Hello, I am interested in many defined regions on the Y chromosome and I would like to check if they are present in single or multiple copy on the human genome. I think the Table Browser would be very helpful to do it using the DGV structural Variation and the Segmental Duplication tracks. However, I am not able to connect my query list of defined regions to the output list of DGV structural variants or duplicated regions. The output file contains a list of different variants but it is really difficult to determine which of my defined regions match with one of these variants and which did not. Actually, these variants are not associated with the defined regions queried and defined regions without structural variation are not visible in the output file. Unfortunately, it is indicated on the page where defined regions are entered that we can name the defined regions but ?the fourth field, name, is optional and for notation purposes only, it is not used in the table browser?.
Could you please tell me if there is another way to connect each defined region to the corresponding result? Thank you very much in advance for your help, Best regards, Caroline Bouakaze _______________________________________________________________________________ Laboratoire d?Anthropologie Moléculaire et Imagerie de Synthèse, UMR5288, CNRS, Toulouse, France _______________________________________________ Genome maillist - [email protected] https://lists.soe.ucsc.edu/mailman/listinfo/genome
