Thank you for your great tools. I have a question: I'm not quite sure how to generate the input matrix from the normalized count table for RNA-Seq, ATAC-Seq, and WBGS data. Could you please explain?
Following an exemple of my data :
For ATAC-seq:
"Chr","Start","End","Bd21-3 D0r1","Bd21-3 D1r1","Bd21-3 D3r1","Bd21-3 D4r1","Bd21-3 D0r2","Bd21-3 D1r2","Bd21-3 D3r2","Bd21-3 D4r2","Bd21-3 D0r3","Bd21-3 D1r3","Bd21-3 D3r3","Bd21-3 D4r3","NA","NA","NA"
1,36222,36622,1,36222,36622,3927.05764014892,3436.04536976362,1978.58390924122,3424.18258835817,4982.43569281856,3728.81215775087,2863.17505667422,4117.86170355401,5108.41645644849,2436.39845482816,1780.36887556699,1716.3170845623
1,61084,61484,1,61084,61484,208.586179565762,129.007399952285,129.64306232078,129.103713699879,139.610953060372,154.586433675601,119.073442810648,103.639480979118,169.635402721379,122.136573116154,131.328532226932,141.551924499984
1,82192,82592,1,82192,82592,152.211536439881,124.558868919448,117.425391526151,132.03788901124,141.844728309338,182.693057980256,108.248584373316,79.5372761002531,146.8655500071,148.373318452216,117.700099637345,111.472140543737
1,82947,83347,1,82947,83347,279.618229904373,161.036823388714,191.410175782512,136.439151978282,254.650378382119,229.537431821348,142.269568033502,126.536575614039,260.714813578495,173.705348431863,155.488026363018,111.472140543737
1,110714,111114,1,110714,111114,515.264238170559,457.308990175686,359.063769464358,374.107352198514,529.404734004931,496.550362715568,398.97335383308,350.68708098748,555.584406228408,446.92938606948,402.658235601442,318.491830124963
1,165233,165633,1,165233,165633,214.22364387835,199.294190271116,142.539492603999,127.636626044199,193.221559035555,159.270871059711,114.434217766077,110.870142442777,198.097718614227,196.323232342262,134.42590327002,161.900013646856
1,215566,215966,1,215566,215966,417.172359131525,426.169272945824,281.006428276454,225.931498974789,489.196779523544,435.65267672215,298.456811200715,333.815537572274,391.641466685599,373.647442199788,282.480239129627,206.134990053101
1,230442,230842,1,230442,230842,153.339029302398,159.257410975579,116.746632037561,108.564486520353,151.896716929685,201.430807516693,112.114605243792,84.357717076026,125.234189928535,132.088442036729,90.44323445817,99.0863471499886
1,231432,231832,1,231432,231832,175.888886552751,104.095626168395,124.891745900646,148.175853223725,138.494065435889,168.639745827929,169.331714126831,257.893592203851,111.572278299967,108.565
RNA-seq and WGBS is the same with geneID instead peak ID.
thank you in advance
Hello,
Thank you for your great tools. I have a question: I'm not quite sure how to generate the input matrix from the normalized count table for RNA-Seq, ATAC-Seq, and WBGS data. Could you please explain?
Following an exemple of my data :
For ATAC-seq:
RNA-seq and WGBS is the same with geneID instead peak ID.
thank you in advance
cheers