CD Genomics has been providing the accurate and affordable whole genome sequencing service for couple of years. We combine both Illumina (short reads) and PacBio (long reads) platforms to achieve whole genome de novo assemblies and re-sequencing for viruses, microbes, plants, animals and humans.
The Introduction of Whole Genome Sequencing
Whole genome sequencing represents the determination of the complete DNA sequence of an organism’s genome at a single time, which entails chromosomal DNA as well as DNA contained in mitochondria and chloroplasts. Whole genome sequencing provides a powerful tool for both de novo sequencing and re-sequencing. De novo sequencing refers to sequencing of a novel genome without reference sequence available. 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. Oxford Nanopore and PacBio sequencing systems enable a faster and more accurate characterization of any species at the nucleotide level.
Whole genome resequencing can identify DNA biomarkers such as single nucleotide polymorphism (SNPs), insertions and deletions (indels), structure variations (SVs), copy number variations (CNVs) and other genetic changes of the sequenced species with high accuracy. It also provides an unprecedented opportunity for characterizing the polymorphic variants in a population, which comprehensively unravels the underlying mechanisms of species origin, development, growth, and evolution. What’s more, whole genome re-sequencing is an indispensable part of genome-wide association study (GWAS), where common genetic variants in different individuals are assessed to determine if a variant is associated with a particular phenotype. GWAS can be broadly used in food safety, agriculture, and pharmacy, especially personalized medicine.
Advantages of Whole Genome Sequencing
Whole Genome Sequencing Workflow
CD Genomics combines both Illumina HiSeq and PacBio systems to provide a fast and accurate whole genome sequencing and bioinformatics analysis for any species. Our highly experienced expert team executes quality management, following every procedure to ensure confident and unbiased results. The general workflow for whole genome sequencing is outlined below.
|Sample requirements and preparation
We provide customized bioinformatics analysis including:
CD Genomics provides full whole genome sequencing service package including sample standardization, library construction, deep sequencing, raw data quality control, genome assembly, and bioinformatics analysis. We can tailor this pipeline to your research interest. If you have additional requirements or questions, please feel free to contact us.
1. How to assure the creditability of assembly results?
Contig N50 and Scaffold N50 are two parameters to describe the “completeness” of a genome assembly. In terms of the quality of assembly results, there are several methods to evaluate it. EST dataset, RNA sequences, or conserved genes can be used to evaluate the completeness of genome assembly. BAC data can be used to test the accuracy.
2. How do we assemble hyper repetitive and heterozygous regions?
Repetitive sequences are abundant in a wide range of species, from microbes to mammals. Repeats have always presented technical challenges for sequence alignment and assembly. As for diploid or polyploid organisms, we generally assemble one set of chromosomes. It is hard to tell which alleles belong to which set of chromosomes in heterozygous regions. We combine the data from HiSeq, PacBio, and Sanger sequencing to ensure the accuracy of genome assembly in hyper repetitive and heterozygous regions.
3. How to estimate the genome size?
There are several ways to estimate the genome size.
ii. Flow cytometry
Flow cytometry is a common approach to estimate the genome size.
iii. Genome survey
Genome survey provides an initial view of a genome, and develop strategies for deep sequencing and genome assembly. This method adopts K-mer analysis to estimate genome size, repetition, and heterozygosis mathematically.
4. What are the advantages of whole genome sequencing over whole exome sequencing?
Whole exome sequencing captures only the exons in a genome, while whole genome sequencing capture nucleotides at the genomic level. Given that the exons only account for 1.5% of a genome size, it suggests that whole genome sequencing can capture more sequence data, not just coding regions. Additionally, mutations in noncoding regions may associate with diseases, such as cancer, which leads more people to the studies of noncoding regions.
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
Journal: Nature Genetics
Impact factor: 27.959
Published: 20 March 2017
Total hip replacement is a treatment for severe hip osteoarthritis, indicated by severe pain and reduced mobility, although radiographic changes may vary. The prior genome-wide association studies (GWAS) of hip osteoarthritis have reported a number of common sequence variants, all conferring small to moderate effects.
In this study, the researchers performed a GWAS to discover the association between end-stage hip osteoarthritis (THR) and sequence variants, based on whole genome sequencing results. The study involved 4,657 Icelandic patients and 207,514 population controls. The authors identified two rare signals that strongly associate with osteoarthritis total hip replacement: (i) a missense variant, c.1141G>C (P.aSP369His), in the COMP gene; (ii) a frameshift mutation, rs532464664 (p.Val330Glyfs*106), in the CHADL gene.
Table 1. Association of c.1141G>C in COMP (0.026%) and the homozygous state of rs532464664 (0.15%)
in CHADL with osteoarthritis in Iceland.
Figure 1. Age at total hip replacement by COMP variant genotype and CHADL variant genotype.
Figure 2. Regional association plot for the CHADL locus.
Figure 3. CHADL gene expression in human joint tissues and primary cells and during mesenchymal stem cell differentiation.
In summary, the authors identified two variants, including a rare missense variant in COMP and a frameshift mutation in CHADL. They strongly associate with osteoarthritis hip replacement and confer substantial risk of THR (odds ration = 16.7 and 7.7, respectively). Theses odds ratio are higher than those previously reported.
Styrkarsdottir U, et al. Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. Nature genetics, 2017, 49(5): 801.