Flye
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De novo assembler for single molecule sequencing reads using repeat graphs
Hi, We have nanopore reads sequenced with the Q20 but when I use nano-hq, there are no contigs assembled. However, when I use nano-raw, I get 4 contigs in the...
Hi, I have sequenced a haploid fungal genome (around 35mb total size, 7 chromosomes, 1 mitochondria) using both Nanopore (R10.4.1 Kit 14 ligation) and Illumina (150bp). I have removed middle...
I have been trying to assemble a 10Mb genome with uncorrected nanopore data (3-4 chromosomes expected). We have a lot of data, is that the reason Flye fails at the...
Hi, Thanks for your great work on enabling de novo assembly on ONT data! I have been working on a snakemake pipeline for assembling and polishing bacterial data, and have...
Hi fenderglass and community, after running metaFlye with no interruptions I received the following Tracebacks and Errors (see below). The main output files should be assembly.fasta, assembly_graph.{gfa|gv} and assembly_info.txt. I...
Hello. I am using Ubuntu and I have tried python versions 3.5, 3.7, 3.9, and 2.7 and each time I get an error that my python version is wrong. I...
Hello, author, thank you for developing the useful tools. I have successfully run it in another small genome of about 230MB, and got a very good assembly result.However, when I...
Hello, I am having problems with the consensus step of Flye 2.9-b1774 installed in anaconda3, where the pipeline aborts with: [2022-04-29 09:50:49] INFO: Starting Flye 2.9-b1774 [2022-04-29 09:50:50] INFO: >>>STAGE:...
Hello, Debian Med wants to help where it can, hoping that bringing the Nanopore and associated software closer to a regular Linux distribution may attract additional eyeballs and help spread...
Hi, This issue is related to the `--polish-haplotypes` subcommand of the `--polish-target` command in the Flye version used by HapDup. Now, given a region, I have the following haplotypes from...