |	119275
                       Number of splices: AT/AC |	2834
               Number of splices: Non-canonical |	16184
                      Mismatch rate per base, % |	0.21%
                         Deletion rate per base |	0.01%
                        Deletion average length |	1.97
                        Insertion rate per base |	0.01%
                       Insertion average length |	1.71
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	1197148
             % of reads mapped to multiple loci |	3.72%
        Number of reads mapped to too many loci |	360103
             % of reads mapped to too many loci |	1.12%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	0.37%
                     % of reads unmapped: other |	0.08%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	504155	504155	504155
N_multimapping	1197148	1197148	1197148
N_noFeature	921815	29710839	1094660
N_ambiguous	622520	1751	62912
UnstrandedReadsAssigned:28901474 PositiveStrandReadsAssigned:733219 NegativeStrandReadsAssigned:29288237
Dataset is classified negative stranded
MeadianReadLen=101 20thPercentileLength=101 echo kmer=97
SRR11216162 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: SRR11216162-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 32,147,112 reads, 29,459,129 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,285 rounds

  52973 SRR11216162.ke.tsv
  35125 SRR11216162.se.tsv
  88098 total
==> SRR11216162.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	98.1627	6.09449
PNS24247	1044	945	54.2683	2.98422
PNS24249	1928	1829	38.1854	1.08492
PNS24246	1044	945	54.2683	2.98422
PNS24248	1044	945	54.2683	2.98422
PNS24244	1471	1372	124.847	4.72867
PNS24243	293	194	0	0
KQK14069	1603	1504	10850.8	374.911
KQK14071	474	375	1512.92	209.652

==> SRR11216162.se.tsv <==
BRADI_1g14170v3	14796
BRADI_1g53295v3	17
BRADI_1g59795v3	626
BRADI_1g07683v3	0
BRADI_1g00485v3	1
BRADI_1g20270v3	310
BRADI_1g74790v3	143
BRADI_1g09890v3	0
BRADI_1g77505v3	436
BRADI_1g48960v3	0
SRR11216162 completed mapping pipeline successfully
