This protocol is available at NGI Uppsala.
Flexible whole genome library preparation with PCR-free workflows from as little as 100 ng DNA and PCR workflows for lower-input samples.
Cost-efficient, high-throughput library preparation for whole-genome sequencing of large sample collections. Only for sample batches of 96.
library preparation genome WGS dna affordableDesign targeted sequencing panels for your regions of interest. Twist Bioscience provides the probes, and NGI handles QC, library prep, and sequencing.
twist bioscience methylation RNA dnaMethod for multiplex protein biomarker analysis (>1000 proteins) with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink RevealMethod for multiplex protein biomarker analysis (5400 proteins) with sequencing readout using the Illumina NovaSeq platform.
Olink biomarker Olink HT proteinNEBNext 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-seqTotal RNA sequencing based on reduced rRNA content and other type of highly abundant RNAs in both prokaryotic and eukaryotic samples.
transcriptomics RNA mRNA illumina RNA-Seq library preparationNGI 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 dnaRuns with methylation sequencing data. It pre-processes raw data from FastQ inputs, aligns the reads and performs extensive quality-control on the results, using either Bismark or bwa-meth/MethylDackel.
methylseq Methyl-Seq BS Bisulfite