Bacterial whole genome sequencing can be divided into bacterial genome de novo sequencing and bacterial genome resequencing, which is a method to obtain the complete genome sequence of bacteria. We can provide bacterial whole genome sequencing and bioinformatics analysis services to help you explore the genetic structure and functions, evolutionary relationships of microbial populations, and the unique biological characteristics of the strain.
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We provide next-generation sequencing and long-read sequencing technologies for bacterial whole genome sequencing, utilizing the advanced Illumina HiSeq, Nanopore MinION, and PacBio SMRT platforms to produce high-quality sequencing data quickly and efficiently. For next-generation sequencing (NGS), the workflow of bacterial genome de novo sequencing includes four steps: (1) the chromosomal DNA is randomly interrupted; (2) different lengths of sequences are selected to construct a library; (3) large-scale sequencing and genomic assembly; (4) fill in the gap. The final assembly level is measured by the assembly indicators. Bacterial whole genome resequencing could be completed based on high-throughput sequencing data of small fragment libraries and reference-based alignment. For long-read sequencing, long-read libraries can easily cross repetitive and GC-rich segments for accurate detection of chromosome structural variations and fusion genes.
With bacterial whole genome sequencing, a large number of single nucleotide polymorphisms (SNPs), insertions and deletions (InDels), and structural variations (SVs) can be discovered or identified. Bacterial whole genome sequencing can also be used for identification of the unique biological characteristics (pathogenic mechanism, symbiotic mechanism, metabolic mechanism) of the strains and molecular strain typing. Bacterial whole genome sequencing is becoming more and more relevant for the medical sector, which is increasingly influencing diagnostics, epidemiology, risk management, and patient care.
Our bioinformatics analysis includes genomic assembly, genomic structure studies, functional annotation, pathogenic microbiology, and comparative genomic analysis.
|Genomic Assembly||Genomic assembly and outcome evaluation|
|Coding/noncoding gene prediction|
|Repetitive sequence analysis|
|Genomic Structure Analysis||Genomic island prediction|
|Detection of CRISPRs|
|Functional Annotation||NR, GO, COG, KEGG, SwissProt, Pfam, TCDB, SignalP, CAZy|
|Pathogenic Microbiology||Drug resistance gene database (ARDB)|
|Virulence factor database (VFDB)|
|The comprehensive antibiotic resistance database (CARD)|
|Comparative Genomic Analysis||Synteny analysis|
|Analysis of gene family evolution|
Sampling kits: We provide a complete range of microbial sampling kits for clients, including microbial collection products, DNA/RNA isolation kits, and accessories for storage and mailing.
Deliverables: Raw sequencing data, assembled and annotated sequences, quality-control dashboard, and the bioinformatics report.