Ambry Genetics has extensive experience with Sequence Capture Services. From Nimblegen's sequence capture 2.1M HD2 and 385K arrays to Agilent’s SureSelect Target Enrichment System, we offer sequence capture services customizable to your needs. We can prepare targeted libraries using either systems for processing on the Illumina® Genome Analyzer IIX. Our team of experts is here to help you reach your project goals.
| Services |
Applications |
| • Library Preparation |
• All Exon Regions |
| • Sequence Capture |
• Candidate Gene Sets |
| • Sequence on GA IIX |
• Pathway Analysis |
| • Data Analysis |
• Large-Scale Genomic Loci |
| • Bioinformatics Support |
• Customization Available |
Sequence capture service
Nimblegen HD2 / 385K
NimbleGen Sequence Capture arrays are high-density, long oligo arrays that enable researchers to target human exome or any specific genomic regions for use with next generation sequencing instruments. 2.1M HD2 and 385K arrays can capture up 30 MB and 5 MB of unique sequence respectively. This array-based process offers significant scalability advantages over current PCR-based methods for targeted enrichment.
Agilent SureSelect
Agilent’s SureSelect Target Enrichment System is a liquid hybridization selection technique that improves the process-efficiency of next-generation sequencing workflow. The SureSelect Target Enrichment System captures up to 3 MB of unique sequence and has sample low input requirements of gDNA, thus allowing researchers’ flexibility to perform highly targeted next-generation sequencing on the most precious of samples. See workflow. Sequence Capture Applications
Ambry Genetics is the First Certified Services Provider for Agilent's SureSelect.
Nimblegen Sequence Capture Arrays
Agilent sureselect target enrichment
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