NGS, also known as high-throughput sequencing, is a DNA sequencing technology which has revolutionized genomic and molecular research and has influenced all fields of biological research, it has become increasingly prevalent in modern society. NGS allows us to sequence DNA and RNA much more accurately, quickly and cheaply. Library sequencing is a technique that encompasses the initial step of attaching adapters, which include elements like index sequences, barcodes, and sequencing primer binding regions, to both ends of the desired target fragments. Subsequently, these prepared fragments are subjected to sequencing using a dedicated sequencer. In contrast, targeted sequencing is characterized by the selective capture of particular genes or regions of interest before the sequencing phase. Notably, the principal methods for executing targeted sequencing comprise hybrid capture and multiplex PCR.

NGS, also known as high-throughput sequencing, is a DNA sequencing technology which has revolutionized genomic and molecular research and has influenced all fields of biological research, it has become increasingly prevalent in modern society. NGS allows us to sequence DNA and RNA much more accurately, quickly and cheaply. Library sequencing is a technique that encompasses the initial step of attaching adapters, which include elements like index sequences, barcodes, and sequencing primer binding regions, to both ends of the desired target fragments. Subsequently, these prepared fragments are subjected to sequencing using a dedicated sequencer. In contrast, targeted sequencing is characterized by the selective capture of particular genes or regions of interest before the sequencing phase. Notably, the principal methods for executing targeted sequencing comprise hybrid capture and multiplex PCR.

• Scalable platform

  Genome sequencing is the methodology employed to employ high-throughput DNA sequencing techniques alongside advanced bioinformatics tools for the compilation and scrutiny of both the functional and structural constituents of an entire genome. This comprehensive approach facilitates the examination of individual disparities and distinctions within populations. Moreover, by executing de novo sequencing and leveraging bioinformatics methodologies, it becomes possible to derive genetic maps for various species.

• Transcriptomics

  The term "transcriptome" encompasses the entirety of transcripts generated by the cells or tissues of a particular species under specific conditions. Leveraging second-generation high-throughput sequencing, it becomes feasible to efficiently and extensively acquire sequence data pertaining to nearly all transcripts and information on differential gene expression within the tissues or organs of a specific species under particular conditions. This approach has found extensive utility across diverse domains, encompassing fundamental research, clinical diagnostics, and pharmaceutical research .

• Experiment design

  Selection of SNP fit for research purpose, and then a selection of platform based on the number of samples and design possibility.

• Genotyping

  Validation of the existence and frequency of known SNPs and discovery or novel SNPs.

• Data

  Provided in Excel format. For SNP discovery, raw data, annotation, LD results are also provided.

We aim to provide the highest level of service, confidentiality and customer support. Our extensive expertise can help expedite your SNP and mutation analysis assays with speed, quality, and reliability. With our services you can either take a deep look into the genome or search for unknown genotype-phenotype connections or genotype already known variations.