FIMO Results

FIMO - Motif search tool

FIMO version 5.5.5, (Release date: Thu Sep 14 08:48:04 2023 +1000)

For further information on how to interpret these results please access https://meme-suite.org/meme/doc/fimo-output-format.html.
To get a copy of the FIMO software please access https://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 MOA1_loss_diff.fa
  
  Database contains 1227 sequences, 29094 residues

  MOTIFS streme_out/streme.xml (DNA)
  
        MOTIF
        WIDTH
        
         BEST POSSIBLE MATCH
        
        1-CWGRAR
        6
        CAGAAA
       
        2-AAAAATG
        7
        AAAAATG
       
        3-HTTTWAAAD
        9
        TTTTTAAAA
       
        4-GAGGAAR
        7
        GAGGAAA
       
        5-CCASTGG
        7
        CCAGTGG
       
Random model letter frequencies (./background):

A 0.311 C 0.189 G 0.189 T 0.311

MOTIF	WIDTH	BEST POSSIBLE MATCH
1-CWGRAR	6	CAGAAA
2-AAAAATG	7	AAAAATG
3-HTTTWAAAD	9	TTTTTAAAA
4-GAGGAAR	7	GAGGAAA
5-CCASTGG	7	CCAGTGG

SECTION I: HIGH-SCORING MOTIF OCCURENCES

There were 12 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
4-GAGGAAR	STREME-4	chr10	+	554326	554332	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr20	+	18466628	18466634	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr15	+	38288334	38288340	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr1	+	45945568	45945574	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr2	-	57133273	57133279	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr16	-	58164363	58164369	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr12	-	98227381	98227387	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr15	+	98736106	98736112	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr7	+	99032154	99032160	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr9	-	110704383	110704389	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr10	+	114697086	114697092	3.85e-05	0.138	GAGGAAG
4-GAGGAAR	STREME-4	chr5	-	134705794	134705800	3.85e-05	0.138	GAGGAAG

DEBUGGING INFORMATION

Command line:

fimo --verbosity 1 --oc fimo_out_4 --bgfile ./background --motif 4-GAGGAAR streme_out/streme.xml MOA1_loss_diff.fa

Settings:


  
    output_directory = fimo_out_4
    MEME file name = streme_out/streme.xml
    sequence file name = MOA1_loss_diff.fa
  
  
    background file name = ./background
    alphabet = DNA
    max stored scores = 100000
  
  
    allow clobber = true
    compute q-values = true
    parse genomic coord. = true
  
  
    text only = false
    scan both strands = true
    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.

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output_directory = fimo_out_4	MEME file name = streme_out/streme.xml	sequence file name = MOA1_loss_diff.fa
background file name = ./background	alphabet = DNA	max stored scores = 100000
allow clobber = true	compute q-values = true	parse genomic coord. = true
text only = false	scan both strands = true	max strand = false
threshold type = p-value	output theshold = 0.0001	pseudocount = 0.1
alpha = 1	verbosity = 1