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Diploid

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Leuven, BE

About Diploid

At Diploid, we turn NGS data into clinical reports or research reports, allowing hospitals, commercial labs and research institutes to outsource human genome interpretation.

Our focus is on 3 major areas:
- Rare disease diagnostics
- Carrier screening
- Cancer

With high-quality diagnostics, fast... Show more »

At Diploid, we turn NGS data into clinical reports or research reports, allowing hospitals, commercial labs and research institutes to outsource human genome interpretation.

Our focus is on 3 major areas:
- Rare disease diagnostics
- Carrier screening
- Cancer

With high-quality diagnostics, fast turn-around times, secure infrastructure, and a personal approach, Diploid is rapidly becoming a trusted partner for genetic departments and commercial labs worldwide.

Over the past few months, we have been working for the following institutes and labs:
- Oxford University Hospitals (UK)
- University of Verona (Italy)
- Otogenetics (US)
- Macrogen (US)
- King Faisal Specialist Hospital (KSA)
- National Reference Lab (UAE)

Diploid's infrastructure received ISO 27001 certification and is HIPAA compliant.

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Our Services (14)


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DNA Sequencing Data Analysis

Price on request
Request a quote for more information about this service.

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Whole Genome Sequencing

Starting at $2,990.00 per sample

Whole Genome Sequencing including clinical report:

We offer WGS followed by clinical interpretation in the fields of rare disease diagnostics, carrier screening and germ-line cancer risk assessment.

Included:
- DNA isolation from blood or saliva
- WGS sequencing at 30x on Illumina HiSeq X Ten
- 350 bp insert DNA... Show more »

Whole Genome Sequencing including clinical report:

We offer WGS followed by clinical interpretation in the fields of rare disease diagnostics, carrier screening and germ-line cancer risk assessment.

Included:
- DNA isolation from blood or saliva
- WGS sequencing at 30x on Illumina HiSeq X Ten
- 350 bp insert DNA library, PE150, Paired-end 2 x 150 (read length)
- Bioinformatic analysis (alignment, statistics of sequencing depth and coverage; SNP/InDel, SV and CNV calling, annotation and statistics)
- Analysis of SNPs, CNVs and SVs
- Clinical report pinpointing the causal variant (rare disease diagnostics) or discussing variants that confer a carrier status (carrier screening)
- Report signed by a PhD and by an MD with specialisation in medical genetics
- TAT of 10-12 weeks

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Human Rare Disease WGS DNA Blood Biofluids Illumina Show 7 more tags Show less

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Whole Exome Sequencing Data Analysis

Price on request
  • Starting from BAM or VCF files
  • Data delivered by secure online upload or by HDD shipment
  • Extensive clinical or research report discussing most relevant variants given the diagnostic/research question
  • Report contains links to publications and other online resources
  • Report signed by a board-certified clinical... Show more »
  • Starting from BAM or VCF files
  • Data delivered by secure online upload or by HDD shipment
  • Extensive clinical or research report discussing most relevant variants given the diagnostic/research question
  • Report contains links to publications and other online resources
  • Report signed by a board-certified clinical geneticist
  • 14 business days turn around time
  • Optional Fast-track service (7 days TAT)
  • First 3 analyses are FREE

See http://www.diploid.com/service for more information

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Human Rare Disease Exome sequencing

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Whole Genome Sequencing Data Analysis

Price on request
  • Starting from BAM or VCF files
  • Data delivered by secure online upload or by HDD shipment
  • Extensive clinical or research report discussing most relevant variants given the diagnostic/research question
  • Report contains links to publications and other online resources
  • Report signed by a board-certified clinical... Show more »
  • Starting from BAM or VCF files
  • Data delivered by secure online upload or by HDD shipment
  • Extensive clinical or research report discussing most relevant variants given the diagnostic/research question
  • Report contains links to publications and other online resources
  • Report signed by a board-certified clinical geneticist
  • 14 business days turn around time
  • Optional Fast-track service (7 days TAT)
  • Optional CNV analysis
  • First analysis is FREE

See http://www.diploid.com/service for more information

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Human Rare Disease WGS

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NGS Data Analysis

Next generation sequencing data analysis
Price on request
  • Starting from BAM or VCF files
  • Data delivered by secure online upload or by HDD shipment
  • Extensive clinical or research report discussing most relevant variants given the diagnostic/research question
  • Report contains links to publications and other online resources
  • Report signed by a board-certified clinical... Show more »
  • Starting from BAM or VCF files
  • Data delivered by secure online upload or by HDD shipment
  • Extensive clinical or research report discussing most relevant variants given the diagnostic/research question
  • Report contains links to publications and other online resources
  • Report signed by a board-certified clinical geneticist
  • 14 business days turn around time
  • Optional Fast-track service (7 days TAT)

See http://www.diploid.com/service for more information

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Human

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Sequencing Data Analysis and Management

Price on request
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Nucleic Acid Services

Price on request
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DNA Sequencing

Price on request
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Nucleic Acid Data Analysis

Price on request
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DNA Services

Price on request
Request a quote for more information about this service.

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Next Generation Sequencing (NGS)

Price on request
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Biology

Price on request
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Nucleic Acid Analysis

Price on request
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Biochemistry & Molecular Biology

Price on request
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