DNBSEQ-T1+

October 9, 2025/in MGI, Sequencing Platforms/by Harshita Sharma

Accelerate high-throughput genomic testing with DNBSEQ-T1+

The DNBSEQ-T1+ is one of the fastest T-level benchtop sequencers available globally—built on MGI’s proven DNBSEQ™ technology for accuracy, scalability, and reliability. Designed for clinical and translational genomics labs, the T1+ supports dual flow cell operation, delivering up to 1.2 terabases (Tb) of sequencing data within 24 hours (600 Gb per flow cell).

For laboratories managing time-sensitive or high-volume projects, this means faster turnaround, improved workflow efficiency, and reduced dependence on external bioinformatics infrastructure. The optional integrated bioinformatics module enables automated secondary analysis immediately after sequencing, helping clinicians and molecular pathologists move from raw data to interpretable results without delay.

In practice, DNBSEQ-T1+ helps streamline comprehensive genomic profiling (CGP), oncology testing, and clinical research pipelines—supporting both diagnostic accuracy and operational consistency across runs.

High-Speed, High-Throughput Sequencing

Generate up to 1.2 Tb of data in a single run with dual flow cell operation.

Choose from FCL, FCM, or FCS flow cells to match your throughput needs—from small clinical batches to large oncology cohorts.

Maintain >93% Q30 and >90% Q40 base quality across read lengths up to PE150.

Complete full runs in as little as 7–24 hours, supporting faster reporting and clinical turnaround.

Versatile Applications Across Clinical Genomics

Flexible read lengths (SE50–PE300) suit NIPT, RNA-Seq, oncology panels, WES, WGS, and methylation studies.

Supports coverage depth from 1 Gb to 120 Gb per sample, enabling both targeted assays and whole-genome workflows.

Ideal for translational and precision medicine—from pathogen detection to tumour profiling.

Integrated DNB Make & Load Technology

DNB M&L (Make & Load) module automates DNB preparation and loading directly within the sequencer.

Delivers consistent, contamination-free results with minimal hands-on time.

Each flow cell operates independently, supporting different read lengths or applications in parallel.

Enables an end-to-end “Make–Sequence–Analyse” workflow that saves time and reduces error.

Smart Configurations and Automated Analysis

Available in two setups: DNBSEQ-T1+ RS (flexible throughput) and T1+ ARS (with built-in bioinformatics).

The ARS configuration automatically triggers advanced data analysis post-run, streamlining bioinformatics pipelines.

Simplifies data interpretation for clinicians and molecular pathologists, improving workflow efficiency and diagnostic accuracy.

Download the DNBSEQ-T1+ brochure for a complete overview of performance metrics, application data, and configuration options. For guidance on how this platform fits your lab’s workflow, Decode Science can walk you through integration and local support options.

Watch How T1+ Works

DNBSEQ-T1+

DNBSEQ-E25

DNBSEQ-G400

DNBSEQ-T7

DNBSEQ-G99

Twist Oncology – DNA CGP Panel

October 8, 2025/in Oncology/by Harshita Sharma

PRODUCTS

Comprehensive Genomic Profiling for Oncology Research

The new Twist Oncology - DNA CGP panel offers 562-gene coverage for complete tumour profiling

Comprehensive Genomic Profiling (CGP) uses next-generation sequencing (NGS) to evaluate multiple clinically relevant biomarkers within a solid tumor. It provides detailed genomic resolution, enabling the detection of single nucleotide variants (SNVs), insertions and deletions (indels), copy number variations (CNVs), select gene fusions, and key cancer genomic signatures such as tumor mutational burden (TMB) and microsatellite instability (MSI).

By consolidating this information into a single assay, CGP offers a complete view of a tumor’s molecular profile, reducing the need for multiple tumor-specific panels or separate testing methods.

Why CGP Matters

Unified Testing Platform

Combines samples from all tumor types into a single test platform, enabling efficient batching and streamlined workflow.

Actionable Insights

Focuses on clinically and research-relevant information, supporting treatment decisions and drug development strategies.

Cost-Effective Efficiency

More efficient and economical than whole-exome sequencing (WES) for oncology, lowering resource use while maintaining comprehensive genomic coverage.

If you’d like to see how this fits your current setup, I can walk you through integration options or pilot testing. The new Twist Oncology – DNA CGP Panel provides 562-gene coverage for comprehensive tumor profiling.

Twist Tumor DNA CGP Panel

Enable improved Tx Selection and enhanced Clinical Research

Fixed Panel + Customisation Options

562 genes analyzed for SNVs and hotspot mutations (+39 genes compared to TSO500)
Microsatellite instability (MSI) detection across ~50 sites
Copy number variation (CNV) analysis for 57 clinically relevant genes
Selected fusions and tumor mutational burden (TMB) scoring for complete tumor profiling

Add custom biomarkers to differentiate your lab’s testing capabilities
Adaptable for specific clinical or research needs

End-to-End Twist NGS Workflow Compatibility:

Library preparations: EF2.0, cfDNA
Hybridization solutions with options for software analytics
Streamlined workflow for enhanced lab efficiency

Now available in Australia and New Zealand through Decode Science.

Example Data Metrics

Example sequencing QC metrics averaged across data down sampled to 2000x raw coverage (32M 2×150 reads). 4.5 Gb of Data is enough for VAF detections ranging ~2%. Data available upon request.

Panel target size	2.4 Mb
Example input	50 ng
Mean Target Coverage	515x
On-Target Rate	77%
Fold-80 Base Penalty	1.32
Duplication Rate	20%
Target bases covered >100x	99.5%

Advantages of Twist Oncology Panel

CONTENT

TSO-500 : Content is locked at 523 genes in 2025 and beyond

Twist CGP : Offers an updated CPG panel of 562 genes with Twist dsDNA probes

CUSTOMISATION

TSO-500 : Not Possible

Twist CGP : Can easily modify content to add genomic features or new biomarkers

COMPATIBILITY

TSO-500 : Product is locked into Illumina Platform Ecosystem

Twist CGP : Twist can enable Illumina short-read platforms and non-Illumina platforms (Ultima, Element, etc.)

WORKFLOW

TSO-500 : Requires an overnight capture + 2nd Hybridization Capture

Twist CGP : Single overnight hybridization capture (Option Trinity on Element)

COMPETITIVE PRICING

TSO-500 : High cost per sample for IVD kit pricing

Twist CGP : Can offer competitive pricing and modular kit options.

MODULAR PRODUCT

TSO-500 : Purchase is an all inclusive kit, no option for purchasing components

Twist CGP : Twist can sell modules, or custom configurations through OEM services

Customer Testimonial

"At LifeStrands Genomics Australia, we rely heavily on Twist’s NGS probes and reagents across nearly all our assays... Twist’s probe design flexibility and scalability have allowed us to tailor both DNA and RNA panels that suit a wide range of solid tumours without compromising sensitivity or turnaround times. We view Twist not just as a vendor, but as a strategic partner in advancing precision oncology."

Dr. Vivek Rathi, MD MSc FRCPA

Medical Director LifeStrands Genomics Australia (Genoox User)

Ready To Order?

As the official distributor for Twist Bioscience in Australia and New Zealand, Decode Science makes accessing CGP Panel straightforward. Our role is to connect your lab with Twist’s advanced technologies, ensuring you get the right custom panel solution for your sequencing projects—delivered locally with support when you need it.

Knock-in Immortalized Cells

March 18, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Knock-in Immortalized Cells

Get CRISPR-Engineered Cell Lines Faster and More Efficiently.

EditCo’s Knock-in Immortalized Cells provide a fast and efficient way to integrate engineered cells into your research, using automated transfection optimization and RNP-based delivery to ensure high editing success with minimal off-target effects.

By eliminating the delays and challenges of DIY CRISPR projects, our cost-effective solution enables you to model more genes and variants across multiple cell lines, accelerating your path to discovery without overspending.

Cost-Effective CRISPR Knock-in Cell Pools – Flexible & Efficient

EditCo’s Knock-in Immortalized Cell Pools provide a high-throughput, budget-friendly solution for introducing precise edits while maintaining a mixed population of edited and unedited cells.

– Optimized transfection for high-efficiency knock-ins
– Supports SNVs, tags, and large insertions with advanced HDR strategies
– Flexible clonal isolation—manage it yourself or opt for our Knock-in Clones
– Comprehensive QC & sequencing reports for reliable validation

Precision-Verified CRISPR Knock-in Clones – Ready for Your Research

EditCo’s Knock-in Immortalized Cell Clones provide a sequence-verified, clonal population for precise, high-quality knock-ins. Whether modifying SNVs, tagging proteins, or inserting large sequences, our automated isolation process ensures you receive a single-cell-derived clone with your desired edit.

– Guaranteed precision with fully validated knock-ins
– Endogenous tagging & SNV editing for functional studies
– Streamlined delivery with complete QC & sequencing reports
– Customizable options including additional clones & intermediate pools

Skip the complexity—get ready-to-use, precision-edited clones with EditCo!

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

Immortalized Cells Portfolio

Knockout Immortalized Cells

Knock-in Immortalized Cells

Let’s Find You an Application That Helps
Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Knockout Immortalized Cells

March 18, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Knockout Immortalized Cells

Reliable, Reproducible CRISPR Editing for Breakthrough Discoveries

Spend Less Time on Editing, More on Innovation: EditCo’s advanced automation eliminates time-consuming steps, allowing you to focus on impactful research.

Superior Performance & Scalability: Our CRISPR platform delivers high knockout efficiencies, ensuring consistent, reproducible results across experiments.

XDel Knockout Cell Pools & Clones

XDel is an advanced CRISPR knockout tool that eliminates uncertainty in gene editing. Using a groundbreaking guide RNA design approach, it provides highly effective, reliable, and repeatable gene knockouts, enabling researchers to speed up their breakthroughs with assurance.

– Higher Efficiency & Consistency: XDel technology ensures superior on-target knockout rates with minimal variability.
– Reduced Off-Target Effects: Achieve precise edits with lower unintended mutations compared to single-guide methods.
– Validated & Scalable: Persistent protein depletion enables direct use in functional assays, drug discovery, and disease modeling.

CRISPR Knockout Cell Pools & Clones

Accelerate your research with high-efficiency CRISPR Knockout Cell Pools & Clones from EditCo. Our cell pools provide a mix of edited and unedited cells for immediate assays, while clonal lines ensure precise gene knockouts with sequence-verified accuracy.

– 50%+ knockout efficiency in cell pools
– Up to 95% protein knockout for functional validation
– Single, double, or triple knockouts available
– Comprehensive QC & sequencing reports included

Knockout Cell Libraries – High-Throughput CRISPR Screening Made Easy

EditCo’s Knockout Cell Libraries enable high-efficiency CRISPR screening with over 90% editing success in a ready-to-use 96-well arrayed format. Designed for functional assays and drug target discovery, our libraries eliminate transfection challenges and infrastructure barriers.

– Multi-guide CRISPR design for precise knockouts
– High-throughput screening with scalable workflows
– Comprehensive QC & sequencing reports included
– Compatible with diverse assays for discovery & validation

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

Immortalized Cells Portfolio

Knockout Immortalized Cells

Knock-in Immortalized Cells

Let’s Find You an Application That Helps
Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Knockout T-cells

March 18, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Knockout CD8+ & CD4+ T Cells

Advanced CRISPR Knock-Ins for iPSC Research

EditCo delivers efficient gene editing with guaranteed >80% efficiency in human primary cells, achieving >90% in many cases, using a smart multi-guide design and a 7-day protocol for results in 2 weeks or faster. Their Primary Cell KO Pools produce functionally consistent cell populations, ideal for drug discovery or biological modeling, while maintaining high viability and functionality. Researchers can use EditCo-supplied cells or their own CD8+/CD4+ T cells, ensuring flexibility and reliability. By minimizing failed experiments and false negatives, EditCo saves time and resources, offering 1M-cell EC Pools for high-quality, rapid, and dependable gene editing.

Image: High editing efficiency across multiple donors.

Image: EditCo KO CD8+ T cell pools can be thawed and expanded for weeks, with or without TCR stimulation.

Next-Level Edited CD8+ T Cells – Powerful, Stable, and Ready for Action

Take your research further with precision-engineered CD8+ T cells that combine high editing efficiency, long-term stability, and exceptional functionality. Designed to maintain their knockout integrity, expand effortlessly post-thaw, and deliver strong antigen-specific responses, these cells are built for performance. Whether you’re exploring immune responses or advancing cell therapy, these edited T cell pools provide the reliability and power you need.

🔬 Unmatched Editing Precision – Achieve over 90% knockout efficiency across multiple donors, maintaining stability before and after cryopreservation.

🧬 Thrives & Expands with Ease – These cells stay healthy and proliferate for weeks, with or without stimulation, ensuring flexibility in your experiments.

⚡ Optimized for Real-World Function – A single round of activation preserves normal function, preventing overstimulation and exhaustion.

🎯 Potent, Targeted Cytotoxicity – Strong antigen-specific activation, with robust CD107a expression, ensures effective tumor-killing potential.

Power up your research with CD8+ T cells engineered to perform when it matters most.

CD4+ T Cells - Stability and Functionality Post-Editing

The editing of CD4+ T cells has shown high efficiency and stability, with a robust ability to maintain functionality after the editing process. The efficiency of the CD4+ T cell editing was determined through ICE analysis, with results demonstrating high editing efficacy across multiple loci while ensuring cell viability during the freezing stage. Post-editing, the cells can be thawed and expanded without loss of functionality or editing efficiency. Cytokine production in edited T cells, including IFNg, IL2, and TNFa, indicates that the editing process does not negatively impact the cells’ ability to produce essential cytokines upon stimulation. These edited pools also show high viability, making them suitable for further downstream assays.

– High editing efficiency of CD4+ T cells determined by ICE analysis.
– No reduction in cell viability after freezing, as indicated by flow cytometry
– Successful expansion and thawing of edited cells without affecting functionality
– Edited cells exhibit high levels of cytokine production (IFNg, IL2, TNFa) post-stimulation
– High viability and expansion potential, with >90% viability after 14 days in culture
– Statistical analysis shows significant cytokine differences between edited and mock cells

Image: Editing Efficiency and Viability for CD4+ T cell pools.

Image: Editing Efficiency leads to protein depletion as shown by flow cytometry

Image: CD4+ pool stability after thaw.

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

Let’s Find You an Application That Helps
Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Gene Knockout Kits

March 18, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Gene Knockout Kits

EditCo Gene Knockout Kits: Reliable and Efficient CRISPR Solutions

EditCo’s Gene Knockout Kit offers a simplified, highly efficient solution for generating human and mouse protein-coding gene knockouts. Unlike traditional CRISPR methods, which rely on a single guide RNA (gRNA) to create random indels, EditCo’s multi-guide approach ensures consistent and precise gene disruption. This method generates fragment deletions at the targeted loci, providing a more reliable and predictable knockout, ultimately enhancing experimental success. With fast delivery times (kits arrive in just 5 days), users can avoid the trial and error of guide screening and proceed quickly with their experiments. The process is streamlined further with an easy online ordering portal, which includes the option to purchase controls, SpCas9 nuclease, and Transfection Optimization kits to complement your knockout experiment. This solution guarantees high knockout efficiency, making gene editing faster and more reliable than ever before.

Guaranteed Knockouts with Multi-Guide CRISPR

EditCo’s Gene Knockout Kit uses a multi-guide gRNA approach to ensure reliable and efficient gene disruption. This method targets a single exon with three spatially coordinated gRNAs, creating multiple double-strand breaks and resulting in large fragment deletions. Compared to single-guide CRISPR, our multi-guide strategy significantly increases knockout efficiency, with over 75% large deletions and a 29.2% improvement in knockout success.

– High Knockout Efficiency: Multi-guide format provides up to 89.9% knockout success across 32 genetic targets.
– Reduced Off-Target Effects: Less occurrence of off-target edits compared to single-guide methods.
– Consistent Results: Fragment deletions lead to sustained protein depletion over time, confirmed through Western blot analysis.
– Reliable Gene Editing: Achieve complete knockout in just 7 days post-transfection.

Image: Better knockout efficiency was found across 32 genetic targets assessed.

Image: EditCo’s Gene Knockout Kit was designed to increase the efficacy of CRISPR-mediated knockouts.

Image: Multi-guide gRNA for each target resulted in >75% large deletion outcomes.

Image: Editing of three genes (CDK9, CINP, COASY) in HEK293 cells (transfected via nucleofection) using the multi-guide approach resulted in high knockout efficiencies, as indicated by Knockout (KO) Scores

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

CRISPR Reagents Portfolio

Gene Knockout kits

Arrayed gRNA Libraries

Let’s Find You an Application That Helps
Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Arrayed gRNA Libraries

March 18, 2025/in EditCo, Partners/by Harshita Sharma

PRODUCTS

Arrayed gRNA Libraries

Smarter, Faster, and More Efficient CRISPR Screening

Achieve unparalleled knockout efficiency with EditCo’s multi-guide CRISPR design. Our Arrayed CRISPR gRNA Libraries eliminate the inefficiencies of traditional loss-of-function screens, offering a reliable and ready-to-transfect solution. With up to three spatially coordinated sgRNAs per gene, our approach ensures higher knockout success, reduces false negatives, and eliminates the need for complex NGS data analysis. Designed for both human and mouse genes, our libraries provide fast delivery, robust quality control, and seamless Sanger sequencing analysis—so you can focus on results, not troubleshooting.

Whole Genome CRISPR Libraries for Comprehensive Gene Editing

EditCo’s Whole Human and Whole Mouse Genome Libraries provide unmatched gene coverage with our multi-guide design, ensuring high editing efficiency across 20,000+ gene targets. Designed for seamless transfection, these libraries reduce false negatives and eliminate time-consuming preparation, making large-scale CRISPR screening easier than ever.

– Comprehensive Coverage: Target the entire human or mouse genome with high knockout efficiency.
– Ready-to-Use Libraries: Pre-plated and transfection-ready, minimizing preparation time.
– Enhanced Stability: Chemically modified sgRNAs resist degradation and prevent immune responses.
– Flexible Formats: Available in 96- or 384-well plates with multi-guide sgRNAs for reliable gene disruption.

Accelerate Target Discovery with Pathway Libraries

EditCo’s 30+ Pathway Libraries, including druggable targets, GPCRs, kinases, and immuno-oncology genes, provide a powerful tool for target identification studies. Designed with our multi-guide CRISPR strategy, these libraries ensure high knockout efficiency and fewer false negatives. Select libraries ship in as little as one week, helping you start your screen faster.

– Diverse Pathway Coverage: Includes key gene sets for drug discovery and functional studies.
– Fast Shipping: Select libraries ready to ship within a week.
– High-Efficiency Knockouts: Multi-guide sgRNAs deliver precise, predictable gene disruption.
– Ready-to-Use Format: Available in 96- or 384-well plates with modified sgRNAs for stability.

Available Gene Pathways

Optimal Knockout Efficiency for High-Throughput Screening

XDel technology delivers precise, high-efficiency knockouts by using a multi-guide RNA strategy that ensures consistent and reliable gene editing. Unlike traditional single-guide methods, XDel induces fragment deletions in early exons, maximizing on-target accuracy while minimizing variability and off-target effects.

Superior editing efficiency – Multi-guide design achieves higher and more consistent knockouts
Reduced off-target effects – XDel minimizes unintended edits compared to single-guide methods
Sustained knockout effects – Gene edits remain stable across multiple cell passages
High viability & protein depletion – Maintains cell health while ensuring effective functional knockouts

Achieve robust genotype and phenotype screening with XDel’s optimized CRISPR knockout technology.

Image: XDel multiple gRNA creates fragment deletions

Image: XDel design includes up to 3 modified sgRNAs (grey bars) that target a single gene of interest

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

CRISPR Reagents Portfolio

Gene Knockout kits

Arrayed gRNA Libraries

Let’s Find You an Application That Helps
Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

SR-X™ Biomarker Detection System

December 10, 2024/in Partners, Quanterix/by Harshita Sharma

PRODUCTS

SR-X™ Biomarker Detection System

THE SR-X™ BIOMARKER DETECTION SYSTEM

The SR-X Ultra-Sensitive Biomarker Detection System leverages advanced Simoa® bead technology to provide researchers with a compact, cost-effective solution for ultra-sensitive biomarker detection. Designed for multiplexing, the SR-X can detect up to four analytes per well with minimal sample volume, optimizing both productivity and sample preservation. A comprehensive range of Simoa assay kits is available, delivering significantly enhanced sensitivity compared to traditional immunoassay methods. This ensures precise detection of biomarkers at both normal and acute levels across various sample types.

Multiplex Measurement of Low-Abundance Circulating Proteins

The SR-X™ system enables multiplex detection of neurodegeneration biomarkers using the Simoa® bead-based assay. Healthy donor sample readings are presented alongside the lower limit of quantification (LLOQ), indicated by dashed lines, for each assay in its validated matrix.

Ready to Order?

Our team can help you in placing the order. Click below to get a quote and fast ordering.

Quanterix Portfolio

Let’s Find You an Application That Helps
Your Research

Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

Or give us a call at:

1300 581 991

Integrated online ordering portal between Twist Bioscience & Decode Science

October 23, 2024/in Instructions/by Harshita Sharma

Integrated online ordering portal between Twist Bioscience & Decode Science!

To streamline the ordering process for your Twist Gene Fragments, Clonal Genes, Oligo Pools, IgG Antibodies and Custom Vector Onboarding, Twist Bioscience has an integrated portal connecting your Twist Bioscience eCommerce account and Decode Science (channel partner for Twist Bioscience in Australia and New Zealand).

All you need to do is:

Open your Twist eCommerce account www.twistbioscience.com, sign in and select what Twist can build for you:

Enter your own Project Name – (Twist recommend giving meaningful names to projects, if you don’t assign one, Twist will use a default name. You can always change it later)

Select start a new project

Upload your sequences, and follow the prompts through on each screen for your selected project for any of Twist’s synthesis services (NGS ordering not currently online yet)

Navigate through each page, each product has different options etc*

*If you are ordering genes and need to codon optimise your sequences, please select the gene to optimise and then click on “Codon Optimization” button on the top right of the next screen.

The platform will then navigate you through the various steps involved. If you have difficulties please contact your Decode team member and they can set up a virtual session to guide you.

Twist also now have a bulk codon optimisation tool available – Codon Optimization Tool | Twist Bioscience

Once you have completed all the details for your project follow the pages through to:

Request quote – this will be provided directly from Decode Science in AUD and include any discount structure, promotional offers etc.

You will receive email notification that Decode Science has received your quotation request and provided a project number Q-xxxxxx, which can be used to keep track of your orders.

Decode Science will email you a quote within 24 hours. If you would like to proceed with the purchase, please request a PO be generated for Decode Science and email through to support@decodescience.co.nz. Credit card payment is also accepted

Decode and Twist will take care of everything else, and you will receive your Twist DNA order delivered to your lab.

– Keep track of your orders in your online account

– Be notified when your order has been despatched to Decode Science

If you have any enquiries, please do not hesitate to contact sales@decodescience.co.nz

Smash the limits of single cell sequencing with Parse

April 29, 2024/in Seminar/by Harshita Sharma

Smash the limits of single cell sequencing.

Join us to learn about Parse’s single cell whole transcriptome technology and recently
launched Evercode V3 Kits. More cells, more samples, more clarity.

Combinatorial barcoding technology strips away the limitations and frustrations of yesterday’s single cell approach. It ditches the specialized instrument, freeing you to pursue unprecedented discoveries. Unleash the potential of single cell. Decode Science and Parse Biosciences invite you to a seminar discussing the advances in fixation-based single cell transcriptomics including our V3 chemistry, TCR/BCR kits, CRISPR Detect and Gene Capture.

MEET THE SPEAKER

John received his PhD at Duke University, where he studied cis-regulatory element activation during limb regeneration. He then spent a few years as a postdoc at the University of California, Merced where he studied early organ formation using single-cell genetic and epigenetic approaches. As a Field Application Scientist at Parse Biosciences, John assists scientists with their single-cell genomics experiments, from experimental design, sample preparation, single-cell library workflows, data analysis, and more.

John’s favorite model organism are zebrafish, both embryos and adults. In his free time John enjoys eating spicy food, and dabbles in growing his own hot chili pepper plants.

Brisbane

Date: 8th September 2025

Seminar : 10:30 AM – 11:30 AM – Translational Research Institute Room 3000

Sydney - DAY 1

SEMINAR 1

Date: 9th September 2025

Time: 10 AM – 11 AM

Location: Westmead Institute of Medical Research (hosted by Genomics Core) L2 WIMR Seminar room

SEMINAR 2

Date: 9th September 2025

Time: 2 PM – 3 PM

Location: UNSW (hosted by Ramaciotti) – AGSM Theatre

Sydney - DAY 2

SEMINAR 1

Date: 10th September 2025

Time: 9:30 AM – 10:30 AM

Location: VCCRI (Victor Chang Cardiac Research Institute) (hosted by Innovation Centre), Level 5 Meeting Room

SEMINAR 2

Date: 10th September 2025

Time: 12:00 PM – 1 PM

Location: Garvan Insitute (hosted by Single Cell Platform) – John Shine Room, Garvan Institute of Medical Research

Canberra

Date: 12th September 2025

Time: TBD

Location: TBD

Melbourne - Day 1

Date: 11th September 2025

Time: TBD

Location: TBD

Melbourne - Day 2

Date: 15th September 2025

Time: TBD

Location: TBD

Adelaide

Date: 16th September 2025

Time: TBD

Location: TBD

Author Archive for: Harshita

About Harshita Sharma

Entries by Harshita Sharma

High-Speed, High-Throughput Sequencing

Versatile Applications Across Clinical Genomics

Integrated DNB Make & Load Technology

Smart Configurations and Automated Analysis

Chris Wicky

Comprehensive Genomic Profiling for Oncology Research

Unified Testing Platform

Actionable Insights

Cost-Effective Efficiency

Chris Wicky

Knock-in Immortalized Cells

Get CRISPR-Engineered Cell Lines Faster and More Efficiently.

Tag and Quantify Your Protein:

Create a Disease Model:

Analyze Gene Regulation:

Uncover Protein Interactions:

Let’s Find You an Application That Helps Your Research

Knockout Immortalized Cells

Reliable, Reproducible CRISPR Editing for Breakthrough Discoveries

Characterize Genes Associated with Neurodegenerative Disease:

Investigate a Protein’s Mechanism of Action:

Expedite Drug Discovery Research:

Thoroughly Confirm Your Phenotype in Multiple Models in Parallel:

Let’s Find You an Application That Helps Your Research

Knockout CD8+ & CD4+ T Cells

Advanced CRISPR Knock-Ins for iPSC Research

Focus on your experiment while they handle CRISPR

Choose your starting point

Transparent and detailed results

Reliable and validated outcomes

Let’s Find You an Application That Helps Your Research

Gene Knockout Kits

EditCo Gene Knockout Kits: Reliable and Efficient CRISPR Solutions

Human and Mouse Knockouts

Multi-Guide sgRNA

Complete CRISPR Solution

Kit Contents

Let’s Find You an Application That Helps Your Research

Arrayed gRNA Libraries

Smarter, Faster, and More Efficient CRISPR Screening

Let’s Find You an Application That Helps Your Research

SR-X™ Biomarker Detection System

THE SR-X™ BIOMARKER DETECTION SYSTEM

Ultra-sensitive Simoa® Bead Technology

Semi-Automated

Convenient

Flexible

Low-maintenance

Let’s Find You an Application That Helps Your Research

Integrated online ordering portal between Twist Bioscience & Decode Science!

Smash the limits of single cell sequencing.

Join us to learn about Parse’s single cell whole transcriptome technology and recently launched Evercode V3 Kits. More cells, more samples, more clarity.

Brisbane

Sydney - DAY 1

Sydney - DAY 2

Canberra

Melbourne - Day 1

Melbourne - Day 2

Adelaide

APPLICATIONS

PARTNERS

COMPANY

SUPPORT

Instant Download

Special October Offer

FREE UMBRELLA

Let’s Find You an Application That Helps
Your Research

Expedite Drug Discovery
Research:

Let’s Find You an Application That Helps
Your Research

Let’s Find You an Application That Helps
Your Research

Let’s Find You an Application That Helps
Your Research

Let’s Find You an Application That Helps
Your Research

Let’s Find You an Application That Helps
Your Research

Join us to learn about Parse’s single cell whole transcriptome technology and recently
launched Evercode V3 Kits. More cells, more samples, more clarity.