Starting /dee2/code/volunteer_pipeline.sh SRR6892966
    current disk space = 1516053540864
    free memory = 1597160824 
SRR6892966 SRAfilesize
9e61d9a28f99590cb066fedda415fd4a  SRR6892966.sra
SRR6892966.sra file validated
SRR6892966 is single end
SRR6892966 is conventional basespace
SRR6892966 read1 length is 50 nt
##FastQC	0.11.5
>>Basic Statistics	pass
#Measure	Value
Filename	SRR6892966_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	53
>>END_MODULE
>>Per base sequence quality	pass
#Base	Mean	Median	Lower Quartile	Upper Quartile	10th Percentile	90th Percentile
1	32.33275	33.0	31.0	34.0	31.0	34.0
2	32.47525	34.0	31.0	34.0	31.0	34.0
3	32.5695	34.0	31.0	34.0	31.0	34.0
4	35.99525	37.0	35.0	37.0	35.0	37.0
5	36.00675	37.0	35.0	37.0	35.0	37.0
6	35.99475	37.0	35.0	37.0	35.0	37.0
7	36.026	37.0	35.0	37.0	35.0	37.0
8	36.04525	37.0	35.0	37.0	35.0	37.0
9	37.722	39.0	37.0	39.0	35.0	39.0
10	37.6505	39.0	37.0	39.0	35.0	39.0
11	37.65025	39.0	37.0	39.0	35.0	39.0
12	37.434	39.0	37.0	39.0	34.0	39.0
13	37.59	39.0	37.0	39.0	35.0	39.0
14	39.08875	40.0	38.0	41.0	36.0	41.0
15	39.02375	40.0	38.0	41.0	36.0	41.0
16	39.00375	40.0	38.0	41.0	35.0	41.0
17	38.9055	40.0	38.0	41.0	35.0	41.0
18	38.823	40.0	38.0	41.0	35.0	41.0
19	38.81275	40.0	38.0	41.0	34.0	41.0
20	38.9305	40.0	38.0	41.0	35.0	41.0
21	38.8865	40.0	39.0	41.0	35.0	41.0
22	38.54375	40.0	38.0	41.0	34.0	41.0
23	39.554	41.0	39.0	41.0	37.0	41.0
24	38.853	40.0	38.0	41.0	35.0	41.0
25	39.7	40.0	40.0	41.0	38.0	41.0
26	39.53575	41.0	40.0	41.0	36.0	41.0
27	40.17275	41.0	40.0	41.0	39.0	41.0
28	39.2405	41.0	40.0	41.0	36.0	41.0
29	38.44075	40.0	38.0	41.0	34.0	41.0
30	38.3305	40.0	38.0	41.0	33.0	41.0
31	38.5685	40.0	38.0	41.0	34.0	41.0
32	39.68125	41.0	40.0	41.0	38.0	41.0
33	40.08475	41.0	40.0	41.0	39.0	41.0
34	34.70375	37.0	31.0	41.0	25.0	41.0
35	33.35575	35.0	30.0	38.0	25.0	39.0
36	36.3465	38.0	36.0	39.0	30.0	40.0
37	38.439	39.0	38.0	40.0	35.0	41.0
38	38.563	40.0	38.0	41.0	35.0	41.0
39	39.18175	40.0	39.0	41.0	36.0	41.0
40	38.82425	40.0	38.0	41.0	35.0	41.0
41	39.5575	41.0	40.0	41.0	37.0	41.0
42	38.5145	40.0	38.0	41.0	34.0	41.0
43	39.06325	40.0	39.0	41.0	36.0	41.0
44	38.8035	40.0	39.0	41.0	35.0	41.0
45	38.85125	41.0	39.0	41.0	35.0	41.0
46	38.8225	41.0	39.0	41.0	35.0	41.0
47	39.1915	41.0	39.0	41.0	36.0	41.0
48	38.244	40.0	38.0	41.0	34.0	41.0
49	37.938	40.0	38.0	41.0	34.0	41.0
50	36.126	38.0	35.0	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
11	1.0
12	0.0
13	0.0
14	2.0
15	0.0
16	3.0
17	1.0
18	1.0
19	1.0
20	3.0
21	2.0
22	2.0
23	7.0
24	5.0
25	9.0
26	15.0
27	9.0
28	16.0
29	23.0
30	39.0
31	45.0
32	53.0
33	69.0
34	114.0
35	184.0
36	266.0
37	454.0
38	784.0
39	1892.0
>>END_MODULE
>>Per base sequence content	fail
#Base	G	A	T	C
1	19.900000000000002	25.174999999999997	24.5	30.425
2	21.425	17.65	27.450000000000003	33.475
3	27.725	21.05	24.3	26.924999999999997
4	26.8	25.275	22.475	25.45
5	25.45	25.650000000000002	22.6	26.3
6	26.900000000000002	22.6	25.724999999999998	24.775
7	26.224999999999998	22.3	28.075	23.400000000000002
8	26.724999999999998	22.175	26.275	24.825
9	28.449999999999996	22.925	25.8	22.825
10	30.049999999999997	22.175	24.2	23.575
11	27.85	23.875	23.45	24.825
12	28.199999999999996	24.65	22.875	24.275
13	25.75	23.825	24.875	25.55
14	26.674999999999997	24.7	24.5	24.125
15	28.225	26.825	24.3	20.65
16	27.55	26.55	24.349999999999998	21.55
17	24.825	26.474999999999998	26.224999999999998	22.475
18	29.275000000000002	24.65	22.900000000000002	23.175
19	26.775	28.975	20.4	23.849999999999998
20	25.324999999999996	29.475	19.400000000000002	25.8
21	10.5	12.55	60.62499999999999	16.325
22	49.175000000000004	2.375	47.55	0.8999999999999999
23	94.80160723254646	1.8583626318432949	2.235057759919638	1.1049723756906076
24	47.01025769326995	48.711533650237676	3.0272704528396295	1.2509382036527394
25	1.25	94.25	2.7	1.7999999999999998
26	1.7000000000000002	46.275	50.025	2.0
27	1.975	0.22499999999999998	95.75	2.0500000000000003
28	2.875	0.42500000000000004	47.3	49.4
29	3.4750000000000005	0.475	48.949999999999996	47.099999999999994
30	3.55	0.8250000000000001	46.7	48.925000000000004
31	50.74999999999999	0.8750000000000001	1.25	47.125
32	96.175	1.0999999999999999	1.225	1.5
33	95.475	1.425	1.125	1.975
34	50.24999999999999	1.7000000000000002	45.45	2.6
35	51.025	2.1999999999999997	44.474999999999994	2.3
36	47.225	2.7	0.6	49.475
37	2.275	3.125	0.3	94.3
38	2.6	50.24999999999999	0.44999999999999996	46.7
39	2.725	95.025	0.65	1.6
40	49.6	47.85	1.0999999999999999	1.4500000000000002
41	93.72500000000001	2.825	1.0250000000000001	2.4250000000000003
42	45.9	49.8	1.325	2.9749999999999996
43	0.8	94.075	1.525	3.5999999999999996
44	0.775	46.775	1.7500000000000002	50.7
45	0.9249999999999999	2.125	48.475	48.475
46	1.6500000000000001	1.8499999999999999	45.725	50.775000000000006
47	1.575	2.65	1.35	94.425
48	1.725	49.175000000000004	1.4500000000000002	47.65
49	48.3	47.05	1.825	2.825
50	45.800000000000004	2.375	47.9	3.925
>>END_MODULE
>>Per sequence GC content	pass
#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	0.5
34	1.0
35	1.0
36	1.0
37	3.0
38	5.0
39	11.5
40	18.0
41	39.0
42	60.0
43	97.5
44	135.0
45	209.5
46	284.0
47	356.0
48	428.0
49	469.0
50	510.0
51	544.0
52	578.0
53	564.0
54	550.0
55	498.5
56	447.0
57	396.5
58	346.0
59	307.5
60	269.0
61	237.0
62	205.0
63	150.0
64	95.0
65	69.0
66	43.0
67	30.5
68	18.0
69	11.5
70	5.0
71	3.5
72	2.0
73	1.0
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	0.0
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	0.44999999999999996
24	0.075
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	0.0
50	0.0
>>END_MODULE
>>Sequence Length Distribution	pass
#Length	Count
50	4000.0
>>END_MODULE
>>Sequence Duplication Levels	pass
#Total Deduplicated Percentage	97.8
#Duplication Level	Percentage of deduplicated	Percentage of total
1	98.74744376278119	96.575
2	0.843558282208589	1.6500000000000001
3	0.17893660531697342	0.525
4	0.10224948875255625	0.4
5	0.025562372188139063	0.125
6	0.025562372188139063	0.15
7	0.051124744376278126	0.35000000000000003
8	0.0	0.0
9	0.025562372188139063	0.22499999999999998
>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
ACACCGATGACGACTGTGAATGGAATTCTCGGGTGCCAAGGAACTCCAGT	9	0.22499999999999998	RNA PCR Primer, Index 1 (100% over 30bp)
CATCGAGTAGACCTTGTTATTGGAATTCTCGGGTGCCAAGGAACTCCAGT	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 30bp)
CCGTCTGCACGTACGTACGTTGGAATTCTCGGGTGCCAAGGAACTCCAGT	7	0.17500000000000002	RNA PCR Primer, Index 1 (100% over 30bp)
TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAGATCATCTCGTATGC	6	0.15	RNA PCR Primer, Index 7 (100% over 50bp)
CCATATGTTCCTTGCCAACCTGGAATTCTCGGGTGCCAAGGAACTCCAGT	5	0.125	RNA PCR Primer, Index 1 (100% over 30bp)
>>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	0.15	0.0	0.0	0.0
2	0.0	0.15	0.0	0.0	0.0
3	0.0	0.15	0.0	0.0	0.0
4	0.0	0.15	0.0	0.0	0.0
5	0.0	0.15	0.0	0.0	0.0
6	0.0	0.15	0.0	0.0	0.0
7	0.0	0.15	0.0	0.0	0.0
8	0.0	0.15	0.0	0.0	0.0
9	0.0	0.15	0.0	0.0	0.0
10	0.0	0.15	0.0	0.0	0.0
11	0.0	0.2	0.0	0.0	0.0
12	0.0	0.325	0.0	0.0	0.0
13	0.0	0.375	0.0	0.0	0.0
14	0.0	0.575	0.0	0.0	0.0
15	0.0	0.875	0.0	0.0	0.0
16	0.0	1.35	0.0	0.0	0.0
17	0.0	1.85	0.0	0.0	0.0
18	0.0	2.8	0.0	0.0	0.0
19	0.0	3.825	0.0	0.0	0.0
20	0.0	4.375	0.0	0.0	0.0
21	0.0	51.625	0.0	0.0	0.0
22	0.0	96.775	0.0	0.0	0.0
23	0.0	96.9	0.0	0.0	0.0
24	0.0	96.975	0.0	0.0	0.0
25	0.0	97.0	0.0	0.0	0.0
26	0.0	97.125	0.0	0.0	0.0
27	0.0	97.4	0.0	0.0	0.0
28	0.0	97.45	0.0	0.0	0.0
29	0.0	97.45	0.0	0.0	0.0
30	0.0	97.45	0.0	0.0	0.0
31	0.0	97.45	0.0	0.0	0.0
32	0.0	97.45	0.0	0.0	0.0
33	0.0	97.45	0.0	0.0	0.0
34	0.0	97.45	0.0	0.0	0.0
35	0.0	97.45	0.0	0.0	0.0
36	0.0	97.475	0.0	0.0	0.0
37	0.0	97.475	0.0	0.0	0.0
38	0.0	97.475	0.0	0.0	0.0
>>END_MODULE
>>Kmer Content	warn
#Sequence	Count	PValue	Obs/Exp Max	Max Obs/Exp Position
GTTGGAA	25	3.6958358E-5	44.0	19
CTCCAGT	215	0.0	39.906975	44
AATGGAA	55	8.843199E-8	32.0	19
TCTGGAA	35	2.6843656E-4	31.428572	20
CCTGGAA	35	2.6843656E-4	31.428572	20
TTGGAAT	90	2.2919266E-10	26.888891	20
GCTGGAA	50	6.483462E-5	26.4	19
ATGGAAT	100	2.3646862E-11	26.4	20
CTGGAAT	145	0.0	25.793104	21
AGTGGAA	55	1.240733E-4	24.0	19
GTGGAAT	75	1.3407134E-6	23.466667	21
GGAACTC	385	0.0	22.285715	40
AATTCTC	400	0.0	22.0	24
AGGAACT	390	0.0	22.0	39
ACTCCAG	390	0.0	22.0	43
AACTCCA	390	0.0	22.0	42
TCTCGGG	400	0.0	22.0	27
TTCTCGG	400	0.0	22.0	26
GAACTCC	390	0.0	22.0	41
GAATTCT	400	0.0	22.0	23
>>END_MODULE
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806248 spots for SRR6892966.sra
Written 3806248 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
Read 3806232 spots for SRR6892966.sra
Written 3806232 spots for SRR6892966.sra
SRR ids: ['SRR6892966.sra']
extra args: ['--split-files', '--defline-qual', '+']
tempdir: /tmp/pfd_cm632bvv
SRR6892966.sra spots: 76124656
blocks: [[1, 3806232], [3806233, 7612464], [7612465, 11418696], [11418697, 15224928], [15224929, 19031160], [19031161, 22837392], [22837393, 26643624], [26643625, 30449856], [30449857, 34256088], [34256089, 38062320], [38062321, 41868552], [41868553, 45674784], [45674785, 49481016], [49481017, 53287248], [53287249, 57093480], [57093481, 60899712], [60899713, 64705944], [64705945, 68512176], [68512177, 72318408], [72318409, 76124656]]
SRR6892966 file size 13183668
SRR6892966 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 SRR6892966 SRR6892966_1.fastq
Input file:	SRR6892966_1.fastq
trimmed:	SRR6892966-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
Thu Dec 12 02:17:20 2024 >> started

Thu Dec 12 02:20:48 2024 >> done (208.347s)
76124656 reads processed; of these:
   10742 ( 0.01%) short reads filtered out after trimming by size control
      21 ( 0.00%) empty reads filtered out after trimming by size control
76113893 (99.99%) reads available; of these:
 2916079 ( 3.83%) trimmed reads available after processing
73197814 (96.17%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	    4710	  0.01%
 19	    7392	  0.01%
 20	    9017	  0.01%
 21	    4650	  0.01%
 22	    2673	  0.00%
 23	   11885	  0.02%
 24	    6067	  0.01%
 25	    7180	  0.01%
 26	    8754	  0.01%
 27	   53144	  0.07%
 28	    7077	  0.01%
 29	    1698	  0.00%
 30	    2415	  0.00%
 31	    5250	  0.01%
 32	    8080	  0.01%
 33	   52720	  0.07%
 34	   92638	  0.12%
 35	   32635	  0.04%
 36	   19390	  0.03%
 37	   34245	  0.04%
 38	   21239	  0.03%
 39	   32671	  0.04%
 40	   14839	  0.02%
 41	  147549	  0.19%
 42	   36497	  0.05%
 43	  268300	  0.35%
 44	   76726	  0.10%
 45	   34261	  0.05%
 46	   71068	  0.09%
 47	  843156	  1.11%
 48	  301653	  0.40%
 49	  696500	  0.92%
 50	73197814	 96.17%
76113893 reads passed initial QC


criterion=sequence-density
sequence-density=97.58
sequence-density-rank=1
fanout-score=48.17
fanout-score-rank=2
prefix-density=97.93
prefix-fanout=48.0
sequence=TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAGATCATCTCGTATGC


criterion=fanout-score
sequence-density=4.26
sequence-density-rank=2
fanout-score=88.63
fanout-score-rank=1
prefix-density=98.09
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 TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAGATCATCTCGTATGC -o SRR6892966 -
Input file:	STDIN
trimmed:	SRR6892966-trimmed.fastq

Parameters used:
-- 3' end adapter sequence (-x):	TGGAATTCTCGGGTGCCAAGGAACTCCAGTCACCAGATCATCTCGTATGC
-- 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
Thu Dec 12 02:30:47 2024 >> started

Thu Dec 12 02:37:14 2024 >> done (386.628s)
74560548 reads processed; of these:
 2222564 ( 2.98%) short reads filtered out after trimming by size control
   53614 ( 0.07%) empty reads filtered out after trimming by size control
72284370 (96.95%) reads available; of these:
71841742 (99.39%) trimmed reads available after processing
  442628 ( 0.61%) untrimmed reads available after processing

Length distribution of reads after trimming:
length	count	percentage
 18	  752873	  1.04%
 19	  446869	  0.62%
 20	34953591	 48.36%
 21	35218913	 48.72%
 22	  133204	  0.18%
 23	   85374	  0.12%
 24	   77675	  0.11%
 25	   70416	  0.10%
 26	   86664	  0.12%
 27	   49272	  0.07%
 28	    9420	  0.01%
 29	    2152	  0.00%
 30	    1396	  0.00%
 31	    1146	  0.00%
 32	    1447	  0.00%
 33	    2198	  0.00%
 34	    9132	  0.01%
 35	   16378	  0.02%
 36	    7514	  0.01%
 37	    8143	  0.01%
 38	    3268	  0.00%
 39	    5402	  0.01%
 40	    1917	  0.00%
 41	    6768	  0.01%
 42	    2790	  0.00%
 43	    6497	  0.01%
 44	    2905	  0.00%
 45	    2663	  0.00%
 46	    4001	  0.01%
 47	    4648	  0.01%
 48	    3367	  0.00%
 49	    2054	  0.00%
 50	  304313	  0.42%


criterion=sequence-density
sequence-density=0.42
sequence-density-rank=1
fanout-score=0.00
fanout-score-rank=20
prefix-density=0.00
prefix-fanout=1.0
sequence=CATCGAGTAGACCTTGTTATTCTCGGGTG


criterion=fanout-score
sequence-density=0.11
sequence-density-rank=6
fanout-score=42.67
fanout-score-rank=1
prefix-density=0.20
prefix-fanout=23.3
sequence=TGGAATTCTCGTATGCCGTCTTCTGCTTGA
                                 Started job on |	Dec 12 02:40:51
                             Started mapping on |	Dec 12 02:40:51
                                    Finished on |	Dec 12 03:09:08
       Mapping speed, Million of reads per hour |	156.64

                          Number of input reads |	73837715
                      Average input read length |	21
                                    UNIQUE READS:
                   Uniquely mapped reads number |	64342573
                        Uniquely mapped reads % |	87.14%
                          Average mapped length |	20.45
                       Number of splices: Total |	2768166
            Number of splices: Annotated (sjdb) |	2724253
                       Number of splices: GT/AG |	2739599
                       Number of splices: GC/AG |	26804
                       Number of splices: AT/AC |	1625
               Number of splices: Non-canonical |	138
                      Mismatch rate per base, % |	0.05%
                         Deletion rate per base |	0.00%
                        Deletion average length |	1.63
                        Insertion rate per base |	0.00%
                       Insertion average length |	1.00
                             MULTI-MAPPING READS:
        Number of reads mapped to multiple loci |	6695551
             % of reads mapped to multiple loci |	9.07%
        Number of reads mapped to too many loci |	735660
             % of reads mapped to too many loci |	1.00%
                                  UNMAPPED READS:
       % of reads unmapped: too many mismatches |	0.00%
                 % of reads unmapped: too short |	2.63%
                     % of reads unmapped: other |	0.16%
                                  CHIMERIC READS:
                       Number of chimeric reads |	0
                            % of chimeric reads |	0.00%
N_unmapped	2799591	2799591	2799591
N_multimapping	6695551	6695551	6695551
N_noFeature	3521853	4073399	62692910
N_ambiguous	1225019	131877	5253
UnstrandedReadsAssigned:59595701 PositiveStrandReadsAssigned:60137297 NegativeStrandReadsAssigned:1644410
Dataset is classified positive stranded
MeadianReadLen=21 20thPercentileLength=20 echo kmer=19
SRR6892966 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: SRR6892966-trimmed.fastq
[quant] finding pseudoalignments for the reads ... done
[quant] processed 73,837,715 reads, 62,241,080 reads pseudoaligned
[   em] quantifying the abundances ... done
[   em] the Expectation-Maximization algorithm ran for 1,293 rounds

  52973 SRR6892966.ke.tsv
  35125 SRR6892966.se.tsv
  88098 total
==> SRR6892966.ke.tsv <==
target_id	length	eff_length	est_counts	tpm
PNS24245	936	837	0	0
PNS24247	1044	945	14.9285	0.366256
PNS24249	1928	1829	91.3192	1.15758
PNS24246	1044	945	14.9285	0.366256
PNS24248	1044	945	14.9285	0.366256
PNS24244	1471	1372	1499.9	25.3459
PNS24243	293	194	1	0.119509
KQK14069	1603	1504	4803.9	74.0538
KQK14071	474	375	358.557	22.1681

==> SRR6892966.se.tsv <==
BRADI_1g14170v3	4900
BRADI_1g53295v3	390
BRADI_1g59795v3	1117
BRADI_1g07683v3	1
BRADI_1g00485v3	43
BRADI_1g20270v3	2130
BRADI_1g74790v3	449
BRADI_1g09890v3	20
BRADI_1g77505v3	1037
BRADI_1g48960v3	1
SRR6892966 completed mapping pipeline successfully
