Hello everyone, I am new to working with the GLASS database, and I have a question regarding the accessibility of Whole Genome Sequencing (WGS) data for identifying non-coding single nucleotide polymorphisms (SNPs) associated with glioma risk. If anyone has experience with this type of data from the GLASS database or knows how to access it, I would greatly appreciate your guidance. Thank you for your assistance. Best regards, Mari Álvarez

Created by María del Mar Álvarez Torres MariAlvarezCU
Hi Mari Álvarez, Unfortunately, we cannot share germline data at this time. Please see the response in the following thread: https://www.synapse.org/#!Synapse:syn17038081/discussion/threadId=8955. Best regards, Kevin

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