Long-read DNA sequencing fully characterized chromothripsis in a patient with Langer–Giedion syndrome and Cornelia de Lange syndrome-4 | Journal of Human Genetics
Long Read Sequencing Market is expected to reach US$ 5,334.68 million by 2028 With Oxford Nanopore Technologies; Tataa Biocenter; Illumina, Inc; Perkinelmer Inc.; F. Hoffmann-La Roche Ltd.; Baseclear B.V.; Bionano Genomics; Longas
Mostly natural sequencing-by-synthesis for scRNA-seq using Ultima sequencing | Nature Biotechnology
Next-gen sequencing company Longas publicly launches
What is Oxford Nanopore Technology (ONT) sequencing? – YourGenome
Our Investment in Inso Biosciences | 2048 Ventures
New generation Sequencing
Nick Loman on Twitter: "@koadman @longastech @torstenseemann Introducing Morphoseq: a way of getting long "virtual" reads from short read platforms like Illumina. The basic principle is to mutagenise sample to actually remove
Whole genome sequencing - Wikipedia
CSI: (Exclusive) Metagenomics: The Sequencing of DNA | Staten Island Technical High School
Advantages of long read assembly. Shown here is a genome sequence with... | Download Scientific Diagram
Sequencing Strategies for Whole Genomes - Genomics Course
Nick Loman on Twitter: "@koadman @longastech @torstenseemann Introducing Morphoseq: a way of getting long "virtual" reads from short read platforms like Illumina. The basic principle is to mutagenise sample to actually remove
Long-Read Sequencing Technology | For challenging genomes
Nick Loman on Twitter: "@koadman @longastech @torstenseemann Introducing Morphoseq: a way of getting long "virtual" reads from short read platforms like Illumina. The basic principle is to mutagenise sample to actually remove
Consistent ultra-long DNA sequencing with automated slow pipetting | BMC Genomics | Full Text
Handling of targeted amplicon sequencing data focusing on index hopping and demultiplexing using a nested metabarcoding approach in ecology | Scientific Reports
Lutz Froenicke on Twitter: "Longas Technologies is going to offer a new synthetic long read technology: MorphoSeq. The scheme looks somewhat similar to the Loop Genomics approach and sequences fragments up to
Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities | Nature Communications
Ultraplexing: increasing the efficiency of long-read sequencing for hybrid assembly with k-mer-based multiplexing | Genome Biology | Full Text
Nick Loman on Twitter: "@koadman @longastech @torstenseemann Introducing Morphoseq: a way of getting long "virtual" reads from short read platforms like Illumina. The basic principle is to mutagenise sample to actually remove
Discover 5 Top BioTech Startups advancing Long-Read Sequencing
UK explores whole-genome sequencing for newborn babies - The Lancet
Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads | Nature Biotechnology
