FIMO Results

FIMO - Motif search tool

FIMO version 5.1.1, (Release date: Wed Jan 29 15:00:42 2020 -0800)

For further information on how to interpret these results please access http://meme-suite.org//doc/fimo-output-format.html.
To get a copy of the FIMO software please access http://meme-suite.org

If you use FIMO in your research, please cite the following paper:
Charles E. Grant, Timothy L. Bailey, and William Stafford Noble, "FIMO: Scanning for occurrences of a given motif", Bioinformatics, 27(7):1017-1018, 2011. [full text]

DATABASE AND MOTIFS

  DATABASE sequence.fasta
  
  Database contains 1 sequences, 30482 residues

  MOTIFS MEME.html (DNA)
  
        MOTIF
        WIDTH
        
         BEST POSSIBLE MATCH
        
        TTAACGAACT
        10
        TTAACGAACT
       
        CKTGCTGC
        8
        CGTGCTGC
       
        AAGAGA
        6
        AAGAGA
       
Random model letter frequencies (--nrdb--):

A 0.282 C 0.222 G 0.229 T 0.267

MOTIF	WIDTH	BEST POSSIBLE MATCH
TTAACGAACT	10	TTAACGAACT
CKTGCTGC	8	CGTGCTGC
AAGAGA	6	AAGAGA

SECTION I: HIGH-SCORING MOTIF OCCURENCES

There were 16 motif occurences with a p-value less than 0.0001. The full set of motif occurences can be seen in the TSV (tab-delimited values) output file fimo.tsv, the GFF3 file fimo.gff which may be suitable for uploading to the UCSC Genome Table Browser (assuming the FASTA input sequences included genomic coordinates in UCSC or Galaxy format), or the XML file fimo.xml.
The p-value of a motif occurrence is defined as the probability of a random sequence of the same length as the motif matching that position of the sequence with as good or better a score.
The score for the match of a position in a sequence to a motif is computed by summing the appropriate entries from each column of the position-dependent scoring matrix that represents the motif.
The q-value of a motif occurrence is defined as the false discovery rate if the occurrence is accepted as significant.
The table is sorted by increasing p-value.

Motif ID	Alt ID	Sequence Name	Strand	Start	End	p-value	q-value	Matched Sequence
TTAACGAACT	MEME-1	NC_009020.1	+	58	67	1.36e-06	0.00828	TTAACGAACT
TTAACGAACT	MEME-1	NC_009020.1	+	21681	21690	1.36e-06	0.00828	TTAACGAACT
TTAACGAACT	MEME-1	NC_009020.1	+	25799	25808	1.36e-06	0.00828	TTAACGAACT
TTAACGAACT	MEME-1	NC_009020.1	+	26122	26131	1.36e-06	0.00828	TTAACGAACT
TTAACGAACT	MEME-1	NC_009020.1	+	28148	28157	1.36e-06	0.00828	TTAACGAACT
TTAACGAACT	MEME-1	NC_009020.1	+	27143	27152	2.79e-06	0.0142	TAAACGAACT
CKTGCTGC	MEME-2	NC_009020.1	+	91	98	9.38e-06	0.228	CGTGCTGC
TTAACGAACT	MEME-1	NC_009020.1	+	27893	27902	1.58e-05	0.0689	AAAACGAACT
CKTGCTGC	MEME-2	NC_009020.1	+	4299	4306	2.03e-05	0.228	CTTGCTGC
TTAACGAACT	MEME-1	NC_009020.1	+	28852	28861	3.13e-05	0.119	TTAACGAATC
CKTGCTGC	MEME-2	NC_009020.1	+	12885	12892	3.59e-05	0.228	CGCGCTGC
CKTGCTGC	MEME-2	NC_009020.1	+	27834	27841	3.59e-05	0.228	CGCGCTGC
CKTGCTGC	MEME-2	NC_009020.1	+	12308	12315	4.56e-05	0.228	GGTGCTGC
CKTGCTGC	MEME-2	NC_009020.1	+	22116	22123	4.56e-05	0.228	GGTGCTGC
TTAACGAACT	MEME-1	NC_009020.1	+	26310	26319	5.13e-05	0.173	TGAGCCAACT
CKTGCTGC	MEME-2	NC_009020.1	+	10265	10272	7.51e-05	0.322	CGTGTTGC

DEBUGGING INFORMATION

Command line:

fimo --oc . --verbosity 1 --thresh 1.0E-4 --norc MEME.html sequence.fasta

Settings:


  
    output_directory = .
    MEME file name = MEME.html
    sequence file name = sequence.fasta
  
  
    background file name = --nrdb--
    alphabet = DNA
    max stored scores = 100000
  
  
    allow clobber = true
    compute q-values = true
    parse genomic coord. = false
  
  
    text only = false
    scan both strands = false
    max strand = false
  
  
    threshold type = p-value
    output theshold = 0.0001
    pseudocount = 0.1
  
  
    alpha = 1
    verbosity = 1

This information can be useful in the event you wish to report a problem with the FIMO software.

Go to top

output_directory = .	MEME file name = MEME.html	sequence file name = sequence.fasta
background file name = --nrdb--	alphabet = DNA	max stored scores = 100000
allow clobber = true	compute q-values = true	parse genomic coord. = false
text only = false	scan both strands = false	max strand = false
threshold type = p-value	output theshold = 0.0001	pseudocount = 0.1
alpha = 1	verbosity = 1