FASTQ to T2T Alignment

Transform your sequencing data into comprehensive Telomere-to-Telomere assemblies

Get 80% off. Use code: CYBERWEEK80

Valid until February 23 2025

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About FASTQ to T2T Conversion

Transform your sequencing data into a comprehensive T2T assembly, providing a complete and detailed representation of your genome. Our service ensures high-quality alignments for advanced genomic analysis.

Key Features

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High-Quality Assembly

Premium T2T assemblies for comprehensive genomic analysis

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Platform Support

Compatible with all major sequencing platforms

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Secure Processing

Safe and efficient handling of your genetic data

How It Works

Share Your Files

Upload your FASTQ files via Google Drive, Dropbox, or any other cloud service

Processing

We align your data to the T2T reference genome

Secure Delivery

Receive your T2T assembly files via secure download link

Supported Platforms

Illumina BGI PacBio Oxford Nanopore
Supported Input Formats

We accept high-throughput sequencing FASTQ files from all major sequencing platforms

Pricing

FASTQ to T2T Alignment

60.00€
80% off with code: CYBERWEEK80
  • ✓ High-quality T2T assembly
  • ✓ Support for all major platforms
  • ✓ Secure file handling
  • ✓ Fast processing
  • ✓ Research-grade output
  • ✓ Technical support
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Important Information

Note: This service is intended for ancestry, research and academic purposes only. It is not suitable for clinical or diagnostic use.

Legal Information

Legal Disclaimer

By using our genomic data service, you acknowledge and agree to the following terms and conditions:

  1. PURPOSE This service is intended solely for ancestry and genealogy research purposes. It is not designed, intended, or suitable for health-related uses or medical purposes.
  2. NO HEALTH PREDICTIONS We explicitly disclaim any responsibility for health predictions or interpretations made from the files provided through this service. Users are strictly prohibited from using our converted data for medical or health-related purposes.
  3. DATA ACCURACY While we strive for accuracy in our imputation process, please be aware of the following limitations: - The imputation process can lead to an error rate of genotypes ranging from 1% to 5%, due to the statistical nature of the process. It is not advisable to utilize the imputed file for health predictions, as there is a chance of encountering false positives/negatives.
  4. THIRD-PARTY USE The compatibility of our imputed files with third-party DNA websites is provided as-is. We do not guarantee the acceptance or proper functioning of our files on all external platforms.
  5. DATA PRIVACY We prioritize the security of your genetic data and provide a link for you to download your imputed data directly from your private account. However, we cannot guarantee absolute security during transmission or storage on your end.
  6. NO WARRANTY This service is provided "as is" without any warranties, express or implied. We do not guarantee the completeness, reliability, or accuracy of the converted data.
  7. LIMITATION OF LIABILITY We shall not be held liable for any direct, indirect, incidental, consequential, or exemplary damages resulting from your use of this service or the data provided.
  8. USER RESPONSIBILITY You are solely responsible for how you use the imputed data. We strongly recommend consulting with qualified professionals for any health-related concerns or interpretations of genetic data.
  9. COMPLIANCE Users must comply with all applicable laws and regulations regarding the use and sharing of genetic information in their jurisdiction.
  10. CHANGES TO SERVICE We reserve the right to modify, suspend, or discontinue any part of this service without prior notice.
  11. By proceeding with our service, you indicate that you have read, understood, and agreed to these terms. If you do not agree with any part of this disclaimer, please do not use our service.

Start Your T2T Analysis Today

Transform your sequencing data into comprehensive genome assemblies

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