Plant and Animal Genome
Reference-Free Genomics

Plant & Animal
De Novo Assembly

Deciphering the blueprint of life from scratch. We combine the "Technology Trinity" to deliver chromosome-scale assemblies for the most complex species.

Biodiversity & Ag-Tech

The Technology Trinity

One platform is never enough for a perfect assembly. We weave together long-reads and spatial mapping to resolve the unresolvable.

PacBio HiFi (CCS)

Combining the accuracy of short-read sequencing with the length of long-reads for near-perfect contig assembly.

Oxford Nanopore (ULR)

Ultra-Long Reads (100kb+) to span the most complex repetitive regions and structural variations.

Hi-C Scaffolding

Capturing 3D chromatin interactions to anchor contigs into chromosome-level pseudomolecules.

>50 MB
Contig N50
Industry-leading assembly contiguity.
>98%
BUSCO Score
Highly complete gene space representation.
Q50+
Accuracy
Near-zero consensus error rate.
Chr-Scale
Resolution
Full chromosomal-level scaffolding.

Assembly
Gold Standards

Building a reference-grade genome requires more than just raw data. Our computational pipeline utilizing Hifiasm, Canu, and Salsa2 ensures that N50 metrics and BUSCO scores exceed international consortium standards.

  • Haplotype-Aware Phase Assembly
  • Gap-Free Centromere & Telomere Resolution
  • High-Confidence Gene Scaffolding
  • Automated Assembly Polishing with Illumina

Conquering Polyploidy & Repeats

Many plant genomes are polyploid (multiple chromosome sets), making assembly extremely difficult. We utilize Oxford Nanopore Ultra-Long reads to span multi-megabase repeats and PacBio HiFi to resolve highly similar haplotypes.

Heterozygosity Handling

Advanced algorithms to separate paternal and maternal alleles in diploid organisms.

Chromosomal Scaffolding

Utilizing Hi-C to map long-range connections and anchor contigs into full chromosomes.

Scientific Agriculture

End-to-End Pipeline

1

Genome Survey

Illumina depth + K-mer analysis

2

Long-Read Assembly

Primary contig generation

3

Hi-C Scaffolding

Chromosome anchoring

4

Gene Annotation

Ab-initio & Homology based

Technical FAQ

Resequencing requires a high-quality reference genome. Use De Novo sequencing for non-model organisms, for species with highly fragmented existing references, or when investigating structural variations that are lost in standard mapping approaches.

Build Your Species' Blueprint.

Join the elite group of researchers publishing chromosome-level reference genomes with our Technology Trinity.

RESEQUENCING_VIEW
Chat on WhatsApp