Samplix provides target enrichment services using the Xdrop™ platform together with Oxford Nanopore and/or Illumina sequencing. The properties of our Xdrop™ platform to target and enrich very long DNA fragments. We are therefore able to perform unique enrichment and sequencing projects, including:
• Identify Genomic Integrations, e.g. viral • Verify CRISPR edits • Sequence of repetitive elements, e.g. tandem repeats • Gap closing in difficult genomes • Phase Haplotypes • Amplify Whole Genomes with uniform coverage
See Xdrop™ example data
Don't hesitate to contact us, using the form below to learn how your project can be helped by our target enrichment and sequencing services
Please enter a valid value
First name Please enter a name
Last name Please enter last name
Email Please enter valid email
Organisation Please enter a company
Country - Afghanistan Albania Algeria Argentina Armenia Australia Austria Azerbaijan Bahrain Bangladesh Belarus Belgium Belize Bhutan Bolivia Bosnia and Herzegovina Botswana Brazil Brunei Bulgaria Cambodia Cameroon Canada Chile China Colombia Congo (DRC) Costa Rica Côte d’Ivoire Croatia Cuba Czech Republic Denmark Dominican Republic Ecuador Egypt El Salvador Eritrea Estonia Ethiopia Faroe Islands Finland France Georgia Germany Greece Greenland Guatemala Haiti Honduras Hong Kong SAR Hungary Iceland India Indonesia Iran Iraq Ireland Israel Italy Jamaica Japan Jordan Kazakhstan Kenya Korea Kuwait Kyrgyzstan Laos Latin America Latvia Lebanon Libya Liechtenstein Lithuania Luxembourg Macao SAR Macedonia, FYRO Malaysia Maldives Mali Malta Mexico Moldova Monaco Mongolia Montenegro Morocco Myanmar Nepal Netherlands New Zealand Nicaragua Nigeria Norway Oman Pakistan Panama Paraguay Peru Philippines Poland Portugal Puerto Rico Qatar Réunion Romania Russia Rwanda Saudi Arabia Senegal Serbia Singapore Slovakia Slovenia Somalia South Africa Spain Sri Lanka Sweden Switzerland Syria Taiwan Tajikistan Thailand Trinidad and Tobago Tunisia Turkey Turkmenistan Ukraine United Arab Emirates United Kingdom United States Uruguay Uzbekistan Venezuela Vietnam Yemen Zimbabwe Please enter country
Your message Please enter a valid value
By registering on this web page, you are consenting and agreeing to collection and use of that information by Samplix in accordance with its Privacy Policy.
“We used Samplix Xdrop™ and Sequencing Services in a project aiming at closing genomic gaps of the herring Y chromosome. We were pleased with the advice we received from Samplix experts regarding experimental design as well as with the speed and quality of the delivered Service”
Prof. Leif Andersson, Uppsala University, Sweden