Automating PacBio SMRTbell Whole Genome Sequencing Library Preps on Miro Canvas
Automating Pacbio WGS Library Prep on the Miro Canvas Long read sequencing plays an important role in generating contiguous, high-quality genomes, for haplotype phasing, structural variant detection, and de novo assemblies. The application...
Automating the Oxford Nanopore Ligation Sequencing Kit on Miro Canvas
Automating the Oxford Nanopore Ligation Sequencing Kit on Miro Canvas Long read sequencing is particularly well suited for detection of large genomic mutations, coverage of long repeat regions that confound short read assemblies, and identification...
Enabling the Twist Human Core Exome Kit on Miro Canvas
Enabling the Twist Human Core Exome Kit on Miro Canvas Whole exome sequencing (WES) provides a unique opportunity to dive deeply into the coding regions of the genome. It plays an important role in generating data for research, and in some...
Personal automation for whole genome sequencing: evaluating digital microfluidics across two different PCR-free protocols.
Solving the problem of rare: automated microfluidics for accurate variant detection by PCR-free WGS of very small human samples
Preimplantation genetic testing (PGT) currently relies on whole genome amplification (WGA) to provide limited information on ploidy. Currently only 30% of genetic etiologies can be identified due to the inability to fully sequence embryos to...
ASHG 2019 Poster
A versatile microfluidic platform for NGS library preparation enables multi-omics studies for a broad range of research samples and laboratory settings.