Successfully executing a 43 color panel is a technically demanding task. One that is made more difficult when there are confounding issues like non-specific binding and cell debris.

Sage Science introduced a novel approach for enriching mitochondrial DNA for sequence analysis without PCR or gradient centrifugation.

Recent article from February 2022 shoes how size selection improved viral read mapping by over 90% for begomoviruses.

Sage Science distributes universal sequencing technology´s TELL-Seq linked-read NGS library prep kits used with very low sample inputs for de novo DNA sequencing, carried out easily in a PCR tube without the need for expensive instrumentation.

Programmable DNA size selection enables new discoveries by helping optimize the library detected by a sequencer. That’s why the 24-sample capacity PippinHT is quickly becoming established as a key tool for a host of research applications and clinical

Integrated DNA extraction, digestion, and size-selection using HLS-CATCH were introduced for addressing the problem of current short-read targeted sequencing of genes with high homology to other regions of the genome.

The BluePippin was used for High Pass DNA size selection prior to library construction. ONT Promethion was used for structural varian detection.Several variant calling tools  were evalueted and compared to short-read sequencing.