Partial mutagenesis disrupts repetitive regions before sequencing, helping measure microsatellite lengths despite amplification instability.
Ribosome stall sequences keep translated proteins attached to coding DNA for massively parallel display, sequencing, and functional screening.
A blocking oligonucleotide protects full-length targets while 5′ exonuclease digests truncated strands for cloning-ready enrichment.
Parallel MDA uses staged primer roles and barcode adjustment to raise single-cell genome throughput while limiting amplification bias.
Mediator molecules move reagents between droplet populations, adjusting concentration to control reaction rates.