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Services/Tier 01

Tier 01 · 5 services

Sequencing & Genomic Analysis

From raw reads to biological insight — WGS to spatial transcriptomics.

Core2 services
Emerging3 services
01

NGS Data Analysis

Core

Summary

End-to-end analysis of short-read sequencing data: whole-genome (WGS), whole-exome (WES), RNA-seq, amplicon panels, and metagenomics — from raw FASTQ to publication-ready results.

Mature, production-ready service

Tools Used

BWA-MEM2STARHISAT2SalmonfastpFastQCMultiQCTrimmomaticPicard

Ideal Client

Research labs, hospitals, and biotech startups with raw sequencing data needing QC, alignment, and downstream analysis.

02

Variant Calling, Annotation & Pathway Analysis

Core

Summary

Germline and somatic variant detection, functional annotation against curated databases, and pathway enrichment — including disease-mutation interpretation for clinical and research contexts.

Mature, production-ready service

Tools Used

GATK HaplotypeCallerDeepVariantMutect2VEPSnpEffANNOVARClinVargnomADKEGG

Ideal Client

Clinical genomics labs, rare-disease diagnostics centres, and oncology research groups.

03

Long-Read Sequencing Analysis

Emerging

Summary

Oxford Nanopore and PacBio HiFi data processing for structural variant discovery, full-length isoform characterisation, and haplotype phasing — resolving regions inaccessible to short reads.

Active R&D — early-adopter pricing

Tools Used

Minimap2Sniffles2PBSVIsoQuantFlyeMedakaWhatsHapNanoStat

Ideal Client

Researchers studying complex or repeat-rich genomic regions, structural rearrangements, or full-length transcript diversity.

04

Single-Cell Analysis

Emerging

Summary

scRNA-seq, scATAC-seq, and multiome (joint RNA + ATAC) workflows — covering clustering, trajectory inference, cell-type annotation, and regulatory network reconstruction at single-cell resolution.

Active R&D — early-adopter pricing

Tools Used

Cell RangerSeuratScanpyArchRSignacHarmonyscVIMonocle3

Ideal Client

Immunology labs, cancer researchers, and developmental biology groups seeking cellular-resolution transcriptomic or epigenomic maps.

05

Spatial Transcriptomics

Emerging

Summary

Analysis of spatially-resolved gene expression from Visium, Stereo-seq, Xenium, and similar platforms — integrating spatial context with cell-type deconvolution and tissue niche identification.

Active R&D — early-adopter pricing

Tools Used

Space RangerSquidpySeuratGiottoBayesSpaceRCTDcell2location

Ideal Client

Pathology labs, tissue atlas consortia, and neuroscience groups needing gene expression maps in spatial context.

Interested in Sequencing & Genomic Analysis?

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