Whole Genome Sequencing
De novo sequencing is sequencing a novel genome where there is no reference sequence available for alignment. It is used to generate accurate reference sequences, even for complex or polyploid genomes and to Identify structural variants and complex rearrangements, such as deletions, inversions, or translocations.
We at National Genomics Core-CDFD have meticulous quality control in each step of the sequencing project. Experts with PhD and International experience are using top-notch technologies to carefully plan and generate high quality, meaningful data.
Whole genome re-sequencing approach can be used to study the underlying mechanisms of species origin, development, growth, and evolution. Whole Genome Resequencing data can be used for comparing the sequence to that of a known reference genome. Re-sequencing of the genome will identify genetic variations such as SNPs and InDels and discover other genetic changes of the sequenced species.
We at National Genomics Core-CDFD have meticulous quality control in each step of the sequencing project. Experts with PhD and International experience are using top-notch technologies to carefully plan and generate high quality, meaningful data.
De novo sequencing is sequencing a novel genome where there is no reference sequence available for alignment. It is used to generate accurate reference sequences, even for complex or polyploid genomes and to Identify structural variants and complex rearrangements, such as deletions, inversions, or translocations.
We at National Genomics Core-CDFD have meticulous quality control in each step of the sequencing project. Experts with PhD and International experience are using top-notch technologies to carefully plan and generate high quality, meaningful data.
