BioSkryb Genomics

BioSkryb Genomics develops single-cell multiomic analysis products and bioinformatics platforms, including the BaseJumper Bioinformatics Platform and ResolveDNA amplification kits.

About BioSkryb Genomics

BioSkryb Genomics develops single-cell multiomic analysis products and bioinformatics platforms, including the BaseJumper Bioinformatics Platform and ResolveDNA amplification kits.

Products

  • BaseJumper Cloud

    Healthcare Data & ResearchFree plan

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    Cloud-based bioinformatics platform for quality control (QC) analysis of whole genome sequencing data and transcriptomic analysis, enabling data processing without a high-perfor...

  • BaseJumper Local

    Healthcare Data & ResearchFree plan

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    Installs key bioinformatics workflows to run on a user's own high-performance computing cluster.

  • BaseJumper Services

    Healthcare Data & ResearchCustom pricing

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    Custom bioinformatics services available through ResolveServices, including custom AI data set generation and preparation and access to application-specific bundled workflows cu...

  • Single-cell and low-input DNA amplification kit providing reproducible recovery of >97% of genomes of single cells and low-input DNA samples using primary template-directed ampl...

  • BaseJumper AI

    Healthcare Data & ResearchCustom pricing

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    Early release offering providing large language model (LLM)-enabled, end-to-end (E2E) workflows for genomic exploration.

  • Enables whole genome and transcriptome sequencing from a single cell, leveraging primary template-directed amplification (PTA) to achieve up to 97% genomic coverage with superio...

  • ResolveServices

    Drug Discovery & BiotechCustom pricing

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    Contract single-cell sequencing service offering end-to-end solutions from cell isolation and nucleic acid amplification through NGS workflows, data analysis, and AI training da...

What customers say

“Among all the whole-genome amplification (WGA) methods we have tested, PTA-based WGA has provided the most accurate output. It reliably stays close to the original 50/50 ratio of allele frequency in heterozygous loci, minimizing allele dropout and false-positive loss of heterozygosity.”
CustomerBioSkryb Genomics customer
“PTA is our method of choice if you want reproducible, efficient, and evenly amplified genomes from single cells for single nucleotide variant detection.”
CustomerBioSkryb Genomics customer

Security and compliance

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