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View additional product information for CarrierSeq™ ECS Kit with Ion 540™ Chips (15 samples/chip) - FAQs (A48023)
17 product FAQs found
No, CarrierSeq samples have only been tested using standard Ion S5 sequencing chemistry.
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No, CarrierSeq libraries have only been tested for manual library preparation.
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The Ion AmpliSeq CarrierSeq ECS Panel consists of two pools.
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The Ion AmpliSeq CarrierSeq ECS Panel targets >14,000 amplicons that cover all coding regions and intro/exon boundaries of 420 target genes implicated in 418 inherited disorders.
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No, CarrierSeq samples are only compatible with the Ion 530 and Ion 540 Chips.
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No, the panel is preconfigured with a set of primers and cannot be altered. However, during analysis in Carrier Reporter Software, you can select which genes you want to report.
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No, CarrierSeq library preparation has only been tested with Ion AmpliSeq Library Kit Plus (Cat. No. A35907, 4488990, A38875).
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No, CarrierSeq samples have only been tested for use with IonCode barcodes.
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No, because the baseline used for analyzing CarrierSeq samples is instrument-specific and chip-specific, CarrierSeq samples cannot be run on an Ion PGM or Ion Proton instrument. They are only compatible with the Ion GeneStudio S5 systems.
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Yes, a local version of Carrier Reporter Software can be installed on an Ion Reporter local server. For more information, please contact a Thermo Fisher Scientific representative.
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Access to Carrier Reporter Software, Cloud version, is included with the purchase of the Ion AmpliSeq CarrierSeq ECS Panel.
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CarrierSeq ECS data can be analyzed using Carrier Reporter Software.
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Yes, difficult-to-characterize target genes due to homology as a result of pseudogenes (GBA and GBAP1 for Gaucher disease research), paralogues (SMN1 and SMN2 for spinal muscular atrophy research), and loci (HBA1 and HBA2 for alpha-thalassemia research) are consolidated in the Ion AmpliSeq CarrierSeq ECS Panel.
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The Ion AmpliSeq CarrierSeq ECS Panel targets >14,000 amplicons that cover all coding regions and intro/exon boundaries of 420 target genes implicated in 418 inherited disorders, and enables the analysis of 28,000 non-benign ClinVar variants for single-nucleotide variants (SNVs), insertions and deletions (indels), and copy number variants (CNVs) by next-generation sequencing (NGS).
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For the complete list of genes on the Ion AmpliSeq CarrierSeq ECS panel, please contact your local Thermo Fisher Scientific representative.
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Yes, the Ion AmpliSeq CarrierSeq ECS Panel is available for purchase separately (Cat. No. A43471, A48036).
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For the CarrierSeq ECS Kit with Ion 540 Chips, Cat. No. A43586, we recommend running 16 samples per chip. For the CarrierSeq ECS Kit with Ion 540 Chips, Cat. No. A48023, we recommend running 15 samples per chip.
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