Short Read Sequencing - Data Linked

Short read sequencing is a high-throughput next-generation sequencing (NGS) approach used to determine the nucleotide sequence of DNA or RNA fragments, enabling detection of genetic variants, gene expression profiles, or genomic features depending on the library preparation strategy employed. This assay involves fragmentation of input nucleic acids, adapter ligation, and amplification prior to sequencing on short-read platforms (such as Illumina), generating millions of short sequence reads (typically 50–300 bp) in parallel. The resulting raw sequencing data are linked to associated metadata and downstream bioinformatic analyses, including quality control, alignment to a reference genome or transcriptome, and quantification or variant calling as appropriate to the experimental design.

SEEK ID: https://fairdomhub.org/assays/2547

Experimental assay

Projects: Hi-IMPAcTB

Investigation: IMPAcTB

Study: Intravenous BCG-mediated protection against tuberculosis requires CD4+ T cells and CD8alpha+ lymphocytes

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Assay type: Experimental Assay Type

Technology type: Technology Type

Organisms: No organisms

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Created: 23rd Jan 2025 at 20:35

Last updated: 27th May 2026 at 20:47

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