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 RNAMethod 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.
parse combinatorial transcriptomics RNA mRNA illumina RNA-Seq single-cellMethod for multiplex protein biomarker analysis (5400 proteins) with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink HTMethod for multiplex protein biomarker analysis with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink ExploreNEBNext 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.
WGBS EM-seq library preparation methylation epigenetics illumina CpGRNA sequencing of mRNAs selected through poly-A enrichment.
illumina RNA-Seq library preparation transcriptomics RNA truseq mRNARNA 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.
illumina RNA-Seq library preparation transcriptomics RNA mRNANGI 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.
transcriptomics RNA illumina spatialNGI 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
spatial transcriptomics RNA illuminaWe 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.
spatial transcriptomics RNA illuminaWe now offer spatially resolved transcriptomics through the 10X Genomics Visium CytAssist, which combines histology with probe-based transcriptomics in a spatial context.
RNA illumina spatial transcriptomicsWe offer spatial transcriptomics through the 10X Genomics Visium method. The method combines histology with unbiased transcriptomics in a spatial context.
RNA illumina spatial transcriptomicsA method to identify open chromatin regions, such as promotor areas, using a transposase.
open chromatin epigenetics illumina ATACseq ATAC-seq Omni-ATAC TN5 ATACCombining short & long reads at the single cell level.
single cell long-read illumina ont chromium 10x Genomics full transcript library preparationProfiling of chromatin accessibility at the single cell level.
epigenetics single cell illumina ATAC-seq dna chromium chromatin 10x Genomics ATAC library preparationProfiling of 3´gene expression and chromatin accessibility in the same cell.
ATAC-seq RNA-Seq ATAC chromium library preparation 10x Genomics transcriptomics single cell RNA mRNA illuminaProfiling of gene expression levels at single-cell resolution.
transcriptomics single cell RNA mRNA illumina RNA-Seq chromium 10x Genomics library preparationSingle-cell profiling of gene expression levels on fixed cells.
illumina RNA-Seq chromium 10x Genomics fixed cells library preparation transcriptomics single cell RNA mRNAA proximity-ligation protocol using a sequence-independent endonuclease, generating data for TAD identification and scaffolding.
illumina de novo chromatin scaffolding library preparation epigenetics TADsNGI now offers High Molecular Weight (HMW) DNA extraction as a service for sequencing projects at or in collaboration with NGI and SciLifeLab.
hmw hmw dna dna extractionSequencing 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.
illumina 16S amplicon targeted library preparationG-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 preparationSPLAT is an in-house developed WGBS library preparation method. This approach enables quick and efficient preparation of WGBS libraries from low-input DNA
epigenetics illumina CpG WGBS Bisulphite single-stranded DNA ssDNA library preparation methylationLow cost library preparation option for gDNA based on bead-linked transposase. Only for full plates of samples.
illumina WGS dna nextera normalization library preparation genomeNGI 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.
dna tagmentation PCR-free library preparation genome illumina WGSGold standard method for shotgun DNA libraries used for whole genome sequencing and metagenomics.
dna library preparation truseq genome illumina WGSLibrary preparation from limited input DNA, used in whole genome sequencing and metagenomics etc.
illumina WGS dna library preparation truseq genomeLibrary 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.
WGS dna library preparation genome illuminaNanopore cDNA sequencing is able to sequence entire transcripts in one go, ideal for detecting isoforms and fusions events.
nanopore assembly long-readNanopore 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.
de novo iso seq sv revio smrt assembly pacbio methylation amplicon hifimiRNA libraries from very low input total RNA samples & degraded total RNA.
illumina library preparation epigenetics RNAGenotyping-by-sequencing without prior genome information.
genome illumina wholegenome dna polymorphism library preparationA platform for human whole exome sequencing (WES) using target enrichment and library preparation for next generation sequencing.
library preparation illumina dna exome targetedWe offer a broad range of microarray options for high-throughput genotyping solutions based on SNP complexity and organism.
infinium SNP illumina genotyping dna arrayThe EPIC BeadChip array allows for the interrogation over 935,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
methylation epigenetics illumina dna array infinium CpG