Lung Cancer Panel 1 EGFR ALK1
- Sample type
- Formalin-fixed, paraffin-embedded (FFPE) tumor tissue block or unstained slides. Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 36,000
Compare available tests
Genomic Sequencing & Technology Services
Exome/Genome/Epigenome Sequencing Services
Catalog role labels reflect current assignments. Test choice, timing and prices require clinician or laboratory confirmation.
- KMLTTB Regulated Laboratory
- ISO 9001:2015 Quality System
- Free Pre-Test Counselor Guidance
- Nationwide & Home Sample Collection
Test comparison
227 tests
Lung Cancer Panel 6 EGFR by Sequencing, ALK by IHC, ROS1 by FISH
- Sample type
- Formalin-fixed, paraffin-embedded (FFPE) tumor tissue block or unstained slides. Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 60,000
MLC1 Gene Mutation Analysis Agrawal Mutation
- Sample type
- Peripheral blood (EDTA tube), Amniotic Fluid, Chorionic villi, or Cord blood.
- Turnaround
- 7–8 Days Typical turnaround time is 7-8 days.
- Price
- KSh 18,000
NGS Homologous Recombinant Deficiency HRR Panel
- Sample type
- Blood sample (typically 5-10ml in an EDTA tube). Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 84,000
NGS TP53 Mutation Analysis
- Sample type
- Bone marrow or peripheral blood sample.
- Turnaround
- 18 Days Results typically take between 15 to 18 days.
- Price
- KSh 80,000
NPM1 Gene Fragment Analysis
- Sample type
- Blood sample (usually EDTA tube). Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 18,000
NRAS Mutation Analysis Codons 12 & 13
- Sample type
- Paraffin-embedded tumor tissue block.
- Turnaround
- 7–8 Days Approximately 7-8 days.
- Price
- KSh 21,000
PDGFR cKIT Gastrointestinal Stromal Tumors
- Sample type
- Paraffin-embedded tumor tissue block.
- Turnaround
- 7–8 Days Approximately 7-8 days.
- Price
- KSh 30,000
Pik3ca Mutation Analysis Exon 7, 9 & 20
- Sample type
- Tumor tissue sample (e.g., paraffin-embedded tissue block or unstained slides). Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 18,000
Preimplantation Genetic Disorder PGD HLA Typing Single Embryo
- Sample type
- Trophectoderm cells from a single embryo obtained during IVF.
- Turnaround
- See timing details Approximately three weeks.
- Price
- KSh 60,000
Targeted Mutation Analysis More Than 2 Mutations
- Sample type
- Peripheral blood, Plasma, Serum, Amniotic fluid, Cord blood, Chorionic villi.
- Turnaround
- 10–15 Days
- Price
- KSh 39,000
Clinical Exome Next Generation Sequencing Test
- Sample type
- Blood sample (typically 5-10ml in an EDTA tube). Confirm specific requirements with the laboratory before booking.
- Turnaround
- 30 Days Results are typically available within 30 days. Confirm exact turnaround time with the laboratory before booking.
- Price
- KSh 90,000
Whole Exome Sequencing WES Test
- Sample type
- Blood sample.
- Turnaround
- 4 Weeks Approximately 4 weeks.
- Price
- KSh 48,000
Carrier Screening
- Sample type
- Blood sample.
- Turnaround
- 4 Weeks Approximately 4 weeks.
- Price
- KSh 120,000
Clinical Exome Sequencing for Couple
- Sample type
- Blood samples from both partners.
- Turnaround
- Timing on request
- Price
- KSh 80,000
Clinical Exome Trio Sequencing
- Sample type
- Blood samples from three individuals (e.g., child and both parents). Confirm specific sample type and volume requirements with the laboratory before collection.
- Turnaround
- Timing on request
- Price
- KSh 120,000
NGS Whole Exome for Couple
- Sample type
- Blood samples from both partners.
- Turnaround
- Timing on request
- Price
- KSh 96,000
LGMD NGS Panel
- Sample type
- Blood sample (usually collected in an EDTA tube). Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 40,000
Whole Exome Sequencing Chromosomal Microarray
- Sample type
- Blood sample (usually collected in an EDTA tube). Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 84,000
Thyroid Prognostication NGS Panel
- Sample type
- Confirm with the laboratory before booking. Typically requires a blood sample or thyroid tissue sample.
- Turnaround
- Timing on request
- Price
- KSh 68,000
Genetic Test Counselling
- Sample type
- No specimen required. This is a consultation service.
- Turnaround
- See timing details Consultation scheduling and duration will be confirmed upon booking.
- Price
- KSh 800
Whole Exome Mitochondrial Genome Sequencing
- Sample type
- Blood sample.
- Turnaround
- 4 Weeks 3 to 4 weeks.
- Price
- KSh 88,000
Human Genome Sequencing and Variant Calling 30X
- Sample type
- Blood sample (typically 5-10ml in an EDTA tube). Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 450,000
Human Exome Sequencing and Analysis SureSelect V6
- Sample type
- Extracted DNA. Confirm with the laboratory before booking.
- Turnaround
- 8 Weeks Approximately 8 weeks.
- Price
- KSh 80,000
Human Exome Sequencing and Analysis Twist Human Core Exome
- Sample type
- Blood sample (typically 5-10ml). Confirm specific requirements with the laboratory before booking.
- Turnaround
- 8 Weeks Approximately 8 weeks. Confirm exact turnaround time with the laboratory before booking.
- Price
- KSh 78,000
Human Exome Sequencing SureSelect V6
- Sample type
- Blood sample (typically 5-10ml). Confirm specific requirements with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 60,000
Human Exome Sequencing Twist Human Core Exome
- Sample type
- Blood sample (typically 5-10ml in an EDTA tube). Confirm specific requirements with the laboratory before booking.
- Turnaround
- See timing details Confirm turnaround time with the laboratory before booking.
- Price
- KSh 56,000
Mitochondrial Genome Sequencing
- Sample type
- Blood sample (EDTA tube). Confirm with the laboratory before booking.
- Turnaround
- Timing on request
- Price
- KSh 40,000
Bacterial Genome De Novo Assembly and Annotation Illumina
- Sample type
- Confirm with the laboratory before booking. Typically requires a sample containing the bacteria, such as blood, tissue, or other relevant bodily fluid.
- Turnaround
- 4 Weeks Results are typically available within 4 weeks.
- Price
- KSh 36,000
Bacterial Genome De Novo Assembly and Annotation Illumina and ONT Hybrid
- Sample type
- Confirm with the laboratory before booking. Typically requires a sample containing the bacteria, such as blood, tissue, or other relevant bodily fluid.
- Turnaround
- Timing on request
- Price
- KSh 90,000
Clinical context
Clinical testing guide & how to choose
Tests in Genomic Sequencing & Technology Services answer different clinical questions. This catalogue supports a conversation with your clinician or counselor; it does not establish a diagnosis or replace an individual assessment.
Choosing a test
A comprehensive panel measures several related markers, while a single-marker test addresses a more focused question. A larger panel is not automatically the right choice. Discuss your symptoms, previous results and referral with a qualified clinician before selecting tests. Results should not be interpreted in isolation.
Before sample collection
Confirm the required tube, sample volume, any fasting instructions and the collection deadline for your chosen test. Tell the collection team about medication and recent treatment. Do not stop prescribed medication unless your clinician advises it. Home collection depends on the sample’s handling and transport requirements.
Common questions
Questions before booking
Should I choose a panel or a single-marker test for Genomic Sequencing & Technology Services?
A comprehensive panel measures several related markers, while a single-marker test addresses a more focused question. A larger panel is not automatically the right choice. Discuss your symptoms, previous results and referral with a qualified clinician before selecting tests. Results should not be interpreted in isolation. Free pre-test counselor guidance is available to help you understand the booking options.
Can I use SHIF/SHA or private insurance for these tests?
Coverage depends on your scheme, the specific test, referral and authorization requirements, and the provider arrangement. Before booking, ask the laboratory and your insurer to verify eligibility, any co-payment, and whether direct billing or reimbursement applies. Listing a test here does not guarantee insurance coverage.
When should I arrange sample collection?
Check the sample and preparation notes for the specific test, then confirm the collection time and reporting deadline with the laboratory. Same-day reporting, where listed, may depend on a collection cutoff and working days. Nationwide and home sample collection are available subject to location, sample suitability and transport arrangements.
Related services
Services in this topic
12 Kb Matepair Library Preparation
Research DNA library preparation for a workflow named 12 Kb mate-pair. The listing does not establish sequencing or data analysis.
Service details →12S rRNA Sequencing
Research sequencing of a 12S mitochondrial rRNA region may support species identification for suitable organisms, depending on the assay and reference data.
Service details →16S rRNA Sequencing
Research-oriented sequencing of the bacterial 16S rRNA gene may support taxonomic characterization of a sample; identification depends on assay coverage and reference data.
Service details →2x150 Hiseq Sequencing 1 Gb
A HiSeq sequencing listing named for 2 × 150 reads and a 1 GB package label. It describes sequence-data generation, not a defined clinical genetic test.
Service details →2x150 Hiseq Sequencing 10 Gb
A HiSeq DNA sequencing listing named for a 2 × 150 configuration and a 10 GB package label. It does not identify a clinical genetic assay or interpretation service.
Service details →2x150 Hiseq Sequencing 20 GB
A HiSeq DNA sequencing listing named for a 2 × 150 configuration and a 20 GB package label. It is not a defined clinical or legal genetic test.
Service details →2x150 Hiseq Sequencing 3 GB
A DNA sequencing listing named for 2 × 150 HiSeq sequencing and a 3 GB package label. It describes a sequencing workflow, not a specified genetic disease test.
Service details →2x150 Hiseq Sequencing 5 Gb
A HiSeq sequencing listing named for 2 × 150 reads and a 5 GB package label. The listing does not establish whole-genome coverage or a clinical genetic test.
Service details →2x150 Hiseq Sequencing One Lane
A listing for 2 × 150 HiSeq DNA sequencing with a one-lane package label. It does not specify a patient genetic assay, analysis service, or clinical report.
Service details →2x150 Miseq Sequencing Flow Cell
A listing for DNA sequencing on an Illumina MiSeq flow cell using a 2 × 150 read configuration. This identifies a sequencing workflow, not a disease-specific genetic test or clinical interpretation.
Service details →2x250 Miseq Sequencing Flow Cell
A listing for MiSeq DNA sequencing with a 2 × 250 paired-end configuration. It does not identify a disease-specific genetic assay, ancestry analysis, or clinical interpretation.
Service details →3 Kb Matepair Library Preparation
Research DNA library preparation for a service named as a 3 Kb mate-pair workflow. It is a preparation step, not sequencing or interpretation.
Service details →7 Kb Matepair Library Preparation
Research DNA library preparation for a workflow named 7 Kb mate-pair. This preparation step does not itself sequence DNA or identify variants.
Service details →Amplicon Library Preparation
Research library preparation for sequencing defined DNA amplicons. The listing does not establish target amplification, sequencing or variant interpretation as included.
Service details →ATAC Sequencing
ATAC-seq for research profiling of chromatin accessibility; the title does not establish clinical analysis or interpretation.
Service details →ATAC Sequencing and Analysis
ATAC-seq for research profiling of chromatin accessibility in an agreed sample; it is not a personal health diagnostic.
Service details →ATAC Sequencing Data Analysis
Research analysis of existing ATAC-seq data to characterize chromatin accessibility. It does not diagnose disease or provide treatment guidance.
Service details →Autosomal STR Fragment Analysis
Autosomal STR fragment analysis examines selected short tandem repeat markers and can support comparison of DNA profiles, including relationship assessment when an appropriate validated method is used.
Service details →Bacterial 16S rRNA V3 V4 Amplicon Sequencing and Analysis
Bacterial 16S rRNA V3-V4 amplicon sequencing and analysis for research microbial-community profiling, not infection diagnosis.
Service details →Bacterial Genome Reference Based Data Analysis Illumina
Research analysis of existing Illumina bacterial genome sequencing data against a reference. It does not test a patient or select antibiotic treatment.
Service details →Bacterial Genome Sequencing and Reference Based Analysis
Research bacterial genome sequencing and reference-based analysis for a defined bacterial-genomics project; it is not an antimicrobial-susceptibility test.
Service details →Bacterial Genome Sequencing De Novo Assembly and Annotation Illumina
Bacterial genome sequencing, de novo assembly and annotation for research; this listing is not a clinical infection or resistance test.
Service details →Bacterial Genome Sequencing De Novo Assembly and Annotation Illumina and ONT Hybrid
Bacterial de novo genome assembly and annotation for research; the catalog's Illumina/ONT hybrid label and current workflow require confirmation.
Service details →Bacterial Stranded Transcriptome Library Preparation
Bacterial stranded transcriptome library preparation is a preparatory service for later sequencing. Its exact protocol and deliverable require confirmation; it is not an expression result or diagnosis.
Service details →Bacterial Stranded Transcriptome Sequencing
Bacterial stranded transcriptome sequencing is named as a research workflow for strand-aware bacterial RNA profiling. Clinical diagnostic or resistance-testing use is not established.
Service details →Bacterial Stranded Transcriptome Sequencing and Analysis
Bacterial stranded transcriptome sequencing is intended to generate strand-aware RNA-sequencing data for bacterial gene-expression research. Confirm the exact workflow and intended use.
Service details →Bacterial Transcriptome De Novo Data Analysis
Bacterial transcriptome de novo data analysis is a bioinformatics service for existing bacterial RNA-sequencing data, not sample testing or sequencing.
Service details →Bacterial Transcriptome Library Preparation
Bacterial transcriptome library preparation is a preparatory service for later RNA sequencing, not sequencing, gene-expression reporting, or a clinical diagnostic by itself.
Service details →Bacterial Transcriptome Reference Based Data Analysis
Bacterial transcriptome reference-based data analysis is a bioinformatics service for suitable existing RNA-sequencing data, not physical sample testing or sequencing.
Service details →Bacterial Transcriptome Sequencing
Bacterial transcriptome sequencing is intended to profile RNA expression in bacterial material for research. It is not established here as a clinical infection or resistance test.
Service details →Bacterial Transcriptome Sequencing and De Novo Analysis
Bacterial transcriptome sequencing and de novo analysis is named as an RNA-sequencing research workflow. The method and scope require confirmation; it is not established as a diagnostic.
Service details →Bacterial Transcriptome Sequencing and Reference Based Analysis
Bacterial transcriptome sequencing with reference-based analysis is intended to examine bacterial RNA expression against a selected reference. Its scope and research use must be confirmed before submission.
Service details →Bacterial V3V4 16S rRNA Amplicon Sequencing
Bacterial 16S V3-V4 amplicon sequencing for research profiling of marker-gene reads; it is not a gut-health or infection diagnosis.
Service details →Bacterial V3V4 16S rRNA Amplicon Sequencing Data Analysis
Research analysis of existing bacterial 16S rRNA V3/V4 amplicon data to characterize bacterial sequence composition. It is not an infection or dysbiosis test.
Service details →Bisulfite Sequencing Data Analysis
Research analysis of bisulfite sequencing data to characterize DNA methylation at covered sites. It does not assess personal disease risk or diagnose conditions.
Service details →Bisulfite Sequencing Library Preparation
Research library preparation for bisulfite sequencing of DNA methylation. Preparation alone does not measure methylation or diagnose a condition.
Service details →Cattle Genome Sequencing 10X
Cattle genome sequencing for a defined genomics project; the 10X title label does not establish disease prediction or livestock performance.
Service details →Cattle Genome Sequencing 30X
Cattle genome sequencing for a defined genomics project; the title's 30X label is not a health, accuracy or productivity guarantee.
Service details →Cattle Genome Sequencing and Variant Calling 10X
Cattle genome sequencing and variant calling for a defined research project; the 10X catalog label does not assure accuracy, disease prediction or livestock outcomes.
Service details →Cattle Genome Sequencing and Variant Calling 30X
Cattle genome sequencing and variant calling for a defined research or breeding-genomics project; the catalog's 30X label is not an accuracy or trait-outcome guarantee.
Service details →ChIP Sequencing
ChIP-seq for research of protein-DNA binding; the title does not establish upstream ChIP preparation, analysis or a clinical test.
Service details →ChIP Sequencing and Analysis
ChIP-seq sequencing and analysis to study protein-DNA binding in a defined research sample; it is not a personal health or disease test.
Service details →ChIP Sequencing Data Analysis
Research analysis of existing ChIP-seq data to identify protein-associated DNA signal under a defined experimental design. It does not measure binding affinity or diagnose disease.
Service details →ChIPSeq Library Preparation
Research library preparation for a ChIP-seq workflow. The listing does not establish chromatin immunoprecipitation, sequencing or binding-site analysis as included.
Service details →Chloroplast Genome Sequencing
Chloroplast genome sequencing for a defined plant-genomics research project; analytical scope beyond sequencing requires confirmation.
Service details →Chloroplast Genome Sequencing and Analysis
Chloroplast genome sequencing and analysis for plant-genomics research; results are sequence data, not a guaranteed species or trait conclusion.
Service details →Chloroplast Genome Sequencing Data Analysis
Research analysis of existing chloroplast genome sequencing data for plant-genomics projects. This is not a specimen sequencing service or a crop-performance test.
Service details →DdRAD Library Preparation
Research library preparation for a double-digest RAD sequencing (ddRAD) workflow. This step does not itself generate sequence or genotype results.
Service details →DdRAD Sequencing 96 Samples
ddRAD sequencing for a defined population-genomics research project; the target organism, project size and analysis are not verified.
Service details →DdRAD Sequencing and Primary Analysis 96 Samples
Research ddRAD sequencing and primary analysis for a defined population-genomics project; it is not a clinical diagnostic.
Service details →ddRAD Sequencing Primary Data Analysis 96 Samples
Research primary analysis of ddRAD sequencing data for a project named for 96 samples. The listing does not establish library preparation or sequencing.
Service details →Diploid Plant Genome De Novo Assembly and Annotation Illumina
Research de novo assembly and annotation of diploid plant genome sequencing data. This listing describes computational analysis, not sample sequencing or guaranteed agricultural outcomes.
Service details →Diploid Plant Genome Reference Based Data Analysis Illumina
Research reference-based analysis of supplied diploid plant genome sequencing data. It does not itself collect tissue or sequence DNA.
Service details →DNA Short Insert Library Preparation
Research library preparation for a short-insert DNA sequencing workflow. Preparation is distinct from sequencing and downstream analysis.
Service details →DNA Viral Genome Sequencing
DNA viral genome sequencing for a defined research project; no clinical diagnostic or outbreak-tracking service is established by this listing.
Service details →DNA Viral Genome Sequencing and Analysis
DNA viral genome sequencing and analysis for a defined research project; this listing is not a patient diagnostic or treatment test.
Service details →DNA Viral Genome Sequencing Data Analysis
Research analysis of supplied DNA-virus sequencing data. It is not a viral infection test and does not provide diagnosis or treatment guidance.
Service details →DNA Viral Metagenome Sequencing and Analysis
Research sequencing and analysis of viral DNA from an agreed input; the listing does not establish a clinical viral diagnostic.
Service details →DNA Viral Metagenome Sequencing Data Analysis
Research analysis of supplied viral metagenomic sequencing data. It does not test for infection or promise detection of viruses missed by other methods.
Service details →Eukaryotic mRNA Sequencing De Novo Data Analysis
Eukaryotic mRNA sequencing de novo data analysis is bioinformatics analysis of existing sequence data, not physical sample testing or sequencing.
Service details →Eukaryotic mRNA Sequencing Library Preparation
Eukaryotic mRNA sequencing library preparation is a preparatory service for later sequencing, not sequencing or a gene-expression result by itself.
Service details →Eukaryotic mRNA Sequencing Library Preparation Ultra Low Input
Ultra-low-input eukaryotic mRNA library preparation is named for preparing libraries from limited input material. No input threshold or sensitivity is independently established; sequencing is a separate step.
Service details →Eukaryotic mRNA Sequencing Reference Based Data Analysis
Eukaryotic mRNA sequencing reference-based data analysis is analysis of existing sequencing data, not physical sample testing or sequencing.
Service details →Eukaryotic SmallRNA Library Preparation
Eukaryotic small-RNA library preparation is a preparatory service for later sequencing; it does not itself analyze expression or provide a clinical result.
Service details →Eukaryotic SmallRNA Sequencing Data Analysis
Eukaryotic small-RNA sequencing data analysis is a bioinformatics service for suitable existing small-RNA sequence data, not DNA sample testing or sequencing.
Service details →Eukaryotic Stranded mRNA Library Preparation
Eukaryotic stranded mRNA library preparation is a preparatory laboratory service intended to make an RNA library for later sequencing. It is not sequencing or a gene-expression result by itself.
Service details →Eukaryotic Stranded Transcriptome Library Preparation Including LncRNA
Eukaryotic stranded transcriptome library preparation including stated lncRNA scope is a preparatory step for later sequencing, not a diagnostic result.
Service details →Eukaryotic Stranded Transcriptome Sequencing and Reference Based Analysis Including lncRNA
This service is named for stranded eukaryotic transcriptome sequencing and reference-based analysis including lncRNA. Its stated scope is research gene-expression profiling, not diagnosis.
Service details →Eukaryotic Stranded Transcriptome Sequencing Including lncRNA
Eukaryotic stranded transcriptome sequencing including lncRNA is named for RNA-expression research. The workflow and transcript coverage require confirmation; diagnostic use is not established.
Service details →Eukaryotic Transcriptome Library Preparation Including LncRNA
Eukaryotic transcriptome library preparation including stated lncRNA scope is a preparatory step for later sequencing, not transcriptome analysis or a diagnostic result.
Service details →Eukaryotic Transcriptome Sequencing and Reference Based Analysis Including LncRNA
Eukaryotic transcriptome sequencing with reference-based analysis, including lncRNA in the stated scope, is intended to profile RNA expression for research. It is not established as a patient diagnostic.
Service details →Eukaryotic Transcriptome Sequencing Including LncRNA
Eukaryotic transcriptome sequencing including lncRNA is intended to profile RNA expression for research. The exact RNA coverage and workflow require confirmation; it is not an established diagnostic.
Service details →Eukaryotic Transcriptome Sequencing Reference Based Data Analysis Including LncRNA
Eukaryotic transcriptome reference-based data analysis including stated lncRNA scope is bioinformatics analysis of existing sequencing data, not sample testing or sequencing.
Service details →Fungal Genome Reference Based Data Analysis Illumina
Research reference-based analysis of supplied fungal genome sequencing data. It does not test for or diagnose a fungal infection.
Service details →Fungal Genome Sequencing and Reference Based Analysis
Fungal genome sequencing and reference-based analysis for a defined research project; it is not an infection or antifungal-susceptibility test.
Service details →Fungal Genome Sequencing De Novo Assembly and Annotation Illumina
Fungal genome de novo assembly and annotation for research; the catalog title does not establish clinical diagnosis or antifungal susceptibility.
Service details →Fungal ITS2 Amplicon Sequencing and Analysis
Research-oriented fungal ITS2 amplicon sequencing and analysis to characterize fungal DNA in an agreed sample; it is not a fungal-infection diagnostic.
Service details →Fungal ITS2 Amplicon Sequencing Data Analysis
Research analysis of existing fungal ITS2 amplicon sequencing data to characterize fungal sequence diversity. It is not a fungal infection test.
Service details →GBS Library Preparation
Research library preparation for a genotyping-by-sequencing (GBS) workflow. It prepares material for later sequencing and does not produce genotypes by itself.
Service details →Genotyping By Sequencing 96 Samples
Genotyping-by-sequencing for a defined genomics research project; the target organism, sample capacity and analysis scope require confirmation.
Service details →Genotyping By Sequencing And Primary Analysis 96 Samples
Genotyping-by-sequencing with primary analysis for a defined research project; the target organism and exact sample capacity require confirmation.
Service details →Genotyping By Sequencing Primary Data Analysis 96 Samples
Research primary analysis of genotyping-by-sequencing data for a project named for 96 samples. This is not individual health testing.
Service details →HiC Sequencing
Hi-C sequencing for research on three-dimensional genome contacts; this listing is not a clinical genetic test.
Service details →HiC Sequencing And Analysis
Hi-C sequencing and analysis for research on three-dimensional chromatin contacts; it is not a genetic-disease diagnostic.
Service details →HiC Sequencing Data Analysis
Research analysis of existing Hi-C sequencing data to characterize genome-wide chromatin contacts. This is not a clinical genetic test.
Service details →Human Bisulfite Sequencing
Human bisulfite sequencing for a defined DNA-methylation research project; the title does not establish analysis or clinical interpretation.
Service details →Human Bisulfite Sequencing and Analysis
Human DNA bisulfite sequencing and analysis for an agreed epigenomics research project, not an individual disease-risk test.
Service details →Human Genome Reference Based Data Analysis Illumina
Research reference-based analysis of supplied human genome sequencing data. It does not assess an individual's health risk or provide clinical interpretation.
Service details →MeDIP Sequencing
MeDIP sequencing for research profiling of methylated-DNA enrichment; it is not an individual cancer-risk or treatment test.
Service details →MeDIP Sequencing and Analysis
MeDIP-seq for research profiling of methylated DNA enrichment; it is not a cancer screen, absolute methylation measurement or treatment test.
Service details →MeDIP Sequencing Data Analysis
Research analysis of existing MeDIP-seq data to identify regions enriched for methylated DNA. It does not make base-resolution calls or diagnose disease.
Service details →MeDIPSeq Library Preparation
Research library preparation for a MeDIP-seq workflow. MeDIP enriches methylated DNA fragments; preparation alone does not measure methylation or diagnose disease.
Service details →Metatranscriptome Sequencing
Metatranscriptome sequencing is intended to profile RNA expressed in a community or mixed sample for research. The organisms, material, and workflow require confirmation.
Service details →Metatranscriptome Sequencing and Analysis
Metatranscriptome sequencing and analysis is named as a research workflow for profiling RNA in a defined sample or community. The exact sample scope is unclear and requires confirmation.
Service details →Metatranscriptome Sequencing Data Analysis
Metatranscriptome sequencing data analysis is a bioinformatics service for existing sequence data from a defined mixed sample, not physical sample testing or sequencing.
Service details →Mitochondrial Genome Sequencing and Analysis
Research sequencing and analysis of mitochondrial DNA for a defined project; this listing does not establish a clinical test for mitochondrial disease.
Service details →Mitochondrial Genome Sequencing Data Analysis
Research analysis of supplied mitochondrial genome sequencing data. It is not a mitochondrial-disease diagnostic test or personal health prediction.
Service details →PacBio Sequel II Library Preparation
Research library preparation named for PacBio Sequel II. Preparation is distinct from sequencing and does not guarantee read length, accuracy or an analytical result.
Service details →Polyploid Plant Genome De Novo Assembly and Annotation Illumina
Polyploid plant genome de novo assembly and annotation is named as an Illumina-related research workflow for complex plant genomes. Species scope and deliverables require confirmation.
Service details →Polyploid Plant Genome Reference Based Data Analysis Illumina
Research reference-based analysis of supplied polyploid plant genome sequencing data. This listing does not establish physical sample testing or sequencing.
Service details →RbcL Sequencing
Research sequencing of the plant rbcL marker may support plant taxonomic identification, subject to assay coverage and reference data.
Service details →Rice Genome Sequencing 10X
Rice genome sequencing for agricultural genomics research; the title's 10X label does not guarantee depth, trait identification or crop performance.
Service details →Rice Genome Sequencing 30X
Rice genome sequencing for a defined crop-genomics research project; 30X does not guarantee coverage, accuracy or crop traits.
Service details →Rice Genome Sequencing and Variant Calling 10X
Rice genome sequencing and variant calling for a defined agricultural research project; the 10X label does not guarantee coverage, accuracy or crop performance.
Service details →Rice Genome Sequencing and Variant Calling 30X
Rice genome sequencing and variant calling for crop-genomics research; the 30X label does not guarantee coverage, accuracy or agricultural outcomes.
Service details →RNA Viral Metagenome Sequencing
RNA viral metagenome sequencing is named as a research workflow for analyzing viral RNA in a sample. Target range and clinical use are not established.
Service details →RNA Viral Metagenome Sequencing and Analysis
RNA viral metagenome sequencing and analysis is named as a broad RNA-virus sequencing service. The sample workflow, detectable targets, analysis, and intended use require confirmation; no diagnostic claim is established.
Service details →RNA Viral Metagenome Sequencing Data Analysis
RNA viral metagenome sequencing data analysis is a bioinformatics service for appropriate existing sequence data, not physical sample testing or sequencing.
Service details →SELEX Sequencing Data Analysis
Research analysis of sequencing data from a defined SELEX experiment, such as comparing sequence enrichment across selection rounds. It is not genetic testing.
Service details →Shotgun Metagenome Sequencing and Analysis
Research shotgun metagenomic sequencing and analysis of microbial-community DNA from an agreed sample, not a clinical microbiome or infection diagnosis.
Service details →Shotgun Metagenome Sequencing Data Analysis
Research analysis of existing shotgun metagenomic sequencing data to characterize microbial DNA in a sample. It is not a clinical microbiome test.
Service details →Vertebrate Genome Reference Based Data Analysis Illumina
Research reference-based analysis of supplied vertebrate genome sequencing data. Species, reference and project outputs require confirmation.
Service details →