We offer short read mapping against a reference genome and bigwig/bedgraph generation using aligners such as bwa and bowtie. Reference genome and aligners will be of your choice and we will recommend a pipeline based on the type of samples you have sequenced with us (such as WGS, exome, ChiP and other targeted approaches).
We offer short read mapping against a reference genome/transcriptome of your choice and counting of reads mapped to a feature (such as gene, exon, miRNA) of choice. Our preferred choice of aligner is HISAT2 but we are happy to accommodate any aligner of your choice. You will receive raw read counts as part of the service based on the type of samples you have sequenced with us (such as Total RNA, mRNA, microRNA and other approaches).
We offer 16S analyses using QIIME2 and MOTHUR pipelines tailored specifically to the region that we target in our new service.
Cost of alignment service
At the moment we charge 100 NOK per sample with a maximum of 1000 per MiSeq run/NextSeq run/one lane of HiSeq data for the above alignment services.
QIIME2 and MOTHUR analyses cost 1000 NOK per MiSeq run and is included in the cost of the amplicon service that we offer.
Do get in touch with us if you wish to use these services at firstname.lastname@example.org
We can offer further analyses specific to your projects on a collaborative basis. If you are interested, please get in touch.
Bioinformatic services request form
Bioinformatic services request form - to provide the NSC with information regarding bioinformatic services that you have requested.