Design 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 bioscienceMethod for multiplex protein biomarker analysis (>1000 proteins) with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink RevealMultiple rounds of barcoding of fixed and permeabilised cells.
RNA mRNA illumina RNA-Seq single-cell parse combinatorial transcriptomicsMethod for multiplex protein biomarker analysis (5400 proteins) with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink HTNEBNext EM-Seq kit is an alternative to whole-genome bisulfite sequencing (WGBS). The enzymatic conversion of unmethylated cytosines in EM-seq is more gentle to DNA than WGBS and results in libraries with more even genome coverage and better coverage of CpG sites across the genome.
library preparation methylation epigenetics illumina CpG WGBS EM-seqRNA sequencing of mRNAs selected through poly-A enrichment.
library preparation transcriptomics RNA truseq mRNA illumina RNA-SeqRNA sequencing of either all RNAs in a sample, or of a RNA sample depleted of for example rRNA by the user.
library preparation RNA truseq illumina rnaseq RNA-SeqTotal RNA sequencing based on reduced rRNA content and other type of highly abundant RNAs in both prokaryotic and eukaryotic samples.
library preparation transcriptomics RNA mRNA illumina RNA-SeqNGI offers multiomic spatial profiling through the AVITI24™ with Teton™ CytoProfiling, which combines high-resolution imaging with simultaneous RNA, protein, and morphology detection in a single run.
RNA illumina spatial transcriptomicsNGI offers high resolution spatial transcriptomics through the 10x Genomics Visium HD 3’, which combines histology with PolyA-based transcriptomics in HD spatial context
transcriptomics RNA illumina spatialWe now offer high resolution spatially resolved transcriptomics through the 10X Genomics Visium HD CytAssist, which combines histology with probe-based transcriptomics in HD spatial context
transcriptomics RNA illumina spatialWe now offer high resolution spatially resolved transcriptomics through the 10X Genomics Visium HD CytAssist, which combines histology with probe-based transcriptomics in HD spatial context
transcriptomics RNA illumina spatialWe now offer spatially resolved transcriptomics through the 10X Genomics Visium CytAssist, which combines histology with probe-based transcriptomics in a spatial context.
illumina spatial transcriptomics RNAWe now offer spatially resolved transcriptomics through the 10X Genomics Visium CytAssist, which combines histology with probe-based transcriptomics in a spatial context.
transcriptomics RNA illumina spatialWe offer spatial transcriptomics through the 10X Genomics Visium method. The method combines histology with unbiased transcriptomics in a spatial context.
spatial transcriptomics RNA illuminaA method to identify open chromatin regions, such as promotor areas, using a transposase.
illumina ATACseq ATAC-seq Omni-ATAC TN5 ATAC open chromatin epigeneticsCombining short & long reads at the single cell level.
10x Genomics full transcript library preparation single cell long-read illumina ont chromiumProfiling of chromatin accessibility at the single cell level.
dna chromium chromatin 10x Genomics ATAC library preparation epigenetics single cell illumina ATAC-seqProfiling of 3´gene expression and chromatin accessibility in the same cell.
single cell RNA mRNA illumina ATAC-seq RNA-Seq ATAC chromium library preparation 10x Genomics transcriptomicsProfiling of gene expression levels at single-cell resolution.
RNA-Seq chromium 10x Genomics library preparation transcriptomics single cell RNA mRNA illuminaSingle-cell profiling of gene expression levels on fixed cells/nuclei.
mRNA FFPE illumina RNA-Seq sequencing chromium 10x Genomics library preparation fixed cells transcriptomics single cell multiplexing RNA probesA proximity-ligation protocol using a sequence-independent endonuclease, generating data for TAD identification and scaffolding.
chromatin scaffolding library preparation epigenetics TADs illumina de novoNGI now offers High Molecular Weight (HMW) DNA extraction as a service for sequencing projects at or in collaboration with NGI and SciLifeLab.
dna extraction hmw hmw dnaSequencing of the 16S gene 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.
targeted library preparation illumina 16S ampliconG-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.
ssDNA library preparation genome illumina WGS dna single-stranded DNASPLAT is an in-house developed WGBS library preparation method. This approach enables quick and efficient preparation of WGBS libraries from low-input DNA
WGBS Bisulphite single-stranded DNA ssDNA library preparation methylation epigenetics illumina CpGLow cost library preparation option for gDNA based on bead-linked transposase. Only for full plates of samples.
nextera normalization library preparation genome illumina WGS dnaNGI can sequence user-prepared libraries on all Illumina instruments. User-prepared libraries orders can only be whole-lane orders. Libraries with custom setups and or custom primers can only be whole flow cells.
illuminaMethod 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.
library preparation truseq genome illumina WGS dnaLibrary 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 cDNA sequencing is able to sequence entire transcripts in one go, ideal for detecting isoforms and fusions events.
assembly long-read nanoporeNanopore instruments can sequence very long continuous fragments of DNA. Sequencing native DNA allows detection of base modifications.
assembly long-read nanoporeNanopore direct RNA sequencing is able to sequence entire transcripts from native RNA, opening up opportunities to detect RNA 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.
revio smrt assembly pacbio methylation amplicon hifi de novo iso seq svGenotyping-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.
dna exome targeted library preparation illuminaWe offer a broad range of microarray options for high-throughput genotyping solutions based on SNP complexity and organism.
illumina genotyping dna array infinium SNPThe EPIC BeadChip array allows for the interrogation over 935,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
epigenetics illumina dna array infinium CpG methylation