Topic 25
reads read sequencing genomics assembly genome nanopore reference long genomes short illumina quality sequence assemblies technologies genomic oxford assembled n50 pacbio sequenced sequences chromosome mb novo complete de length bioinformatics coverage high species repetitive chromosomes genes accurate contigs annotation whole annotated error draft accuracy variants generated contig technology hi completeness haplotype resource dna regions mapping kb busco data contiguity pipeline using bp resources coding transcriptome will genetic calling ont generation available 99 samples scaffold level scaffolds single gene copy variant comparative next alignment cost platform raw assemble generate transcripts methods gb throughput platforms contiguous scale valuable present diploid transcript pacific
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