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Webinars by BGI Genomics

Novel Clinical Translational & Spatial Genomics Tools - Journey towards Precision Medicine

Novel Clinical Translational & Spatial Genomics Tools - Journey towards Precision Medicine

Novel Clinical Translational & Spatial Genomics Tools - Journey towards Precision Medicine

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In this webinar we discuss in depth Translational and Spatial Genomics applications, and BGI & MGI's current journey in Diagnostics and Single Cell Sequencing development.

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The Complete Guide to RNA Sequencing

Novel Clinical Translational & Spatial Genomics Tools - Journey towards Precision Medicine

Novel Clinical Translational & Spatial Genomics Tools - Journey towards Precision Medicine

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In this webinar you will learn common quality challenges with DNA sample preparation in WGS, research goals and coverage requirement, common questions regarding WGS bioinformatic analysis and more.

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The Complete Guide to RNA Sequencing

Novel Clinical Translational & Spatial Genomics Tools - Journey towards Precision Medicine

Unravelling COVID-19 Complexity: Sequencing Strategies & Solutions for SARS-CoV-2 Research

The Complete Guide to RNA Sequencing

In this webinar BGI’s RNA Project Expert draws from her decade of experience managing 1000s of RNA sequencing projects and gives a comprehensive overview of RNA sequencing.

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Unravelling COVID-19 Complexity: Sequencing Strategies & Solutions for SARS-CoV-2 Research

Unravelling COVID-19 Complexity: Sequencing Strategies & Solutions for SARS-CoV-2 Research

Unravelling COVID-19 Complexity: Sequencing Strategies & Solutions for SARS-CoV-2 Research

Unravelling COVID-19 Complexity: Sequencing Strategies and Solutions for SARS-CoV-2 Research

Genetic diversity of SARS-CoV-2 from evolutionary analysis. Sequencing solutions and research strategies about the molecular epidemiology for clinical research, vaccine development and drug R&D.

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"Dr. Tom" Data Visualisation Solution

Unravelling COVID-19 Complexity: Sequencing Strategies & Solutions for SARS-CoV-2 Research

Application of 10x Genomics + DNBSEQ™ Technology for Cost-Effective Single Cell Solutions

Advanced, intuitive multi-omics data visualisation system for efficient analysis&discovery:"Dr. Tom"

Advanced and intuitive multi-omics data visualisation system for efficient analysis and discovery: "Dr. Tom"

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Application of 10x Genomics + DNBSEQ™ Technology for Cost-Effective Single Cell Solutions

Unravelling COVID-19 Complexity: Sequencing Strategies & Solutions for SARS-CoV-2 Research

Application of 10x Genomics + DNBSEQ™ Technology for Cost-Effective Single Cell Solutions

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Introduction of single cell sequencing, available technologies and their respective advantages. Combining 10X Genomics technology and DNBSEQ™ Sequencing Technology for highly cost-efficient single cell sequencing, with a real world case study of data example.

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Quantitative Proteomics for Biomarker Discovery Research

Quantitative Proteomics for Biomarker Discovery Research

Quantitative Proteomics for Biomarker Discovery Research

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Different quantitative proteomics approaches, with common questions and challenges in proteomics experiment design.

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Webinars by MGI

MGI Revolutionizes MPS Analysis by Novel Bioinformatics

Understanding COVID19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Understanding COVID19 Pathogenesis with Single-Cell Atlas of Non-human Primate

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Take advantage of our state-of-the-art MGI Bioinformatics to improve your MPS analysis. Gain first-hand knowledge on the latest BIT products with our core BIT managers.

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Understanding COVID19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Understanding COVID19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Understanding COVID19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Understanding COVID-19 Pathogenesis with Single-Cell Atlas of Non-human Primate, Dr. Longqi Liu

Join Dr. Longqi Liu to discover the latest research applying single-cell techniques to dissect mechanisms underlying COVID-19 pathology. 

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MGI After-sales Service Introduction

Understanding COVID19 Pathogenesis with Single-Cell Atlas of Non-human Primate

MGI Canada Virtual Symposium - CoolMPS, DNBSEQ and More

MGI after-sales service introduction webinar

Introduction of MGI global Service Centres. With rapid international expansion of the service and support teams, MGI is committed to providing the best product experience for customers everywhere. 

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MGI Canada Virtual Symposium - CoolMPS, DNBSEQ and More

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

MGI Canada Virtual Symposium - CoolMPS, DNBSEQ and More

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MGI’s DNA Nanoball Sequencing (DNBSEQ) platforms generate high quality data for various applications. Hear from Canada’s genomics leaders at BC Cancer, UBC, and McGill on their experiences with the MGI platforms.

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Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

An Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

DNBSEQ-T7 has achieved major breakthroughs: the first 4-chip sequencing platform, completing PE150 at full load within 24 hours, generating 6Tb of data per day, and completing up to 60 whole human genomes per day. MGI presents the cancer genetic testing experience based on DNBSEQ-T7.

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COVID-19 Publications Based on MGI Sequencing Platform

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

MGI Webinar: COVID-19 Publications Based on MGI Sequencing Platform

Recent COVID-19 publications based on applications of MGI high-throughput sequencing platforms and discuss novel topics e.g. evolution of SARS-CoV-2 separately from SARS, similar infection mode of COVID-19 to SARS, potential immune mechanism. 

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DNBSEQ-G50 Full Performance Upgrade

DNBSEQ-G50 Full Performance Upgrade

DNBSEQ-G50 Full Performance Upgrade

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MGI's DNBSEQ-G50 sequencer now has a major upgrade, with improvements to flexibility, turnaround time and performance. Check out these new improvements.

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Webinars by MGI

Understanding COVID-19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Understanding COVID-19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Understanding COVID-19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Understanding COVID-19 Pathogenesis with Single-Cell Atlas of Non-human Primate, Dr. Longqi Liu

Join Dr. Longqi Liu to discover COVID-19 pathogenic mechanisms, based on a Single-Cell transcriptomic atlas of non-human primate tissues generated by MGI's high-throughput sequencing platform DNBelab C4 Pocket Single-Cell Lab. 

Register to Attend

MGI After-sales Service Introduction

Understanding COVID-19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Understanding COVID-19 Pathogenesis with Single-Cell Atlas of Non-human Primate

MGI after-sales service introduction webinar

Introduction of MGI global Service Centres. With rapid international expansion of the service and support teams, MGI is committed to providing the best product experience for customers everywhere. 

View on demand

MGI Canada Virtual Symposium - CoolMPS, DNBSEQ and More

Understanding COVID-19 Pathogenesis with Single-Cell Atlas of Non-human Primate

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

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MGI’s disruptive DNA Nanoball Sequencing (DNBSEQ) platforms generate high quality data for a variety of applications. Hear from Canada’s genomics leaders at BC Cancer's Michael Smith Genome Sciences Centre, University of British Columbia, and McGill Genome Centre on their experiences with MGIDNBSEQ platforms.

View on demand

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

An Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

DNBSEQ-T7 has achieved major breakthroughs: the first 4-chip sequencing platform, completing PE150 at full load within 24 hours, generating 6Tb of data per day, and completing up to 60 whole human genomes per day. MGI presents the cancer genetic testing experience based on DNBSEQ-T7.

View on demand

COVID-19 Publications Based on MGI Sequencing Platform

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

COVID-19 Publications Based on MGI Sequencing Platform

MGI Webinar: COVID-19 Publications Based on MGI Sequencing Platform

Recent COVID-19 publications based on applications of MGI high-throughput sequencing platforms and discuss novel topics e.g. evolution of SARS-CoV-2 separately from SARS, similar infection mode of COVID-19 to SARS, potential immune mechanism. 

View on Demand

DNBSEQ-G50 Full Performance Upgrade

Introduction to DNBSEQ-T7 and Advanced Cancer Genetic Testing

COVID-19 Publications Based on MGI Sequencing Platform

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MGI's DNBSEQ-G50 sequencer now has a major upgrade, with improvements to flexibility, turnaround time and performance. Check out these new improvements.

View on demand

Technology Webinars

MGI DNBSEQ™ Sequencing Technology

stLFR: A Novel & Cost-effective Approach to Genome Assembly

stLFR: A Novel & Cost-effective Approach to Genome Assembly

MGI DNBSEQ webinar

The webinar discusses:  

  • A introduction to MGI (00:00) 
  • MGI single stranded circular library (05:24) 
  • The generation and loading of DNA nanoball (07:37) 
  • Combinatorial probe anchor synthesis (18:01) 
  • The basic data analysis workflow (23:23) 

Watch it here

stLFR: A Novel & Cost-effective Approach to Genome Assembly

stLFR: A Novel & Cost-effective Approach to Genome Assembly

stLFR: A Novel & Cost-effective Approach to Genome Assembly

single-tube long fragment read (stLFR) webinar

In this webinar, MGI introduces single-tube long fragment read (stLFR), a technology that enables sequencing of data from long DNA molecules using economical second-generation sequencing technology. It was demonstrated that how stLFR brings a drastic improvement of de novo assembly results for several economically important plant and pest genomes with short-read sequencing technology on the MGISEQ-2000.

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Design of Experiments and WGS Library Preparation

stLFR: A Novel & Cost-effective Approach to Genome Assembly

Design of Experiments and WGS Library Preparation

MGI sequencing platform webinar

This webinar introduces MGI sequencing platform library construction methods and tools, sequencing strategy, depth calculation and cost, and bioinformatics analysis tools. 

  • 00:00 – 20:24: Intro&experimental design based on MGI platform 
  • 20:24 – 33:55: WGS library preparation workflow 
  • 33:55 – 34:54: Summary 
  • 34:54 – End:  How to find the resources?

Watch it here

Preimplantation Genetic Screening Total Solution

Multiplexed Single Cell Genomics with CoolMPSTM Sequencing

Design of Experiments and WGS Library Preparation

MGI PGS Total Solution webinar

This webinar introduces both PGS (Preimplantation Genetic Screening) for detecting embryonic chromosomal CNVs and PGD (Preimplantation Genetic Diagnosis) for inherited monogenic diseases with haplotype phasing. The integration and customization of these two tests as an one-stop solution s showcased, including: sample preparation, library preparation, sequencing, data analysis, and reporting. 

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Quality Control for DNBSEQTM Platforms

Multiplexed Single Cell Genomics with CoolMPSTM Sequencing

Multiplexed Single Cell Genomics with CoolMPSTM Sequencing

MGI Quality Control for DNBSEQ Platforms webinar

This webinar introduces quality control key points on DNBSEQ platform, including sample QC, fragmented DNA QC, PCR products QC and DNA nanoball QC. In addition, it also introduces MGI's flagship product DNBSEQ-G400RS genetic sequencer, e.g. preparation of sequencing reagents as well as best practices and UI demo on it.

Watch it here

Multiplexed Single Cell Genomics with CoolMPSTM Sequencing

Multiplexed Single Cell Genomics with CoolMPSTM Sequencing

Multiplexed Single Cell Genomics with CoolMPSTM Sequencing

CoolMPS and DNBSEQ webinar

CoolMPSTM and the non-coding Alzheimer’s transcriptome: A 10-billion read puzzle

Dr. Andreas Keller, Dpt. of Neurology and Neurological Sciences, Stanford University; 

Ms. Gracie Gordon, PhD candidate, Department of Medicine and Institute for Human Genetics, University of California, San Francisco (UCSF)

watch it here

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