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We reviewed 3 live results for séquençage exome and narrowed them down to the 3 options that look most worth comparing first.
The options are Exome Sequencing, TruSeq RNA Exome 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: Illumina
Description
TruSeq RNA Exome, formerly known as the TruSeq RNA Access Library Prep Kit, is an Illumina sequencing library preparation and enrichment solution. It provides an economical, reproducible workflow for sequencing human coding RNA from degraded or low-input samples, including formalin-fixed paraffin-embedded (FFPE) tissues. Utilizing biotinylated capture probes targeting coding RNA without requiring poly-A tails, the kit enables stranded transcriptome analysis, novel transcript discovery, and gene fusion detection from as little as 10 ng total RNA.
Best for
Genomics researchers, Molecular biology laboratories, Sequencing RNA from FFPE tissue samples and Low-input human coding transcriptome 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 | #2TruSeq RNA Exome | #3Exome Diagnostics |
|---|---|---|---|
| Source | CeGaT GmbH | Illumina | 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. | TruSeq RNA Exome, formerly known as the TruSeq RNA Access Library Prep Kit, is an Illumina sequencing library preparation and enrichment solution. It provides an economical, reproducible workflow for sequencing human coding RNA from degraded or low-input samples, including formalin-fixed paraffin-embedded (FFPE) tissues. Utilizing biotinylated capture probes targeting coding RNA without requiring poly-A tails, the kit enables stranded transcriptome analysis, novel transcript discovery, and gene fusion detection from as little as 10 ng total RNA. | 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 | Genomics researchers, Molecular biology laboratories, Sequencing RNA from FFPE tissue samples and Low-input human coding transcriptome analysis | physicians, clinical geneticists, identifying genetic causes of rare diseases and evaluating heterogeneous symptoms |
| Action | CeGaT GmbH | Illumina | CeGaT GmbH |
| Rate this product |
"Exome Sequencing from CeGaT GmbH."
Note: TopFind AI compiles product and service information for general comparison purposes only.