Microcoding and flow cytometry as a high-throughput fungal identification system for Malassezia species

Keyphrases

• Identification System 100%
• Flow Cytometry 100%
• High-throughput 100%
• Malassezia 100%
• Species Identification 100%
• Precise Identification 100%
• Targeted Sequencing 100%
• Fungal Identification 100%
• Epidemiology 50%
• Human Animals 50%
• Domestic Animals 50%
• Multiplex 50%
• Pathogenic Species 50%
• Hybrid Analysis 50%
• Luminex 50%
• Simultaneous Detection 50%
• Sequence Analysis 50%
• Group-specific 50%
• Culture-based 50%
• Nucleic Acid Hybridization 50%
• PCR Amplification 50%
• Multiplex PCR (mPCR) 50%
• Amplicon 50%
• Fluorochrome 50%
• Internal Transcribed Spacer 1 (ITS1) 50%
• Ribosomal RNA 50%
• Dermatological Diseases 50%
• D1-D2 Region 50%
• Capture Probe 50%
• Flow Cytometric 50%
• Covalently Bound 50%
• Non-target 50%
• Suspension Culture 50%
• Comprehensive Identification 50%
• Fluorescent Beads 50%
• Single Array 50%
• Mismatch Discrimination 50%
• Uniplex PCR 50%
• Multiple Arrays 50%
• Microcode 50%
• K-plex 50%
• Specific Capture 50%
• Reporter Molecules 50%

Biochemistry, Genetics and Molecular Biology

• New Species 100%
• Malassezia 100%
• Fungus Identification 100%
• Flow Cytometry 100%
• Protein Sequencing 50%
• Multiplex Polymerase Chain Reaction 50%
• Internal Transcribed Spacer Region 50%
• Nucleic Acid Hybridization 50%
• Domestic Animal 50%
• Amplicon 50%
• New Genus 50%
• Shotgun Sequencing 50%
• Suspension Cell Culture 50%
• Species Identification 50%
• Ribosomal RNA 50%

Immunology and Microbiology

• New Species 100%
• Malassezia 100%
• Fungus Identification 100%
• Nucleic Acid Hybridization 50%
• New Genus 50%
• Multiplex Polymerase Chain Reaction 50%
• Amplicon 50%
• Sequence Analysis 50%
• Species Identification 50%
• Suspension Cell Culture 50%
• Domestic Animal 50%
• Ribosomal RNA 50%
• Cohort Effect 50%
• Ribosome RNA 50%