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We reviewed 3 live results for human exome sequencing and narrowed them down to the 3 options that look most worth comparing first.
The options are Human Whole Exome Sequencing, GENEQUALITY® Whole Exome Sequencing Kit and Exome Sequencing.
Source: Genomics Core Leuven
Description
Human Whole Exome Sequencing is a specialized genomic sequencing service provided by Genomics Core Leuven. The service sequences the full human exome utilizing the SeqCap EZ Exome v3 capture kit from Nimblegen alongside Illumina sequencing technology. It requires high-quality DNA input of more than 500 ng and delivers comprehensive data outputs including raw fastq-files, aligned BAM-files, and annotated SNP vcf-files for scientific analysis.
Best for
Researchers, Genomics laboratories, Exome sequencing and SNP variant discovery
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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 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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| Compare | #1Human Whole Exome Sequencing | #2GENEQUALITY® Whole Exome Sequencing Kit | #3Exome Sequencing |
|---|---|---|---|
| Source | Genomics Core Leuven | AB ANALITICA Srl | CeGaT GmbH |
| Description | Human Whole Exome Sequencing is a specialized genomic sequencing service provided by Genomics Core Leuven. The service sequences the full human exome utilizing the SeqCap EZ Exome v3 capture kit from Nimblegen alongside Illumina sequencing technology. It requires high-quality DNA input of more than 500 ng and delivers comprehensive data outputs including raw fastq-files, aligned BAM-files, and annotated SNP vcf-files for scientific analysis. | 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 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, Genomics laboratories, Exome sequencing and SNP variant discovery | Clinical diagnostic laboratories, Genetics researchers, Whole exome sequencing and Mitochondrial genome analysis | researchers, physicians, rare disease research and tumor profiling |
| Action | Genomics Core Leuven | AB ANALITICA Srl | CeGaT GmbH |
| Rate this product |
"Human Whole Exome Sequencing from Genomics Core Leuven."
Note: TopFind AI compiles product and service information for general comparison purposes only.