Software

• 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? 
• Why do some of the processed reads from the Long Ranger Basic pipeline not have barcodes associated with them?