Molecular Design Lab Launch platform

MOLECULAR DESIGN Lab (MDL)

From sequence to scientific decision

A research platform that connects sequence context, assay design, peptide analysis, molecular engineering and scientific reporting in one connected workflow.

Illustrative interface
01 Sequence Define biological target
→
02 Design Configure assay parameters
→
03 Analysis Review scientific candidates
→
04 Decision Interpret and report

CONNECTED RESEARCH WORKFLOW

Keep scientific context connected from input to interpretation

01

Sequence

Start from a sequence, accession, transcript or defined target region and confirm the biological context.

02

Design

Configure assay or molecular design parameters while preserving the context of the original target.

03

Analysis

Compare candidate results using relevant metrics, constraints, predictions and quality checks.

04

Scientific decision

Select, interpret and document results with their parameters, warnings and limitations visible.

COMPLETE RESEARCH TOOLSET

Explore every Molecular Design Lab research workflow

Each tool has a defined role in the research process. Start with the scientific question, review the expected input and output, and move to the next workflow without losing the context needed for interpretation.

ASSAY & MOLECULAR DESIGN

Plan assays, design primers and guides, build constructs and review design quality.

01

Design Assay

Plan Standard PCR or RT-qPCR from biological target selection through transcript context, design constraints and downstream primer generation.

InputGene · RefSeq transcript · DNA sequence OutputAssay strategy & design context OpenDesign Assay →
02

Primer Design

Generate and compare research-oriented PCR primer pairs using configurable amplicon-size, melting-temperature and GC-content constraints.

InputDNA template · Tm/GC/product constraints OutputRanked primer-pair candidates NextAssay QC & Specificity →
03

RT-qPCR Primer Design

Design and prioritize transcript-aware RT-qPCR primer pairs with exon-aware ranking, genomic-DNA risk review and optional hydrolysis-probe candidates.

InputTranscript/cDNA · exon context OutputRT-qPCR primer & probe candidates OpenRT-qPCR Designer →
04

Assay QC & Specificity

Review a primer pair before wet-lab use using sequence QC, Tm balance, 3′ complementarity, intended-target validation and specificity screening.

InputPrimer pair · intended target · reference panel OutputQC summary & specificity evidence OpenRun Assay QC →
05

Multiplex Panel Designer

Design multiple primer pairs as one coordinated PCR or targeted-amplicon panel, review cross-primer conflicts and organize compatible pools.

InputMultiple targets · panel constraints OutputPrimer sets · compatibility & pool plan OpenMultiplex Designer →
06

CRISPR Guide Designer

Scan a user-supplied DNA sequence for SpCas9 or Cas12a guide candidates, compare transparent sequence-level checks and continue to validation-primer design.

InputDNA sequence · nuclease · optional target position OutputRanked guide candidates OpenCRISPR Designer →
07

Plasmid Designer

Build or inspect a plasmid, visualize the construct, screen restriction sites, plan cloning primers and preserve a reproducible design record.

InputBackbone · insert · FASTA/GenBank OutputConstruct map & cloning plan OpenPlasmid Designer →
08

Advanced Vector Designer

Plan a research vector architecture from the biological goal, host and payload while reviewing module compatibility and construct logic.

InputVector goal · host · payload · optional backbone OutputProposed vector architecture NextPlasmid Designer →
09

Multi-Site Assembly

Plan complex multi-fragment and multi-site construct assembly using research workflows such as Gibson or Golden Gate with sequence-partitioning support.

InputBackbone · fragments · insertion sites OutputAssembly plan & construct handoff OpenAssembly Designer →
VARIANT & GENOMIC WORKFLOWS

Move from individual or batched variants to experimental context, candidate prioritization and assay design.

10

Variant → Experiment

Translate a defined sequence variant into transcript, genomic and experimental context, then hand validated information to downstream design workflows.

InputGene/transcript · variant OutputMapped research context & handoffs OpenVariant Workflow →
11

Batch VCF Analysis

Upload GRCh38 or GRCh37 VCF variants for batched consequence analysis, evidence filtering and selection of variants for deeper experimental workflows.

InputVCF · genome assembly OutputAnnotated & filtered variant set NextVariant → Experiment →
12

Cohort Analysis

Analyze multi-sample VCF genotype information, depth and allele fractions across trio, tumor-normal or case-control research contexts.

InputMulti-sample VCF · study roles OutputCohort-level candidate prioritization OpenCohort Analysis →
13

Variant-aware Primers

Design experimental primer candidates around a validated local variant, including flanking, allele-specific, indel-junction and probe-oriented workflows.

InputValidated sequence window · exact REF/ALT OutputVariant-aware assay candidates NextAssay QC & Specificity →
PEPTIDE, STRUCTURE & IMMUNOLOGY

Characterize sequences, compare predicted presentation and examine structural context for candidate interpretation.

14

Peptide Analysis

Evaluate peptide or protein sequences using physicochemical properties and candidate-level sequence analysis for downstream research prioritization.

InputPeptide · protein sequence OutputPhysicochemical profile & candidates NextMHC / HLA Prediction →
15

MHC / HLA Prediction

Prioritize peptide candidates by predicted binding to selected human HLA or mouse MHC targets and compare rank and affinity-related outputs.

InputPeptides · HLA/MHC alleles OutputPredicted binding prioritization OpenMHC / HLA Prediction →
16

3D Structure & Binding

Examine three-dimensional structural and binding context as an additional research layer when interpreting molecular candidates and interactions.

InputMolecular target or sequence context OutputStructural visualization & interaction context Open3D Structure & Binding →

WORKSPACE, LEARNING & BETA

Everything around the analysis is part of the workflow too

Use the workspace to preserve context and reproducibility, then use the learning and beta resources when you need guidance, limitations or feedback channels.

PRODUCT WALKTHROUGH

One connected path from biological input to scientific reporting

A typical MDL workflow keeps the target context, design settings, candidate evidence, warnings and reporting information connected throughout the research process.

01

Select the biological target

Start from a sequence, accession, transcript or defined target region and confirm the biological context before design.

02

Configure the design

Define the relevant design parameters while keeping advanced options available when additional control is needed.

03

Review candidate results

Compare candidates using relevant metrics, design constraints, quality indicators and method context.

04

Inspect warnings and limitations

Review specificity concerns, sequence limitations and other issues that may affect candidate selection or interpretation.

05

Prepare the research report

Preserve the selected candidate, parameters, warnings and interpretation context for later review and reporting.

SCIENTIFIC CLARITY

Scientific results are more useful when their context remains visible

MDL is designed to keep the information needed to interpret a computational result connected to the result itself.

01

Source & biological context

Keep accession, transcript, sequence region, strand and relevant biological context connected to downstream design decisions.

02

Parameters & assumptions

Keep important design settings, thresholds and assumptions visible so results can be reviewed and reproduced more transparently.

03

Methods & versions

Record the computational method, software version and relevant database or reference context alongside the analysis.

04

Warnings & limitations

Surface specificity concerns, prediction limits and design warnings before candidate selection, export or interpretation.

05

Interpretation

Distinguish calculated properties, computational predictions and experimental evidence rather than presenting them as equivalent.

RESEARCH USE

Computational design supports scientific decision-making

Molecular Design Lab is intended to support research workflows. Computational outputs should be interpreted in biological context and experimentally validated where appropriate.

LEARNING RESOURCES

Understand the principles behind molecular design decisions

Explore practical guidance across primer and assay design, variant analysis, molecular engineering, CRISPR, multiplex PCR, immunology, structural analysis and reproducible research workflows.

PRIMER DESIGN

Principles of PCR primer design

Review target selection, primer properties, design constraints and candidate evaluation for PCR workflows.

Open →
RT-qPCR

Transcript-aware RT-qPCR design

Explore transcript context, exon structure, genomic-DNA risk and design considerations for quantitative PCR assays.

Open →
ASSAY QC

Specificity and assay quality

Understand sequence QC, primer-pair compatibility, intended-target validation and specificity screening before wet-lab use.

Open →
VARIANT ANALYSIS

From genetic variant to experimental validation

Follow a variant from sequence and transcript context through evidence review, genomic validation and assay planning.

Open →
CRISPR GUIDE DESIGN

CRISPR guide selection & edit-validation strategy

Learn how PAM recognition, guide position, sequence quality and candidate ranking influence CRISPR guide selection, and how selected guides can be carried forward to validation-primer design.

Open →
MOLECULAR ENGINEERING

Plasmid, vector and multi-site assembly design

Explore construct architecture, vector-module compatibility, cloning strategy and multi-fragment assembly planning.

Open →
MULTIPLEX PCR

Designing compatible primer panels

Learn how primer-pair interactions, Tm compatibility, amplicon constraints and pool assignment affect multiplex panel design.

Open →
IMMUNOLOGY & STRUCTURE

Peptide, MHC/HLA & structural analysis

Connect peptide properties, predicted MHC/HLA binding and 3D structural context when prioritizing research candidates.

Open →
REPRODUCIBILITY

From analysis to scientific report and handoff

Preserve parameters, warnings, evidence context and workflow state so results can be reviewed, reported and continued reproducibly.

Open →

FREQUENTLY ASKED QUESTIONS

Common questions about Molecular Design Lab.

Who is Molecular Design Lab designed for?

MDL is designed for researchers, molecular biologists, biotechnologists, immunologists, laboratory scientists and students working with sequence-based molecular research workflows.

Which research workflows does MDL support?

Current workflows include primer and RT-qPCR design, assay assessment, peptide analysis, MHC/HLA prediction, molecular and vector design, project workflows and scientific reporting.

Are computational results equivalent to experimental evidence?

No. Calculated properties and computational predictions should be interpreted in their biological context and experimentally validated where appropriate.

Can different MDL tools be used as part of one workflow?

Compatible MDL tools are designed to support connected workflows so that biological context, design parameters, selected candidates and reporting information can move between relevant stages.

Can results be included in scientific reports?

Several MDL workflows support structured scientific reports or exports that preserve selected results, design parameters and relevant interpretation context.

What do MDL evidence labels mean?

MDL uses distinct terms for different kinds of information. A calculated property is derived directly from supplied data or a defined formula. A computational prediction is a model- or rule-based estimate. A researcher decision records a documented human choice within the workflow. Experimental evidence comes from laboratory or other independently generated observations. These categories should not be treated as equivalent.

What do Captured and Missing mean in the scientific report?

Captured means that the item is documented in the current research snapshot. It does not mean experimentally validated or scientifically confirmed. Missing means the item is not documented in the current snapshot; it does not by itself mean the evidence does not exist elsewhere.

How should research data be handled?

Some workspace features, including Run History, reliability logs and recovery checkpoints, use storage in this browser. Recovery checkpoints may contain the complete active research snapshot, including biological sequences or other research content. Browser-local storage is not a cloud or institutional backup. Export data that must be retained, and review the applicable data-handling conditions before sending confidential or sensitive information to any external service.

Which MDL tool should I start with?

Start with the scientific question and the type of input you already have. Use Design Assay for assay planning, Primer Design or RT-qPCR for sequence-based primer design, Variant → Experiment for a defined variant, Batch VCF or Cohort Analysis for variant sets, Protein Sequence Analyzer or Protein → Peptide Designer for protein-derived workflows, and the User Guide when you are unsure which route fits your task.

Does MDL include restriction analysis and virtual gel planning?

Yes. Restriction Enzyme Analyzer maps recognition and cut sites and predicts digest fragments from a supplied DNA sequence. Virtual Gel Electrophoresis can then be used to visualize expected fragment separation. These are computational planning tools; enzyme conditions and experimental gel behavior should still be checked independently.

What can the protein and peptide tools do?

Protein Sequence Analyzer helps inspect sequence properties and annotated sequence features. Protein → Peptide Designer generates peptide windows for downstream screening, while Peptide Analysis evaluates candidate-level properties. Selected peptides can be carried into relevant MHC/HLA workflows. Computationally attractive candidates are not evidence of biological activity.

What does MHC / HLA Prediction tell me?

MHC / HLA Prediction prioritizes peptide candidates using predicted binding to supported human HLA or mouse MHC targets. Binding predictions are screening evidence only: they do not by themselves establish antigen processing, presentation, immunogenicity or an experimental immune response.

What does Population Coverage estimate?

Population Coverage estimates HLA coverage from supplied epitope-to-HLA restrictions and a cited population allele-frequency dataset. The result depends on the supplied frequencies, represented alleles and model assumptions. Missing alleles are not evidence of zero frequency, and modeled population coverage is not an individual-level prediction.

How should CRISPR Guide Designer results be interpreted?

CRISPR Guide Designer ranks candidate guides from a user-supplied DNA sequence using transparent sequence-level checks and the selected nuclease context. Candidate ranking supports research planning but does not establish editing efficiency, specificity or biological outcome. Selected guides should be independently evaluated and experimentally validated.

What is Provenance & Evidence used for?

Provenance & Evidence helps review the active research snapshot for source context, accessions, datasets, methods, versions, parameters, warnings and other traceability information. Better provenance improves reproducibility and review, but provenance completeness does not prove scientific, clinical or regulatory validity.

Does MDL automatically choose the best scientific candidate?

No. MDL can calculate, predict, compare and organize candidate information, but candidate selection remains a researcher decision. Scientific Decision is designed to keep compared candidates, warnings, provenance and the researcher's rationale visible rather than silently converting a score into a scientific conclusion.

How should I cite or preserve an MDL analysis?

Preserve the relevant input context, accession or reference sequence, important parameters, method or database information when available, warnings, selected outputs and retrieval or analysis date. Scientific Report, Run History, Project Workspace, Provenance & Evidence and export functions can help retain this context. Keep independent copies when a durable institutional research record is required.

Can MDL outputs be used directly for clinical or diagnostic decisions?

No. Molecular Design Lab is intended for research workflows. Computational predictions, design candidates, workflow-completeness records and software-generated reports do not establish clinical validity, diagnostic performance, treatment suitability or regulatory compliance.

MOLECULAR DESIGN Lab

Move from molecular input to a documented scientific workflow

Explore connected tools for sequence analysis, assay design, candidate evaluation, molecular engineering and scientific reporting.