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 samplingCost-efficient, high-throughput library preparation for whole-genome sequencing of large sample collections. Only for sample batches of 96.
genome WGS dna affordable library preparationFlexible whole genome library preparation with PCR-free workflows from as little as 100 ng DNA and PCR workflows for lower-input samples.
Design targeted sequencing panels for your regions of interest. Twist Bioscience provides the probes, and NGI handles QC, library prep, and sequencing.
dna twist bioscience methylation RNAFull length sequencing of the 16S gene provides a significantly higher taxonomic resolution compared to sequencing of isolated regions.
library preparation illumina 16S amplicon targetedSequencing of the 16S V3/V4 region to study bacterial diversity and composition in a sample.
library preparation illumina 16S amplicon targetedSequencing of PCR amplicons to study genetic variation within small target regions.
amplicon targeted library preparation illumina 16SG-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.
genome illumina WGS dna single-stranded DNA ssDNA library preparationLow cost library preparation option for gDNA based on bead-linked transposase. Only for full plates of samples.
dna nextera normalization library preparation genome illumina WGSMethod for shotgun DNA libraries used for whole genome sequencing and metagenomics.
PCR-free library preparation genome illumina WGS dna tagmentationGold standard method for shotgun DNA libraries used for whole genome sequencing and metagenomics.
WGS dna library preparation truseq genome illuminaLibrary preparation from limited input DNA, used in whole genome sequencing and metagenomics etc.
WGS dna library preparation truseq genome illuminaLibrary 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.
illumina WGS dna library preparation genomeNanopore instruments can sequence very long continuous fragments of DNA. Sequencing native DNA allows detection of base modifications.
long-read nanopore assemblyPacBio 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.
smrt assembly pacbio methylation amplicon hifi de novo iso seq sv revioGenotyping-by-sequencing without prior genome information.
wholegenome dna polymorphism library preparation genome illuminaA 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
methylation base modifications basecalling pod5Basic 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.
human data WES WGS sarek cancer