NEW RELEASE LISDESK 2026 Engine — Integrated Illumina NovaSeq & DRAGEN Bioinformatic Pipelines Explore Genomic Module →
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Precision Genomics

Genomics & Next-Gen Sequencing (NGS) Informatics

Bridging high-throughput sequencers with clinical interpretation and variant classification

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Key Metric
Automated FASTQ-to-VCF bioinformatic pipeline orchestration
ACMG / AMP Guidelines CAP Molecular Pathology CLIA NGS Validation FDA Part 11

Solution Overview

Modeled after state-of-the-art sequencing workflows (such as Illumina Connected Analytics and DRAGEN pipelines), our Genomics module orchestrates sample library prep, flow cell loading, run metrics, secondary bioinformatic pipelines, and tertiary clinical variant curation (ACMG/AMP guidelines) into compliant clinical molecular reports.

Documented Performance Metrics

65% Faster
Variant Curation Speed
Streamlined evidence curation for pathogenic classifications
Direct
Sequencer Integration
Direct automated run folder parsing and sample sheet dispatch
100% Traceable
Audit Trail
Complete bioinformatic versioning, pipeline checksums, and sign-offs

End-to-End Operational Lifecycle

How specimens flow seamlessly through this module from intake to verified release.

1
Extraction & Library Prep

DNA/RNA quantification, normalization calculations, and index assignment.

2
Sequencing Run Orchestration

Automated sample sheet generation and push to Illumina sequencers.

3
Bioinformatics & QC

Automated FASTQ demultiplexing, alignment, variant calling, and coverage analytics.

4
Clinical Interpretation & Sign-out

ACMG classification workbench, oncologist curation, and PDF clinical report delivery.

Architectural Capabilities

Library preparation pooling, index balancing, and flow cell mapping
Direct API orchestration with Illumina NovaSeq, NextSeq, and MiSeq sequencers
Secondary analysis pipeline trigger (BWA-MEM, GATK, DRAGEN) with QC metrics tracking (Q30, coverage depth)
ACMG / AMP guidelines variant interpretation workbench with ClinVar and gnomAD links
Automated clinical genomic reporting with therapy associations and clinical trial matches
CONSULTATION
Schedule Genomics & Next-Gen Sequencing (NGS) Informatics Walkthrough

Our clinical specialists will review your current instrumentation and showcase direct bidirectional interfaces.

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