Bioinformatics
Technologies: Next Generation Sequencing & SoftGenetics’NextGENe® software
Applications: Analysis for: Whole Genome Sequencing, Exome Sequencing, mRNA Sequencing, ChiP Sequencing, SNP Discovery, miRNA or Small RNA Sequencing, de novo Sequencing, Resequencing, Sequence Capture, Indel & Structural Variant Discovery
Ambry Genetics can help you interpret and view the vast amount of data from your Next Generation Sequencing experiments. Now 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 generation 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 generation sequencing projects and bioinformatics needs.
Bioinformatics Deliverables:
- • Assembly (reference-guided or de novo)
- • Hybrid Assembly (combined analysis of data from multiple sequencing platforms)
- • Distribution Report - (includes coverage by direction and read lengths)
- • Variant Report (variants, dBSNP)
- • Comparison Reports
- • Splicing Reports
- • Structural Variation Report
- • ChIP-seq analysis report
- • Small RNAs discovery/ quantification
- • Expression Report
- • Peak Identification Report
- • Analysis of non-mapping reads
- • Run Summaries
- • Post-run sorting of barcoded/indexed samples
- • Custom Reports available
Recognized as a leading
Agilent Certified Solutions Provider.
We are proud to be an
Illumina Certified Service Provider.
Ambry Genetics utilizes
NextGene Sequencing Software.
Established as an Agilent SureSelect© Certified Provider.
Ambry Genetics utilizes
RainDance Technologies.
Bioinformatics Support Powered by SoftGenetics Analysis Software.
