Discover how broad multiplex reference panels covering influenza-lineage groups, respiratory targets, enteric targets, plus bacterial and fungal markers support assay development, verification, and quality control without clinical claims.
Multiplex Reference Panels That Cover Influenza-Lineage, Respiratory, Enteric, and Microbial Targets
When you build or validate a multiplex detection workflow PCR, digital PCR, sequencing, hybrid capture, or automated classification the biggest risk isn’t sensitivity. It’s coverage:
- Will your design hold up across subtypes and lineages ?
- Will it stay stable across instrument changes and operator variation ?
- Can you prove performance using a consistent reference set ?
That’s why advanced teams rely on multi-target reference panels: curated libraries that include influenza-lineage groups (H1/H3/H5/H7/H9 and B-lineages), respiratory targets, enteric targets, and broader microbial markers, plus selected fungi and toxin markers.
What This Panel Actually Represents ?
Your catalog is essentially a structured diversity library that includes:
1) Influenza-lineage Groups (A and B)
-Multiple H-subtype families (examples include H1/H3 and additional H groups)
-Multiple geographically and temporally distinct isolates
-B-lineage groupings such as Victoria-like and Yamagata-like variants
Why it matters: Influenza-like genomes are highly variable. A wide isolate set is perfect for primer/probe stress testing, alignment benchmarking, and dropout detection during multiplex design.
2) Respiratory Target Families
-Syncytial-type A and B groups
-Parainfluenza-type groups
-“Partial lung” labeled entries (useful as challenging diversity members)
Why it matters: Respiratory panels often face high sequence similarity among neighboring groups. A diverse library helps confirm:
3) Enteric / Gastro-Associated Target Families
-Norovirus-type entries
-Rotavirus Group A variants
-Several enterovirus-type groupings and sub-groups
Why it matters: Enteric workflows often deal with mixed backgrounds and complex sample matrices. A broad reference set helps validate:
4) DNA Target Families With Many Subtypes
For example: adenovirus-type groups and herpes-family groups, plus related lineages).
Why it matters: These families are useful for:
-assessing subtype discrimination
-evaluating conserved vs variable region designs
-benchmarking classification confidence thresholds
5) Bacterial Markers
-Streptococcus pneumoniae, Legionella, Bordetella pertussis, Neisseria meningitidis
-Klebsiella pneumoniae, Staphylococcus aureus, Streptococcus pyogenes
-Haemophilus influenzae, Mycobacterium tuberculosis
-Pseudomonas aeruginosa, Acinetobacter baumannii, Neisseria gonorrhoeae
-Helicobacter pylori (and other common QC-relevant bacteria)
Why it matters: Bacterial targets are key for evaluating:
-multiplex primer compatibility
-off-target amplification risk
-mixed-panel specificity (when many taxa exist in one test)
6) Fungal Markers + Toxin Marker
fungi such as:
-Candida albicans, Candida glabrata
-Cryptococcus neoformans
-Aspergillus fumigatus
- …and a toxin marker: aflatoxin
Why it matters: Adding fungi + toxin markers helps teams validate:
-cross-kingdom specificity (bacteria vs fungi)
-extraction method differences
-reporting logic when targets span multiple classes
1) Influenza-lineage Groups (A and B)
-Multiple H-subtype families (examples include H1/H3 and additional H groups)
-Multiple geographically and temporally distinct isolates
-B-lineage groupings such as Victoria-like and Yamagata-like variants
Why it matters: Influenza-like genomes are highly variable. A wide isolate set is perfect for primer/probe stress testing, alignment benchmarking, and dropout detection during multiplex design.
2) Respiratory Target Families
-Syncytial-type A and B groups
-Parainfluenza-type groups
-“Partial lung” labeled entries (useful as challenging diversity members)
Why it matters: Respiratory panels often face high sequence similarity among neighboring groups. A diverse library helps confirm:
3) Enteric / Gastro-Associated Target Families
-Norovirus-type entries
-Rotavirus Group A variants
-Several enterovirus-type groupings and sub-groups
Why it matters: Enteric workflows often deal with mixed backgrounds and complex sample matrices. A broad reference set helps validate:
4) DNA Target Families With Many Subtypes
For example: adenovirus-type groups and herpes-family groups, plus related lineages).
Why it matters: These families are useful for:
-assessing subtype discrimination
-evaluating conserved vs variable region designs
-benchmarking classification confidence thresholds
5) Bacterial Markers
-Streptococcus pneumoniae, Legionella, Bordetella pertussis, Neisseria meningitidis
-Klebsiella pneumoniae, Staphylococcus aureus, Streptococcus pyogenes
-Haemophilus influenzae, Mycobacterium tuberculosis
-Pseudomonas aeruginosa, Acinetobacter baumannii, Neisseria gonorrhoeae
-Helicobacter pylori (and other common QC-relevant bacteria)
Why it matters: Bacterial targets are key for evaluating:
-multiplex primer compatibility
-off-target amplification risk
-mixed-panel specificity (when many taxa exist in one test)
6) Fungal Markers + Toxin Marker
fungi such as:
-Candida albicans, Candida glabrata
-Cryptococcus neoformans
-Aspergillus fumigatus
- …and a toxin marker: aflatoxin
Why it matters: Adding fungi + toxin markers helps teams validate:
-cross-kingdom specificity (bacteria vs fungi)
-extraction method differences
-reporting logic when targets span multiple classes