PIPELINE 01
Genomics
Reliable pipelines for every genomic application.
Input
FASTQBAMVCF
Outputs
Germline variants
HaplotypeCaller / DeepVariant
Somatic variants
Mutect2 / DeepSomatic
PGx report
86-gene panel
HLA types
High-resolution typing
ACACTTTCTC
GGGCUGGCAT
TAGGCTTCCC
GUAUCGAACT
UGCUTUUCTA
UGGGACGUCG
UCCUTGTACG
ATTAACCUUG
AAGCGUTUGC
GUTGCCGGUC
GUUTUAGGUU
CGAUGUAUGU
ACATATUGUT
GGTAGUTAUA
TUGCTCTATC
AATGAGCTGA
GCTATUUTUA
TGGGAGTGGT
BetaFrom Raw Data to Real Decisions
NGS analysis made easier, and actionable.
Experience a true point-and-click environment for complex omics. Seq4Life™ removes the technical barriers to discovery with automated pipelines, built-in AI guidance, and clinical-grade reporting — no bioinformatics expertise required.
GenomicsTranscriptomicsEpigenomicsPharmacogenomicsHLA TypingAI Assistant
!
Beta Release: Seq4Life is in active development. If you encounter any issues, please use the contact form so we can investigate and resolve them. We appreciate your patience as we refine the platform.
Analysis Pipelines
Three pipelines. One platform.
Dedicated automated pipelines for every NGS data type — pick what you need, run it in one click.
PIPELINE 02
Transcriptomics
Go beyond the sequence to see how genes are behaving.
Input
FASTQ
Outputs
Bulk RNA expression
Differential analysis
Single-cell (scRNA)
High-resolution maps
PIPELINE 03
Epigenomics
Decode the "switches" that control the genome.
Input
FASTQBAM
Outputs
ATAC-Seq peaks
Chromatin accessibility
ChIP-Seq peaks
Histone modifications
Methylation map
Bisulfite-Seq analysis
Built for Labs
The "No-Code" Lab Experience
Everything you need to go from raw sequencing data to a lab-ready report — without writing a single line of code.
app.seq4life.com/runs/2847
Pipelines
- Genomics
- Transcriptomics
- Epigenomics
- Pharmacogenomics
- HLA Typing
+ New Run
Run #2847
Germline Variant Calling
Pipeline progress100%
sample.maf summary
14,283
Variants
986
Pathogenic
42
Drug-gene
report.pdf
Downloadvariants.vcf
Convert → TXTannotations.maf
Convert → TXTAI Assistant
Found 3 high-impact variants worth review.
Want me to summarize the PGx panel?
Ask anything…
1
2
3
4
5
- 1
Point-and-Click Workflow
A zero-code interface that launches sophisticated pipelines without deep bioinformatics training.
- 2
Secondary Data Insights
View the "inner life" of your data without the friction — instantly see contents of MAF, BAM, CRAM, VCF files on screen.
- 3
Lab-Ready Reporting
Skip manual formatting. Generate comprehensive Clinical PDF Reports designed for lab validation.
- 4
Seamless Data Utility
Built-in intermediate file converters (VCF → TXT) keep your data in the format you need.
- 5
AI-Assistant Guidance
An integrated AI provides real-time summaries and helps you interpret results instantly.
How It Works
From sample to insight in three steps
step-1.run
Drop files or pull from cloud
FASTQBAMVCF
S3·GCS·Azure
Upload your data — or "Pull from cloud"
Drop FASTQ, BAM, or VCF files into the secure platform, or connect S3 / GCS / Azure to pull directly.
step-2.run
Choose pipeline
Genomics✓
Transcriptomics
Epigenomics
Select your pipeline
Choose Genomics, Transcriptomics, or Epigenomics. No bioinformatics expertise needed — hit Run.
step-3.run
Run complete
2h 14mreport.pdf
↓ Downloadvariants.vcf
850 KBsummary.maf
412 KBGet actionable results
Receive automated interpretations, interactive visualizations, and downloadable clinical-grade reports.
Pricing
Flexible pricing for every stage of genomics analysis
From individual analyses to enterprise-scale pipelines.
Choose what works for you.
Pay Per Report
Best for
Individuals, researchers, small labs
$49
per report after first 5 free
- First 5 reports free
- No upfront commitment
- Full platform access
- Pay only to download outputs
- Ideal for occasional or exploratory use
Most Popular
Enterprise Subscription
Best for
Labs, hospitals, large organizations
From $1,999
per month, volume-based
Up to 50 / mo$1,999
51–100 / mo$3,799
100+ / moCustom
- Full platform access
- Dedicated support & onboarding
- Custom workflows & integrations
- Flexible data retention
- White-label options available
Custom Plan
Best for
Growing teams and startups
Talk to us
tailored to your needs
- Mix & match pipelines and reports
- Volume-based pricing
- Flexible usage based on your needs
- Priority support
- Flexible data retention, white-label options
All plans include the full Seq4Life™ platform — pipelines, AI assistance, and clinical-grade reports.
Our partners & collaborators
Start in minutes
Raw data in.
Real decisions out.
First 5 reports are free. No credit card. No bioinformatics expertise. Just upload and analyze.
FASTQ
BAM
VCF
report.pdf
variants.vcf
summary.maf