Methods to scaffold contigs together and correct genome assembly errors.
A proximity-ligation protocol using a sequence-independent endonuclease, generating data for TAD identification and scaffolding.
chromatin scaffolding library preparation epigenetics TADs illumina de novoNanopore instruments can sequence very long continuous fragments of DNA. Sequencing native DNA allows detection of base modifications.
nanopore assembly long-readPacBio SMRT sequencing generates reads tens of kilobases in length enabling high quality genome assembly, structural variant analysis, amplicon resequencing, full-length transcript isoform sequencing, full-length 16S rRNA sequencing and amplification free epigenetic characterization.
methylation amplicon hifi de novo iso seq sv revio smrt assembly pacbio