Starting /dee2/code/volunteer_pipeline.sh SRR1033809
    current disk space = 1548129669120
    free memory = 1599454628 
SRR1033809 SRAfilesize
0b60b343797a1c3476e0d562460b4336  SRR1033809.sra
SRR1033809.sra file validated
SRR1033809 is single end
SRR1033809 is conventional basespace
SRR1033809 read1 length is 35 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR1033809_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	50
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	70.99725	71.0	71.0	71.0	71.0	71.0
2	70.67175	71.0	71.0	71.0	71.0	71.0
3	70.69175	71.0	71.0	71.0	71.0	71.0
4	70.7975	71.0	71.0	71.0	71.0	71.0
5	70.69675	71.0	71.0	71.0	71.0	71.0
6	70.85125	71.0	71.0	71.0	71.0	71.0
7	70.72275	71.0	71.0	71.0	71.0	71.0
8	70.515	71.0	71.0	71.0	71.0	71.0
9	70.84675	71.0	71.0	71.0	71.0	71.0
10	70.67125	71.0	71.0	71.0	71.0	71.0
11	70.72225	71.0	71.0	71.0	71.0	71.0
12	70.31525	71.0	71.0	71.0	71.0	71.0
13	70.255	71.0	71.0	71.0	71.0	71.0
14	69.66925	71.0	71.0	71.0	71.0	71.0
15	70.34625	71.0	71.0	71.0	71.0	71.0
16	70.2595	71.0	71.0	71.0	71.0	71.0
17	70.08925	71.0	71.0	71.0	71.0	71.0
18	70.3485	71.0	71.0	71.0	71.0	71.0
19	70.33025	71.0	71.0	71.0	71.0	71.0
20	70.1375	71.0	71.0	71.0	71.0	71.0
21	70.324	71.0	71.0	71.0	71.0	71.0
22	70.295	71.0	71.0	71.0	71.0	71.0
23	69.918	71.0	71.0	71.0	71.0	71.0
24	70.056	71.0	71.0	71.0	71.0	71.0
25	69.87875	71.0	71.0	71.0	71.0	71.0
26	69.26725	71.0	71.0	71.0	70.0	71.0
27	69.9915	71.0	71.0	71.0	71.0	71.0
28	69.302	71.0	71.0	71.0	71.0	71.0
29	68.52725	71.0	71.0	71.0	61.0	71.0
30	70.0145	71.0	71.0	71.0	71.0	71.0
31	68.89675	71.0	71.0	71.0	65.0	71.0
32	69.99075	71.0	71.0	71.0	71.0	71.0
33	69.70375	71.0	71.0	71.0	71.0	71.0
34	69.2945	71.0	71.0	71.0	71.0	71.0
35	68.8265	71.0	71.0	71.0	64.0	71.0
>>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
42	1.0
43	0.0
44	1.0
45	0.0
46	0.0
47	0.0
48	0.0
49	0.0
50	0.0
51	0.0
52	2.0
53	0.0
54	1.0
55	0.0
56	1.0
57	0.0
58	1.0
59	1.0
60	5.0
61	10.0
62	11.0
63	17.0
64	25.0
65	54.0
66	51.0
67	137.0
68	241.0
69	491.0
70	1270.0
71	1680.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	40.949999999999996	58.95	0.075	0.025
2	30.049999999999997	30.8	19.275000000000002	19.875
3	38.275	22.175	20.200000000000003	19.35
4	33.7	31.5	19.1	15.7
5	24.05	31.7	17.2	27.05
6	25.6	21.224999999999998	37.4	15.775
7	29.599999999999998	28.749999999999996	20.549999999999997	21.099999999999998
8	20.3	19.55	37.075	23.075000000000003
9	23.525	31.924999999999997	27.275	17.275
10	39.25	19.275000000000002	20.025000000000002	21.45
11	24.25	17.549999999999997	31.775	26.424999999999997
12	24.675	19.3	28.075	27.950000000000003
13	31.81590795397699	25.41270635317659	16.58329164582291	26.18809404702351
14	28.57857857857858	36.53653653653654	20.145145145145147	14.73973973973974
15	31.73173173173173	26.601601601601605	18.543543543543546	23.123123123123122
16	26.876876876876878	36.93693693693694	19.344344344344343	16.84184184184184
17	27.988994497248626	24.96248124062031	31.21560780390195	15.832916458229116
18	36.66166166166166	23.523523523523522	17.792792792792792	22.02202202202202
19	40.965965965965964	17.34234234234234	25.900900900900904	15.79079079079079
20	29.87987987987988	21.57157157157157	32.78278278278278	15.765765765765765
21	23.48087021755439	28.257064266066518	30.857714428607153	17.404351087771943
22	27.224999999999998	18.375	28.349999999999998	26.05
23	27.888944472236116	28.23911955977989	25.912956478239117	17.958979489744873
24	22.025	18.075	39.35	20.549999999999997
25	13.356678339169584	15.08254127063532	52.32616308154077	19.23461730865433
26	18.734367183591797	11.755877938969485	29.139569784892444	40.37018509254627
27	49.0622655663916	8.802200550137535	26.356589147286826	15.778944736184048
28	18.70935467733867	11.605802901450724	47.148574287143575	22.536268134067033
29	17.983991995998	35.842921460730366	20.38519259629815	25.78789394697349
30	26.663331665832917	6.078039019509754	47.44872436218109	19.809904952476238
31	46.54827413706853	5.877938969484743	24.212106053026513	23.36168084042021
32	13.838838838838837	4.3043043043043046	23.84884884884885	58.008008008008005
33	16.966966966966968	1.9019019019019021	28.803803803803802	52.327327327327325
34	40.94094094094094	0.8758758758758759	34.80980980980981	23.373373373373376
35	10.11011011011011	0.2752752752752753	56.63163163163163	32.98298298298298
>>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	0.5
17	1.0
18	1.0
19	1.0
20	1.0
21	0.5
22	0.0
23	0.0
24	1.0
25	2.0
26	2.0
27	1.5
28	1.0
29	1.0
30	7.5
31	14.0
32	14.0
33	23.0
34	32.0
35	32.0
36	56.5
37	81.0
38	81.0
39	110.0
40	139.0
41	207.0
42	275.0
43	275.0
44	336.5
45	398.0
46	398.0
47	481.0
48	564.0
49	564.0
50	693.0
51	822.0
52	822.0
53	915.0
54	1008.0
55	1008.0
56	701.5
57	395.0
58	395.0
59	278.0
60	161.0
61	111.5
62	62.0
63	62.0
64	43.5
65	25.0
66	25.0
67	18.0
68	11.0
69	11.0
70	8.5
71	6.0
72	6.0
73	3.5
74	1.0
75	1.0
76	1.0
77	1.0
78	1.0
79	0.5
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	0.0
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	0.05
14	0.1
15	0.1
16	0.1
17	0.05
18	0.1
19	0.1
20	0.1
21	0.025
22	0.0
23	0.05
24	0.0
25	0.05
26	0.05
27	0.025
28	0.05
29	0.05
30	0.05
31	0.05
32	0.1
33	0.1
34	0.1
35	0.1
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
35	4000.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	72.6
#Duplication Level	Percentage of deduplicated	Percentage of total
1	92.32093663911846	67.025
2	4.235537190082645	6.15
3	1.0674931129476584	2.325
4	0.7575757575757576	2.1999999999999997
5	0.30991735537190085	1.125
6	0.17217630853994492	0.75
7	0.03443526170798898	0.17500000000000002
8	0.10330578512396695	0.6
9	0.06887052341597796	0.44999999999999996
>10	0.7575757575757576	10.299999999999999
>50	0.13774104683195593	6.2
>100	0.03443526170798898	2.7
>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
GGGGATGTAGCTCAGATGGTTCGTATGCCGTCTTC	108	2.7	No Hit
GACACGACTCTCGGCAACGGATATCTTCGTATGCC	78	1.95	No Hit
AGTTCTACAGTCCGACGATCTCGTATGCCGTCTTC	68	1.7000000000000002	Illumina PCR Primer Index 1 (95% over 22bp)
GACACGACTCTCGGCAACGGATATCTCTCGTATGC	51	1.275	No Hit
GGGGATGTAGCTCAGATGGTATCGTATGCCGTCTT	51	1.275	No Hit
ACGACTCTCGGCAACGGATATCTTCGTATGCCGTC	50	1.25	No Hit
GACACGACTCTCGGCAACGGATATTCGTATGCCGT	30	0.75	No Hit
GGGGATGTAGCTCAGATGGTAGAGTCGTATGCCGT	29	0.7250000000000001	No Hit
AGAATCTTGATGATGCTGCATTCGTATGCCGTCTT	28	0.7000000000000001	No Hit
GACACGACTCTCGGCAACGGATATCGTATGCCGTC	27	0.675	No Hit
ACGACTCTCGGCAACGGATATCTCTCGTATGCCGT	24	0.6	No Hit
GGGGATGTAGCTCAGATGGTCGTATGCCGTCTTCT	23	0.575	No Hit
ACACGACTCTCGGCAACGGATATCTTCGTATGCCG	19	0.475	No Hit
AACGAACGAACGATTTGAACTCGTATGCCGTCTTC	18	0.44999999999999996	No Hit
GGGGATGTAGCTCAGATGGTAGATCGTATGCCGTC	18	0.44999999999999996	No Hit
GGGGATGTAGCTCAGATGGTAGTCGTATGCCGTCT	16	0.4	No Hit
GACACGACTCTCGGCAACGGATATCTCGTATGCCG	16	0.4	No Hit
GGGGATGTAGCTCAAATGGTATCGTATGCCGTCTT	13	0.325	No Hit
GCGTCTGTAGTCCAACGGTTTCGTATGCCGTCTTC	13	0.325	No Hit
GACACGACTCTCGGCAACGGATTCGTATGCCGTCT	13	0.325	No Hit
GGGGATGTAGCTCAGATGGTAGAGCTCGTATGCCG	13	0.325	No Hit
AGGGCTATAGCTCAGTTCGGTCGTATGCCGTCTTC	11	0.27499999999999997	No Hit
ACACGACTCTCGGCAACGGATATCTCTCGTATGCC	11	0.27499999999999997	No Hit
GGGGATGTAGCTCAAATGGTAGAGTCGTATGCCGT	10	0.25	No Hit
ACGACTCTCGGCAACGGATATCTCGTATGCCGTCT	10	0.25	TruSeq Adapter, Index 25 (95% over 22bp)
ACGACTCTCGGCAACGGATATTCGTATGCCGTCTT	10	0.25	No Hit
GGGGATGTAGCTCAAATGGTAGATCGTATGCCGTC	10	0.25	No Hit
AGTTCTACAGTCCGACGATCATCGTATGCCGTCTT	9	0.22499999999999998	No Hit
ACCTGCTCTGATACCATGTTGTGATCGTATGCCGT	9	0.22499999999999998	No Hit
GCGTCTGTAGTCCAACGGTTATCGTATGCCGTCTT	8	0.2	No Hit
ACACGACTCTCGGCAACGGATATTCGTATGCCGTC	8	0.2	No Hit
ACGAACGAACGATTTGAACTCGTATGCCGTCTTCT	8	0.2	No Hit
GGTAGTTCGACCGCGGAATTCGTATGCCGTCTTCT	7	0.17500000000000002	No Hit
ACGACTCTCGGCAACGGATATCTCGTCGTATGCCG	6	0.15	No Hit
GGGATGTAGCTCAGATGGTATCGTATGCCGTCTTC	6	0.15	No Hit
GGGATGTAGCTCAGATGGTTCGTATGCCGTCTTCT	6	0.15	No Hit
GGGGATGTAGCTCAAATGGTTCGTATGCCGTCTTC	6	0.15	No Hit
GAAAAGAAACGAAGATCGCGTTCGTATGCCGTCTT	6	0.15	No Hit
GGGATTGTAGTTCAATTGGTCAGAGTCGTATGCCG	5	0.125	No Hit
ACCGGGCACATTAGTGTCTGTCGTATGCCGTCTTC	5	0.125	No Hit
GCGTCTGTAGTCCAACGGTTAGTCGTATGCCGTCT	5	0.125	No Hit
GGTGGCTGTAGTTTAGTGGTGAGAATCGTATGCCG	5	0.125	No Hit
ACACGACTCTCGGCAACGGATATCTCGTATGCCGT	5	0.125	No Hit
GGTGGCTGTAGTTTAGTGGTGAGATCGTATGCCGT	5	0.125	No Hit
GGTGGCTGTAGTTTAGTGGTCGTATGCCGTCTTCT	5	0.125	No Hit
GGTAGTTCGACCGCGGAATTTTCGTATGCCGTCTT	5	0.125	No Hit
GTTCTACAGTCCGACGATTCGTATGCCGTCTTCTG	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
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
AGCTCAG	20	0.005388326	29.0	9
GACACGA	25	4.303467E-4	29.0	1
TCAGATG	20	0.005388326	29.0	12
CTCAGAT	20	0.005388326	29.0	11
GGGGATG	20	0.005388326	29.0	1
GCTCAGA	20	0.005388326	29.0	10
ACACGAC	30	0.0012503903	24.166668	2
CACGACT	30	0.0012503903	24.166668	3
GATCGTA	35	0.0030680934	20.714287	23
ACTCGTA	40	0.0066521973	18.125	23
GGCAACG	40	0.0066521973	18.125	13
TCGGCAA	40	0.0066521973	18.125	11
CTCTCGG	40	0.0066521973	18.125	8
ACTCTCG	40	0.0066521973	18.125	7
GCAACGG	40	0.0066521973	18.125	14
TCTCGGC	40	0.0066521973	18.125	9
CTCGGCA	40	0.0066521973	18.125	10
ACGACTC	40	0.0066521973	18.125	4
CGGCAAC	40	0.0066521973	18.125	12
AACGGAT	40	0.0066521973	18.125	16
>>END_MODULE
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371484 spots for SRR1033809.sra
Written 371484 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
Read 371470 spots for SRR1033809.sra
Written 371470 spots for SRR1033809.sra
SRR ids: ['SRR1033809.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_ya11bgqa
SRR1033809.sra spots: 7429414
blocks: [[1, 371470], [371471, 742940], [742941, 1114410], [1114411, 1485880], [1485881, 1857350], [1857351, 2228820], [2228821, 2600290], [2600291, 2971760], [2971761, 3343230], [3343231, 3714700], [3714701, 4086170], [4086171, 4457640], [4457641, 4829110], [4829111, 5200580], [5200581, 5572050], [5572051, 5943520], [5943521, 6314990], [6314991, 6686460], [6686461, 7057930], [7057931, 7429414]]
SRR1033809 file size 1027402
SRR1033809 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 SRR1033809 SRR1033809_1.fastq
Input file:	SRR1033809_1.fastq
trimmed:	SRR1033809-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 00:57:02 2024 >> started

Sat Dec  7 00:57:07 2024 >> done (4.457s)
7429414 reads processed; of these:
      0 ( 0.00%) short reads filtered out after trimming by size control
      0 ( 0.00%) empty reads filtered out after trimming by size control
7429414 (100.00%) reads available; of these:
7429414 (100.00%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 35	7429414	100.00%
7429414 reads passed initial QC


criterion=sequence-density
sequence-density=44.11
sequence-density-rank=1
fanout-score=35.50
fanout-score-rank=2
prefix-density=84.78
prefix-fanout=18.5
sequence=TCGTATGCCGTCTTCTGCTTGAAAA


criterion=fanout-score
sequence-density=4.63
sequence-density-rank=3
fanout-score=40.18
fanout-score-rank=1
prefix-density=5.56
prefix-fanout=33.4
sequence=GCTCGTATGCCG
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 TCGTATGCCGTCTTCTGCTTGAAAA -o SRR1033809 -
Input file:	STDIN
trimmed:	SRR1033809-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TCGTATGCCGTCTTCTGCTTGAAAA
-- 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 00:57:19 2024 >> started

Sat Dec  7 00:57:26 2024 >> done (7.420s)
7099218 reads processed; of these:
 193163 ( 2.72%) short reads filtered out after trimming by size control
   6401 ( 0.09%) empty reads filtered out after trimming by size control
6899654 (97.19%) reads available; of these:
6462791 (93.67%) trimmed reads available after processing
 436863 ( 6.33%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	 247032	  3.58%
 19	 283052	  4.10%
 20	 496213	  7.19%
 21	1538800	 22.30%
 22	 395553	  5.73%
 23	 611451	  8.86%
 24	1839637	 26.66%
 25	 368303	  5.34%
 26	 301960	  4.38%
 27	 195295	  2.83%
 28	 106195	  1.54%
 29	  50907	  0.74%
 30	  14568	  0.21%
 31	  11370	  0.16%
 32	   2455	  0.04%
 33	      0	  0.00%
 34	      0	  0.00%
 35	 436863	  6.33%


criterion=sequence-density
sequence-density=13.66
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=15
prefix-density=0.00
prefix-fanout=1.0
sequence=TCGCTTGGTGCAGATCGGGACTCGTATGCCG


criterion=fanout-score
sequence-density=0.19
sequence-density-rank=16
fanout-score=150.99
fanout-score-rank=1
prefix-density=1.33
prefix-fanout=21.7
sequence=CGTATGCCGTCTTC
                                 Started job on |	Dec 07 00:57:42
                             Started mapping on |	Dec 07 00:57:43
                                    Finished on |	Dec 07 00:58:05
       Mapping speed, Million of reads per hour |	1183.07

                          Number of input reads |	7229850
                      Average input read length |	23
                                    UNIQUE READS:
                   Uniquely mapped reads number |	2871753
                        Uniquely mapped reads % |	39.72%
                          Average mapped length |	22.19
                       Number of splices: Total |	56320
            Number of splices: Annotated (sjdb) |	6259
                       Number of splices: GT/AG |	53852
                       Number of splices: GC/AG |	1388
                       Number of splices: AT/AC |	4
               Number of splices: Non-canonical |	1076
                      Mismatch rate per base, % |	0.57%
                         Deletion rate per base |	0.02%
                        Deletion average length |	1.23
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.01
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	1564621
             % of reads mapped to multiple loci |	21.64%
        Number of reads mapped to too many loci |	2212010
             % of reads mapped to too many loci |	30.60%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	7.00%
                     % of reads unmapped: other |	1.04%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	2793476	2793476	2793476
N_multimapping	1564621	1564621	1564621
N_noFeature	1559433	1663059	2759901
N_ambiguous	11734	2681	1081
UnstrandedReadsAssigned:1300586 PositiveStrandReadsAssigned:1206013 NegativeStrandReadsAssigned:110771
Dataset is classified positive stranded
MeadianReadLen=23 20thPercentileLength=21 echo kmer=19
SRR1033809 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: SRR1033809-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 7,229,850 reads, 1,602,585 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 940 rounds

  52973 SRR1033809.ke.tsv
  35125 SRR1033809.se.tsv
  88098 total
==> SRR1033809.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	0	0
PNS24243	293	194	0	0
KQK14069	1603	1504	6	2.37492
KQK14071	474	375	0	0

==> SRR1033809.se.tsv <==
BRADI_1g14170v3	7
BRADI_1g53295v3	1
BRADI_1g59795v3	0
BRADI_1g07683v3	0
BRADI_1g00485v3	0
BRADI_1g20270v3	10
BRADI_1g74790v3	11
BRADI_1g09890v3	1
BRADI_1g77505v3	0
BRADI_1g48960v3	0
SRR1033809 completed mapping pipeline successfully
