Next-Generation Sequencing Service

End-to-end solution for your tissue and liquid biopsy samples

DiaCarta’s Next-Generation Sequencing service is an end-to-end solution for your tissue and liquid biopsy samples. With a streamlined workflow and dedicated in-house team, we offer quick turnaround time from sample to result.

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Standard or Customized Workflows

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Expertise in sample extraction, prep and QC

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Reliable Services

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Rapid Turn-around Time

Next-Generation Sequencing Service Offerings

Sample & Library Preparation

  • DNA/RNA extraction and library construction
  • High-quality sequencing libraries for all types of samples including FFPE tissues and ctDNA in liquid biopsies
  • Constructed libraries are compatible with all Illumina sequencing platforms
  • All libraries are verified for quality and yield

Next-Generation Sequencing

  • Whole genome sequencing
  • Exome sequencing
  • mRNA sequencing
  • Small RNA (miRNA, shRNA) sequencing
  • ChlP sequencing
  • Amplicon sequencing
  • 16S metagenomics sequencing
  • Disease panel sequencing

Genome Annotation

Our scalable annotation pipeline can deliver annotated data rapidly. We use sophisticated algorithms to annotate any type of genome.

  • Rapid pipeline
  • Customizable data delivery
  • Export support

Bioinformatics Support

Our expert bioinformatics support accommodates any analysis types. We work with you to ensure that you are getting the right analysis while keeping your data secure.

  • Dedicated bioinformatics team
  •  Cost-effective with quick delivery of data
  • Flexible analysis format

Next-Generation Sequencing Service Applications

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Variant (SNP & Indel) Discovery

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Differential Gene Expression Analysis

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Novel Isoform (Alternative & Splicing) Identification

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16S rRNA Metagenomics Analysis

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Structural Variation Discovery

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Peak Analysis (ChlP-Seq)

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De Novo Genome & Transcriptome Assembly

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Whole Genome Metagenomics Analysis

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Exome Sequencing Analysis

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Small & miRNA Sequencing Analysis

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Gap-Closure Analysis (Genome Finishing)

Streamlined Workflow for Next-Generation Sequencing Service

Step 1: Sample & Library Prepartion

Step 2: Next-Generation Sequencing

Step 3: De Novo Assembly

Step 4: Report

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