Questions & Answers
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- Should I use Long Ranger, Supernova, or other tools to analyze 10x linked reads?
- Why does the longranger basic pipeline only output one FASTQ file when I gave it paired-end data?
- Why do I see 0|0 genotypes in my Long Ranger output?
- Why is my molecule size less than what I expected for my Chromium Genome library?
- How many barcodes does Long Ranger need to call a structural variant?
- What is the resolution (size of chromosomal rearrangement) that Long Ranger can detect with linked-read data?