Let Ambry Genetics help you interpret and view the vast amount of data from your Next Generation Sequencing projects. Now also powered by SoftGenetics’ NextGENe software, overall analysis, assemblies, alignments and annotations are easier to do and to view than ever before. We offer custom bioinformatics for next gen sequencing which provides excellent SNP comparison reports, individual variant reports, indel detection reports, de novo assemblies and contigs, whole genome assemblies, transcriptome, ChIP analysis and much more. Inquire about standard workflows or customization for your genomics projects. Our genomics team is always available to discuss your next gen sequencing projects and bioinformatics needs.
APPLICATIONS |
BIOINFORMATICS DELIVERABLES
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| • Whole Genome Sequencing |
• Assembly (reference-guided or de novo) |
| • Exome Sequencing |
• Distribution Report - (Includes coverage by direction read lengths) |
| • mRNA Sequencing |
• Variant Report (variants, dBSNP) |
| • ChiP Sequencing |
• Comparison Reports |
| • SNP Discovery |
• Splicing Reports |
| • miRNA or Small RNA Sequencing |
• Structural Variation Report |
| • De Novo Sequencing |
• ChIP-Seq Analysis Report |
| • Resequencing |
• Small RNAs Discovery/Quantification |
| • Sequence Capture |
• Expression Report |
| • Indexing/Barcoding |
• Peak Identification Report |
| • Indel & Structural Variant Discovery |
• Analysis of Non-Mapping Reads |
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• Run Summaries |
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• Post-Run Sorting of Barcoded/Indexed Samples |
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• Hybrid Assembly (combined analysis of data from multiple sequencing platforms) |
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All reports viewable in Excel.Custom reports available. |
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100 Columbia #200, Aliso Viejo, CA 92656