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Human Research

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Human Research
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Human genomics is at the forefront of understanding complex diseases, genetic disorders, and personalized medicine. By sequencing genomes or exomes, researchers can identify genomic alterations that contribute to rare diseases, cancer, and complex disorders such as diabetes or heart disease. Rapid sequencing technologies enable high-resolution insights into genetic variants, allowing for better diagnostics and targeted therapeutic strategies.

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Our sequencing services for Human Research includes:

DNA Sequencing Whole Genome (Short Read, Long Read, Hybrid), Enrichment (Whole Exome, Amplicon and Targeted), Single Cell DNA, Genome Mapping, Genotyping (Based on SNP, ddRAD, Microsatellites)
RNA Sequencing Total RNA, mRNA, Small RNA, Long Non-Coding, IncRNA, Iso Sequencing
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