-
Notifications
You must be signed in to change notification settings - Fork 2
Home
In a hurry? Check out our Quickstart guide
Regulatory proteins, such as Transcription Factors (TFs), are key genomic elements which promote or reduce the expression of genes by binding short, evolutionary conserved DNA sequences, often referred to as motifs. Mutations occurring in DNA motifs have been shown to have deleterious effects on the transcriptional landscape of the cell (Li & Ovcharenko, 2015; Guo et al., 2018). The recent introduction of Genome Variation Graphs (VG) (Garrison et al., 2018) allowed to represent in a single and efficient data-structure the genomic variation present within a population of individuals.
GRAFIMO (GRAph-based Finding of Individual Motif Occurrences) is a command-line tool that extends the traditional Position Weight Matrix (PWM) scanning procedure to VGs. GRAFIMO can search the occurrences of a given PWM in many genomes in a single run, accounting for the effects that SNPs, indels and potentially any structural variation (handled by VG) have on found potential motif occurrences. As result, GRAFIMO produces a report containing the statistically significant motif candidates found, reporting their frequency within the haplotypes embedded in the scanned VG and if they contain genomic variants or belong to the reference genome sequence.
For any bug report, doubts or improvement suggestions, do not hesitate to open an issue!
- Required softwares and dependencies
- Install GRAFIMO via pip
- Install GRAFIMO via source code
- Install GRAFIMO via Bioconda (Linux users only)
- Use GRAFIMO via Docker (All Operating Systems including Windows and MacOS)
Looking for an hands-on tutorial? Check out our practical tutorials.
In this section will be presented how to run GRAFIMO and some advanced options. Here we assume that the genome variation graph (VG) has been built constructing a VG for each chromosome. If you have a single whole genome variation graph, substitute -d argument with -g followed by the path to your whole genome VG. If you do not have a genome variation graph, here is described how to construct it with GRAFIMO.
Note that in both cases the XG and GBWT indexes must be stored in the same location.
Doubts on building genomes as single whole genome variation graph or constructing a VG for each chromosome? Check out our discussion.
GRAFIMO requires three mandatory arguments:
- path to a directory containing the chromosomes VGs (XG and GBWT indexes) or path to the whole genome variation graph (XG and GBWT indexes). See VG's wiki for further details on XG and GBWT indexes.
- path to PWM motif file in MEME or JASPAR format
- BED file containing a set of genomic regions, where GRAFIMO will search the potential motif occurrences
To run GRAFIMO from command-line
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file
By default GRAFIMO will create a directory in the current location called grafimo_out_PID_MOTIFID, containing the results. For further details on result files see Results description section.
For each potential motif occurrence GRAFIMO computes a log-likelihood score, a P-value and a q-value. Such measures are weighted by a background probability distribution. By default, GRAFIMO assumes a uniform background distribution for nucleotides. The user can specify a different background distribution in a text file and give it to GRAFIMO using -k option. An example of background file is
A 0.2951
C 0.2047
T 0.2955
G 0.2048
Assume that our background distribution has been written in a file named bg_nt, then we call GRAFIMO with
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file -k path/to/bg_nt
For an example of background files accepted by GRAFIMO, take a look at bg_nt in tutorials/findmotif_tutorial/data directory.
By default GRAFIMO applies a threshold of 1e-4 on the P-value of each retrieved potential motif occurrence. So, will be reported the motif candidates with an associated P-value smaller than 1e-4. The threshold can be changed by using the -t option. For example, let us set a threshold of 1e-3 on the P-values
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file -t 1e-3
GRAFIMO, besides P-values, computes q-values for the motif occurrences candidates. The user can apply a threshold on q-values, rather than on P-values, by using the --qvalueT option. --qvalueT option can be used in combination with -t to define a threshold value different from 1e-4. Let us apply a threshold of 1e-5 on q-values
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file --qvalueT -t 1e-5
GRAFIMO by default reports only those potential motif occurrences which are found in at least one of the haplotypes encoded in the VG. GRAFIMO allows to include in the final report also those motif occurrences (surviving the threshold on statistical significance) which are not observed in the haplotypes encoded in the VG, but which can be obtained from the set of genomic variants, used to construct the genome variation graph. In order to do this, we use the --recomb option
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file --recomb
It is possible to limit GRAFIMO search for potential motif occurrences to a subset of chromosomes by using the -c option. Let us assume we are interested only in what is happening on chr2, chr10 and chrX. In order to do this, we call GRAFIMO from command-line with
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file --chroms-find 2 10 X
As mentioned in "How to run GRAFIMO" section, by default, GRAFIMO creates a directory named grafimo_out_PID_MOTIFID, which contains the results. To store GRAFIMO results in a different directory (can be both a new or an already existing directory), we call GRAFIMO with -o option
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file -o /path/to/my/output/directory
GRAFIMO allows also to explore the VG structure for a user-defined number of regions (the top n regions, starting from the one containing the potential binding site with most significant P-value). GRAFIMO will create a PNG image for each one of the best n regions. The images will be stored in results directory, inside top_graphs folder. Let us assume we want to inspect the structure of the best 10 regions. In order to do this, we call GRAFIMO with --top-graph option
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file --top-graph 10
It is also possible to visualize results directly on stdout, without writing report files. Note that on the stdout will be printed only the content of the TSV report. To do this, we call GRAFIMo from command-line with -f option
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file -f
By default, GRAFIMO will use all available cores. As discussed here, the user can set a smaller number of used cores, in order to limit the amount of required resources. For example, to run GRAFIMO using just four cores, we type
grafimo findmotif -d /path/to/my/xg/and/gbwt/directory -m /path/to/my/motif -b /path/to/my/bed/file --cores 4
For more options available when running GRAFIMO, type from command-line
grafimo -h
GRAFIMO results are reported in three files (stored in output directory):
- tab-delimited report (TSV report)
- HTML report
- GFF3 report
The TSV report contains all the statistically significant potential motif occurrence found by GRAFIMO (according to the applied threshold). Each retrieved motif occurrence has a log-likelihood score, a P-value, a q-value, its DNA sequence, a flag value stating if a sequence is part of the reference or has been found in the haplotypes and the number of haplotype sequences where the motif candidate sequence occurs. An example of TSV report is the following
motif_id motif_alt_id sequence_name start stop strand score p-value q-value matched_sequence haplotype_frequency reference
1 MA0139.1 CTCF chr22:43481590-43481860 43481733 43481714 - 21.26229508196724 4.403657357543095e-08 0.004175283686980911 AAGCCAGCAGGGGGCACAG 5096 ref
2 MA0139.1 CTCF chr22:19038291-19038561 19038422 19038441 + 19.245901639344254 1.9442011615088443e-07 0.005962538354344465 TGGCCAGCAAGGGGCACTG 4 non.ref
3 MA0139.1 CTCF chr22:19038291-19038561 19038422 19038441 + 19.114754098360663 2.1268826066771178e-07 0.005962538354344465 CGGCCAGCAAGGGGCACTG 5092 ref
4 MA0139.1 CTCF chr22:40856678-40856948 40856891 40856910 + 18.295081967213093 3.6764803446618004e-07 0.005962538354344465 TCCCCTCCAGGGGGCGACG 5096 ref
5 MA0139.1 CTCF chr22:11285607-11285877 11285804 11285785 - 18.213114754098342 3.8774723287177635e-07 0.005962538354344465 ATACCGCCAGGTGGCAGCA 5096 ref
6 MA0139.1 CTCF chr22:22125904-22126174 22126044 22126063 + 18.13114754098359 4.088625891963074e-07 0.005962538354344465 CAGCCTGCAGATGGCACAG 5096 ref
7 MA0139.1 CTCF chr22:20146797-20147067 20147010 20147029 + 17.688524590163922 5.4295945317287e-07 0.005962538354344465 CGGCCCGCAGGGGGCGGAT 5092 ref
8 MA0139.1 CTCF chr22:34842682-34842952 34842827 34842846 + 17.672131147540995 5.486120126825257e-07 0.005962538354344465 GAGCCAGTAGGGGACAGCG 146 non.ref
9 MA0139.1 CTCF chr22:42532903-42533173 42533062 42533081 + 17.622950819672155 5.659801842459994e-07 0.005962538354344465 GGGCCACCAGAGGGCTCCT 5096 ref
10 MA0139.1 CTCF chr22:34842682-34842952 34842827 34842846 + 17.44262295081967 6.331282484526275e-07 0.006002942174878742 GAGCCAGTAGGGGACAGTG 4950 ref
This report can be easily processed for a downstream analysis.
The HTML report has the same content of the TSV, but it can be loaded and viewed on the most commonly used web browsers.
The GFF3 report can be loaded on the UCSC Genome Browser as a custom track. For example, this allows a fast linking between the genomic variants used to build the VG and those present in annotated databases like dbSNP or ClinVar.
Li, Shan, and Ivan Ovcharenko. "Human enhancers are fragile and prone to deactivating mutations." Molecular biology and evolution 32.8 (2015): 2161-2180.
Guo, Yu Amanda, et al. "Mutation hotspots at CTCF binding sites coupled to chromosomal instability in gastrointestinal cancers." Nature communications 9.1 (2018): 1-14.
Garrison, Erik, et al. "Variation graph toolkit improves read mapping by representing genetic variation in the reference." Nature biotechnology 36.9 (2018): 875-879.