Parameters
input_file_cond1: 20090724_LUd3_1_hg19_ensembl59_G_iCLIP_TIA1_HeLa_bedGraph-cDNA-hits-in-genome.bed.gz
input_file_cond1_res_type: single hits in whole-genome, cDNA counts
input_file_cond2: 20090724_LUd3_1_hg19_ensembl59_M_iCLIP_TIA1_HeLa_bedGraph-cDNA.bed.gz
input_file_cond2_res_type: multiple hits in transcribed genome, cDNA counts
mapped_to: hg19
annot_ver: ensembl59
window_size: 250
MA_window_size: 15

Differential analysis

MA plots are used for differential analysis of condition 1 (cond1) vs. condition 2 (cond2).
Data (bedGraphs) from two conditions are quantile-normalized first, then put into a MA-plot.
A sliding window of 15% of A axis span is used to calculate z-scores (of M).

Positive z-score indicates over-representation of counts in condition 1.
Negative z-score indicates over-representation of counts in condition 2.

Because bedGraph format uses the sign to indicate strand, results are split into two bedGraphs. Magnitude equals to the absolute value of z-score and sign indicates strand:

A third bedGraph is also produced showing only windows centered at peaks of high-density smoothed absolute z-values.

MA plots

M=log(count_cond1/count_cond2), A=log(count_cond1)+log(count_cond2).


Top 30 regions with highest density of difference (z-scores) in counts

Click on region to automatically upload the two bedGraphs with z-scores of differential analysis and start exploring in UCSC browser.

smoothed_abs_z_scorez_scoreAMnormalized count in condition 1normalized count in condition 2regiongene_namesense relative
to window
seg_typeseg_biotype
154.646.442.846.5268.71430.75chr14+:62213716..62214216HIF1Asame3UTRprotein_coding
151.93-5.372.96-5.271.2548.24chr1+:17222299..17222799U1-ENSG00000207005samencRNAsnRNA
136.88-4.734.23-4.47488.5833chr10-:33189349..33189849ITGB1same3UTRprotein_coding
133.83-5.483.93-5.212.592.6662chr11-:61731877..61732377FTH1same3UTRprotein_coding
123.05-7.502.74-7.480.589.5417chr12+:20704146..20704646AC112777.1samencRNArRNA_pseudogene
112.51-4.763.30-4.59248.24chr1-:16840451..16840951U1-ENSG00000206652samencRNAsnRNA
100.75-5.313.16-5.161.553.5833chr14-:21679017..21679517HNRNPCsame3UTRprotein_coding
97.71-6.622.55-6.710.57142959.986chr7+:44840850..44841350PPIAsameORFprotein_coding
94.685.243.965.0990.62.66667chr1-:45976674..45977174PRDX1same3UTRprotein_coding
91.78-5.771.72-5.450.521.8247chr1-:228763725..2287642255S_rRNA-ENSG00000201321samencRNArRNA
89.41-5.721.59-5.170.518.0222chr12+:98115282..98115782U6-ENSG00000206899samencRNAsnRNA
86.68-5.882.06-6.130.535.0167chr12+:42848319..42848819Y_RNA-ENSG00000207142samencRNAmisc_RNA
82.45-4.162.85-4.091.7529.8117chr1+:226259013..226259513H3F3Asame3UTRprotein_coding
80.137.432.847.5196.54920.529412chr16-:87866030..87866530SLC7A5same3UTRprotein_coding
78.80-5.712.25-6.050.58333338.6937chr7+:148680644..148681144Y_RNA-ENSG00000202354samencRNAmisc_RNA
78.28-5.942.19-6.380.541.7851chr1+:38010739..38011239SNIP1antiintronprotein_coding
77.953.763.453.7239.6253chr1+:169101418..169101918ATP1B1same3UTRprotein_coding
77.356.363.426.2693.73681.225chr1-:153515923..153516423S100A4sameORFprotein_coding
76.286.043.315.9778.36761.25chr3+:41281284..41281784CTNNB1same3UTRprotein_coding
73.99-5.801.81-5.610.524.4333chr13+:82264659..82265159PTMAP5same3UTRprotein_coding
72.90-5.841.95-5.900.529.8333chr1+:220428047..220428547RAB3GAP2antiintronprotein_coding
72.753.744.103.6460.66674.86458chr11-:65622285..65622785CFL1same3UTRprotein_coding
72.674.303.304.2743.3822.25chr1-:26227062..26227562STMN1sameORFprotein_coding
71.44-5.062.62-5.071.0588235.6454chr4-:91759751..91760251TMSL3same3UTRprotein_coding
70.76-5.811.84-5.690.525.8083chr10+:99192188..99192688PGAM1sameORFprotein_coding
70.5010.234.489.80666.6590chr11+:65272059..65272559intersameinter
69.535.252.395.6136.66490.75chr14-:102547723..102548223HSP90AA1same3UTRprotein_coding
69.314.612.145.1025.750.75chr12-:123745716..123746216CDK2AP1same3UTRprotein_coding
67.862.384.452.3248.79580chr15+:45009998..45010498B2Msame3UTRprotein_coding
67.23-5.602.21-5.980.58333336.9103chr7-:22549848..22550348EEF1A1P6samencRNApseudogene
Download full list in tab-delimited format.

Other measures of (dis)similarity

x-links in condition 1: 208288
x-links in condition 2: 138370
All x-link positions (union): 346314
Positions shared by both conditions (intersection): 344
Jaccard index (intersection/union): 0.0010

x-link position similarity

For each x-link in condition 1 (condition 2), look for nearest x-link in condition 2 (condition 1). Draw histogram of distances to closest neighbors.

Average distances (full span), all include distance 0: Average distances (-200..200 window), all include distance 0: [eps]
Download graphs in tab-delimited format.

Count similarity

For each x-link position with specific value stored in input bedGraph for condition 1 (condition 2) look if same position in bedGraph for condition 2 (condition 1) has a non-zero value.

[eps]
Download graphs in tab-delimited format.

k-mers similarity

For k-mer analyses performed with same parameters on both conditions, report on similarity of results.
Similarity is measured by correlation of z-scores of all k-mers, and number of top k-mers shared by both conditions.

Available k-mer analyses:
comparedanalysis parametersconditionanalysis id
Falsechromosomes=whole genome, intervals=[(-30, -10), (10, 30)], k=5, random_perms=100, report_for_region=(-50, 50), valid_region_types=['ncRNA', '3UTR', '5UTR', 'intron', 'ORF']condition 170962
Falsechromosomes=whole genome, intervals=[(-30, -10), (10, 30)], k=5, random_perms=100, report_for_region=(-50, 50), valid_region_types=['ncRNA', 'ORF', '3UTR', '5UTR', 'intron']condition 148438
Falsechromosomes=whole genome, intervals=[(-50, 50)], k=5, random_perms=100, report_for_region=(-50, 50), valid_region_types=['ncRNA', 'ORF', '3UTR', '5UTR', 'intron']condition 155403
Skipping this comparison because no analysis with same parameters in both conditions exist.

RNAmaps similarity

For RNAmap analyses performed with same parameters on both conditions, report on similarity of results.
RNAmaps are compared by normalizing them first to sum 1.0 and then taking the average squared absolute difference (units are squared abs. difference per 1000 positions).

Available RNAmap analyses:
comparedanalysis parametersconditionanalysis id
Falsechromosomes=whole genome, maxD_flanking=1000, maxD_within=300, maxU_flanking=-1000, maxU_within=-300, smoothing=0condition 148439
Falsechromosomes=whole genome, maxD_flanking=1000, maxD_within=300, maxU_flanking=-1000, maxU_within=-300, smoothing=5condition 170963
Skipping this comparison because no analysis with same parameters in both conditions exist.