FAQs
- Does the Tapestri Platform support detection of VDJ?
- How do I find the version number of DNA Pipeline?
- How do I access an existing Pipeline account?
- Can I test Pipeline if I am not a customer?
- Can I install the Tapestri Pipeline locally?
- How do I delete a panel file in Pipeline?
- What are ITDs?
- Can I use my servers for data storage?
- Which genotype caller does Pipeline use?
- What files do I need to run Pipeline?
- What files does DNA Pipeline generate?
- Which format does the .vcf file conform to?
- Can Designer panel files be used with Pipeline?
- What is the Tapestri barcode structure?
- How is the doublet rate calculated?
- Can I use another pipeline for processing data?
- Where can I find demo datasets?
- Which sequence aligner does Pipeline use?
- What are typical processing times for Pipeline?
- What are blacklisted variants?
- Are my files uploading to BlueBee?
- Why aren’t my files uploading?
- What are the QC error messages?
- Can Tapestri Pipeline detect CNVs?
- Are single-cell RNA-seq applications enabled?
- What are the ADO rate, doublet rate, and LOD?
- Does Pipeline demultiplex samples or cells?
- How does Pipeline call cells?
- Does Pipeline call only somatic mutations?
- How does Pipeline call genotypes?