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Genomics & NGS

Precision genomic solutions for discovery and diagnostics

Home Genomics & NGS
01

Consultation & Quote

Discuss project goals and NGS strategy

02

Sample Submission

Receive collection kits & ship to lab

03

NGS & Bioinformatics

Sequencing, QC, and data analysis

Genomics NGS Lab

Next-Generation Sequencing (NGS) Services

Complete Bio Solutions Inc offers comprehensive NGS solutions powered by Illumina NovaSeq 6000, NextSeq 2000, and PacBio platforms. Our services span whole genome sequencing (WGS), whole exome sequencing (WES), targeted panels, RNA-Seq, and single-cell transcriptomics. Each project includes rigorous quality control, bioinformatics analysis, and variant interpretation. Our CLIA-certified laboratory ensures data integrity for both research and clinical applications.

NGS Workflow & Quality Assurance

We follow optimized protocols from library preparation to final report. Every run includes spike-in controls, replicate samples, and alignment metrics. Bioinformatics pipelines are validated against reference genomes (GRCh38/hg38) and include variant calling, annotation, and filtering.

  • Library prep using KAPA / Illumina / Twist kits (DNA, RNA, FFPE)
  • High-depth sequencing: WGS 30-60x, WES 100x+, panels 500-2000x
  • Comprehensive QC: Q30 scores, alignment rates, coverage uniformity

Frequently Asked Questions about NGS

We accept genomic DNA (≥100 ng at 10 ng/µl), whole blood (2-3 ml in EDTA), saliva, tissue, FFPE sections (4-5 sections, 10 µm), and cell pellets. Detailed protocols are provided. For low-input samples, we offer amplification and optimization.
Standard turnaround: 2-3 weeks for targeted panels, 3-4 weeks for whole exome, and 4-5 weeks for whole genome sequencing. Express service (add 25%) is available for urgent projects.
Yes. We deliver raw FASTQ files, aligned BAM files, VCF files, and a comprehensive report with variant annotations (ANNOVAR, ClinVar, gnomAD). Custom analysis (pathway enrichment, copy number variation) is available.