What fields are required for probe sequences?
Provide a unique identifier for each probe and the probe sequence using only A, T, C, and G bases.
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NGS Panels
Custom Panel Submission Tool
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- What is the Custom Panel Submission Tool?
- What types of designs are supported?
- Are Twist Probes DNA/RNA?
- How large can my panel be?
- How do I access ‘How-to videos’?
- How do I access the quick tour guides?
- Does this tool create my custom panel design?
- Are my designs automatically generated?
- I made a mistake in my submission, what should I do?
- I would like to make edits or changes to my previous submission, what should I do?
- How do I start a new panel design?
- How do I update an existing panel?
- My genome/build of interest is not listed as an option?
- What are Advanced Features?
- What types of targets can I include in my panel?
- How do I submit my complex variants such as MSIs, CNVs, Large Indels or Structural rearrangements such as gene fusions?
- How do I use the UploadFile option?
- What are 0-based coordinates?
- How do I customize default targeting settings for gene symbols?
- Why do you target different transcript databases by default?
- Why do you target all transcripts?
- What are the options for regions to cover within each gene?
- I am only interested in a specific transcript(s) for my gene, how do I specify this?
- I have individual gene requirements, how do I input these?
- What is tiling in the context of Genes?
- My target is difficult to capture/sequence, what do I do?
- My gene of interest has pseudogenes, how do I ensure specific capture?
- How do I input genomic coordinates?
- What is tiling in the context of genomic coordinates?
- How do I input SNPs?
- How do I input probe sequences?
- What fields are required for probe sequences?
- How do I review my design?
- What information is needed to submit my design?
- Where can I get more help?
