Nanopore sequencing services
Based on the innovative technology of Oxford Nanopore Technologies (ONT), BaseClear offers ultra fast and long-read sequencing services. Read lengths are determined by preparation, the longest single...
BaseClear offers high quality sequencing services using the latest platform from Pacific Biosciences, the PacBio Sequel II. With this PacBio platform BaseClear offers real-time sequencing of single molecules with read lenghts up to 30.000 base pairs. This long-read data has added value for de novo assembly, targeted sequencing, detection of structural variation and the direct detection of base modification. PacBio sequencing is often used for closing the genomes of bacteria, fungi and other organisms.
Sequencing on the PacBio platforms can be used in addition to our services based on the Illumina or Nanopore platforms. True whole genome sequencing with the PacBio systems provides complete and accurate views of all types of genomic variation, revealing SNPs/SNVs, structural variants, mobile elements, haplotypes and variants in low-complexity regions. This allows us to:
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Based on the innovative technology of Oxford Nanopore Technologies (ONT), BaseClear offers ultra fast and long-read sequencing services. Read lengths are determined by preparation, the longest single...
BaseClear offers Illumina sequencing services on the NovaSeq 6000 and MiSeq systems. These systems employs Illumina sequencing by synthesis (SBS) technology, which is the most widely adopted...
BaseClear offers complete solutions for both De Novo genome analysis and re-sequencing projects. With our many years of experience, highly qualified specialists and innovative technologies we can...
With our complete suite of microbial genomics solutions, we can be your one-stop shop. Our solutions range from study design consultancy, to data generation and data interpretation. Contact us to...