De Novo Sequencing
De novo sequencing refers to sequencing a novel genome where there is no reference sequence available for alignment. The coverage quality of de novo assembly depends on the size and continuity of the contigs.
De novo sequencing generates the first genome map for a species, thus providing a valuable reference sequence for re-sequencing. Our usage of Oxford Nanopore and PacBio sequencing systems enable a faster and more accurate characterization of any species at the nucleotide level.
Bio Basic Asia Pacific combines Illumina HiSeq, PacBio systems and Oxford Nanopore to provide a fast and accurate de novo sequencing and bioinformatics analysis for any species.
Our highly experienced expert team executes quality management, following every procedure to ensure reliable results.
Sequencing Platforms
HiSeq 4000, X Ten / NovaSeq 6000 / PacBio Sequel, RSII
For more information and quotation, kindly contact us at NGS@biobasic-asia.com
Bioinformatics Analysis
- Data Quality Control
- Genome Preliminary Assemblies
- Genome Annotation
Advantages
- Generates accurate reference sequences, even for complex or polyploid genomes
- Provides useful information for mapping genomes of novel organisms or finishing genomes of known organisms
- Identifies structural variants and complex rearrangements, such as deletions, inversions, or translocations
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