info@SeqMatic.com
Mon - Fri 9AM - 7PM PST

1.510.870.0965

Whole Genome (WGS) Sequencing Services

Home > Services > Whole Genome Sequencing (WGS)

Whole Genome Sequencing Services

A comprehensive genome mapping of the DNA exon & intron regions

Whole genome sequencing services (WGS) are critical to the expansion of understanding complexities of genetic applications across research fields, from personalized medicine to evolutionary studies, agricultural, environmental and cancer research.

SeqMatic offers comprehensive whole genome sequencing services for the analysis of human, animal, plant, and microbe samples. WGS generates extensive genome variation data that is widely used in genomic research, including the documentation of single-nucleotide polymorphisms (SNPs), insertions and deletions (InDels), structural variations (SVs), and copy number variations (CNVs). Combined with our in-depth bioinformatics pipeline, SeqMatic ensures a quick turnaround time for sequencing and produces publication-ready data.

Applications of Whole Genome Sequencing

Human

Human

Animal & Plants

Animal & Plants

Microbes

Microbes

Testing of genetic disorders

Population genetics research

Generation of reference genomes

Rare disease mutations

Agricultural breeding programs

Microbial identification

Cancer genomics

Genome-wide association studies (GWAS)

Comparative genomic studies

Tracking of infectious disease outbreaks

Genomics Comparison Table

	HUMAN	ANIMAL & PLANTS	MICROBIAL
Comprehensive Genome Assessment (>30x)	x	x	x
Clinical-grade sequencing	x
Single-nucleotide polymorphisms (SNPs)	x	x	x
Insertions and deletions (InDels)	x	x	x
Structural Variations (SVs)	x	x	x
Copy number variations (CNVs)	x	x
Repeated sequences analysis with long-reads technology	x	x	x
In-depth bioinformatic analysis and generation of publication-ready data	x	x	x
Experience working with animal sample types, including horse, bees, mice, pigs and many other		x
Experience with biosafety (BSL2) sample types	x		x
Stringent Quality Control from library preparation to data analysis	x	x	x

“SeqMatic exhibits the best in sequencing performance, customer service, and turnaround. My experience in getting several runs completed was an absolute pleasure, and I would recommend SeqMatic to anyone with sequencing needs!”

Customer F.G.

San Francisco, CA

This list is an extraction of all research topics listed in Google Scholar, where SeqMatic is cited as a CRO Laboratory Service Provider.

Ward, L.M., Lingappa, U.F., Grotzinger, J.P. et al. “Microbial mats in the Turks and Caicos Islands reveal diversity and evolution of phototrophy in the Chloroflexota order Aggregatilineales.” Environmental Microbiome 15, 9 (2020).
Ward, L.M., Fischer, W.W. and McGlynn, S.E., “Candidatus Anthektikosiphon siderophilum OHK22, a new member of the chloroflexi family Herpetosiphonaceae from Oku-okuhachikurou Onsen. Microbes and environments“, (2020) 35(3), p.ME20030.
Ward, L.M., Shih, P.M., Hemp, J., Kakegawa, T., Fischer, W.W. and McGlynn, S.E., “Phototrophic methane oxidation in a member of the Chloroflexi phylum.” (2019) BioRxiv, p.531582.
Cherry, J.J., DiDonato, C.J., Androphy, E.J., Calo, A., Potter, K., Custer, S.K., Du, S., Foley, T.L., Gopalsamy, A., Reedich, E.J. and Gordo, S.M., “In vitro and in vivo effects of 2, 4 diaminoquinazoline inhibitors of the decapping scavenger enzyme DcpS: context-specific modulation of SMN transcript levels.” (2017) PLoS One, 12(9), p.e0185079.
Ward, L.M., Idei, A., Nakagawa, M., Ueno, Y., Fischer, W.W. and McGlynn, S.E., “Geochemical and metagenomic characterization of Jinata Onsen, a Proterozoic-analog hot spring, reveals novel microbial diversity including iron-tolerant phototrophs and thermophilic lithotrophs.” (2019) Microbes and environments, 34(3), pp.278-292.
Find other Research Publications from around the world!

Optimize Your Results

Solutions are custom-made according to research needs

Pre-Submission

Planning & Consultation – Assurance of de-identified sample submission and handling

Sample Submission

Nucleic Acid Extraction – We accept a wide range of sample types

Library Preparation

Library Generation – Amplified cDNA is used for sequence libraries’ construction

Sequencing

Different platforms for different data outputs

Data Analysis

Custom Bioinformatics

Non-model organisms & Viral Genomes

Whole Exome Sequencing (WES)

Service Portfolio

PRODUCT HIGHLIGHT

TailorMix Dual-Indexed PhiX

Check Product Highlights