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We reviewed 3 live results for whole exome sequencing and narrowed them down to the 3 options that look most worth comparing first.
The options are Whole Exome Sequencing, GENEQUALITY® Whole Exome Sequencing Kit and Whole Exome Sequencing.
Source: GENEWIZ
Description
GENEWIZ provides whole exome sequencing (WES) services for human and mouse samples across research-use-only and CLIA-certified, CAP-accredited clinical applications. The next-generation sequencing service targets protein-coding regions using hybridization capture technologies, including the Twist Human Comprehensive Exome. Available sequencing coverage options range from 50x for germline variant discovery to 100x and over 200x for somatic mutations and tumor mutational burden detection. The end-to-end workflow on Illumina platforms covers hybridization capture, 2x150 bp sequencing with high Q30 quality guarantees, and bioinformatics analysis for SNVs, INDELs, gene fusions, and CNVs.
Best for
Biomedical researchers, Clinical geneticists, Germline variant discovery and Somatic mutation 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: GENEWIZ
Description
Whole Exome Sequencing (WES) from GENEWIZ by Azenta Life Sciences provides comprehensive next-generation sequencing solutions targeting protein-coding regions to investigate genetic variations in cancers, Mendelian diseases, and complex disorders. The service offers customizable human and mouse exome sequencing for research use only, alongside clinical-grade workflows performed in a CLIA-certified and CAP-accredited laboratory. Features include flexible coverage tiers from 50x to over 200x, hybridization capture technology, Illumina 2×150 bp sequencing with guaranteed Q30 data quality, and end-to-end sample-to-analysis bioinformatics support.
Best for
Biomedical researchers, Clinicians and geneticists, Investigating genetic variations in complex disorders and cancers and Germline variant and somatic mutation discovery
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| Compare | #1Whole Exome Sequencing | #2GENEQUALITY® Whole Exome Sequencing Kit | #3Whole Exome Sequencing |
|---|---|---|---|
| Source | GENEWIZ | AB ANALITICA Srl | GENEWIZ |
| Description | GENEWIZ provides whole exome sequencing (WES) services for human and mouse samples across research-use-only and CLIA-certified, CAP-accredited clinical applications. The next-generation sequencing service targets protein-coding regions using hybridization capture technologies, including the Twist Human Comprehensive Exome. Available sequencing coverage options range from 50x for germline variant discovery to 100x and over 200x for somatic mutations and tumor mutational burden detection. The end-to-end workflow on Illumina platforms covers hybridization capture, 2x150 bp sequencing with high Q30 quality guarantees, and bioinformatics analysis for SNVs, INDELs, gene fusions, and CNVs. | 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. | Whole Exome Sequencing (WES) from GENEWIZ by Azenta Life Sciences provides comprehensive next-generation sequencing solutions targeting protein-coding regions to investigate genetic variations in cancers, Mendelian diseases, and complex disorders. The service offers customizable human and mouse exome sequencing for research use only, alongside clinical-grade workflows performed in a CLIA-certified and CAP-accredited laboratory. Features include flexible coverage tiers from 50x to over 200x, hybridization capture technology, Illumina 2×150 bp sequencing with guaranteed Q30 data quality, and end-to-end sample-to-analysis bioinformatics support. |
| Best for | Biomedical researchers, Clinical geneticists, Germline variant discovery and Somatic mutation profiling | Clinical diagnostic laboratories, Genetics researchers, Whole exome sequencing and Mitochondrial genome analysis | Biomedical researchers, Clinicians and geneticists, Investigating genetic variations in complex disorders and cancers and Germline variant and somatic mutation discovery |
| Action | GENEWIZ | AB ANALITICA Srl | GENEWIZ |
| Rate this product |
"Whole Exome Sequencing from GENEWIZ."
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