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We reviewed 3 live results for ce ivd exome kit and narrowed them down to the 3 options that look most worth comparing first.
The options are Exome Sequencing, GENEQUALITY® Whole Exome Sequencing Kit and Exome Diagnostics.
Source: CeGaT GmbH
Description
CeGaT GmbH provides comprehensive Whole Exome Sequencing (WES) services, sequencing protein-coding genomic regions using Illumina paired-end platforms and Twist Bioscience target enrichment. Processed in an accredited laboratory in Tübingen, Germany, the service supports research in rare diseases, oncology, and population genetics across human and mouse samples. Deliverables include structured project reports, FASTQ data, and scalable bioinformatic analysis levels utilizing the Illumina DRAGEN Bio-IT Platform with standard turnaround times of 15 days.
Best for
researchers, physicians, rare disease research and tumor profiling
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Source: AB ANALITICA Srl
Description
GENEQUALITY® Whole Exome Sequencing Kit by AB ANALITICA is a CE-IVD certified device compliant with EU Regulation 2017/746 (IVDR) for preparing NGS genomic libraries enriched for the human exome and mitochondrial genome. Validated on whole blood DNA (10ng to 500ng) and Illumina platforms such as NovaSeq6000 and NextSeq500/550, it covers approximately 42Mb across 19,441 genes to detect single nucleotide variants, insertions, deletions, single nucleotide polymorphisms, and copy number variations for genetic disease analysis.
Best for
Clinical diagnostic laboratories, Genetics researchers, Whole exome sequencing and Mitochondrial genome analysis
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Source: CeGaT GmbH
Description
CeGaT Exome Diagnostics offers comprehensive genetic testing designed to identify the causes of rare diseases in patients with complex, heterogeneous symptoms. Utilizing ExomeXtra®, the service combines whole exome sequencing, whole genome sequencing depth, and array-CGH resolution copy number variant detection. The diagnostic portfolio includes Trio ExomeXtra®, Single ExomeXtra®, ExomeFocus®, and Prenatal ExomeXtra®, featuring infection screening, mitochondrial genome analysis, actionable medical reports reviewed by human genetics specialists, and complimentary reassessment services.
Best for
physicians, clinical geneticists, identifying genetic causes of rare diseases and evaluating heterogeneous symptoms
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| Compare | #1Exome Sequencing | #2GENEQUALITY® Whole Exome Sequencing Kit | #3Exome Diagnostics |
|---|---|---|---|
| Source | CeGaT GmbH | AB ANALITICA Srl | CeGaT GmbH |
| Description | CeGaT GmbH provides comprehensive Whole Exome Sequencing (WES) services, sequencing protein-coding genomic regions using Illumina paired-end platforms and Twist Bioscience target enrichment. Processed in an accredited laboratory in Tübingen, Germany, the service supports research in rare diseases, oncology, and population genetics across human and mouse samples. Deliverables include structured project reports, FASTQ data, and scalable bioinformatic analysis levels utilizing the Illumina DRAGEN Bio-IT Platform with standard turnaround times of 15 days. | GENEQUALITY® Whole Exome Sequencing Kit by AB ANALITICA is a CE-IVD certified device compliant with EU Regulation 2017/746 (IVDR) for preparing NGS genomic libraries enriched for the human exome and mitochondrial genome. Validated on whole blood DNA (10ng to 500ng) and Illumina platforms such as NovaSeq6000 and NextSeq500/550, it covers approximately 42Mb across 19,441 genes to detect single nucleotide variants, insertions, deletions, single nucleotide polymorphisms, and copy number variations for genetic disease analysis. | CeGaT Exome Diagnostics offers comprehensive genetic testing designed to identify the causes of rare diseases in patients with complex, heterogeneous symptoms. Utilizing ExomeXtra®, the service combines whole exome sequencing, whole genome sequencing depth, and array-CGH resolution copy number variant detection. The diagnostic portfolio includes Trio ExomeXtra®, Single ExomeXtra®, ExomeFocus®, and Prenatal ExomeXtra®, featuring infection screening, mitochondrial genome analysis, actionable medical reports reviewed by human genetics specialists, and complimentary reassessment services. |
| Best for | researchers, physicians, rare disease research and tumor profiling | Clinical diagnostic laboratories, Genetics researchers, Whole exome sequencing and Mitochondrial genome analysis | physicians, clinical geneticists, identifying genetic causes of rare diseases and evaluating heterogeneous symptoms |
| Action | CeGaT GmbH | AB ANALITICA Srl | CeGaT GmbH |
| Rate this product |
"Exome Sequencing from CeGaT GmbH."
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