This guide provides detailed instructions for preparing Nextera Mate Pair DNA libraries for paired-end sequencing using Illumina's advanced technology.
It outlines two distinct protocols:
The document covers essential aspects including workflow overviews, best practices for sample handling and reagent use, DNA input recommendations, and guidance on sequencing and data analysis.
Designed for research use, this guide ensures proper and safe application of the Nextera Mate Pair Sample Preparation Kit.
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Illumina Nextera Mate Pair Library Prep Reference Guide A comprehensive reference guide detailing the Illumina Nextera Mate Pair Library Prep protocol for generating mate pair libraries from genomic DNA for paired-end sequencing. Covers gel-free and gel-plus protocols, DNA input recommendations, and technical assistance. |
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Illumina TruSeq Synthetic Long-Read DNA Library Prep Guide A comprehensive guide from Illumina detailing the protocol for preparing TruSeq Synthetic Long-Read DNA libraries for genomic analysis, including long-read assembly and phasing applications. |
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Illumina TruSeq Bovine Parentage Reference Guide for DNA Sequencing Comprehensive guide to preparing DNA libraries for bovine parentage analysis using the Illumina TruSeq Bovine Parentage Kit, covering protocols, input recommendations, and technical assistance. |
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Illumina MiSeq System: Denature and Dilute Libraries Guide A comprehensive guide from Illumina detailing the procedures for denaturing and diluting DNA libraries for sequencing on the MiSeq system, including protocols for various normalization methods and PhiX control preparation. |
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Illumina NextSeq 500 系统指南 - 高通量测序仪操作手册 Illumina NextSeq 500 系统指南提供了关于该高通量测序仪的全面操作、维护和故障排除信息。本手册专为科研用户设计,涵盖仪器组件、软件功能(如 NCS、BaseSpace Sequence Hub、Local Run Manager、RTA)以及测序流程,旨在帮助用户高效利用 NextSeq 500 进行外显子组、全基因组和转录组测序。 |
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Illumina Local Run Manager Germline Variant Analysis Module Workflow Guide for NextSeq 550Dx This document provides a workflow guide for the Illumina Local Run Manager Germline Variant Analysis Module on the NextSeq 550Dx instrument. It details the process of setting up runs, entering sample information, importing manifests, performing analysis, and viewing results, specifically for germline variant detection in DNA from peripheral whole blood specimens. The guide also covers output file formats, folder structures, base calling, index diversity, revision history, and technical assistance. |
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Illumina DNA Prep with Enrichment Dx Kit: Targeted DNA Library Preparation The Illumina DNA Prep with Enrichment Dx Kit is a comprehensive solution for preparing DNA sequencing libraries from both peripheral whole blood and formalin-fixed, paraffin-embedded (FFPE) tissue samples. This kit is designed to enrich libraries for specific genomic regions of interest, enabling targeted sequencing applications. It supports DNA from whole blood and FFPE tissues, utilizes user-supplied probe panels for target enrichment, and is compatible with Illumina sequencing systems. |
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NovaSeq 6000: Guía para Desnaturalizar y Diluir Librerías para Secuenciación Esta guía proporciona instrucciones detalladas para desnaturalizar y diluir librerías genómicas y de ARN para su secuenciación en el sistema Illumina NovaSeq 6000. Cubre protocolos estándar y Xp, incluyendo variaciones para TruSight Oncology 500 ctDNA y HT. |