Results 71 to 80 of about 11,169 (113)

Accelerating SARS-CoV-2 genomic surveillance in a routine clinical setting with nanopore sequencing

open access: yesInternational Journal of Medical Microbiology
Background: SARS-CoV-2 genomic analysis has been key to the provision of valuable data to meet both epidemiological and clinical demands. High-throughput sequencing, generally Illumina-based, has been necessary to ensure the widest coverage in global ...
Sergio Buenestado-Serrano   +11 more
doaj   +1 more source

Barcode Sequencing by Illumina NGS v1

open access: yes
This protocol details the extraction of genomic DNA from cells and barcode sequencing by NGS.
Nicholas A. Popp   +4 more
openaire   +1 more source

Full-length 16S rRNA gene sequencing by PacBio improves taxonomic resolution in human microbiome samples

open access: yesBMC Genomics
Background Sequencing variable regions of the 16S rRNA gene (≃300 bp) with Illumina technology is commonly used to study the composition of human microbiota.
Elena Buetas   +7 more
doaj   +1 more source

Primed and ready: nanopore metabarcoding can now recover highly accurate consensus barcodes that are generally indel-free

open access: yesBMC Genomics
Background DNA metabarcoding applies high-throughput sequencing approaches to generate numerous DNA barcodes from mixed sample pools for mass species identification and community characterisation.
Jia Jin Marc Chang   +5 more
doaj   +1 more source

Comparative analysis of illumina and oxford nanopore sequencing platforms for 16S rRNA profiling of respiratory microbial communities

open access: yesScientific Reports
The respiratory microbiome plays a crucial role in health and disease, necessitating accurate characterization through high-throughput sequencing technologies.
Guillem Macip   +12 more
doaj   +1 more source

Evaluation of somatic copy number variation detection by NGS technologies and bioinformatics tools on a hyper-diploid cancer genome

open access: yesGenome Biology
Background Copy number variation (CNV) is a key genetic characteristic for cancer diagnostics and can be used as a biomarker for the selection of therapeutic treatments.
Daniall Masood   +25 more
doaj   +1 more source

P597: All for One Clinical Genomics Network: Linking Canadian diagnostic laboratories to share genome-wide sequencing data to support rare disease diagnosis

open access: yesGenetics in Medicine Open
E. Magda Price   +14 more
doaj   +1 more source

Candida auris sequencing by Illumina miSeq using Illumina DNA Prep v1

open access: yes
Candida auris sequencing is becoming more important for public health and surveillance. This protocol is designed to guide individuals experienced in sequencing in setting up a SOP for sequencing C. auris. This protocol is designed for Illumina short-read sequencing.
openaire   +1 more source

My Seq Illumina sequencer and Next Generation Sequencing technologies

open access: yes, 2016
Overview of next generation sequencing (NGS) technologies:Illumina MySeqIllumina technologies comparison MySeq, NextSeq, HiSeq.PacBio.Ion Torrent.Oxford Nanopore.
openaire   +1 more source

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