Fig. 3From: High contiguity de novo genome assembly and DNA modification analyses for the fungus fly, Sciara coprophila, using single-molecule sequencingPost-assembly work flow. Chosen assemblies were scaffolded, polished, gap-filled, filtered, anchored into chromosomes where possible, and classified as X or autosomal by coverage. Repeats were identified. RNA-seq was used for transcriptome assembly and gene annotation. Single-molecule datasets were used to investigate DNA modificationsBack to article page