Long-read sequencing solutions

Accuracy with deep insights: HiFi Long-read sequencing solutions

Achieve unparalleled accuracy and comprehensive insights with MedGenome's long-read solutions on the PacBio Revio.

Long-read sequencing for multiple applications

Experience MedGenome's advanced capabilities in de novo genome assemblies, full-length transcriptome sequencing, and comprehensive variant detection with PacBio HiFi technology

While short-read sequencing has been an advantage for genomics study, it struggles to resolve repetitive regions, assemble complex structural variants, and fully capture isoform diversity. PacBio HiFi sequencing solves these issues with highly accurate long reads, enabling comprehensive profiling of genetic variation, including SNVs, Indels, SVs, and complex regions. MedGenome provides unparalleled capabilities with both short-read and PacBio long-read solutions, supporting highly contiguous genome assemblies, structural variant detection, full-length transcript sequencing, epigenetic profiling, and haplotype phasing, providing comprehensive genomic insights for diverse research needs.

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PacBio HiFi Long-read sequencing solutions

Streamlined long-read DNA and RNA sequencing workflows: unified solutions to save time and effort

De novo Genome Assembly and Annotation
De novo Genome Assembly and Annotation
  • Reference-quality genome assembly: highly accurate and contiguous genome assemblies.
  • Comprehensive genome annotation: complete and accurate gene models including identification of isoforms and alternative splicing.
Human variant detection
Human variant detection
  • Unparalleled variant detection: Identify challenging structural variants and variants in complex regions of the genome.
  • Comprehensive genomic coverage: Uniform genome-wide coverage, minimizing biases and enabling confident variant calling in GC-rich and repetitive regions.
  • Haplotype resolution: Resolve variants on homologous chromosomes, providing insights into allele-specific expression and compound heterozygosity.
Full-length RNA sequencing
Full-length RNA sequencing
  • Isoform diversity: quantify all gene isoforms, including novel ones.
  • Fusion gene detection: characterize fusion genes, crucial for understanding cancer development.
  • Long non-coding RNA (lncRNA) analysis: identify and characterize lncRNAs, important regulatory molecules often missed by short-read sequencing.
Single-cell full-length RNA Seq
Single-cell full-length RNA Seq
  • Deconvolute cellular heterogeneity: Profile full-length transcriptomes to reveal diversity and rare cell types.
  • Discover novel cell states: Track isoform changes for insights into differentiation and disease.
  • Link transcriptomic variation: Correlate isoform expression with cell markers to understand functional consequences.

how to order

Starting a project with MedGenome

MedGenome's customer portal allows for easy sample submission and sample tracking during lab processing. Using our portal ensures data QC, raw data and interactive analysis reports are delivered securely.

Our process is simple

Request a quote Request a quote
We create your project file We create your project
Upload sample details Upload sample details
Submit documents and ship samples Submit documents and ship samples
We process and analyze your samples We process and analyze your samples
Your data is delivered to you Your data is delivered to you

Resources

White papers and technical resources

Resource Video
Video
WES/WGS Report Walkthrough
Whitepaper
Whitepaper
Denovo Genome Assembly Solutions at MedGenome

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