Your Trusted Partner
Welcome to HaystackLabs, your go-to partner in genome sequencing. As an NABL-accredited laboratory under ISO 15189:2022, we deliver accurate, reliable, and secure sequencing data. Using advanced technologies and streamlined workflows, we provide comprehensive genomic and transcriptomic sequencing services through a seamless, transparent process, ensuring data integrity, compliance, and timely delivery. Our solutions offer global accessibility and consistent quality for laboratories and institutions seeking dependable sequencing services.
Why choose HaystackLabs?
Achieve unparalleled precision and efficiency in genomic solutions with HaystackLabs, your trusted sequencing partner.
Streamlined registration and logistics
Library preparation expertise
Real-time status updates
Timely progress notifications
Secure data access
Streamlined registration and logistics
Library preparation expertise
Real-time status updates
Timely progress notifications
Secure data access
Streamlined registration and logistics
Library preparation expertise
Real-time status updates
Timely progress notifications
Secure data access
SEQUENCING SERVICES
Explore the diverse range of services we offer to help navigate the health journey.
Whole Exome Sequencing (WES)
We analyse crucial genetic information from the protein coding region of the genome to identify health conditions with precision.
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Whole Genome Sequencing (WGS)
We decode the entire genomic blueprint to identify disease causing mutations and deliver comprehensive solutions.
Learn More
Meta Genomics
We analyse microbial communities to identify species and their antibiotic resistant genes and extend personalised intervention strategies.
Learn More
Targeted Sequencing
We utilise the targeted sequencing approach to enrich specific DNA/RNA molecules to enhance diagnostic accuracy while simplifying the analysis.
Learn More
Metatranscriptome Sequencing
Capture active RNA signals from entire microbial communities to understand functional activity. Reveal metabolic pathways, gene expression patterns, and host–microbe interactions with depth and clarity.
Learn More
Genotyping-by-Sequencing (GBS)
A cost-efficient approach for genome-wide SNP discovery across large populations. Ideal for agricultural genomics, and genetic diversity studies through rapid, reduced-complexity sequencing.
Learn More
Long-Read Sequencing
Sequence continuous DNA fragments to resolve structural variants, repeats, and full-length transcripts. Perfect for de novo assemblies and comprehensive genome analysis, complementing short-read workflows.
Learn More
Transcriptome Sequencing
Decode the dynamic gene expression landscape with high-quality RNA-seq workflows. From differential expression to novel transcript discovery, generate publication-ready insights with speed, precision, and expert analytical support.
Learn More
Customised Bioinformatics
Tailored, modular pipelines aligned to your project goals across genomics and multi-omics. We deliver fast, publication-ready insights from complex datasets.
Learn More
Non-Invasive Prenatal Testing (NIPT)
A highly sensitive blood-based test analysing cell-free fetal DNA to screen for trisomies, sex-chromosome aneuploidies, and microdeletions. Enables early, safe, and informed prenatal risk assessment.
Learn More
Whole Exome Sequencing (WES)
We analyse crucial genetic information from the protein coding region of the genome to identify health conditions with precision.
Learn More
Whole Genome Sequencing (WGS)
We decode the entire genomic blueprint to identify disease causing mutations and deliver comprehensive solutions.
Learn More
Meta Genomics
We analyse microbial communities to identify species and their antibiotic resistant genes and extend personalised intervention strategies.
Learn More
Targeted Sequencing
We utilise the targeted sequencing approach to enrich specific DNA/RNA molecules to enhance diagnostic accuracy while simplifying the analysis.
Learn More
Metatranscriptome Sequencing
Capture active RNA signals from entire microbial communities to understand functional activity. Reveal metabolic pathways, gene expression patterns, and host–microbe interactions with depth and clarity.
Learn More
Genotyping-by-Sequencing (GBS)
A cost-efficient approach for genome-wide SNP discovery across large populations. Ideal for agricultural genomics, and genetic diversity studies through rapid, reduced-complexity sequencing.
Learn More
Long-Read Sequencing
Sequence continuous DNA fragments to resolve structural variants, repeats, and full-length transcripts. Perfect for de novo assemblies and comprehensive genome analysis, complementing short-read workflows.
Learn More
Transcriptome Sequencing
Decode the dynamic gene expression landscape with high-quality RNA-seq workflows. From differential expression to novel transcript discovery, generate publication-ready insights with speed, precision, and expert analytical support.
Learn More
Customised Bioinformatics
Tailored, modular pipelines aligned to your project goals across genomics and multi-omics. We deliver fast, publication-ready insights from complex datasets.
Learn More
Non-Invasive Prenatal Testing (NIPT)
A highly sensitive blood-based test analysing cell-free fetal DNA to screen for trisomies, sex-chromosome aneuploidies, and microdeletions. Enables early, safe, and informed prenatal risk assessment.
Learn More
Whole Exome Sequencing (WES)
We analyse crucial genetic information from the protein coding region of the genome to identify health conditions with precision.
Learn More
Whole Genome Sequencing (WGS)
We decode the entire genomic blueprint to identify disease causing mutations and deliver comprehensive solutions.
Learn More
Meta Genomics
We analyse microbial communities to identify species and their antibiotic resistant genes and extend personalised intervention strategies.
Learn More
Targeted Sequencing
We utilise the targeted sequencing approach to enrich specific DNA/RNA molecules to enhance diagnostic accuracy while simplifying the analysis.
Learn More
Metatranscriptome Sequencing
Capture active RNA signals from entire microbial communities to understand functional activity. Reveal metabolic pathways, gene expression patterns, and host–microbe interactions with depth and clarity.
Learn More
Genotyping-by-Sequencing (GBS)
A cost-efficient approach for genome-wide SNP discovery across large populations. Ideal for agricultural genomics, and genetic diversity studies through rapid, reduced-complexity sequencing.
Learn More
Long-Read Sequencing
Sequence continuous DNA fragments to resolve structural variants, repeats, and full-length transcripts. Perfect for de novo assemblies and comprehensive genome analysis, complementing short-read workflows.
Learn More
Transcriptome Sequencing
Decode the dynamic gene expression landscape with high-quality RNA-seq workflows. From differential expression to novel transcript discovery, generate publication-ready insights with speed, precision, and expert analytical support.
Learn More
Customised Bioinformatics
Tailored, modular pipelines aligned to your project goals across genomics and multi-omics. We deliver fast, publication-ready insights from complex datasets.
Learn More
Non-Invasive Prenatal Testing (NIPT)
A highly sensitive blood-based test analysing cell-free fetal DNA to screen for trisomies, sex-chromosome aneuploidies, and microdeletions. Enables early, safe, and informed prenatal risk assessment.
Learn More
Testimonials
Feedbacks about our service from the bottom of heart
![[object Object]](/assets/testimonials/ashit.png)
Dr. Ashit Naik
MBBS, MD, Pain Physician and Intensivist, Shri Medishine Hospital, Raipur
infexn®-NGS has improved how I diagnose infections in patients. It has helped identify pathogens which were previously undiagnosed by conventional methods and has helped create personalized treatments and also in saving lives. infexn®-NGS is reliable and has an effective impact for patient care.
![[object Object]](/assets/testimonials/alfia.jpg)
Dr. Alfia Alim
Consultant Microbiologist & Head of Infection Control, Mediversal Multi-Super Specialty Hospital
Reliable and timely diagnosis of pathogens in critically ill patients still poses major problems for intensive care medicine. Using Next Generation Sequencing (NGS) in combination with bioinformatic algorithms, this process is able to detect DNA fragments of pathogens in the patient's blood to identify the cause of the sepsis with highest specificity and sensitivity, NGS offered by HaystackAnalytics (infexn®-NGS) has a detection rate five to six times better than that of culture-based procedure with far less turn around time.
![[object Object]](/assets/testimonials/verma.png)
Dr. Nikhileshwar Prasad Verma
MBBS, MD, FICP
infexn®-NGS is a time-saving procedure to identify and choose antibiotics properly.
Dr. Ashit Naik
MBBS, MD, Pain Physician and Intensivist, Shri Medishine Hospital, Raipur
infexn®-NGS has improved how I diagnose infections in patients. It has helped identify pathogens which were previously undiagnosed by conventional methods and has helped create personalized treatments and also in saving lives. infexn®-NGS is reliable and has an effective impact for patient care.
Dr. Alfia Alim
Consultant Microbiologist & Head of Infection Control, Mediversal Multi-Super Specialty Hospital
Reliable and timely diagnosis of pathogens in critically ill patients still poses major problems for intensive care medicine. Using Next Generation Sequencing (NGS) in combination with bioinformatic algorithms, this process is able to detect DNA fragments of pathogens in the patient's blood to identify the cause of the sepsis with highest specificity and sensitivity, NGS offered by HaystackAnalytics (infexn®-NGS) has a detection rate five to six times better than that of culture-based procedure with far less turn around time.
Dr. Nikhileshwar Prasad Verma
MBBS, MD, FICP
infexn®-NGS is a time-saving procedure to identify and choose antibiotics properly.
Dr. Ashit Naik
MBBS, MD, Pain Physician and Intensivist, Shri Medishine Hospital, Raipur
infexn®-NGS has improved how I diagnose infections in patients. It has helped identify pathogens which were previously undiagnosed by conventional methods and has helped create personalized treatments and also in saving lives. infexn®-NGS is reliable and has an effective impact for patient care.
Dr. Alfia Alim
Consultant Microbiologist & Head of Infection Control, Mediversal Multi-Super Specialty Hospital
Reliable and timely diagnosis of pathogens in critically ill patients still poses major problems for intensive care medicine. Using Next Generation Sequencing (NGS) in combination with bioinformatic algorithms, this process is able to detect DNA fragments of pathogens in the patient's blood to identify the cause of the sepsis with highest specificity and sensitivity, NGS offered by HaystackAnalytics (infexn®-NGS) has a detection rate five to six times better than that of culture-based procedure with far less turn around time.
Dr. Nikhileshwar Prasad Verma
MBBS, MD, FICP
infexn®-NGS is a time-saving procedure to identify and choose antibiotics properly.
Partnership
Working with the best
Webinars
Sequencing Landscape: Full Spectrum of Sequencing Technologies from Short-read to Long-read Sequencing
Harold
Field Application Scientist, MGI
Dr. Ravi Kumar Chilukoti
Head - India & South Asia Technical Support & PM, MGI, A member of BGI Group
Dr. Amrutraj Zade
Head - Research & Development, HaystackAnalytics
Connect With Us
We are here to answer your questions. Discover how we can support your needs by reaching out to us today!