Resolve Training
Cell Preparation | FACS Plate Alignment and Best Practices
Cell preparation is crucial for downstream processing of single cells for using BioSkryb’s ResolveDNA® and ResolveOME™ kits. This video provides Fluorescent Activated Cell Sorting (FACS) plate alignment instructions and best practices for upstream cell preparation.
ResolveDNA V2 with D100 | Whole Genome Amplification from Single Cells using Automation
Product: 100545
ResolveDNA enables whole genome amplification from single cells producing double-stranded DNA that may be used as input for many applications including next generation single-cell DNA sequencing. In this video, automation with the Hewlett Packard (HP) D100 is used to perform the ResolveDNA V2 protocol. Set up instructions for the HP D100 are also included.
Real time monitoring may be done with ResolveDNA V2. Please, contact techsupport@BioSkryb.com for additional information.
ResolveDNA V2 Manual Method | Whole Genome Amplification from Single Cells
Product: 100545
ResolveDNA enables whole genome amplification from single cells producing double-stranded DNA that may be used as input for many applications including next generation single-cell DNA sequencing. In this video, the instructions and methods for performing the ResolveDNA V2 protocol are provided.
Real time monitoring may be done with ResolveDNA V2. Please, contact techsupport@BioSkryb.com for additional information.
ResolveDNA V1 | Whole Genome Amplification from Single Cells
Product: 100136
ResolveDNA enables whole genome amplification from single cells producing double-stranded DNA that may be used as input for many applications including next generation single-cell DNA sequencing. In this video, the instructions and methods for performing the ResolveDNA V1 protocol are provided.
ResolveOME | Day 1
Product: 100500
ResolveOME is a unified method to amplify the whole genome and full-length transcriptome from single cells. In this video, the full-length transcriptome and whole genome amplification ResolveOME Day 1 protocol instructions are provided.
ResolveOME Day 2 | Nucleic Acid Separation and Purification
Product: 100500
ResolveOME is a unified method to amplify the whole genome and full-length transcriptome from single cells. This video provides the protocol instructions for ResolveOME Day 2, in which the cDNA and DNA fractions are separated and purified for library preparation.
ResolveOME Day 3 | NGS Library Prep for cDNA and DNA
Product: 100500
The NGS library preparation kits are used to make NGS libraries with unique dual indices for multiplexing via next generation DNA sequencing. This video includes the library preparation instructions used in the ResolveOME protocol.
Cell Preparation | FACS Plate Alignment and Best Practices
Cell preparation is crucial for downstream processing of single cells for using BioSkryb’s ResolveDNA® and ResolveOME™ kits. This video provides Fluorescent Activated Cell Sorting (FACS) plate alignment instructions and best practices for upstream cell preparation.
ResolveDNA V2 with D100 | Whole Genome Amplification from Single Cells using Automation
Product: 100545
ResolveDNA enables whole genome amplification from single cells producing double-stranded DNA that may be used as input for many applications including next generation single-cell DNA sequencing. In this video, automation with the Hewlett Packard (HP) D100 is used to perform the ResolveDNA V2 protocol. Set up instructions for the HP D100 are also included.
Real time monitoring may be done with ResolveDNA V2. Please, contact techsupport@BioSkryb.com for additional information.
ResolveDNA V2: Manual Method | Whole Genome Amplification from Single Cells
Product: 100545
ResolveDNA enables whole genome amplification from single cells producing double-stranded DNA that may be used as input for many applications including next generation single-cell DNA sequencing. In this video, the instructions and methods for performing the ResolveDNA V2 protocol are provided.
Real time monitoring may be done with ResolveDNA V2. Please, contact techsupport@BioSkryb.com for additional information.
ResolveDNA V1 | Whole Genome Amplification from Single Cells
Product: 100136
ResolveDNA enables whole genome amplification from single cells producing double-stranded DNA that may be used as input for many applications including next generation single-cell DNA sequencing. In this video, the instructions and methods for performing the ResolveDNA V1 protocol are provided.
Cell Preparation | FACS Plate Alignment and Best Practices
Cell preparation is crucial for downstream processing of single cells for using BioSkryb’s ResolveDNA® and ResolveOME™ kits. This video provides Fluorescent Activated Cell Sorting (FACS) plate alignment instructions and best practices for upstream cell preparation.
ResolveOME | Day 1
Product: 100500
ResolveOME is a unified method to amplify the whole genome and full-length transcriptome from single cells. In this video, the full-length transcriptome and whole genome amplification ResolveOME Day 1 protocol instructions are provided.
ResolveOME Day 2 | Nucleic Acid Separation and Purification
Product: 100500
ResolveOME is a unified method to amplify the whole genome and full-length transcriptome from single cells. This video provides the protocol instructions for ResolveOME Day 2, in which the cDNA and DNA fractions are separated and purified for library preparation.
ResolveOME Day 3 | NGS Library Prep for cDNA and DNA
Product: 100500
The NGS library preparation kits are used to make NGS libraries with unique dual indices for multiplexing via next generation DNA sequencing. This video includes the library preparation instructions used in the ResolveOME protocol.
BaseJumper Bioinformatics Platform
The BaseJumper Bioinformatics Platform, powered by BioSkryb Genomics, is designed to provide bioinformatics analysis and interactive visualization at scale. Uncovering biomarkers and mechanisms of disease demands high volumes of complex data and the ability to quickly slice layers of analyses. Since multi-omic data can be generated across a single cell, organization and mapping of the results are necessary to empower interplay of molecular features. BaseJumper brings speed and ease of use directly into the hands of its users, shifting time from computation to interpretation of results.
BaseJumper Demo
Users can access BaseJumper through the online portal. They can build their datasets from multiomic analyses and select pre-designed bioinformatics workflows. Computational workflows are computed in the cloud, decreasing the dependence on users’ access to computing resources. Data are displayed in easy-to-interpret and ready-to-export formats that can be readily used in scientific posters, presentations, and publications.