Starting /dee2/code/volunteer_pipeline.sh SRR921326
    current disk space = 1547750924288
    free memory = 1600617700 
SRR921326 SRAfilesize
e184feea48af1df8df09a8665896dc40  SRR921326.sra
SRR921326.sra file validated
SRR921326 is single end
SRR921326 is conventional basespace
SRR921326 read1 length is 35 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR921326_1.fastq
File type	Conventional base calls
Encoding	Sanger / Illumina 1.9
Total Sequences	4000
Sequences flagged as poor quality	0
Sequence length	35
%GC	49
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	32.62975	39.0	36.0	40.0	2.0	40.0
2	33.95425	39.0	35.0	40.0	12.0	40.0
3	34.04425	39.0	36.0	40.0	13.0	40.0
4	33.914	39.0	35.0	40.0	12.0	40.0
5	33.9115	39.0	36.0	40.0	12.0	40.0
6	34.796	39.0	36.0	40.0	20.0	40.0
7	34.7165	39.0	36.0	40.0	19.0	40.0
8	34.6525	39.0	35.0	40.0	19.0	40.0
9	34.5505	39.0	35.0	40.0	18.0	40.0
10	34.55575	39.0	35.0	40.0	18.0	40.0
11	36.048	39.0	35.0	40.0	31.0	40.0
12	36.0545	39.0	35.0	40.0	31.0	40.0
13	36.1255	39.0	35.0	40.0	31.0	40.0
14	36.1345	39.0	35.0	40.0	31.0	40.0
15	36.213	39.0	35.0	40.0	31.0	40.0
16	36.157	39.0	35.0	40.0	31.0	40.0
17	36.22825	39.0	35.0	40.0	31.0	40.0
18	36.08425	39.0	35.0	40.0	31.0	40.0
19	35.97175	39.0	35.0	40.0	31.0	40.0
20	35.94275	39.0	34.0	40.0	31.0	40.0
21	35.78525	39.0	35.0	40.0	31.0	40.0
22	35.494	39.0	34.0	40.0	29.0	40.0
23	35.29325	39.0	34.0	40.0	28.0	40.0
24	35.36725	39.0	34.0	40.0	29.0	40.0
25	35.27425	39.0	34.0	40.0	29.0	40.0
26	34.81625	38.0	33.0	40.0	27.0	40.0
27	34.814	38.0	33.0	40.0	27.0	40.0
28	34.69775	38.0	33.0	40.0	27.0	40.0
29	34.4985	38.0	33.0	40.0	27.0	40.0
30	34.35175	38.0	33.0	40.0	26.0	40.0
31	34.2925	38.0	33.0	40.0	25.0	40.0
32	34.12475	38.0	32.0	40.0	25.0	40.0
33	34.0835	38.0	32.0	40.0	25.0	40.0
34	33.78625	38.0	31.0	40.0	25.0	40.0
35	33.6605	38.0	31.0	40.0	24.0	40.0
>>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
>>END_MODULE
>>Per sequence quality scores	pass
#Quality	Count
2	96.0
3	1.0
4	0.0
5	0.0
6	1.0
7	1.0
8	0.0
9	2.0
10	2.0
11	8.0
12	2.0
13	2.0
14	1.0
15	8.0
16	4.0
17	9.0
18	8.0
19	11.0
20	25.0
21	25.0
22	39.0
23	58.0
24	74.0
25	115.0
26	128.0
27	140.0
28	44.0
29	30.0
30	37.0
31	31.0
32	55.0
33	68.0
34	88.0
35	112.0
36	177.0
37	345.0
38	597.0
39	1633.0
40	23.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	22.394282310899342	26.474091721262656	24.95533055390113	26.176295413936867
2	24.975	28.050000000000004	22.6	24.375
3	21.925	20.225	23.35	34.5
4	21.7	24.425	37.525	16.35
5	20.5	24.05	20.325	35.125
6	22.125	35.325	23.849999999999998	18.7
7	21.275	36.85	18.525	23.35
8	21.575	39.425	20.025000000000002	18.975
9	24.6	32.975	22.85	19.575
10	40.725	22.75	17.8	18.725
11	28.125	33.324999999999996	18.95	19.6
12	34.5	29.15	18.9	17.45
13	41.375	24.375	16.45	17.8
14	23.7	41.275	17.375	17.65
15	28.050000000000004	33.275	20.7	17.974999999999998
16	22.825	33.775	22.95	20.45
17	34.725	23.375	23.025000000000002	18.875
18	37.0	21.825	19.650000000000002	21.525
19	29.325000000000003	21.675	19.2	29.799999999999997
20	22.05	27.55	29.225	21.175
21	24.275	22.05	34.025	19.650000000000002
22	36.675000000000004	24.4	16.400000000000002	22.525000000000002
23	24.7	22.175	18.725	34.4
24	33.050000000000004	25.575	24.125	17.25
25	37.925	23.575	19.725	18.775
26	29.075	21.025	31.25	18.65
27	34.225	24.625	20.0	21.15
28	34.1	22.45	22.15	21.3
29	21.05	35.825	19.35	23.775
30	22.175	27.975	30.95	18.9
31	29.15	34.125	17.599999999999998	19.125
32	26.75	22.175	20.3	30.775000000000002
33	24.3	25.6	20.599999999999998	29.5
34	23.674999999999997	22.175	34.825	19.325
35	27.05	35.825	20.349999999999998	16.775000000000002
>>END_MODULE
>>Per sequence GC content	warn
#GC Content	Count
0	1.0
1	2.0
2	3.0
3	3.0
4	3.5
5	4.0
6	4.0
7	6.0
8	8.0
9	8.0
10	5.0
11	2.0
12	2.0
13	5.5
14	9.0
15	9.0
16	8.0
17	7.0
18	7.0
19	11.5
20	16.0
21	18.5
22	21.0
23	21.0
24	23.5
25	26.0
26	26.0
27	38.5
28	51.0
29	51.0
30	70.5
31	90.0
32	90.0
33	115.0
34	140.0
35	140.0
36	166.0
37	192.0
38	192.0
39	229.0
40	266.0
41	326.0
42	386.0
43	386.0
44	442.5
45	499.0
46	499.0
47	510.5
48	522.0
49	522.0
50	465.0
51	408.0
52	408.0
53	352.0
54	296.0
55	296.0
56	274.5
57	253.0
58	253.0
59	220.5
60	188.0
61	173.5
62	159.0
63	159.0
64	143.5
65	128.0
66	128.0
67	126.0
68	124.0
69	124.0
70	104.0
71	84.0
72	84.0
73	71.5
74	59.0
75	59.0
76	40.5
77	22.0
78	22.0
79	19.0
80	16.0
81	14.0
82	12.0
83	12.0
84	8.5
85	5.0
86	5.0
87	3.5
88	2.0
89	2.0
90	1.0
91	0.0
92	0.0
93	0.5
94	1.0
95	1.0
96	0.5
97	0.0
98	0.0
99	0.0
100	0.0
>>END_MODULE
>>Per base N content	warn
#Base	N-Count
1	16.05
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
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
35	4000.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	86.05000000000001
#Duplication Level	Percentage of deduplicated	Percentage of total
1	95.2643811737362	81.975
2	1.6560139453805929	2.85
3	0.9877977919814062	2.55
4	0.5520046484601976	1.9
5	0.3486345148169669	1.5
6	0.31958163858221966	1.6500000000000001
7	0.17431725740848344	1.05
8	0.08715862870424172	0.6
9	0.2324230098779779	1.7999999999999998
>10	0.3776873910517141	4.125
>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
ATTTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	19	0.475	No Hit
CTCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	16	0.4	No Hit
ATGTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	15	0.375	No Hit
AAGTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	14	0.35000000000000003	No Hit
CTTTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	13	0.325	No Hit
CCGTCTCATGGAGAGTTCGATCCTGGCTCAGGATG	13	0.325	No Hit
AATTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	13	0.325	No Hit
ACCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	11	0.27499999999999997	No Hit
TCTTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	11	0.27499999999999997	No Hit
CACTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	10	0.25	No Hit
CCATCTCATGGAGAGTTCGATCCTGGCTCAGGATG	10	0.25	No Hit
CTGTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	10	0.25	No Hit
AAATCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	10	0.25	No Hit
TACTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	9	0.22499999999999998	No Hit
AGCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	9	0.22499999999999998	No Hit
CTCTCTCATGGAGAGTTCGATCCTGGCTCAGGATG	9	0.22499999999999998	No Hit
TGCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	9	0.22499999999999998	No Hit
TTTTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	9	0.22499999999999998	No Hit
NATTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	9	0.22499999999999998	No Hit
TTCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	9	0.22499999999999998	No Hit
NACTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	9	0.22499999999999998	No Hit
GCCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	8	0.2	No Hit
AACTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	8	0.2	No Hit
NTGTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	8	0.2	No Hit
NGCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	7	0.17500000000000002	No Hit
NTTTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	7	0.17500000000000002	No Hit
GCTTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	7	0.17500000000000002	No Hit
TTATCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	7	0.17500000000000002	No Hit
NTCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	7	0.17500000000000002	No Hit
ATCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	7	0.17500000000000002	No Hit
NCTTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
ACTTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
ACATCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
CCCTCTCATGGAGAGTTCGATCCTGGCTCAGGATG	6	0.15	No Hit
ACGTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
GACTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
TCGTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
TCCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
TATTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
CGCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
GCATCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	6	0.15	No Hit
CATTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	5	0.125	No Hit
AGCTACCTGGTTGATCCTGCCAGTAGTCATATGCT	5	0.125	No Hit
CAATCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	5	0.125	No Hit
AACTCTCATGGAGAGTTCGATCCTGGCTCAGGATG	5	0.125	No Hit
TGGTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	5	0.125	No Hit
TAATCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	5	0.125	No Hit
AGGTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	5	0.125	No Hit
CCATCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	5	0.125	No Hit
GGCGCGACCCCAGGTCAGGCGGGACTACCCGCTGA	5	0.125	No Hit
GGCTCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	5	0.125	No Hit
CTATCAAAAGAGGAAAGGCTTGCGGTGGATACCTA	5	0.125	No Hit
TGCTACCTGGTTGATCCTGCCAGTAGTCATATGCT	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	0.025	0.0	0.0	0.0	0.0
2	0.075	0.0	0.0	0.0	0.0
3	0.075	0.0	0.0	0.0	0.0
4	0.125	0.0	0.0	0.0	0.0
5	0.15	0.0	0.0	0.0	0.0
6	0.15	0.0	0.0	0.0	0.0
7	0.15	0.0	0.0	0.0	0.0
8	0.15	0.0	0.0	0.0	0.0
9	0.15	0.0	0.0	0.0	0.0
10	0.15	0.0	0.0	0.0	0.0
11	0.175	0.0	0.0	0.0	0.0
12	0.2	0.0	0.0	0.0	0.0
13	0.25	0.0	0.0	0.0	0.0
14	0.25	0.0	0.0	0.0	0.0
15	0.25	0.0	0.0	0.0	0.0
16	0.275	0.0	0.0	0.0	0.0
17	0.275	0.0	0.0	0.0	0.0
18	0.275	0.0	0.0	0.0	0.0
19	0.275	0.0	0.0	0.0	0.0
20	0.275	0.0	0.0	0.0	0.0
21	0.275	0.0	0.0	0.0	0.0
22	0.275	0.0	0.0	0.0	0.0
23	0.275	0.0	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
ATCCTGG	25	4.447609E-4	28.8375	20
ATCTCAT	20	0.005538505	28.8375	3
TCGATCC	25	4.447609E-4	28.8375	17
GAGGAAA	20	0.005538505	28.8375	10
GATACCT	20	0.005538505	28.8375	28
TCAGGAT	25	4.447609E-4	28.8375	28
AAGAGGA	20	0.005538505	28.8375	8
GCGGTGG	20	0.005538505	28.8375	22
AGGAAAG	20	0.005538505	28.8375	11
TGGAGAG	25	4.447609E-4	28.8375	9
ATGGAGA	25	4.447609E-4	28.8375	8
CTGGCTC	25	4.447609E-4	28.8375	23
GAGTTCG	25	4.447609E-4	28.8375	13
GGATACC	20	0.005538505	28.8375	27
AGAGTTC	25	4.447609E-4	28.8375	12
TCAAAAG	20	0.005538505	28.8375	4
AAAAGAG	20	0.005538505	28.8375	6
AGGCTTG	20	0.005538505	28.8375	16
GGCTTGC	20	0.005538505	28.8375	17
AAGGCTT	20	0.005538505	28.8375	15
>>END_MODULE
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686960 spots for SRR921326.sra
Written 686960 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
Read 686952 spots for SRR921326.sra
Written 686952 spots for SRR921326.sra
SRR ids: ['SRR921326.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_t3yenjmy
SRR921326.sra spots: 13739048
blocks: [[1, 686952], [686953, 1373904], [1373905, 2060856], [2060857, 2747808], [2747809, 3434760], [3434761, 4121712], [4121713, 4808664], [4808665, 5495616], [5495617, 6182568], [6182569, 6869520], [6869521, 7556472], [7556473, 8243424], [8243425, 8930376], [8930377, 9617328], [9617329, 10304280], [10304281, 10991232], [10991233, 11678184], [11678185, 12365136], [12365137, 13052088], [13052089, 13739048]]
SRR921326 file size 2003950
SRR921326 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 SRR921326 SRR921326_1.fastq
Input file:	SRR921326_1.fastq
trimmed:	SRR921326-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 00:06:41 2024 >> started

Sat Dec  7 00:06:53 2024 >> done (11.857s)
13739048 reads processed; of these:
   76000 ( 0.55%) short reads filtered out after trimming by size control
   28578 ( 0.21%) empty reads filtered out after trimming by size control
13634470 (99.24%) reads available; of these:
  540129 ( 3.96%) trimmed reads available after processing
13094341 (96.04%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	    9315	  0.07%
 19	   16797	  0.12%
 20	   37715	  0.28%
 21	    8213	  0.06%
 22	   14307	  0.10%
 23	   21329	  0.16%
 24	   39531	  0.29%
 25	   96656	  0.71%
 26	   14289	  0.10%
 27	   22232	  0.16%
 28	   36558	  0.27%
 29	   51672	  0.38%
 30	  101342	  0.74%
 31	   12446	  0.09%
 32	   14162	  0.10%
 33	   19895	  0.15%
 34	   23670	  0.17%
 35	13094341	 96.04%
13634470 reads passed initial QC


criterion=sequence-density
sequence-density=11.65
sequence-density-rank=1
fanout-score=44.88
fanout-score-rank=1
prefix-density=11.44
prefix-fanout=44.9
sequence=TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTTCGGGGAGT


criterion=fanout-score
sequence-density=11.65
sequence-density-rank=1
fanout-score=44.88
fanout-score-rank=1
prefix-density=11.44
prefix-fanout=44.9
sequence=TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTTCGGGGAGT
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 TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGCGACGAAATGCTTCGGGGAGT -o SRR921326 -
Input file:	STDIN
trimmed:	SRR921326-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TCAAAAGAGGAAAGGCTTGCGGTGGATACCTAGGCACCCAGAGACGAGGAAGGGCGTAGCAAGC
-- 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 00:07:11 2024 >> started

Sat Dec  7 00:07:22 2024 >> done (11.119s)
11362058 reads processed; of these:
 1309957 (11.53%) short reads filtered out after trimming by size control
    3147 ( 0.03%) empty reads filtered out after trimming by size control
10048954 (88.44%) reads available; of these:
  203739 ( 2.03%) trimmed reads available after processing
 9845215 (97.97%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	    8373	  0.08%
 19	   13762	  0.14%
 20	   29252	  0.29%
 21	    7707	  0.08%
 22	   12339	  0.12%
 23	   16240	  0.16%
 24	   30641	  0.30%
 25	   69560	  0.69%
 26	   11607	  0.12%
 27	   17396	  0.17%
 28	   24633	  0.25%
 29	   40635	  0.40%
 30	   85303	  0.85%
 31	   54979	  0.55%
 32	  142993	  1.42%
 33	   11136	  0.11%
 34	   18239	  0.18%
 35	 9454159	 94.08%


criterion=sequence-density
sequence-density=4.77
sequence-density-rank=1
fanout-score=38.37
fanout-score-rank=1
prefix-density=4.69
prefix-fanout=38.4
sequence=TCTCATGGAGAGTTCGATCCTGGCTCAGGATG


criterion=fanout-score
sequence-density=4.77
sequence-density-rank=1
fanout-score=38.37
fanout-score-rank=1
prefix-density=4.69
prefix-fanout=38.4
sequence=TCTCATGGAGAGTTCGATCCTGGCTCAGGATG
                                 Started job on |	Dec 07 00:07:52
                             Started mapping on |	Dec 07 00:07:52
                                    Finished on |	Dec 07 00:08:03
       Mapping speed, Million of reads per hour |	4032.45

                          Number of input reads |	12321366
                      Average input read length |	30
                                    UNIQUE READS:
                   Uniquely mapped reads number |	8421982
                        Uniquely mapped reads % |	68.35%
                          Average mapped length |	30.46
                       Number of splices: Total |	677612
            Number of splices: Annotated (sjdb) |	643867
                       Number of splices: GT/AG |	665917
                       Number of splices: GC/AG |	8416
                       Number of splices: AT/AC |	387
               Number of splices: Non-canonical |	2892
                      Mismatch rate per base, % |	0.32%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.36
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.17
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	1883631
             % of reads mapped to multiple loci |	15.29%
        Number of reads mapped to too many loci |	798347
             % of reads mapped to too many loci |	6.48%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	9.48%
                     % of reads unmapped: other |	0.40%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	2015753	2015753	2015753
N_multimapping	1883631	1883631	1883631
N_noFeature	470652	647466	8095629
N_ambiguous	164465	14617	1220
UnstrandedReadsAssigned:7786865 PositiveStrandReadsAssigned:7759899 NegativeStrandReadsAssigned:325133
Dataset is classified positive stranded
MeadianReadLen=31 20thPercentileLength=31 echo kmer=27
SRR921326 Starting Kallisto single end mapping to ensembl reference transcriptome. kmer=27

[quant] fragment length distribution is truncated gaussian with mean = 100, sd = 20
[index] k-mer length: 27
[index] number of targets: 52,972
[index] number of k-mers: 66,546,128
[index] number of equivalence classes: 124,662
[quant] running in single-end mode
[quant] will process file 1: SRR921326-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 12,321,366 reads, 7,287,366 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,149 rounds

  52973 SRR921326.ke.tsv
  35125 SRR921326.se.tsv
  88098 total
==> SRR921326.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	0	0
PNS24249	1928	1829	10.1241	1.15536
PNS24246	1044	945	0	0
PNS24248	1044	945	0	0
PNS24244	1471	1372	96.8759	14.7379
PNS24243	293	194	0	0
KQK14069	1603	1504	3202.86	444.493
KQK14071	474	375	1854.6	1032.27

==> SRR921326.se.tsv <==
BRADI_1g14170v3	5382
BRADI_1g53295v3	29
BRADI_1g59795v3	144
BRADI_1g07683v3	0
BRADI_1g00485v3	1
BRADI_1g20270v3	143
BRADI_1g74790v3	35
BRADI_1g09890v3	5
BRADI_1g77505v3	71
BRADI_1g48960v3	1
SRR921326 completed mapping pipeline successfully
