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NGS principles involve variant detection through sequencing and analysis of DNA or RNA samples.
NGS (Next Generation Sequencing) is a high-throughput technology used for DNA or RNA sequencing.
Variant detection involves identifying differences in DNA or RNA sequences compared to a reference genome.
NGS principles include library preparation, sequencing, and bioinformatics analysis.
Variant calling algorithms are used to id...
Variant calling is a process of identifying differences between a sample and a reference genome.
Variant calling is used in genomics to identify genetic variations that may be associated with disease or other traits.
It involves comparing a sample genome to a reference genome to identify differences, or variants, such as single nucleotide polymorphisms (SNPs) or insertions/deletions (indels).
Variant calling can be done u...
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