DNA sequencing is a laboratory process used to determine the exact order of nucleotides within a DNA molecule. It involves using special enzymes to break apart the DNA molecule and then using a specialized sequencing machine to read the sequence of the four nucleotides, which are adenine (A), thymine (T), guanine (G) and cytosine (C). The resulting sequence of nucleotides can then be compared to known sequences in order to identify differences in the DNA sequence and potentially diagnose genetic conditions or link individuals to specific traits.

Free DNA Sequencing Includes free shipping. 3 FREE single pass DNA sequencing reactions. Clinical genetic analysis through ACGT Molecular diagnostics. Aim is to assist healthcare professionals in their diagnoses and treatment of genetic diseases. Ngs technologies hold powerful potential for discovery in genetic and genomic research .

Gene codes is an international software firm specializing in bioinformatics software for DNA sequence analysis. Its scientist-friendly software tools hold the dominant share in the DNA sequencing sector. The company's products are unrivaled in forensic DNA identification for mass fatalities .

MicroGenDX is a global leader in next-gen DNA sequencing diagnostics of infection. The laboratory has run over 500,000 tests at our state-of-the-art, CAP-accredited, CLIA-licensed molecular diagnostic facility. Our advanced instrumentation, including Illumina miseq sequencers, provides the industry’s most informative microbial diagnostics .

DNA Sequencing Includes Free shipping. 3 FREE single pass DNA sequencing reactions. Molecular Diagnostics clinical genetic analysis. Aim is to assist healthcare professionals in their diagnoses and treatment of genetic diseases. Clinical sample analysis through ACGT Molecular diagnostics - assisting healthcare professionals .

Dna-chip was founded by regis professor Chris toumazou in 2003. He invented a way of detecting protons released during DNA synthesis. Optics-free, label-free method shifted DNA sequencing from expensive genome centres into the mainstream of local labs and primary care clinics .

Universal sequencing technology (UST) was established by a group of NGS technology veterans from Roche/454. UST TELL-Seq enables short-read 2nd generation sequencing platforms to produce super long-read results. The company has filed more than 20 patent applications covering linked read and single-cell library preparation chemistry .

RevoluGen is a privately held scientific research and development company commercialising molecular tools. The company’s products have particular applications in delivering HMW-DNA in record time for long-read DNA sequencing as well many other nucleic acid applications. Fire monkey significantly improves long read sequencing results by extracting long-fragment DNA with minimal small fragment DNA .

Loop Genomics is a platform technology for long-read DNA sequencing. Loop Genomics technology transforms short-read DNA sequencers into high-throughput, long-read, single-molecule DNA sequencing machines. Loop Genomics long-read DNA sequencing technology provides phased sequencing solutions across a diverse repertoire of research and clinical applications. Sequencing of partial rRNA gene sequences results in reduced phylogenetic resolution. Full-length, high-throughput, phased sequencing that covers all 16S variable regions is becoming the gold standard for profiling the microbiome. Achieve the highest resolution microbial community profiling with long-read, next-generation sequencing of the microbiome. Characterizing polymorphisms in HLA genes inside and outside of the protein-coding regions is important for organ transplantation compatibility testing and for strengthening causality association studies.  The length of homologous sequences between HLA alleles extends beyond the capabilities of short-read sequencing platforms, resulting in diploid ambiguities and a reliance on imputation.  Sequence full-length HLA DNA and/or RNA with phased, high throughput, long-read sequencing that resolves allelic discrimination and diploid ambiguity. Viral genetic variability is a major determinant of viral drug resistance and viral vaccine efficacy.  Accurately mapping viral genetic variability is a critical step in choosing the optimal course of therapy and developing efficacious vaccines.  Key mutations are typically located throughout long stretches of viral genomes, making the retrieval of critical phased data challenging using short-read sequencing technology.  Use phased, high-throughput DNA sequencing technology to map key mutations at the quasi-species level and generate a complete phased map of viral populations.

Synbio Technologies is a DNA sequencing, synthesis, and engineering technology platform.

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