Can you search for HLA alleles including the HLA nomenclature for a high resolution HLA NGS data, including specific phenotypes?
Does the Mastermind capture those CNVs from the large scale cancer genomics projects?
Does Mastermind also work for fusions, inversions, and translocations?
In addition to the CNV feature, is it possible to search according to the Tier classification for somatic variants?
If I search for a deletion in a certain region, would it also show any duplication associated with that region?
Do you index articles based on legacy exon numbering, as well as systematic versus custom exon numbering?
How did you solve the problem which is caused by changes in the reference genome (different genome coordinates)?
How are various transcripts accounted for in CNV search?
Can you search for other types of structural variations?
What transcripts does Mastermind match to?
What genome build is this based on?
How does the CNV diagram work when there are 50-1000+ genes?
Can you filter out cancer-related CNV?
Can you filter CNV search results by phenotype?
How is CNV overlap defined?
How are published CNVs displayed?
What is visualized in the CNV Diagram?
Can I search for both losses and gains in one search?