Webinar

UltraSensitive Residual Leukemia Detection with Patient-Specific Duplex Sequencing

Dr. Jesse Salk reviews using Duplex Sequencing to measure ultra-rare mutations from carcinogens, aging, and the earliest stages of cancer.

Broader framework for high-efficiency target enrichment, by Ramsey Zeitoun

Dr. Ramsey Zeitoun discusses how Twist’s suite of NGS Solutions maximize sequencing efficiency by enabling coverage and uniformity

Emily Leproust presents at ASHG 2020

Broad Institute implements Twist Custom Exomes for cfDNA | AGBT 2019

Brendan Blumenstiel, Broad Institute of MIT and Harvard, describes the development of a target enrichment workflow for cell free DNA

Capabilities of the Twist NGS Methylation Detection System

Clinical rapid whole exome sequencing with a Twist

How Radboud University Medical Center integrate exome sequencing to study disease

Weizmann Institute Discusses Epitranscriptome Screening

Dr. Schraga Schwartz speaks about epitranscriptome screening for the characterization of the pseudouridine landscape on mammalian RNA

HudsonAlpha Institute uses Twist Custom Panels for Deep Exome Sequencing of FFPE Samples | AGBT 2018

Dr. Shawn Levy discusses the superior performance of Twist probes for high capture efficiency using diverse samples

Helix upgrades to Twist Custom Exomes for broader genetic insights | AGBT 2019

Dr. William Lee discusses design and optimization of an enhanced medical exome using Twist technology

No More Arrays: Genotyping by Sequencing Enables Economical and Improved Association Studies

Using Twist technology to efficiently enrich 1.4 million SNP targets for ancient DNA analysis

Increasing the throughput of NGS sequencing through rational design and empirical validation of 10,

Using the Twist Pan Viral Panel to Enhance Viral Whole-genome Sequencing I AGBT 2018

Mike Wiley discusses his project using the Twist Pan Viral Panel to identify targets to create better diagnostics for Liberia

Ensuring high resolution CNV detection

Implementation of Twist Products in Clinical Genomics

Comprehensive identification of multiple respiratory viruses including SARS-CoV-2 in a single assay

The COVID-19 pandemic has highlighted the urgent need for genomic tools that can accurately and fully characterize samples

Transformación de exoma clínico dirigido a secuenciación completa del exoma, de manera rentable

Aumento en la calidad de secuenciado utilizando el Kit de Exoma Twist’s Human Core sin afectar los costos.

AGBT 2019: Data-Driven Development of a High-Throughput Target Enrichment System

Ramsey Zeitoun of Twist's R&D team revealed new data on the latest target enrichment technologies in the Twist Portfolio at AGBT 2019

Blueprint Genetics evaluates Twist Custom Panels for hereditary disease | AGBT 2019

Dr. Pertteli Salmenperä of Blueprint Genetics details the importance of coverage uniformity in NGS testing of hereditary disorders

Shedding Light on Dark Genes

Enhanced targeted resequencing by optimizing the combination of enrichment technology and DNA fragment length

Targeted Epigenome Sequencing of cfDNA to Improve Sensitivity for Early Cancer Detection

Discover how the Cancer Research UK early detection program engaged with the Twist Targeted Methylation Sequencing Alpha Program to enable the analysis of cancer markers in cell-free DNA

CHOP uses Twist Custom Panels on challenging samples | AGBT 2019

Dr. Renata Pellegrino discusses how to improve sequencing on challenging samples using Twist technology

Improved mutation detection with targeted sequencing

Detecting known and novel mutations in a host's SARS-CoV-2 population by ultra-deep sequencing with unique molecular barcodes

Foundation Medicine NGS Video: Christine Malbeouf I AGBT 2018

Dr. Christine Malbeouf compares capture methods for FFPE RNA-sequencing using Twist technology

Emily Leproust, PhD | Introduction to Twist Bioscience | AGBT 2019

Dr. Emily Leproust discusses how Twist Bioscience is leading the way in target enrichment

UPenn uses Twist Custom Panels for canine cancer detection

Find out how custom panels for target enrichment have been developed for precision veterinary oncology.

U of Verona | Enhanced Targeted Reseq. by DNA Insert Length Optimization | Dr Delledonne | AGBT 2019

Dr. Delledonne of University of Verona describes how DNA fragment length impacts NGS data quality.

Weill Cornell uses Twist Panels for Sequencing Age-Related Mutation Patterns

Dr. Duane Hassane discusses clonal hematopoiesis (CH) and preleukemia using Twist technology

Launching an NGS Assay for Estimating Genetic Ancestry and Providing Health Insights

Discover How Ancestry recently made the shift to Twist Custom Panels

Various challenges in clinical genomic testing

Accurate CRC Detection by Targeted MethylSeq of ctDNA

Sequencing 100,000s of Humans: Lessons, Challenges, Hopes

Sequencing 100,000s of Humans: Lessons, Challenges, Hopes

Changing paradigm on Therapeutics targeting Membrane Proteins: from antigen production to candidate validation

Demystifying End-to-End DNA Sequencing Solutions

AZ700: Exploratory NGS Panel for Use in Translational Oncology

AZ700: Exploratory NGS Panel for Use in Translational Oncology

Unlocking precision medicine through expert NGS panel design

DNA methylation signatures for cardiovascular and metabolic disease

感染症ウイルス検出の新時代 A New Era of Detection of Viruses Causing Infectious Diseases

Twist Corporate Satellite Symposium - ESHG 2024

Dream it, sequence it: New Sequencing technologies to enable your brightest discoveries

Sequencing The Future Together @ ESHG 2023

Evolution of Clinical Genomics: How technology drives change in diagnostic practise

Finding new causes of hereditary breast cancer: Resolving the role of inherited promoter hypermethylation

From Poultry to Peanuts: Low-Coverage WGS to uncover important traits in Chickens and Production Plants

Twist Exome 2.0 Webinar

Thoughtfully Curated Content Paired with Best-in-class Performance

A Custom Hybrid Capture-based NGS Assay to Detect Circulating Tumor DNA

Maartje Geerlings | Radboud

Enabling Clinical Trials and Translational Studies with Twist

Shubha Anand | University of Cambridge

TWIST custom and cost-effective NGS panels - MedGenome Experience

Artificial Intelligence in Drug Discovery & Development

Ancient DNA panel improves protocol for degraded samples: the Altwies mother-child burial

Unlocking precision medicine through expert NGS panel design_

OneShot: Advancing Forensic Biology with Integrated Genetic and Epigenetic Sequencing

Screening, diagnosis, prediction - Genomic data for the whole of life

Predicting prognosis using circulating tumor DNA in uveal melanoma

Sensitive Methylation Sequencing of ctDNA for early Cancer Detection

Twist Targeted Panels in Clinical Genetic Diagnostics

Partnering for IVDR Compliance: On-Demand Webinar

Discover collaborative insights from Twist Bioscience and Platomics on IVDR compliance. Watch this expert-led webinar on-demand today!

Genomic profiling including DNA methylation analysis for challenging cancers of unknown primary

'Yeastern' Medicine: Brewing nightshade drugs with genetically modified yeast using whole-cell engineering

DNA methylation biomarker discovery for complex diseases using Twist Human Methylome

Developing Blood Biopsy Technology Using a New Canine Exome Capture

Metagenomics in lung tumor tissue using shotgun sequencing with high nucleotide diversity

Microfluidic Nano-Scale qPCR for Ultra-Sensitive and Quantitative Detection of SARS-CoV-2

Microfluidic Nano-Scale qPCR for Ultra-Sensitive and Quantitative Detection of SARS-CoV-2

Connecting Plant Trait Genotypes to Phenotypes using WGS Skim-Seq

Long-Read Capture with Twist Target Enrichment

Mapping All Viruses on Earth and a Few for Mars

Mapping All Viruses on Earth and a Few for Mars

Writing The Future Of Cancer Research - Panel Discussion Part 2

Academia Genómica de Twist Bioscience

Experimente una uniformidad superior y un menor coste de secuenciación con los paneles personalizados de enriquecimiento de regiones de interés con Twist Bioscience.

ESHG 2025: Unleash the Power of Your Samples: Next-Level Sequencing with Twist Bioscience

Precision with a Purpose: Benchmark 659 for Cancer Care - Powered by Twist Bioscience

Hit Two Birds with One Stone: Hybrid-capture

Hit Two Birds with One Stone: Hybrid-capture

Targeted capture through Twist cfDNA LP Kit enables sensitive detection of mutations from cell-free DNA

From Womb to Wheeze: Investigating the Epigenetic Predisposition to Respiratory Disease.

Writing the Future of Infectious Disease

Writing the Future of Infectious Disease

Capabilities of the New Twist NGS Methylation Detection System

An end-to-end solution for library preparation, conversion and target enrichment of genomic samples to identify regions of methylation.

Principles and Applications of Methylome Analysis for Cancer and Other Disease Research.

Comprehensive Omics Analysis to Explore Applications in Clinical Oncology

Comprehensive Omics Analysis to Explore Applications in Clinical Oncology

Evolution of Exome Targeted Re-sequencing Analysis: A Comparative Study of Various Methods (Japanese)

Capturing the Resistome: a Culture-free Approach Based on ARESdb

Capturing the Resistome: a Culture-free Approach Based on ARESdb

Genomic Surveillance of Emerging Viruses in Massachusetts and West Africa

Genomic Surveillance of Emerging Viruses in Massachusetts and West Africa

Raising the Bar for NGS Target Enrichment @ ESHG 2022

From Bones to Genomes: Genetic Investigation of Late Iron Age Individuals from North and South of the Alps

Unlock the Full Potential of RNA-Seq

Faster Answers, Fewer Steps: Streamline Your Targeted Sequencing with Trinity Freestyle™

Characterization of Transgene Status in Genome Edited Plant Lines Using Target Capture Sequencing Technology

Sathya Jali | Pairwise Plants

Pairing Pet Dogs With New Genomics Technologies Accelerates Cancer Diagnostic Development

Elinor Karlsson & Kate Megquier

Comprehensive analysis of CRISPR/Cas3 genome editing by Twist Custom Panel

#WeMakeDNA - Epigenomics approach to rare disease and cancer screening

Collaborating for Cocktails: The Coronavirus Immunotherapeutics Consortium (CoVIC)

Collaborating for Cocktails: The Coronavirus Immunotherapeutics Consortium (CoVIC)

A PCR-Free Hybrid Capture Approach for Detection of Pathogenic Repeat Expansions

Master IVDR Compliance Anytime, On-Demand Webinar

Learn expert strategies for IVDR compliance with Twist Bioscience. Watch at your own pace today!

Research of Epigenetics and Epigenetic Age in Iwate Tohoku Medical Megabank Organization

Leading the way in Sample Prep- Corporate workshop presentation at AMP 2020

Culture-independent sequencing in Australian public health microbiology

The Next Generation of Targeted Methylation Sequencing

The Next Generation of Targeted Methylation Sequencing

Low-coverage Whole-genome Sequencing Improves Precision and Speed of Genomics-assisted Crop Improvement

Josh Clevenger

The utility of exome sequencing analysis

Dr. Júlia Baptista discusses the utility of exome sequencing analysis in solving rare genetic disorders: the Exeter experience

Towards new-generation diagnostic schemes utilizing targeted RNASeq and robotics-based DNA Methylation Seq

Garantizando la identificación de CNV de alta resolución

Descubra cómo la plataforma SOPHiA y el kit Twist Human Core Exome proporcionan una solución fiable y eficaz para la detección de CNV

Saving Lives by Detecting Cancer Early

Saving Lives by Detecting Cancer Early | Ken Chahine | Helio Health

Demystifying End-to-End DNA Sequencing Solutions

Validating a diagnostic cfDNA NGS assay

SARS-CoV-2 Variants: How to "Capture" them

SARS-CoV-2 Variants: How to "Capture" them

A Cost-Effective Pan-Genome-Based Platform for Genotype Imputation, QTL Mapping, and Breeding Support

Development of a Universal Pan-pathogen Infectious Disease Diagnostic

Development of a Universal Pan-pathogen Infectious Disease Diagnostic

Panel-based sequencing strategies for infectious diseases

The role of clinical exome sequencing in the genome world

TwinStrand Biosciences discusses Duplex Sequencing

Dr. Jesse Salk reviews using Duplex Sequencing to measure ultra-rare mutations from carcinogens, aging, and the earliest stages of cancer.

Developing an Integrated MRD Assay to Transform Oncology

Targeted Sequencing-based Genotyping as a Competitive Alternative to Genotyping Arrays

Exoma completo, una estrategia eficiente para el estudio de leucemias familiares

Improving Targeted Methylation Sequencing

Séminaire NGS & Virologie : Innovations et applications I French Virology Application Seminar

Development and Application of Methods for Targeted Long-Read Methylation Analysis from Small Amount of DNA

(Presented in Japanese Language)

Leading the Way in Target Enrichment: Targeted Methylation Sequencing

Writing the Future of Human Genetics

On Demand Webinar: Population-Based Genomic Newborn Screening: Results of BabyDetect Study

Harnessing the Power of Surveillance Testing on Small Residential College Campuses

Harnessing the Power of Surveillance Testing on Small Residential College Campuses

Increasing the Precision of Precision Medicine for Children with High-risk Cancer

Increasing the Precision of Precision Medicine for Children with High-risk Cancer

Horsehair whorls

Rakan Naboulsi | Swedish University of Agricultural Sciences

The Evolution of Clinical Genomics at VCGS: Past, Present & Future

The Evolution of Clinical Genomics at VCGS: Past, Present & Future

Raising the Bar in NGS with Twist Bioscience

Analysis of Somatic Mosaicism through Comprehensive Genomic and Epigenomic Profiling of Small Samples

Faster Answers, Fewer Steps: Streamline Your Targeted Sequencing with Trinity Freestyle™

Deciphering Cancer Mutations and Clinical Applications through NGS and Technological Innovations

DNA methylation based liquid biopsy for multi-cancer detection.

Cell-Free DNA methylation analysis for cancer detection

Advancements in Epigenetic Analysis tools for Disease Research

Expanding the Toolbox for Agrigenomics

Paul Doran

Low coverage whole genome sequencing improves precision and speed of genomics-assisted crop improvement

Low cost per sample with Twist’s HT 96-Plex Library Prep kit

Targeted DNA-Seq und Whole-Exome-Seq zirkulierender zellfreier DNA zur Lymphom-Diagnostik

Clinical metagenomics for improved surveillance and diagnosis of infections in New South Wales, Australia

Addressing the challenges of high-throughput SARS-CoV-2 testing

Custom enrichment for RNA sequencing of liquid biopsies

Believe in Better: Leading the Way in Target Enrichment

#WeMakeDNA - Synthetic Biology for the Study of Infectious Diseases

Annual Meeting of Molecular Biology Society of Japan 2020