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Scientific Posters

Scalable Long-Read, Low-Coverage Human Whole Genome Sequencing (lcWGS) for Genotype Imputation

An Efficient Enzyme-Based Library Workflow for Multiplexed Long Read Whole Genome Sequencing

A Novel Engineered Transposase (TnX™) for Improved Performance in Genomic Applications

A Novel Transposase-based Method for Multiplexed Long Read Library Construction

Ultra-High Throughput Sequencing for Synthetic Biology Discovery

LongPlex™ – Enabling Highly Scalable PacBio HiFi Target Capture Assays with Multiplexed Long Fragment Transposition

Automated, Multiplexed Preparation of up to 384 Plasmid Libraries Supports a 24-Hour End-to-End Sequencing Workflow Using the Opentrons Flex

An Optimal Strategy for Internalizing Ultra-high Throughput Plasmid Sequencing

An Automated Workflow for Multiplexed NGS Library Construction in Low-Coverage Whole-Genome Sequencing of Cannabis sativa

Robust, Scalable, Low-Coverage Whole Genome Sequencing for High-Throughput Crop Genotyping

Comparison of a Transformational One-Step Library Prep Method for High-Throughput, Multiplexed Sequencing

Multiplexed phasing of clinically relevant long human PCR amplicons with short reads

Multiplexed NGS-based QC Tools for QC Assays in Genome Editing Applications

Imputation of loss-of-function genotypes using low coverage WGS in a cattle population

Scalable sample extraction and multiplexed library preparation for high-throughput crop genotyping via low-coverage whole genome sequencing

Full-length single-cell RNA-sequencing method with streamlined cDNA synthesis and one-step tagmentation chemistry

Fast and highly sensitive full-length single-cell RNA-sequencing using FLASH-seq

A transformational one-step library preparation method for multiplexed plasmid and amplicon sequencing

Efficient single-cell sequencing for full-length transcripts to decipher subclonal structure of melanoma

Normalizing UDI library construction for sensitive genomic applications

Scalable multiplexed library preparation for low-depth sequencing and genotype imputation

plexWell Low Pass 384 Library Preparation Kit for Microbiome Applications

plexWell Low Pass 384 Library Preparation Kit: Cost-effective high-throughput low pass genotyping

Normalizing NGS library preparation improves full-length single-cell RNAseq analysis

High-throughput library preparation for low-pass sequence-based genotyping pipelines

plexWell: Powerful multiplexed library prep for diverse NGS applications

Phased NGS library generation via tethered synaptic complexes

Material Safety Data Sheets

MSDS seqWell kits

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