Resources

Publications

Sequencing the pandemic: rapid and high-throughput processing and analysis of COVID-19 clinical samples for 21st century public health

A novel next-generation sequencing and analysis platform to assess the Identity of recombinant adeno-associated viral preparations from viral DNA extracts

Profiling SARS-CoV-2 mutation fingerprints that range from the viral pangenome to individual infection quasispecies | MedRxiv

Application Notes

Low-Pass Whole-Genome Sequencing on the Element AVITI™ System Enables Cost-Effective Genotyping

Scalable Transposase-based Multiplexed Library Prep on the Element AVITI™ System with plexWell™

PW096

Low-pass whole-genome sequencing enabled by scalable library prep offers a competitive alternative to microarray-based genotyping

Efficient and highly multiplexed whole viral genome sequencing of SARS-CoV-2 samples

Scalable, true multiplexed library preparation enables high-performance, high-throughput plasmid sequencing

PW096

Scientific Posters

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

Multiplexed NGS-based QC Tools for 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

A novel multiplexed library construction method that streamlines sample preparation prior to targeted hybrid capture

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

Resolution at scale: plexWell Rapid Single Cell for highly multiplexed plate-based scRNA-seq

A novel, fully integrated scRNA-seq workflow enables streamlined library preparation with sensitive and robust transcript detection

PW096

plexWell Low Pass 384 Library Preparation Kit: Microbiome Applications

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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

PW096

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

plexWell: Powerful multiplexed library prep for diverse NGS applications

PW096

Phased NGS library generation via tethered synaptic complexes

Product Brochures

purePlex Product Brochure

plexWell Rapid Single Cell RNA Library Prep Kits

plexWell Library Preparation Kits

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Troubleshooting Guide

plexWell Troubleshooting Guide

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Kit User Guides

purePlex DNA Library Prep Kit User Guide

plexWell Rapid Single Cell User Guide

plexWell 96/384 User Guide

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plexWell Low-pass 384 User Guide

plexWell Plus 24 User Guide

plexWell WGS 24 User Guide

Index List

purePlex Kit Master Index List

plexWell Kits Master Index List

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Sample Sheets

PWGS 24 Sample Sheet Template

PWP24 Sample Sheet Template

Technical Data Sheets

plexWell WGS Tech Data Sheet

plexWell Tech Data Sheet

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Material Safety Data Sheets

MSDS plexWell kit

Certificates

ISO 9001:2015 Certificate

Services

Sample Submission Requirements

Sample Submission Form