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hi everyone my name is janet and i am a bioinformatics masteramp;#39;s student at the university of british columbia and bc cancer genome sciences center today iamp;#39;ll be presenting efficient targeted error resolution and automated finishing of long read genome sequence assemblies long read sequencing technologies such as from oxford nanopore and pacific biosciences have been increasingly used in genomic research over the past several years as these platforms have dramatically developed and improved long reads can span several thousands to even millions of nucleotides in length and this provides valuable long-range genomic information for genome assembly this information aids in resolving repetitive regions identifying structural variants and docHubing chromosome level continuity however the low accuracy of long reads remains a major limitation to their application as this affects the accuracy of data and pain from them such as genome assemblies this is an issue because accurate g