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Dear Navin-Lab,
I wanted to know how the InferCNA plot is generated logic-wise.
Is it true that the calculated genomic bins per chromosome are generated as heatmap-tiles to fill the relative chromosome length within the plot (so that the chromosomal regions are appropriately sized to their length in comparison).
What I want to specifically know, the heatmap tiles are not necessarily representative of the exact chromosomal location of the color highlighted CNV.
So, regardless how much of the chromosome is actually covered by the prediction, the information is sorted by positional occurrence and stretched over the chromosmal region in the graph.
Is this correct?
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