412 results found in Access Array System

• faq

  What is the process for redesigning assays?

  Redesigned primers or additional primers can be ordered through D3 at d3.fluidigm.com/account/login. …

• faq

  What species and targets do you design assays to?

  Advanta™ NGS Library Prep Assays are designed to human species for targets with an associated RefSeq ID, gene name, target sequence, or genome coordinate. …

• faq

  How do I arrange credit terms?

  Our credit application includes your organization’s contact and credit information, trade references and latest financial statements. Complete the form and email it to credit@fluidigm.com. …

• Publications

  High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencing

  To identify disease-causing mutations within coding regions of 11 known NPHP genes (NPHP1-NPHP11) in a cohort of 192 patients diagnosed with a nephronophthisis-associated ciliopathy, at low cost. …

• Publications

  High throughput HLA genotyping using 454 sequencing and the Fluidigm Access Array™ system for simplified amplicon library preparation

  The human leukocyte antigen (HLA) class I and class II loci are the most polymorphic genes in the human genome; distinguishing the thousands of HLA alleles is challenging. …

• product insert

  LP—48.48 Control Line Fluid Product Insert 

• faq

  How should I store my SNP Type genotyping assays?

  As supplied, forward and reverse primers should be stored at −20 °C. …

• User Guide

  D3 Assay Design User Guide 

  D3 Assay Design User Guide 100-6812 r06

• faq

  How can I see prices?

  Simply register your account and request access to online shopping and ordering. …

• faq

  Can I sequence Access Array products on the Ion Torrent sequencer? Do you have a protocol?

  Yes, libraries generated from the Access Array system can be used on the Ion Torrent PGM Sequencer. …

• Publications

  Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance

  Chronic myelomonocytic leukemia (CMML) is a clonal hematopoietic malignancy characterized by myeloproliferative or myelodysplastic features. …

• Publications

  Targeted PCR-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation (CDG)

  Congenital disorders of glycosylation (CDG) are a heterogeneous group of disorders caused by deficient glycosylation, primarily affecting the N-linked pathway. …

• Publications

  CYBERTRACK2.0: zero-inflated model-based cell clustering and population tracking method for longitudinal mass cytometry data

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• Publications

  Dramatic reduction of sequence artefacts from DNA isolated from formalin-fixed cancer biopsies by treatment with uracil-DNA glycosylase

  Non-reproducible sequence artefacts are frequently detected in DNA from formalinfixed and paraffin-embedded (FFPE) tissues. However, no rational strategy has been developed for reduction of sequence artefacts from FFPE DNA as the underlying causes of the artefacts are poorly understood. …

• Quick Reference

  Control Line Fluid Loading Procedure 

• product insert

  Advanta NGS Preamp Reagent Kit—96 Rxn Product Insert 

• Quick Reference

  Advanta NGS Library Preparation on the LP 48.48 IFC with Access Array Quick Reference 

• Protocol

  Advanta NGS Library Preparation with Access Array Protocol 

• technical note

  Multiplex of Oncogene Target-Specific Panels Technical Note 

• User Guide

  Access Array for Ion Torrent PGM Sequencing System User Guide