Easy exome sequencing

Harness the power of the Ion AmpliSeq™ Exome solution to identify relevant variants in your research

Fill out and submit the form below to download a PDF of the following case study:

Whole-Exome Sequencing for Complex Pediatric-onset Disorders
Featured Researcher: Dr. Christian Marshall

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Please indicate which research techniques you are performing (check all that apply)*

 Exome sequencing
 Fragment sequencing
 Genome sequencing
 Mate-paired sequencing
 Paired-end sequencing
 Small genome sequencing
 Small Ggenome sequencing - 16s metagenomics
 Small genome sequencing - de novo
 Small genome sequencing - microbial ID
 Target enrichment
 Targeted DNA sequencing - gene or regions of interest
 Targeted DNA sequencing - HLA typing research
 Targeted DNA sequencing - mitochondrial
 Targeted RNA sequencing
 Transcriptome sequencing

Please indicate which applications you are performing (check all that apply) *

 Mutation / Variant Discovery
 Mutation / Variant Screening
 Clone verification
 BAC sequencing
 De novo sequencing
 Fosmid or cosmid sequencing
 Structural variation (CNV, translocations, indel)
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