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Now every lab can get access to high-quality, fast-turnaround targeted next-generation sequencing.
Learn more about: Transcriptome sequencing Exome sequencing Targeted NGS
The Ion Torrent Certified Service Provider program is a global network of validated service providers that enable researchers in small and medium-sized laboratories to get high-quality next-generation sequencing data generated on the Ion Torrent sequencers from small amounts of input material with very fast turnaround. Three types of services are offered by our certified service providers: exome, transcriptome and targeted gene panel sequencing.
The service provider network also offers an ideal, low-risk option for a lab to evaluate the sequencing results from an Ion Torrent sequencer before investing in one of their own.
Application | Ion AmpliSeq exome | Ion AmpliSeq transcriptome | Ion Torrent whole transcriptome |
---|---|---|---|
Boston University | • | ||
The Boston University Microarray and Sequencing Resource specializes in Ion Ampliseq™ Transcriptome sequencing and RNA-Seq, but also provides all next-generation sequencing services supported by Ion Torrent™ platforms. We provide sequencing services for a wide range of species using the Ion Proton™ and Ion PGM™ instruments and all supported Ion Torrent protocols. We offer the same services to researchers outside of Boston University on an available-resource basis. Please contact us at BuMicroarrayCore@gmail.com Boston University Microarray and Sequencing Resource Core Facility | |||
Cedars Sinai | • | • | • |
![]() The Genomics Core offers sequencing for your research applications for microbiome profiling, transcriptome analyses, and targeted resequencing with rapid turnaround times using both an Ion Torrent™ Personal Genome Machine and an Ion Proton™ Sequencer. These sequencers are designed to deliver better, faster, and less expensive data than current next-generation sequencing machines. Our experienced team of wet lab and bioinformatic scientists strive to provide high-quality results as evidenced by our recent publications in Nature Genetics, Science, BMC Genomics, and AJHG. Cedars Sinai | |||
Children's Hospital Los Angeles | • | ||
The Molecular Pathology Genomics (MPG) Core is integrally positioned within Children's Hospital Los Angeles' Department of Pathology and Laboratory Medicine and Center and acts as the molecular research core to the University of Southern California’s Norris Cancer Center. Our highly skilled staff and faculty expertise allow us to provide exceptional service and act as a facilitator and driver of future genomic innovation. Molecular Pathology Genomics Core at CHLA | |||
Claritas Genomics | • | ||
Claritas Genomics is a full-service clinical research laboratory, originally part of Boston Children’s Hospital. We offer clinincal research services to ordering scientists, hospitals, and researchers. Claritas offers a full range of cllinical research services. Claritas Genomics | |||
The Hospital for Sick Kids | • | ||
The Centre for Applied Genomics (TCAG) is dedicated to conducting and promoting groundbreaking research in genomics including service and training support for academic, government, and private sector scientists worldwide. The Centre's services include sequencing, informatics, microarrays, cytogenomics, biobanking, and statistical analysis. A variety of sequencing applications are undertaken, including whole exome and whole genome, metagenomics, amplicon re-sequencing, transcriptome, and the sequencing of immunoprecipitated or methylated DNA. Sick Kids – The Centre for Applied Genomics | |||
Kashi Laboratories | • | ||
Kashi Laboratories is a fully accredited clinical research laboratory specializing in a range of customized genomic and transplant-related research. The laboratory uses and develops molecular markers associated with a variety of acute and chronic disorders. Kashi Laboratories | |||
Memorial Sloan-Kettering Cancer Center | • | ||
The Genomics Core Lab (GCL) at MSKCC is a full-service microarray and sequencing facility. The GCL supports basic and clinical research by providing DNA and RNA analysis services from experimental design and sample preparation to basic data analysis and training. Since its inception in January 2001, the GCL has processed more than 15,000 samples and served over 150 New York state research laboratories and numerous out-of-state research institutions. Memorial Sloan-Kettering Cancer Center | |||
The Molecular Resource Center | • | ||
The Molecular Resource Center (MRC) is one of the University of Tennessee's Centers of Excellence. It was founded in 1985 to promote and develop the use of molecular biology in basic and clinical research programs at The University of Tennessee Health Science Center. Today, the MRC houses a full range of molecular, biochemical and immunological facilities through its core laboratories. Molecular Resource Center - University of Tennessee | |||
Ohio State University | • | • | • |
![]() The OSU Pharmacogenomics Core Laboratory is an integral part of The OSU College of Medicine Center for Pharmacogenomics. The Center for Pharmacogenomics supports molecular genetics and genomics technologies, biomarker development, and clinical research of complex disorders. The Pharmacogenomics Core Laboratory has developed new approaches for the discovery of genetic variants, with a focus on gene regulation, including innovative genome-scale technologies such as massively-parallel sequencing and data integration. Investigators from different scientific disciplines join forces to explore research of applications on cardiovascular, central nervous system (CNS), infectious diseases, and cancer. OSU Pharmacogenomics Core Laboratory | |||
PrimBio Research Institute | • | ||
PrimBio Research Institute is committed to providing innovative technology and platforms for your genetic analysis. PrimBio was founded to advance genomic research by providing high-quality results with fast turnaround time and competitive pricing. PrimBio Research Institute | |||
Roswell Park Cancer Institute | • | ||
Our mission at Roswell Park Cancer Institute is to understand cancer. Our Genomics Shared Resource (GSR) is a broadly functioning facility that provides an integrated set of tools and services for genomic research analysis. Roswell Park Cancer Institute | |||
RUCDR Infinite Biologics | • | ||
RUCDR Infinite Biologics is a full service bio-repository and analytical services program that currently serves federal, foundation and industry clients. RUCDR provides kit manufacturing, study logistics, sample processing, sample storage and analytical services to support any component of the sample life cycle needed for small and large research studies alike. Analytical services include, but are not limited to, PCR/QPCR/Digital PCR, Microarray and Next-Gen sequencing technologies. RUCDR Infinite Biologics | |||
University of British Columbia | • | ||
![]() The Centre for Brain Health within the University of British Columbia integrates clinical research in the areas of neuroscience, neurology, and psychiatry bringing together all the multidisciplinary areas of brain health. We implement cutting edge research to identify the molecular causes of neurological and neurodegenerative diseases. Centre for Brain Health - University of British Columbia | |||
University of New Mexico | • | • | |
The Keck-UNM Genomics Resource (KUGR) is a shared resource that provides access to microarrays, real-time PCR, and next-generation sequencing technologies, coupled with expert bioinformatics analysis. In collaboration with the laboratory of Dr. Jeremy Edwards, KUGR can perform a variety of next-generation sequencing assays using the Ion Torrent™ PGM™ instrument. These include ChIP-seq, RNA-seq and targeted sequencing assays. This platform is also used for Comprehensive Cancer Panel Assays, which perform multiplex targeted sequencing of all exons from over 400 known cancer-relevant genes, starting with very small amounts of material (such as FFPE samples). Keck-UNM Genomics Resource – University of New Mexico | |||
WuXi AppTec | • | ||
WuXi AppTec provides global solutions and a seamless, high-quality, single-source approach for discovery and clinical research. With a 25-year history, WuXi AppTec supports the comprehensive needs of clinical research worldwide. Leveraging Life Technologies Ion PGM™ and Ion Proton™ next-generation sequencing platforms and an expert technical team, WuXi AppTec offers customer-focused programs to meet your exacting clinical research needs, including high-quality exome sequencing. WuXi AppTec |
Application | Ion AmpliSeq gene panels | Ion AmpliSeq exome | Ion AmpliSeq transcriptome | Ion Torrent whole transcriptome |
---|---|---|---|---|
Cellcall Ltd | • | |||
![]() We at Cellcall offer the full range of basic research and clinical research services which can be delivered using Life Technologies' PGM™ and Ion Proton™ platforms. We can handle complex projects, both large and small. Our scientists and IT experts are at your disposal. Cellcall Ltd | ||||
CeMIA | • | |||
![]() CeMIA staff is skilled in the development and implementation of projects in the fields of molecular and cellular biology. We can assist you in projects based on RNA/DNA extraction techniques, PCR/real-time PCR applications, DNA methylation, Sanger sequencing, next generation sequencing and other molecular biology applications in our fully equipped facilities. Address: 31 Str. Markrigianni, Larissa, Greece | ||||
Centogene AG | • | |||
![]() Centogene is a worldwide leader in the field of genetic diagnostics for rare hereditary diseases - with the largest test portfolio worldwide. Testing samples from over 90 different countries worldwide allows Centogene a unique insight into epidemiological genetic differences, which is crucial in the medical result interpretation process. Centogene's in depth medical expertise is supported by the application of cutting-edge technologies including next generation sequencing, whole exome sequencing (CentoXome®), whole genome sequencing and innovative biomarkers for selected diseases. Centogene has developed a comprehensive mutation database (CentoMD®) that is pillar to offering high quality diagnostic reporting and medical interpretation, thoroughly interpret each patient's sequence data. Contact person: Doreen Niemann | ||||
Clinical Research Facility, University of Edinburgh | • | |||
The Clinical Research Facility, University of Edinburgh is staffed and equipped to offer secure receipt, processing, archiving, and analysis of biological samples. With well-defined SOPs and sophisticated automation, the facility offers high quality and high throughput genetic analysis for clinical research projects. This includes sequencing, genotyping, gene expression, and epigenetics research services on a variety of platforms including the Ion PGM™ and Ion Proton™ sequencers. Clinical Research Facility Edinburgh, University of Edinburgh | ||||
FASTERIS SA-DNA Sequencing Services | • | • | • | |
We are a Swiss biotechnology company, providing worldwide Next-Generation and Sanger DNA sequencing services for private and academic laboratories, since 2003. Fasteris has one of the longest experience in Next-Generation Sequencing (NGS). We developed a broad range of NGS applications such as re-sequencing and de novo assembly of whole genomes, transcriptomes, small RNAs, metagenomes, exomes, ChIP-SEQ. Our bioinformatics team helps researchers finding the relevant biological information for their projects. FASTERIS SA – DNA Sequencing Services | ||||
Genetracer Biotech | • | • | ||
Genoinseq | • | |||
Genoinseq, the Next-Gen Sequencing Unit, is Biocant’s unit specialized in the field of omics. The unit grants access to the full potential of state-of-the-art next generation sequencing equipment, high-throughput genotyping and bioinformatics data analysis for your research. We have a multidisciplinary team of experts in sequencing, genotyping, and bioinformatics, delivering personalized solutions, from consultancy in experimental design to large-scale data analysis with user-friendly outputs. Genoinseq provides services to companies and research groups in the field of Life Sciences, collaborates in R&D projects with other companies or institutes and has its own R&D program aimed towards innovation in scientific and technical aspects of sequencing and data analysis. Genoinseq – Next-Generation Sequencing Unit | ||||
GENOMAX | • | |||
GENOMAX - the Strasbourg medical campus Next-Generation Sequencing platform - provides human exome, genome and RNA research sequencing services based on SOLiD®, Ion Torrent™ PGM™ and Ion Proton™ NGS sequencers coupled with a proprietary, highly efficient, bioinformatics pipeline. GENOMAX | ||||
Institut Cochin Dx | • | |||
The genomic core of Institut Cochin (genomIC) provide academic and private research teams with long experience in state-of-the-art genomic capabilities. GenomIC is an ISO 9001 facility that delivers high quality data in the areas of real time PCR and microarray analysis (genotyping and expression analysis using Genechip Affymetrix® GeneChip® technology). GenomIC offers a variety of next generation sequencing research applications including whole exome sequencing, targeted resequencing (using amplified or captured targets), transcriptome sequencing using Ion PGM™ and Ion Proton™ sequencers. Institut Cochin | ||||
InterGenetics | • | |||
InterGenetics is a scientific group directed for the past 40 years by medical geneticist Constantinos Pangalos, offering specialized clinical research and laboratory genetics services in Greece as well as abroad. Address: Vas. Sofias Avenue 120,115 26 Athens | ||||
MAD: Dutch Genomics Service & Support Provider, University of Amsterdam | • | |||
![]() The MAD: Dutch Genomics Service & Support Provider has been the genomics expertise center of the University of Amsterdam since the year 2000. We operate as a non-profit, global service provider offering microarray services, and next-generation sequencing services using the Ion Proton™ system, providing bioinformatics support for academic, and industrial research & development projects. Our multidisciplinary team of experts is specialized in tailor-made services & support in the field of mRNA/small-RNA sequencing and prokaryotic genome sequencing. Contact Person: Dr. Selina van Leeuwen | ||||
The National Genomics Infrastructure, Uppsala Genome Center | • | |||
The Uppsala Genome Center (UGC) is a part of The National Genomics Infrastructure (NGI), a sequencing service facility with the ambition to establish technologies for Massive Parallel Sequencing (MPS) and provide MPS as a service. UGC offers sequencing service with different applications and different technologies. We operate with the Applied BioSystems SOLiD® 5500 system, Ion PGM™ sequencer and Ion Proton™ semiconductor for MPS. As a complement to the short read MPS platforms we can offer service on RSII from Pacific Biosciences. UGC also offers Sanger Sequencing as a service. The National Genomics Infrastructure, Uppsala Genome Center | ||||
NIMGENETICS | • | |||
NIMGenetics is a fully licensed analytical centre with a trusted clinical research genetics unit. Our scientific-medical team, accredited by the Spanish Association of Human Genetics, is specialized in the development and application of high-resolution genomic systems that enable reliable and precise clinical research. Our missions are: (1) To ease clinical researchers´ access to the latest scientific advances in genomic tools, such as Next Generation Sequencing, for the improvement of future health care. (2) To offer researchers, in addition to an extensive range of genomic tools, a customized service that starts with the design and selection of the most appropriate genomic approaches and ends with a complete analysis. NIMGENETICS | ||||
Stellenbosch University | • | |||
The DNA Sequencing Unit forms part of the Stellenbosch University Central Analytical Facilities and offers a range of analytical services on a not-for-profit basis. The DNA sequencing core offers services using the Ion S5™, Ion Proton™, and Applied Biosystems™ 3730xl sequencers. Contact: Carel van Heerden | ||||
University Hospital, Lund, Sweden | • | |||
University Hospital Department of Clinical Genetics, Lund, Sweden Contact: Tord Jonson | ||||
University of Leicester | • | |||
![]() Address: Dr Caroline Cowley, Manager of Leicester Molecular Diagnostics, Leicester Cancer Research Centre, University of Leicester, Room 303A, 3rd Floor Robert Kilpatrick Building, Leicester Royal Infirmary, Leicester, LE1 5WW, UK | ||||
University of Natural Resources and Life Sciences, Vienna, Austria | • | |||
Application | Ion AmpliSeq exome | Ion AmpliSeq transcriptome | Ion Torrent whole transcriptome |
---|---|---|---|
MACROGEN | • | ||
Mission Biotech | • | ||
TheragenEtex Bio Institute | • | ||
TheragenEtex Bio Institute was established on September 2009 aiming for improvement of human health and welfare in the future through research using human genome sequencing and analysis. TheragenEtex is establishing and expanding genome database, providing genome bioinformatics solution and conducting Biomarker detection and to support researcher's genome based product developments. TheragenEtex Bio Institute | |||
Yamagata University | • | • | |
![]() The Genome Informatics Unit and Biochemical Analysis Center within the Yamagata University Faculty of Medicine (YUM) integrates research areas of community-based cohort studies, genetics, and molecular biology. The Unit provides DNA and RNA sequencing services on the Ion PGM™ and Ion Proton™ sequencers from experimental design to data analysis. Phone: +81-23-628-5410 (DNA-seq) / +81-23-628-5474 (RNA-seq) Email: h-satoh@med.id.yamagata-u.ac.jp (DNA-seq) / harukiochi@med.id.yamagata-u.ac.jp (RNA-seq) | |||
Yourgene Bioscience | • | ||
Yourgene Bioscience provides sequencing and bioinformatics solutions for research at major institutions, universities and hospitals in Taiwan and Asia Pacific regions. With an integrated team of experienced molecular biologists and bioinformaticians, Yourgene is highly motivated to provide quality sequencing data and analysis for all our valuable clients. Yourgene Bioscience |
Application | Ion AmpliSeq exome | Ion AmpliSeq transcriptome | Ion Torrent whole transcriptome |
---|---|---|---|
Boston University | • | ||
The Boston University Microarray and Sequencing Resource specializes in Ion Ampliseq™ Transcriptome sequencing and RNA-Seq, but also provides all next-generation sequencing services supported by Ion Torrent™ platforms. We provide sequencing services for a wide range of species using the Ion Proton™ and Ion PGM™ instruments and all supported Ion Torrent protocols. We offer the same services to researchers outside of Boston University on an available-resource basis. Please contact us at BuMicroarrayCore@gmail.com Boston University Microarray and Sequencing Resource Core Facility | |||
Cedars Sinai | • | • | • |
![]() The Genomics Core offers sequencing for your research applications for microbiome profiling, transcriptome analyses, and targeted resequencing with rapid turnaround times using both an Ion Torrent™ Personal Genome Machine and an Ion Proton™ Sequencer. These sequencers are designed to deliver better, faster, and less expensive data than current next-generation sequencing machines. Our experienced team of wet lab and bioinformatic scientists strive to provide high-quality results as evidenced by our recent publications in Nature Genetics, Science, BMC Genomics, and AJHG. Cedars Sinai | |||
Children's Hospital Los Angeles | • | ||
The Molecular Pathology Genomics (MPG) Core is integrally positioned within Children's Hospital Los Angeles' Department of Pathology and Laboratory Medicine and Center and acts as the molecular research core to the University of Southern California’s Norris Cancer Center. Our highly skilled staff and faculty expertise allow us to provide exceptional service and act as a facilitator and driver of future genomic innovation. Molecular Pathology Genomics Core at CHLA | |||
Claritas Genomics | • | ||
Claritas Genomics is a full-service clinical research laboratory, originally part of Boston Children’s Hospital. We offer clinincal research services to ordering scientists, hospitals, and researchers. Claritas offers a full range of cllinical research services. Claritas Genomics | |||
The Hospital for Sick Kids | • | ||
The Centre for Applied Genomics (TCAG) is dedicated to conducting and promoting groundbreaking research in genomics including service and training support for academic, government, and private sector scientists worldwide. The Centre's services include sequencing, informatics, microarrays, cytogenomics, biobanking, and statistical analysis. A variety of sequencing applications are undertaken, including whole exome and whole genome, metagenomics, amplicon re-sequencing, transcriptome, and the sequencing of immunoprecipitated or methylated DNA. Sick Kids – The Centre for Applied Genomics | |||
Kashi Laboratories | • | ||
Kashi Laboratories is a fully accredited clinical research laboratory specializing in a range of customized genomic and transplant-related research. The laboratory uses and develops molecular markers associated with a variety of acute and chronic disorders. Kashi Laboratories | |||
Memorial Sloan-Kettering Cancer Center | • | ||
The Genomics Core Lab (GCL) at MSKCC is a full-service microarray and sequencing facility. The GCL supports basic and clinical research by providing DNA and RNA analysis services from experimental design and sample preparation to basic data analysis and training. Since its inception in January 2001, the GCL has processed more than 15,000 samples and served over 150 New York state research laboratories and numerous out-of-state research institutions. Memorial Sloan-Kettering Cancer Center | |||
The Molecular Resource Center | • | ||
The Molecular Resource Center (MRC) is one of the University of Tennessee's Centers of Excellence. It was founded in 1985 to promote and develop the use of molecular biology in basic and clinical research programs at The University of Tennessee Health Science Center. Today, the MRC houses a full range of molecular, biochemical and immunological facilities through its core laboratories. Molecular Resource Center - University of Tennessee | |||
Ohio State University | • | • | • |
![]() The OSU Pharmacogenomics Core Laboratory is an integral part of The OSU College of Medicine Center for Pharmacogenomics. The Center for Pharmacogenomics supports molecular genetics and genomics technologies, biomarker development, and clinical research of complex disorders. The Pharmacogenomics Core Laboratory has developed new approaches for the discovery of genetic variants, with a focus on gene regulation, including innovative genome-scale technologies such as massively-parallel sequencing and data integration. Investigators from different scientific disciplines join forces to explore research of applications on cardiovascular, central nervous system (CNS), infectious diseases, and cancer. OSU Pharmacogenomics Core Laboratory | |||
PrimBio Research Institute | • | ||
PrimBio Research Institute is committed to providing innovative technology and platforms for your genetic analysis. PrimBio was founded to advance genomic research by providing high-quality results with fast turnaround time and competitive pricing. PrimBio Research Institute | |||
Roswell Park Cancer Institute | • | ||
Our mission at Roswell Park Cancer Institute is to understand cancer. Our Genomics Shared Resource (GSR) is a broadly functioning facility that provides an integrated set of tools and services for genomic research analysis. Roswell Park Cancer Institute | |||
RUCDR Infinite Biologics | • | ||
RUCDR Infinite Biologics is a full service bio-repository and analytical services program that currently serves federal, foundation and industry clients. RUCDR provides kit manufacturing, study logistics, sample processing, sample storage and analytical services to support any component of the sample life cycle needed for small and large research studies alike. Analytical services include, but are not limited to, PCR/QPCR/Digital PCR, Microarray and Next-Gen sequencing technologies. RUCDR Infinite Biologics | |||
University of British Columbia | • | ||
![]() The Centre for Brain Health within the University of British Columbia integrates clinical research in the areas of neuroscience, neurology, and psychiatry bringing together all the multidisciplinary areas of brain health. We implement cutting edge research to identify the molecular causes of neurological and neurodegenerative diseases. Centre for Brain Health - University of British Columbia | |||
University of New Mexico | • | • | |
The Keck-UNM Genomics Resource (KUGR) is a shared resource that provides access to microarrays, real-time PCR, and next-generation sequencing technologies, coupled with expert bioinformatics analysis. In collaboration with the laboratory of Dr. Jeremy Edwards, KUGR can perform a variety of next-generation sequencing assays using the Ion Torrent™ PGM™ instrument. These include ChIP-seq, RNA-seq and targeted sequencing assays. This platform is also used for Comprehensive Cancer Panel Assays, which perform multiplex targeted sequencing of all exons from over 400 known cancer-relevant genes, starting with very small amounts of material (such as FFPE samples). Keck-UNM Genomics Resource – University of New Mexico | |||
WuXi AppTec | • | ||
WuXi AppTec provides global solutions and a seamless, high-quality, single-source approach for discovery and clinical research. With a 25-year history, WuXi AppTec supports the comprehensive needs of clinical research worldwide. Leveraging Life Technologies Ion PGM™ and Ion Proton™ next-generation sequencing platforms and an expert technical team, WuXi AppTec offers customer-focused programs to meet your exacting clinical research needs, including high-quality exome sequencing. WuXi AppTec |
Application | Ion AmpliSeq gene panels | Ion AmpliSeq exome | Ion AmpliSeq transcriptome | Ion Torrent whole transcriptome |
---|---|---|---|---|
Cellcall Ltd | • | |||
![]() We at Cellcall offer the full range of basic research and clinical research services which can be delivered using Life Technologies' PGM™ and Ion Proton™ platforms. We can handle complex projects, both large and small. Our scientists and IT experts are at your disposal. Cellcall Ltd | ||||
CeMIA | • | |||
![]() CeMIA staff is skilled in the development and implementation of projects in the fields of molecular and cellular biology. We can assist you in projects based on RNA/DNA extraction techniques, PCR/real-time PCR applications, DNA methylation, Sanger sequencing, next generation sequencing and other molecular biology applications in our fully equipped facilities. Address: 31 Str. Markrigianni, Larissa, Greece | ||||
Centogene AG | • | |||
![]() Centogene is a worldwide leader in the field of genetic diagnostics for rare hereditary diseases - with the largest test portfolio worldwide. Testing samples from over 90 different countries worldwide allows Centogene a unique insight into epidemiological genetic differences, which is crucial in the medical result interpretation process. Centogene's in depth medical expertise is supported by the application of cutting-edge technologies including next generation sequencing, whole exome sequencing (CentoXome®), whole genome sequencing and innovative biomarkers for selected diseases. Centogene has developed a comprehensive mutation database (CentoMD®) that is pillar to offering high quality diagnostic reporting and medical interpretation, thoroughly interpret each patient's sequence data. Contact person: Doreen Niemann | ||||
Clinical Research Facility, University of Edinburgh | • | |||
The Clinical Research Facility, University of Edinburgh is staffed and equipped to offer secure receipt, processing, archiving, and analysis of biological samples. With well-defined SOPs and sophisticated automation, the facility offers high quality and high throughput genetic analysis for clinical research projects. This includes sequencing, genotyping, gene expression, and epigenetics research services on a variety of platforms including the Ion PGM™ and Ion Proton™ sequencers. Clinical Research Facility Edinburgh, University of Edinburgh | ||||
FASTERIS SA-DNA Sequencing Services | • | • | • | |
We are a Swiss biotechnology company, providing worldwide Next-Generation and Sanger DNA sequencing services for private and academic laboratories, since 2003. Fasteris has one of the longest experience in Next-Generation Sequencing (NGS). We developed a broad range of NGS applications such as re-sequencing and de novo assembly of whole genomes, transcriptomes, small RNAs, metagenomes, exomes, ChIP-SEQ. Our bioinformatics team helps researchers finding the relevant biological information for their projects. FASTERIS SA – DNA Sequencing Services | ||||
Genetracer Biotech | • | • | ||
Genoinseq | • | |||
Genoinseq, the Next-Gen Sequencing Unit, is Biocant’s unit specialized in the field of omics. The unit grants access to the full potential of state-of-the-art next generation sequencing equipment, high-throughput genotyping and bioinformatics data analysis for your research. We have a multidisciplinary team of experts in sequencing, genotyping, and bioinformatics, delivering personalized solutions, from consultancy in experimental design to large-scale data analysis with user-friendly outputs. Genoinseq provides services to companies and research groups in the field of Life Sciences, collaborates in R&D projects with other companies or institutes and has its own R&D program aimed towards innovation in scientific and technical aspects of sequencing and data analysis. Genoinseq – Next-Generation Sequencing Unit | ||||
GENOMAX | • | |||
GENOMAX - the Strasbourg medical campus Next-Generation Sequencing platform - provides human exome, genome and RNA research sequencing services based on SOLiD®, Ion Torrent™ PGM™ and Ion Proton™ NGS sequencers coupled with a proprietary, highly efficient, bioinformatics pipeline. GENOMAX | ||||
Institut Cochin Dx | • | |||
The genomic core of Institut Cochin (genomIC) provide academic and private research teams with long experience in state-of-the-art genomic capabilities. GenomIC is an ISO 9001 facility that delivers high quality data in the areas of real time PCR and microarray analysis (genotyping and expression analysis using Genechip Affymetrix® GeneChip® technology). GenomIC offers a variety of next generation sequencing research applications including whole exome sequencing, targeted resequencing (using amplified or captured targets), transcriptome sequencing using Ion PGM™ and Ion Proton™ sequencers. Institut Cochin | ||||
InterGenetics | • | |||
InterGenetics is a scientific group directed for the past 40 years by medical geneticist Constantinos Pangalos, offering specialized clinical research and laboratory genetics services in Greece as well as abroad. Address: Vas. Sofias Avenue 120,115 26 Athens | ||||
MAD: Dutch Genomics Service & Support Provider, University of Amsterdam | • | |||
![]() The MAD: Dutch Genomics Service & Support Provider has been the genomics expertise center of the University of Amsterdam since the year 2000. We operate as a non-profit, global service provider offering microarray services, and next-generation sequencing services using the Ion Proton™ system, providing bioinformatics support for academic, and industrial research & development projects. Our multidisciplinary team of experts is specialized in tailor-made services & support in the field of mRNA/small-RNA sequencing and prokaryotic genome sequencing. Contact Person: Dr. Selina van Leeuwen | ||||
The National Genomics Infrastructure, Uppsala Genome Center | • | |||
The Uppsala Genome Center (UGC) is a part of The National Genomics Infrastructure (NGI), a sequencing service facility with the ambition to establish technologies for Massive Parallel Sequencing (MPS) and provide MPS as a service. UGC offers sequencing service with different applications and different technologies. We operate with the Applied BioSystems SOLiD® 5500 system, Ion PGM™ sequencer and Ion Proton™ semiconductor for MPS. As a complement to the short read MPS platforms we can offer service on RSII from Pacific Biosciences. UGC also offers Sanger Sequencing as a service. The National Genomics Infrastructure, Uppsala Genome Center | ||||
NIMGENETICS | • | |||
NIMGenetics is a fully licensed analytical centre with a trusted clinical research genetics unit. Our scientific-medical team, accredited by the Spanish Association of Human Genetics, is specialized in the development and application of high-resolution genomic systems that enable reliable and precise clinical research. Our missions are: (1) To ease clinical researchers´ access to the latest scientific advances in genomic tools, such as Next Generation Sequencing, for the improvement of future health care. (2) To offer researchers, in addition to an extensive range of genomic tools, a customized service that starts with the design and selection of the most appropriate genomic approaches and ends with a complete analysis. NIMGENETICS | ||||
Stellenbosch University | • | |||
The DNA Sequencing Unit forms part of the Stellenbosch University Central Analytical Facilities and offers a range of analytical services on a not-for-profit basis. The DNA sequencing core offers services using the Ion S5™, Ion Proton™, and Applied Biosystems™ 3730xl sequencers. Contact: Carel van Heerden | ||||
University Hospital, Lund, Sweden | • | |||
University Hospital Department of Clinical Genetics, Lund, Sweden Contact: Tord Jonson | ||||
University of Leicester | • | |||
![]() Address: Dr Caroline Cowley, Manager of Leicester Molecular Diagnostics, Leicester Cancer Research Centre, University of Leicester, Room 303A, 3rd Floor Robert Kilpatrick Building, Leicester Royal Infirmary, Leicester, LE1 5WW, UK | ||||
University of Natural Resources and Life Sciences, Vienna, Austria | • | |||
Application | Ion AmpliSeq exome | Ion AmpliSeq transcriptome | Ion Torrent whole transcriptome |
---|---|---|---|
MACROGEN | • | ||
Mission Biotech | • | ||
TheragenEtex Bio Institute | • | ||
TheragenEtex Bio Institute was established on September 2009 aiming for improvement of human health and welfare in the future through research using human genome sequencing and analysis. TheragenEtex is establishing and expanding genome database, providing genome bioinformatics solution and conducting Biomarker detection and to support researcher's genome based product developments. TheragenEtex Bio Institute | |||
Yamagata University | • | • | |
![]() The Genome Informatics Unit and Biochemical Analysis Center within the Yamagata University Faculty of Medicine (YUM) integrates research areas of community-based cohort studies, genetics, and molecular biology. The Unit provides DNA and RNA sequencing services on the Ion PGM™ and Ion Proton™ sequencers from experimental design to data analysis. Phone: +81-23-628-5410 (DNA-seq) / +81-23-628-5474 (RNA-seq) Email: h-satoh@med.id.yamagata-u.ac.jp (DNA-seq) / harukiochi@med.id.yamagata-u.ac.jp (RNA-seq) | |||
Yourgene Bioscience | • | ||
Yourgene Bioscience provides sequencing and bioinformatics solutions for research at major institutions, universities and hospitals in Taiwan and Asia Pacific regions. With an integrated team of experienced molecular biologists and bioinformaticians, Yourgene is highly motivated to provide quality sequencing data and analysis for all our valuable clients. Yourgene Bioscience |
For Research Use Only. Not for use in diagnostic procedures.