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DNA Whole Genome Sequencing (WGS)

Generate a comprehensive mapping of exon and intron regions of the genome

SeqMatic offers comprehensive Whole Genome Sequencing (WGS) 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.

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HumanAnimal & PlantsMicrobes 
  • Testing of genetic disorders
  • population genetics research
  • generation of reference genomes
  • rare disease mutations
  • agricultural breeding programs
  • microbial identification
  • cancer forms
  • genome-wide association studies (GWAS)
  • comparative genomic studies
  • tracking of infectious disease outbreaks
   

Optimize Your Results

Solutions are custom-made according to research needs

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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

Service Portfolio

PRODUCT HIGHLIGHT

TailorMix Dual-Indexed PhiX