slow-wave-sleep 发表于 2025-3-27 00:43:14
Ultralow-Input Genome Library Preparation for Nanopore Sequencing with Droplet MDAencing is a promising technology for genome assembly due to its limitless long reads, recommended input of 1 μg for the Ligation Sequencing Kit often precludes the use of this technology. Here, I detail an unbiased droplet-based multiple displacement amplification of picogram order of DNA to realizeAdrenal-Glands 发表于 2025-3-27 03:37:19
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Analysis of Tandem Repeat Expansions Using Long DNA Readsdisease-causing repeats in the human genome. Long read sequencers enable us to directly analyze repeat length and sequence content by covering whole repeats; they are therefore considered suitable for the analysis of long tandem repeats. Here, we describe an expanded repeat analysis using target seqAGOG 发表于 2025-3-27 21:16:29
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Long-Read Whole-Genome Sequencing Using a Nanopore Sequencer and Detection of Structural Variants in of diseases, including cancers. In this section, we introduce experimental and computational procedures for conducting long-read whole-genome sequencing (WGS) of cancer genomes from fresh frozen tissues/cells. We also demonstrate the analysis of SVs in cancer genomes using long-read WGS data from lNebulizer 发表于 2025-3-28 03:22:42
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Nanopore Sequencing Data Analysis of 16S rRNA Genes Using the GenomeSync-GSTK Systemintroduces the GenomeSync-GSTK system for bacterial species identification in a given sample using nanopore sequencing data of 16S rRNA genes as an example. GenomeSync is a collection of genome sequences designed to provide easy access to genomic data of the species as demanded. GSTK (genome searchconduct 发表于 2025-3-28 11:41:32
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