High-throughput full-genome or targeted sequencing of DNA from organisms with an existing reference genome.
Adaptive sampling is an Oxford Nanopore Technologies (ONT) method for real-time targeted sequencing. The method enables enrichment or depletion of specific genomic regions during sequencing without additional library preparation steps.
nanopore adaptive samplingDesign targeted sequencing panels for your regions of interest. Twist Bioscience provides the probes, and NGI handles QC, library prep, and sequencing.
methylation RNA dna twist bioscienceFull length sequencing of the 16S gene provides a significantly higher taxonomic resolution compared to sequencing of isolated regions.
16S amplicon targeted library preparation illuminaSequencing of the 16S V3/V4 region to study bacterial diversity and composition in a sample.
illumina 16S amplicon targeted library preparationSequencing of PCR amplicons to study genetic variation within small target regions.
library preparation illumina 16S amplicon targetedG-SPLAT is a library preparation technique designed for low-quality or limited-input DNA, with applications in whole-genome sequencing, metagenomics, and and other challenging sequencing projects.
illumina WGS dna single-stranded DNA ssDNA library preparation genomeLow cost library preparation option for gDNA based on bead-linked transposase. Only for full plates of samples.
library preparation genome illumina WGS dna nextera normalizationMethod for shotgun DNA libraries used for whole genome sequencing and metagenomics.
genome illumina WGS dna tagmentation PCR-free library preparationGold standard method for shotgun DNA libraries used for whole genome sequencing and metagenomics.
genome illumina WGS dna library preparation truseqLibrary preparation from limited input DNA, used in whole genome sequencing and metagenomics etc.
library preparation truseq genome illumina WGS dnaLibrary preparation for DNA, ideal for preparing libraries from small amounts of input material. Works well for shotgun libraries, ChIP DNA and FFPE samples, amongst others.
library preparation genome illumina WGS dnaNanopore instruments can sequence very long continuous fragments of DNA. Sequencing native DNA allows detection of base modifications.
assembly long-read nanoporePacBio SMRT sequencing generates reads tens of kilobases in length enabling high quality genome assembly, structural variant analysis, amplicon resequencing, full-length transcript isoform sequencing, full-length 16S rRNA sequencing and amplification free epigenetic characterization.
amplicon hifi de novo iso seq sv revio smrt assembly pacbio methylationGenotyping-by-sequencing without prior genome information.
library preparation genome illumina wholegenome dna polymorphismA platform for human whole exome sequencing (WES) using target enrichment and library preparation for next generation sequencing.
library preparation illumina dna exome targetedQuality control, Basecalling and multiplexing of sequencing reads generated by Oxford Nanopore sequencers.
long-read nanoporeAdditional compute intensive nanopore raw data processing services provided by NGI
pod5 methylation base modifications basecallingBasic quality-control monitoring of Illumina FastQ sequence data.
QC fastqc fastq screen checkqcRuns with illumina DNA-sequencing data, WGS or targeted sequencing e.g. WES. Aligns to the reference genome, gives QC metrics, does variant-calling and finishes with annotation.
WGS sarek cancer human data WES