2025-01-16151 Pages3680 USD
Short-read sequencing is a high-throughput technology used to determine the nucleotide sequence of DNA or RNA fragments that are relatively short in length, typically ranging from 50 to 300 base pairs. This technology has revolutionized genomics research by enabling rapid and cost-effective sequencing of large genomes, transcriptomes, and metagenomes. Short-read sequencing platforms, such as Illumina's sequencing systems, generate millions to billions of short reads in a single run, allowing researchers to analyze genetic variations, gene expression patterns, and microbial diversity with high accuracy and efficiency. The data produced by short-read sequencing is crucial for various applications in fields such as biomedical research, agriculture, forensics, and personalized medicine.
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