Send us sequencing data you already have, from any provider or public repository. We agree a written analysis plan with you first, then deliver a report, publication-ready figures, result tables and re-runnable code. For research institutes, hospitals and pharma teams.
Data from your own lab, another provider or a public repository. Send FASTQ, BAM, count matrices, Seurat/h5ad objects or accession numbers and tell us what you want to compare; you receive a written plan and quote within one working day. No minimum order.
Send data, get a planDNA, RNA, single-cell, spatial, protein and metabolite samples. Sequencing is run in our laboratory and partner sequencing facilities; analysis is done by our bioinformatics team. Sample-to-report projects currently accept samples shipped within mainland China.
Sequencing servicesStandard pipelines are the starting point; the customisation is in the plan, the parameters and the interpretation.
We start from what you want to show, how samples are grouped and where you plan to publish. If the design cannot support a conclusion, we say so at the planning stage and propose what can be done instead.
Analyses, thresholds, deliverables, timeline and price go into a written plan before work starts. At delivery each item is checked against that plan.
QC thresholds, clustering resolution, annotation references and statistical models are chosen for your data, and the reasons are written into the report.
A single figure or only the analyses a reviewer asked for is fine; the scope of revisions is agreed in the plan.
Each page lists the analyses, what you provide, what you receive, typical turnaround and FAQs.
All three examples were run on public data. Reports, figures, tables and code can be downloaded and every number can be recomputed. No client data is used.
Public data GEO GSE147507 · human bronchial epithelial cells, SARS-CoV-2 vs mock, n = 3 each
QC, PCA, sample correlation, DESeq2 differential expression, volcano and heatmap, Hallmark enrichment, plus a methods paragraph.
Public data 10x Genomics PBMC 10k v3 · human peripheral blood mononuclear cells
QC thresholds with reasons, clustering, marker genes, cell-type annotation and proportions, with annotated result tables.
Public data SRA SRR2584866 · E. coli REL606 long-term evolution experiment clone
Read QC, alignment, coverage, SNP/InDel calling and filtering, functional annotation, with the full re-runnable pipeline.
Tell us the data type, sample groups and the question.
Same dayScope, deliverables, timeline and price in writing.
Within 1 working dayRun to plan; parameters and intermediate results are kept.
Typically 5–15 working daysMethods, results and figures checked item by item.
Report, figures, tables, code and methods text; questions answered.
Turnaround depends on the project and is fixed in the written plan; population studies and multi-omics integration typically take 15–25 working days.
All items are part of our company history; see the full timeline.
Sequencing is run in our laboratory and partner sequencing facilities, with analysis by our bioinformatics team. Sample-to-report projects currently accept samples shipped within mainland China.
Biomarker discovery and data analysis support for clinical research samples.
Learn moreTell us the data type and the comparison you need. You will receive a written plan and quote within one working day. Or email contact@healthswiftech.com.
