Start your analyses with prebuilt workflows for human, mouse and rat genomics, or build your own custom, shareable workflows. Analyze whole transcriptome and exome sequencing data, targeted amplicon sequencing data and more.
Analyze your T/B cell receptor data, import IMGT reference segments and visualize clonotyped reads as alignments and Sankey plots
Easily calculate TMB score, detect MSI status and calculate HRD score
Upload your data to QCI Interpret and QCI Interpret Translational, including TMB and MSI status, SNVs, InDels, CNVs, fusions and inversions
Includes copy number variant calling, structural variant calling and regional ploidy detection
Create methylation-level heat maps, predict methylation profiles and create your own databases, which can be used to predict profiles
Is your sample processing taking too long? Simplify your workflow with LightSpeed, our new module that offers optimized read mapping and variant calling pipelines. Get quick and reliable results on your existing computer – without any special hardware.
Upload your raw FASTQ files
LightSpeed carries out adapter trimming, read mapping, deduplication, local realignment, UMI grouping, primer trimming, quality control and variant calling
Begin your analyses, or use our template workflows for whole-genome sequencing (WGS), whole-exome sequencing (WES) and targeted data analysis
