Service introduction

        Genome de novo sequencing, also known as de novo genome sequencing, is a method of sequencing the entire genome of a species without relying on a reference genome. This can be used to study the genome of a newly discovered species or to generate a more accurate and complete genome assembly of a species with a complex or highly repetitive genome.

Technical procedures

Services provided

        We offer a variety of services related to genome de novo sequencing, including:

        Genome survey: This service provides an overview of the genome, including its size, GC content, and repetitiveness.

        Genome assembly statistics: This service provides information about the quality of the genome assembly, such as the average read depth and the N50 length of the contigs.

        Genome annotation and gene function classification: This service assigns genes to functional categories and predicts their functions.

        Comparative genomics and evolutionary analysis: This service compares the genome to other genomes to identify similarities and differences.

Assembly evaluation standards

Sample requirements