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DNA sequencers determine nucleotide sequences for molecular biology, genetic engineering, hereditary disease studies, genome sequencing, and DNA cloning. Selection depends on sequencing method, throughput, accuracy, read length, workflow compatibility, and ease of use. Technologies include Sanger and high-throughput sequencing with fluorescence, pyrosequencing, or nanopore detection.
View product category →Next Generation Sequencing enables high-throughput, parallel analysis of DNA fragments for genomics research, molecular diagnostics, personalized medicine, and biological research. Selection can consider throughput, read length, coverage depth, and workflow compatibility. Short reads support broad genomic mapping but can complicate reconstruction of complex structures.
View product category →All 2 product categories
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