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 cluster_8_coord_nodup.txt.fa
  
  Database contains 967 sequences, 29010 residues

  MOTIFS streme_out/streme.xml (DNA)
  
        MOTIF
        WIDTH
        
         BEST POSSIBLE MATCH
        
        1-WTCCCAGMHT
        10
        TTCCCAGCAT
       
        2-GTGACTCATH
        10
        GTGACTCATA
       
        3-TCAGMA
        6
        TCAGAA
       
        4-TGCCAAA
        7
        TGCCAAA
       
Random model letter frequencies (./background):

A 0.304 C 0.196 G 0.196 T 0.304

MOTIF	WIDTH	BEST POSSIBLE MATCH
1-WTCCCAGMHT	10	TTCCCAGCAT
2-GTGACTCATH	10	GTGACTCATA
3-TCAGMA	6	TCAGAA
4-TGCCAAA	7	TGCCAAA

SECTION I: HIGH-SCORING MOTIF OCCURENCES

There were 9 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-TGCCAAA	STREME-4	chr17	+	8285040	8285046	6.43e-05	0.329	tgccaaa
4-TGCCAAA	STREME-4	chr6	+	13559765	13559771	6.43e-05	0.329	TGCCAAA
4-TGCCAAA	STREME-4	chr10	+	18966464	18966470	6.43e-05	0.329	tgccaaa
4-TGCCAAA	STREME-4	chr16	+	47094181	47094187	6.43e-05	0.329	TGCCAAA
4-TGCCAAA	STREME-4	chr10	-	47391842	47391848	6.43e-05	0.329	TGCCAAA
4-TGCCAAA	STREME-4	chr14	-	59348344	59348350	6.43e-05	0.329	TGCCAAA
4-TGCCAAA	STREME-4	chr3	-	129657841	129657847	6.43e-05	0.329	TGCCAAA
4-TGCCAAA	STREME-4	chr4	-	152799619	152799625	6.43e-05	0.329	TGCCAAA
4-TGCCAAA	STREME-4	chr1	-	185818626	185818632	6.43e-05	0.329	TGCCAAA

DEBUGGING INFORMATION

Command line:

fimo --verbosity 1 --oc fimo_out_1 --bgfile ./background --motif 4-TGCCAAA streme_out/streme.xml cluster_8_coord_nodup.txt.fa

Settings:


  
    output_directory = fimo_out_1
    MEME file name = streme_out/streme.xml
    sequence file name = cluster_8_coord_nodup.txt.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_1	MEME file name = streme_out/streme.xml	sequence file name = cluster_8_coord_nodup.txt.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