DNA Sequencing

Reveals the precise order of building blocks (nucleotides) in a DNA molecule, providing crucial information about genes and genetic variations.

Whole Genome Sequencing

Whole Genome Sequencing (WGS) provides a comprehensive analysis of an organism's entire genetic blueprint, encompassing both coding and non-coding regions. It facilitates the identification of genetic variants, aiding in research and clinical applications. It also finds use in personalized medicine as it offers detailed genetic insights that can guide tailored treatments

Whole Genome Sequencing

Whole Exome Sequencing

Whole Exome Sequencing (WES) offers a comprehensive view of exonic regions of the genome allowing the detection of a wide range of genetic variants

Whole Exome Sequencing

Amplicon Sequencing

Amplicon Sequencing is a highly targeted approach that allows researchers to analyze genetic variation in specific regions of the genome. Amplicon sequencing helps detect rare somatic mutations in complex samples, such as those with mixed tumor and germline DNA. It also has lower sequencing costs and turnaround times compared to more comprehensive approaches such as whole-genome sequencing.

Amplicon Sequencing

ChIP Sequencing

ChipSeq is a combination of the chromatin immunoprecipitation technique with massively parallel sequencing. Chromatin immunoprecipitation allows the identification of specific DNA sequences that are bound to proteins of interest in vivo. ChIPSeq can be used to map DNA-binding proteins and histone modifications in a genome-wide manner at single base-pair resolution

ChIP Sequencing

DNA Sequencing

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