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Genome & Omics Marketplace
Personal genome apps, lab sequencing services and repeatable data analysis
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152 products · Sign in to view pricing
Genome Import & Conversion
Convert FASTQ/BAM into a compact analysis-ready VCF
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Ancestry Composition
Explore population affinity across reference populations
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Paternal Y Tree
Trace paternal haplogroup branches and migration context
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Maternal Migration
Explore maternal haplogroup history through mtDNA
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Surname & Lineage
Combine optional family records with paternal-line evidence
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Family Tree
Build a private, permissioned genetic family tree
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Genetic Relatives
Discover consented matches through shared DNA segments
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Ancient DNA Affinity
Compare selected markers with published ancient samples
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Nutrition & Metabolism
Personalized nutrition patterns from selected variants
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Dietary Preferences
Explore taste, caffeine, lactose and food-response traits
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Vitamins & Micronutrients
Understand selected nutrient-related genetic tendencies
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Running Genetics
Training signals from ACTN3, ACE and VO₂max models
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Fitness & Recovery
Explore fitness response, recovery and injury-related traits
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Skin Profile
Explore pigmentation, sensitivity and aging-related traits
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Sleep Rhythm
Explore genetic signals related to sleep and chronotype
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Genetic Traits
A collection of observable, non-medical inherited traits
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Physiological Traits
Explore selected non-diagnostic body-response traits
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Lifestyle Guidance
Turn wellness traits into practical daily considerations
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Environment Response
Explore selected traits related to common exposures
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Behavioral Traits
Explore research-stage behavioral trait associations
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Disease Risk Library
Evidence library for clinician-guided risk conversations
Professional review
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Carrier Screening Navigator
Professional workflow for inherited-condition carrier findings
Professional review
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Medication Guide
Evidence-linked pharmacogenomic review for professionals
Professional review
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Hereditary Risk Library
Curated knowledge for inherited-risk conversations
Professional review
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Cancer Genetics Library
Research and professional evidence for hereditary cancer
Professional review
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HLA & Blood Group
Professional typing workflow from compatible sequencing data
Professional review
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Physical Exam Assistant
Organize genome-informed questions for a professional visit
Professional review
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FASTQ Quality Control
Automated read QC, contamination checks and MultiQC summary
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Bulk RNA Expression
Quantify gene and transcript expression from RNA-seq
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Differential Expression
Compare experimental groups with reproducible RNA-seq statistics
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Pathway Enrichment
Run GO, KEGG and GSEA with interactive visualizations
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miRNA & Small RNA
Quantify known and candidate small RNAs
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Single-cell RNA-seq
Cell QC, clustering, markers and cell-type exploration
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Spatial Transcriptomics
Explore spatial expression, domains and tissue context
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WGS/WES Secondary Analysis
Research-grade alignment, variant calling and QC
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16S & Metagenomics
Profile research microbiome composition and pathways
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Methylation Research
Process supported methylation sequencing or array data
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Targeted RNA & Fusion Research
Research workflow for targeted expression and fusion candidates
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Custom Bioinformatics Pipeline
Package a validated lab workflow as a repeatable Kepler app
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Human Whole-genome Sequencing
Germline WGS from sample receipt through variant-ready research data.
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Tumor–Normal Whole-genome Sequencing
Matched tumor and normal WGS for somatic research workflows.
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Human Whole-exome Sequencing
Exome capture and germline research analysis for individuals or cohorts.
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Tumor Whole-exome Sequencing
Tumor-only or matched tumor-normal exome research analysis.
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Animal & Plant Genome Resequencing
Population-scale resequencing, variant discovery and annotation.
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Animal & Plant De Novo Genome
Hybrid or long-read assembly, polishing and genome assessment.
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Microbial Whole-genome Sequencing
Whole-genome sequencing for bacterial and fungal isolates.
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Human Long-read Whole Genome
Long-read WGS for structural variation, phasing and complex regions.
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Long-read Target Enrichment
Targeted long-read sequencing of selected genomic regions.
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Target Capture Sequencing
Custom or fixed content capture panels for focused research.
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Custom Amplicon Sequencing
High-depth sequencing of custom DNA amplicons.
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Population Genomics & Evolution
Population structure, selection, migration and demographic history.
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Genome-wide Association Study
Genotype QC, imputation and association testing for research cohorts.
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Genetic Map Construction
Linkage map construction for breeding and trait studies.
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BSA & QTL Mapping
Bulked segregant and quantitative trait locus analysis.
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CNV & Structural Variant Research
Research detection and annotation of CNVs and structural variants.
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Mitochondrial Genome & Enrichment
Mitochondrial enrichment, variant analysis and haplogroup-ready output.
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Variant Annotation & Prioritization
Annotate and prioritize research variants with versioned databases.
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Splice-effect Prediction
Research prediction of candidate variant effects on RNA splicing.
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Comprehensive Tumor DNA + RNA
Combined DNA variants, RNA fusions and expression from tumor samples.
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Homologous Recombination Deficiency
Genomic instability and homologous recombination research metrics.
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ctDNA Liquid-biopsy Research
Low-frequency variant research from plasma cell-free DNA.
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Hereditary Cancer Research Panel
Research analysis of inherited cancer-predisposition genes.
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BRCA1/2 Research
Focused BRCA1/2 SNV, indel and CNV research workflow.
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Myeloid Neoplasm Research
DNA/RNA research panel for myeloid-associated alterations.
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Myeloproliferative Neoplasm Research
Focused research of variants associated with myeloproliferative neoplasms.
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Childhood Cancer Research Panel
DNA/RNA panel analysis for pediatric cancer research cohorts.
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Cancer Hotspot Panel
High-depth analysis of recurrent cancer-associated hotspots.
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Pan-cancer Research Panel
Broad multi-tumor DNA/RNA research profiling.
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FFPE DNA/RNA Analysis
QC-aware tumor analysis designed for FFPE-derived nucleic acids.
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Multi-cancer Liquid-biopsy Panel
Multi-gene liquid-biopsy research with low-frequency calling.
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Core Solid-tumor Panel
Focused tissue-panel research for common actionable alterations.
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CNV Panel of Normals
Build a reusable normal baseline for panel-based CNV research.
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Eukaryotic Reference RNA-seq
Reference-guided gene and transcript analysis for eukaryotic samples.
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De Novo Transcriptome
Transcript assembly and annotation when no suitable reference exists.
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Prokaryotic RNA-seq
Strand-aware bacterial or archaeal expression analysis.
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Long Non-coding RNA
Coding and long non-coding transcript discovery and comparison.
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Circular RNA
Circular RNA discovery, quantification and host-gene context.
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Whole Transcriptome
Joint mRNA, lncRNA, circRNA and small-RNA research package.
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Full-length Transcriptome
Isoform discovery, alternative transcripts and annotation improvement.
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Stranded Total RNA
Strand-specific coding and non-coding RNA profiling.
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RNA Exome Enrichment
Capture-based transcript analysis for degraded or low-input RNA.
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Targeted RNA Expression
Focused expression measurement for a defined gene panel.
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Immune-response RNA Panel
Targeted immune-response expression profiling for research studies.
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Alternative Splicing Analysis
Detect and compare exon usage and transcript-splicing events.
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Single-nucleus RNA-seq
Nucleus-level expression analysis for frozen or difficult tissues.
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Single-cell ATAC-seq
Chromatin accessibility, clustering and regulatory element analysis.
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Single-cell ATAC + Gene Expression
Joint chromatin accessibility and gene expression in matched cells.
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Single-cell Immune Repertoire
Paired TCR/BCR clonotype and cell-state analysis.
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Single-cell Protein + RNA
Joint antibody-derived tag and transcriptome analysis.
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Visium Spatial Transcriptomics
Spatial gene-expression mapping with histology alignment.
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FFPE Spatial Transcriptomics
Probe-based spatial profiling for FFPE tissue sections.
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High-resolution Spatial Transcriptomics
High-density spatial expression and tissue-domain analysis.
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Spatial Proteogenomics
Integrated spatial RNA and protein-marker analysis.
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Spatial Mapping & Image Integration
Map single-cell states into tissue coordinates and morphology.
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Cell Trajectory & Communication
Pseudotime, lineage and ligand–receptor research analysis.
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16S / 18S / ITS Amplicon
Community diversity and taxonomic profiling from marker genes.
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Full-length 16S / ITS
Higher-resolution taxonomic profiling with full-length amplicons.
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Absolute-abundance Microbiome
Combine sequencing and spike-in controls for absolute abundance.
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Shotgun Metagenomics
Species, genes and pathways from untargeted microbial DNA.
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Host-associated Metagenomics
Research profiling of host-associated microbial communities.
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Environmental Metagenomics
Community and functional analysis for soil, water and other environments.
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Metagenome-assembled Genomes
Assembly, binning, quality assessment and genome annotation.
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Antimicrobial Resistance Genes
Research detection and context analysis of resistance genes.
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Metatranscriptomics
Active microbial genes and pathway expression in communities.
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Metaviromics
Viral community discovery, annotation and diversity research.
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Microbial Enrichment Plus
Host-depleted microbial enrichment and DRAGEN-based analysis.
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Viral Surveillance
Consensus genomes, lineages and surveillance-ready outputs.
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SARS-CoV-2 Surveillance
Amplicon QC, consensus sequence and lineage research analysis.
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Influenza A/B Amplicon
Whole-genome amplicon analysis for influenza surveillance research.
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Respiratory Pathogen Research
Targeted respiratory pathogen identification and AMR-marker research.
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Urinary Pathogen & AMR Research
Research identification of urinary pathogens and resistance markers.
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Comparative Microbial Genomics
Pan-genome, phylogeny, virulence and resistance comparison.
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Whole-genome Bisulfite Sequencing
Genome-wide cytosine methylation analysis at base resolution.
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Targeted Methylation Capture
High-depth methylation analysis of selected regulatory regions.
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Five-base DNA Sequencing
Joint genetic and methylation information from a single workflow.
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ChIP-seq
Protein–DNA binding and histone-mark enrichment analysis.
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Bulk ATAC-seq
Open-chromatin peaks, motifs and differential accessibility.
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Methylation Array Analysis
Array QC, normalization, cell composition and differential methylation.
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Genotyping Array Analysis
Genotype calling, sample QC, ancestry-ready and imputation-ready output.
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PGx Star-allele Research
Research star-allele calling from compatible pharmacogenomic arrays.
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Cytogenetics Array Research
Research CNV, LOH and chromosomal pattern analysis.
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Polygenic Score Research
Versioned polygenic score calculation for approved research cohorts.
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Duet DNA Multiomics
Joint canonical-base and modified-cytosine analysis from one library.
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Differential Methylation
Group comparison of methylation sites, regions and pathways.
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High-plex Protein Profiling
High-plex serum or plasma protein quantification and QC.
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Olink Proteomics
Targeted high-plex protein quantification for research cohorts.
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DIA Proteomics
Data-independent acquisition protein identification and quantification.
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4D-DIA / Astral Proteomics
High-depth, high-throughput DIA proteome analysis.
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Blood Proteome
Depletion-aware serum or plasma proteome profiling.
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TMT / iTRAQ Quantitative Proteomics
Isobaric-label multiplex protein quantification.
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Label-free Proteomics
Label-free protein identification, quantification and comparison.
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Phosphoproteomics
Phosphopeptide enrichment, site localization and pathway analysis.
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Protein Modification Profiling
Research analysis of selected post-translational modifications.
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Metaproteomics
Community protein identification and functional profiling.
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Targeted Proteomics
PRM/SRM quantification of selected proteins or peptides.
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Untargeted LC-MS Metabolomics
Broad metabolite feature detection, annotation and statistics.
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Untargeted GC-MS Metabolomics
Volatile and derivatized metabolite profiling by GC-MS.
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Targeted Metabolomics
Absolute or relative quantification of a defined metabolite panel.
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Lipidomics
Lipid species identification, quantification and pathway analysis.
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Plant Metabolomics
Plant-focused extraction, annotation and differential metabolite analysis.
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Volatile Metabolomics
Headspace volatile compound profiling and comparison.
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Natural-product & TCM Metabolomics
Compound profiling and group comparison for natural-product research.
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Spatial Metabolomics
Tissue-coordinate metabolite imaging and region comparison.
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Broad-spectrum Metabolomics
Large-panel metabolite detection with standardized annotation.
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Transcriptome + Proteome
Integrate RNA expression and protein abundance across matched samples.
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Transcriptome + Metabolome
Link gene-expression changes with metabolites and pathways.
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Proteome + Metabolome
Connect protein modules with differential metabolites.
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Microbiome + Metabolome
Associate microbial taxa and functions with metabolite profiles.
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Microbiome + Host Transcriptome
Study microbial features together with host gene expression.
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Transcriptome + Proteome + Metabolome
Three-layer molecular integration for matched research samples.
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Microbiome + Transcriptome + Metabolome
Integrate community, host expression and metabolic phenotype.
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Causal Multi-omics Association
Mediation, Mendelian-randomization-ready and causal-network research.
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