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Document No.: Version: Effective Date: Page No.:Illumine sequencing library pools on a HSEQ 2500 (external)MCCRDSOP0009 1.2 12/01/2014-Page 1 of 101.0 PURPOSE/SCOPE This Standard Operating Procedure
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How to fill out illumina sequencing library pools

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Step 1: Prepare the DNA samples by quantifying and normalizing them to the desired concentration.
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Step 2: Design and order the appropriate sequencer-specific adapters and indexes for your library preparation workflow.
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Step 3: Prepare the library pool by combining equal amounts of each DNA sample. The volume of each sample depends on the desired library yield and the recommended input requirements of the sequencing platform.
04
Step 4: Add the sequencer-specific adapters and indexes to the library pool. This allows for multiplexing of multiple samples in a single sequencing run.
05
Step 5: Size-select the library pool to remove any unwanted fragments or primer dimers using methods such as gel purification or bead-based size selection.
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Step 6: Amplify the library pool using PCR to enrich for the adapter-ligated DNA fragments and to add additional sequences required for cluster generation on the sequencer.
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Step 7: Purify the amplified library pool to remove any remaining PCR artifacts, such as primer dimers and nonspecific products.
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Step 8: Quantify the final library pool using a fluorometric-based method or quantitative PCR (qPCR) to determine the concentration and validate the quality of the library.
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Step 9: Proceed with downstream applications, such as cluster generation and sequencing, following the manufacturer's instructions for your specific sequencing platform.

Who needs illumina sequencing library pools?

01
Researchers and scientists conducting genetic and genomic studies.
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Biotechnology companies involved in genetic research and development.
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Clinical laboratories performing genetic testing and diagnostics.
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Pharmaceutical companies studying genetic variants and personalized medicine.
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Academic institutions conducting research in the field of genomics and genetics.
06
Plant and animal breeders interested in studying genetic traits and improving crop yields or livestock production.
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Forensic scientists analyzing DNA evidence in criminal investigations.
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Environmental scientists studying microbial communities and biodiversity using DNA sequencing techniques.
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Illumina sequencing library pools are collections of DNA libraries that are prepared for sequencing using Illumina sequencing technology.
Researchers or laboratories conducting DNA sequencing experiments using Illumina technology are required to file illumina sequencing library pools.
Illumina sequencing library pools can be filled out by providing detailed information about the DNA libraries being sequenced, including sample names, barcodes, and sequencing protocols.
The purpose of illumina sequencing library pools is to organize and prepare DNA samples for high-throughput sequencing using Illumina technology.
Information such as sample names, barcodes, sequencing protocols, and quality control metrics must be reported on illumina sequencing library pools.
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