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2 changes: 1 addition & 1 deletion docs/_sources/ologram.rst.txt
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Expand Up @@ -228,7 +228,7 @@ As the computation of multiple overlaps can be RAM-intensive, if you have a very


Itemset mining details
-------------------------
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~


In broad strokes, the custom itemset algorithm MODL (Multiple Overlap Dictionary Learning) will perform many matrix factorizations on the matrix of true overlaps to identify relevant correlation groups of genomic regions. Then a greedy algorithm based on how much these words improve the reconstruction will select the utmost best words. MODL is only used to filter the output of OLOGRAM : once it returns a list of interesting combination, OLOGRAM will compute their enrichment as usual, but for them only. Each combination is of the form [Query + A + B + C] where A, B and C are BED files given as --more-bed. You can also manually specify the combinations to be studied with the format defined in OLOGRAM notes (below).
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180 changes: 90 additions & 90 deletions docs/coverage.html

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4 changes: 2 additions & 2 deletions docs/editing.html
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Expand Up @@ -436,7 +436,7 @@ <h2>discretize_key<a class="headerlink" href="#discretize-key" title="Permalink
</pre></div>
</div>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk join_attr -i simple.gtf -j simple.join_mat -k gene_id -m | gtftk discretize_key -k S1 -d S1_d -n 2 -l A,B | gtftk select_by_key -k feature -v gene
|-- 17:11-INFO-discretize_key : Categories: [&#39;A&#39;, &#39;B&#39;]
|-- 17:25-INFO-discretize_key : Categories: [&#39;A&#39;, &#39;B&#39;]
chr1 gtftk gene 125 138 . + . gene_id &quot;G0001&quot;;
chr1 gtftk gene 180 189 . + . gene_id &quot;G0002&quot;;
chr1 gtftk gene 50 61 . - . gene_id &quot;G0003&quot;; S1 &quot;0.2322&quot;; S2 &quot;0.4&quot;; S1_d &quot;A&quot;;
Expand All @@ -455,7 +455,7 @@ <h2>discretize_key<a class="headerlink" href="#discretize-key" title="Permalink
<p>The <em>profile</em> command that could be used to asses the associated epigenetic marks of these 10 gene classes.</p>
</div>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk join_attr -i mini_real.gtf.gz -H -j mini_real_counts_ENCFF630HEX.tsv -k gene_name -n exprs -t gene | gtftk discretize_key -k exprs -p -d exprs_class -n 10 -l A,B,C,D,E,F,G,H,I,J | gtftk tabulate -k exprs_class -Hn | sort | uniq -c
|-- 17:12-INFO-discretize_key : Categories: [&#39;A&#39;, &#39;B&#39;, &#39;C&#39;, &#39;D&#39;, &#39;E&#39;, &#39;F&#39;, &#39;G&#39;, &#39;H&#39;, &#39;I&#39;, &#39;J&#39;]
|-- 17:25-INFO-discretize_key : Categories: [&#39;A&#39;, &#39;B&#39;, &#39;C&#39;, &#39;D&#39;, &#39;E&#39;, &#39;F&#39;, &#39;G&#39;, &#39;H&#39;, &#39;I&#39;, &#39;J&#39;]
96 A
83 B
89 C
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4 changes: 1 addition & 3 deletions docs/index.html
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Expand Up @@ -136,9 +136,7 @@ <h1>Table of content<a class="headerlink" href="#table-of-content" title="Permal
<li class="toctree-l1"><a class="reference internal" href="ologram.html">Commands from section ‘ologram’</a><ul>
<li class="toctree-l2"><a class="reference internal" href="ologram.html#ologram">ologram</a></li>
<li class="toctree-l2"><a class="reference internal" href="ologram.html#ologram-multiple-overlaps">ologram (multiple overlaps)</a></li>
</ul>
</li>
<li class="toctree-l1"><a class="reference internal" href="ologram.html#itemset-mining-details">Itemset mining details</a><ul>
<li class="toctree-l2"><a class="reference internal" href="ologram.html#itemset-mining-details">Itemset mining details</a></li>
<li class="toctree-l2"><a class="reference internal" href="ologram.html#ologram-merge-stats">ologram_merge_stats</a></li>
<li class="toctree-l2"><a class="reference internal" href="ologram.html#ologram-modl-treeify">ologram_modl_treeify</a></li>
<li class="toctree-l2"><a class="reference internal" href="ologram.html#ologram-merge-runs">ologram_merge_runs</a></li>
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4 changes: 2 additions & 2 deletions docs/information.html
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Expand Up @@ -69,10 +69,10 @@ <h2>apropos<a class="headerlink" href="#apropos" title="Permalink to this headli
<p><strong>Description:</strong> Search in all command description files those related to a user-defined keyword.</p>
<p><strong>Example:</strong> Search all commands related to promoters.</p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk apropos -k promoter
|-- 17:12-INFO-apropos : &gt;&gt; Keyword &#39;promoter&#39; was found in the following command:
|-- 17:25-INFO-apropos : &gt;&gt; Keyword &#39;promoter&#39; was found in the following command:
- coverage.
- ologram.
- divergent.
- coverage.
</pre></div>
</div>
<p><strong>Arguments:</strong></p>
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14 changes: 7 additions & 7 deletions docs/miscellaneous.html
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Expand Up @@ -69,13 +69,13 @@ <h2>control_list<a class="headerlink" href="#control-list" title="Permalink to t
<p><strong>Description:</strong> Returns a list of gene matched for expression based on reference values. Based on a reference gene list (or more generally IDs) this command tries to extract a set of other genes/IDs matched for signal/expression. The –reference-gene-file contains the list of reference IDs while the –inputfile contains a tuple gene/signal for all genes.</p>
<p><strong>Example:</strong></p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk control_list -i mini_real_counts_ENCFF630HEX.tsv -r mini_real_control_1.txt -D -V 2 -s -l -p 1 -ju -if example_13.png -pf png
|-- 17:12-INFO-control_list : 0 duplicate lines have been deleted in reference file.
|-- 17:12-INFO-control_list : Found 50 genes of the reference in the provided signal file
|-- 17:12-INFO-control_list : All reference genes were found.
|-- 17:12-INFO-control_list : Searching for genes with matched signal.
|-- 17:12-INFO-control_list : Preparing a dataframe for plotting.
|-- 17:12-INFO-control_list : Saving diagram to file : example_13.png
|-- 17:12-INFO-control_list : Be patient. This may be long for large datasets.
|-- 17:26-INFO-control_list : 0 duplicate lines have been deleted in reference file.
|-- 17:26-INFO-control_list : Found 50 genes of the reference in the provided signal file
|-- 17:26-INFO-control_list : All reference genes were found.
|-- 17:26-INFO-control_list : Searching for genes with matched signal.
|-- 17:26-INFO-control_list : Preparing a dataframe for plotting.
|-- 17:26-INFO-control_list : Saving diagram to file : example_13.png
|-- 17:26-INFO-control_list : Be patient. This may be long for large datasets.
</pre></div>
</div>
<a class="reference external image-reference" href="_static/example_13.png"><img alt="_images/example_13.png" src="_images/example_13.png" /></a>
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38 changes: 18 additions & 20 deletions docs/ologram.html
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Expand Up @@ -102,8 +102,8 @@ <h2>ologram<a class="headerlink" href="#ologram" title="Permalink to this headli
</div>
<p><strong>Example:</strong> Perform a basic annotation. We are searching whether H3K4me3 peaks tends to be enriched in some specific genomic elements. The bars in the bar plot diagram will be ordered according to ‘summed_bp_overlaps_pvalue’.</p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk ologram -i hg38_chr1.gtf.gz -p ENCFF112BHN_H3K4me3_chr1.bed -c hg38_chr1.genome -u 1500 -d 1500 -D -pf example_pa_01.pdf -k 8 -j summed_bp_overlaps_pvalue
|-- 17:12-WARNING-ologram : Using only 8 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
|-- 17:13-WARNING-ologram : Computing log(p-val) for a Neg Binom with mean &gt;= var ; var was set to mean+1 (start_codon)
|-- 17:26-WARNING-ologram : Using only 8 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
|-- 17:26-WARNING-ologram : Computing log(p-val) for a Neg Binom with mean &gt;= var ; var was set to mean+1 (start_codon)
</pre></div>
</div>
<br>
Expand All @@ -118,7 +118,7 @@ <h2>ologram<a class="headerlink" href="#ologram" title="Permalink to this headli
<br>
<br><p><strong>Example:</strong> We are now using the gene_biotype key (note that a list of keys can be provided). This will tell us whether H3K4me3 tends to be located in particular transcripts (protein coding, LncRNAs…). The –no-basic-feature argument tells ologram not to test basic genomic elements (gene, transcripts…).</p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk select_by_key -i mini_real.gtf.gz -k gene_biotype -v protein_coding,lincRNA,antisense,processed_transcript | gtftk ologram -m gene_biotype -p ENCFF112BHN_H3K4me3_K562_sub.bed -c hg38 -D -n -pf example_pa_02.pdf -k 8 -j summed_bp_overlaps_pvalue
|-- 17:14-WARNING-ologram : Using only 8 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
|-- 17:27-WARNING-ologram : Using only 8 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
</pre></div>
</div>
<br>
Expand All @@ -137,8 +137,8 @@ <h2>ologram<a class="headerlink" href="#ologram" title="Permalink to this headli
</div>
<p><strong>Example:</strong> A more complex example where the key is created on the fly. Expression data are loaded as a novel key using the join_attr command and associated to gene features. This novel key (exprs) is then discretized to created 6 classes of genes with increasing expression (based on percentiles, -p) which are tested for enrichment in H3K36me3.</p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk join_attr -i mini_real.gtf.gz -H -j mini_real_counts_ENCFF630HEX.tsv -k gene_name -n exprs -t exon | gtftk discretize_key -k exprs -p -d exprs_class -n 6 -u | gtftk ologram -p ENCFF119BYM_H3K36me3_K562_sub.bed -c hg38 -D -n -m exprs_class -pf example_pa_03.pdf -k 8 -j summed_bp_overlaps_pvalue
|-- 17:15-INFO-discretize_key : Categories: [&#39;[0.0_183.0]&#39;, &#39;(183.0_549.0]&#39;, &#39;(549.0_1018.0]&#39;, &#39;(1018.0_1631.0]&#39;, &#39;(1631.0_3139.0]&#39;, &#39;(3139.0_41703.0]&#39;]
|-- 17:15-WARNING-ologram : Using only 8 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
|-- 17:28-INFO-discretize_key : Categories: [&#39;[0.0_183.0]&#39;, &#39;(183.0_549.0]&#39;, &#39;(549.0_1018.0]&#39;, &#39;(1018.0_1631.0]&#39;, &#39;(1631.0_3139.0]&#39;, &#39;(3139.0_41703.0]&#39;]
|-- 17:28-WARNING-ologram : Using only 8 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
</pre></div>
</div>
<br>
Expand All @@ -153,8 +153,8 @@ <h2>ologram<a class="headerlink" href="#ologram" title="Permalink to this headli
<br>
<br><p><strong>Example:</strong> Using the add_exon_nb, we add the exon number transcript-wise (numbering from 5’ to 3’) and discretize this novel key into 5 classes tested for enrichment.</p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk add_exon_nb -k exon_nbr -i mini_real.gtf.gz | gtftk discretize_key -p -d exon_nbr_cat -n 5 -k exon_nbr | gtftk ologram -p ENCFF112BHN_H3K4me3_K562_sub.bed -c hg38 -D -n -m exon_nbr_cat -pf example_pa_04.pdf -k 8 -j summed_bp_overlaps_pvalue
|-- 17:16-INFO-discretize_key : Categories: [&#39;[1.0_2.0]&#39;, &#39;(2.0_4.0]&#39;, &#39;(4.0_6.0]&#39;, &#39;(6.0_12.0]&#39;, &#39;(12.0_107.0]&#39;]
|-- 17:16-WARNING-ologram : Using only 8 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
|-- 17:29-INFO-discretize_key : Categories: [&#39;[1.0_2.0]&#39;, &#39;(2.0_4.0]&#39;, &#39;(4.0_6.0]&#39;, &#39;(6.0_12.0]&#39;, &#39;(12.0_107.0]&#39;]
|-- 17:29-WARNING-ologram : Using only 8 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
</pre></div>
</div>
<br>
Expand Down Expand Up @@ -182,14 +182,14 @@ <h2>ologram (multiple overlaps)<a class="headerlink" href="#ologram-multiple-ove
<p><strong>Simple example:</strong></p>
<p>Comparing the query (-p) against two other BED files, analyzing multiple overlaps.</p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk ologram -z -w -q -c simple_07.chromInfo -p simple_07_peaks.bed --more-bed simple_07_peaks.1.bed simple_07_peaks.2.bed --more-bed-multiple-overlap
|-- 17:16-WARNING : Converting to bed6 format (simple_07_peaks.bed).
|-- 17:16-WARNING : Converting to bed6 format (simple_07_peaks.1.bed).
|-- 17:16-WARNING : Converting to bed6 format (simple_07_peaks.2.bed).
|-- 17:16-WARNING-ologram : Using only 1 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
|-- 17:16-WARNING-ologram : --more-bed-labels was not set, automatically defaulting to --more-bed file names.
|-- 17:16-WARNING-ologram : [Query + simple_07_peaks_1 + ... ]: there may be a poor fit for this feature. Check fit quality in the results. This is likely due to there being too few regions.
|-- 17:16-WARNING-ologram : [Query + simple_07_peaks_1 + simple_07_peaks_2 + ... ]: there may be a poor fit for this feature. Check fit quality in the results. This is likely due to there being too few regions.
|-- 17:16-WARNING-ologram : Computing log(p-val) for a Neg Binom with mean &gt;= var ; var was set to mean+1 ([Query + simple_07_peaks_1 + simple_07_peaks_2 + ... ])
|-- 17:30-WARNING : Converting to bed6 format (simple_07_peaks.bed).
|-- 17:30-WARNING : Converting to bed6 format (simple_07_peaks.1.bed).
|-- 17:30-WARNING : Converting to bed6 format (simple_07_peaks.2.bed).
|-- 17:30-WARNING-ologram : Using only 1 threads, but 16 cores are available. Consider changing the --nb-threads parameter.
|-- 17:30-WARNING-ologram : --more-bed-labels was not set, automatically defaulting to --more-bed file names.
|-- 17:30-WARNING-ologram : [Query + simple_07_peaks_1 + ... ]: there may be a poor fit for this feature. Check fit quality in the results. This is likely due to there being too few regions.
|-- 17:30-WARNING-ologram : [Query + simple_07_peaks_1 + simple_07_peaks_2 + ... ]: there may be a poor fit for this feature. Check fit quality in the results. This is likely due to there being too few regions.
|-- 17:30-WARNING-ologram : Computing log(p-val) for a Neg Binom with mean &gt;= var ; var was set to mean+1 ([Query + simple_07_peaks_1 + simple_07_peaks_2 + ... ])
</pre></div>
</div>
<p><strong>Detailed example:</strong></p>
Expand Down Expand Up @@ -219,9 +219,8 @@ <h2>ologram (multiple overlaps)<a class="headerlink" href="#ologram-multiple-ove
<br><p>As the computation of multiple overlaps can be RAM-intensive, if you have a very large amount of candidate genomic feature sets (hundreds) we recommend selecting less candidates among them first by running a pairwise analysis.</p>
<p><strong>MODL itemset mining algorithm:</strong> By default, OLOGRAM-MODL will compute the enrichment of all n-wise combinations that are encountered in the real data it was passed. This however can add up to 2**N combinations and make the result hard to read. Furthermore, in biological data noise is a real problem and can obscure the relevant combinations. As such, we also give the option to use a custom itemset mining algorithm on the true overlaps to identify interesting combinations.</p>
</div>
</div>
<div class="section" id="itemset-mining-details">
<h1>Itemset mining details<a class="headerlink" href="#itemset-mining-details" title="Permalink to this headline"></a></h1>
<h2>Itemset mining details<a class="headerlink" href="#itemset-mining-details" title="Permalink to this headline"></a></h2>
<p>In broad strokes, the custom itemset algorithm MODL (Multiple Overlap Dictionary Learning) will perform many matrix factorizations on the matrix of true overlaps to identify relevant correlation groups of genomic regions. Then a greedy algorithm based on how much these words improve the reconstruction will select the utmost best words. MODL is only used to filter the output of OLOGRAM : once it returns a list of interesting combination, OLOGRAM will compute their enrichment as usual, but for them only. Each combination is of the form [Query + A + B + C] where A, B and C are BED files given as –more-bed. You can also manually specify the combinations to be studied with the format defined in OLOGRAM notes (below).</p>
<p>Unlike classical association rules mining algorithms, this focuses on mining relevant bio complexes/clusters and correlation groups (item sets), and you should not request more than 20-30 combinations. As a matrix factorization based algorithm, it is designed to be resistant
to noise which is a known problem in biological data. Its goal is to extract meaningful frequent combinations from noisy data. As a result however, it is biased in favor of the most abundant combinations in the data, and may return correlation groups if you ask for too few words (ie. if AB, BC and AC are complexes, ABC might be returned).</p>
Expand Down Expand Up @@ -436,6 +435,7 @@ <h1>Itemset mining details<a class="headerlink" href="#itemset-mining-details" t
<p>The resulting flags_matrix is a NumPy array that can be edited, and on which MODL can be run.</p>
<p>Since the results of MODL only depend on the true intersections and not on the shuffles, you can run MODL with 1 shuffle or on a manually computed matrix as above to pre-select interesting combinations, and then run the full analysis on many shuffles. We then recommend selecting the combinations that interest you in the resulting tsv file, using MODL’s selection as a starting point and adding or removing some combinations based on your own needs (eg. adding all the highest fold changes, or all particular combinations containing the Transcription Factor X that you are studying).</p>
<p>It is also possible to run any itemset miner you wish on this matrix. An implementation of apriori is provided in the <cite>pygtftk.stats.intersect.modl.apriori.Apriori</cite> class.</p>
</div>
<div class="section" id="ologram-merge-stats">
<h2>ologram_merge_stats<a class="headerlink" href="#ologram-merge-stats" title="Permalink to this headline"></a></h2>
<p><strong>Description:</strong> Several tsv files resulting from <em>OLOGRAM</em> analyses can be merged into a single diagram report using the merge_ologram_stats.</p>
Expand Down Expand Up @@ -614,9 +614,7 @@ <h3><a href="index.html">Table of Contents</a></h3>
<li><a class="reference internal" href="#">Commands from section ‘ologram’</a><ul>
<li><a class="reference internal" href="#ologram">ologram</a></li>
<li><a class="reference internal" href="#ologram-multiple-overlaps">ologram (multiple overlaps)</a></li>
</ul>
</li>
<li><a class="reference internal" href="#itemset-mining-details">Itemset mining details</a><ul>
<li><a class="reference internal" href="#itemset-mining-details">Itemset mining details</a></li>
<li><a class="reference internal" href="#ologram-merge-stats">ologram_merge_stats</a></li>
<li><a class="reference internal" href="#ologram-modl-treeify">ologram_modl_treeify</a></li>
<li><a class="reference internal" href="#ologram-merge-runs">ologram_merge_runs</a></li>
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12 changes: 6 additions & 6 deletions docs/selection.html
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Expand Up @@ -447,8 +447,8 @@ <h2>random_list<a class="headerlink" href="#random-list" title="Permalink to thi
<p><strong>Example:</strong> Select randomly 3 transcripts.</p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk random_list -n 3 -i simple.gtf | gtftk count
transcript 3
exon 5
CDS 5
exon 7
CDS 3
</pre></div>
</div>
<p><strong>Arguments:</strong></p>
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<p><strong>Example:</strong> Select randomly 1 transcript per gene (<em>-m 1</em>).</p>
<div class="highlight-text notranslate"><div class="highlight"><pre><span></span>$ gtftk random_tx -m 1 -i simple.gtf | gtftk select_by_key -k feature -v gene,transcript| gtftk tabulate -k gene_id,transcript_id
gene_id transcript_id
G0001 G0001T002
G0001 G0001T001
G0002 G0002T001
G0003 G0003T001
G0004 G0004T001
G0004 G0004T002
G0005 G0005T001
G0006 G0006T002
G0006 G0006T001
G0007 G0007T001
G0008 G0008T001
G0009 G0009T002
G0009 G0009T001
G0010 G0010T001
</pre></div>
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