Open DO-T opened 3 years ago
For polyploid genomes, you need to use the -mono
parameter to evaluate subgenomes independently, otherwise, you will get overcorrected LAI values due to high LTR identity between subgenomes, resulting in low LAI. See discussions here: https://github.com/oushujun/LTR_retriever/issues/83
For the Illumina assembly, my wild guess is that it may not have homeologous LTRs assembled and resolved between subgenomes, so that the genome-wide LTR identity is lower than expectation and the final LAI correction overcorrected it to an unrealistic high value.
Shujun
We will retest it in this way and thanks for your help!
Hi! I have used hifiasm(0.14-r312) on HiFi-reads only to assemble an allotetraploid plant(coverage ~50x). The options : -t48 -l0 were used in this assembly. All output files were generated successfully. The hifi-assembled-genome contig N50 reaches to ~13Mb and BUSCO score reaches to ~98%. The LTR Assembly Index(LAI), however, was less than 10. My sample was highly homozygous and its ancestors were diverged about 5 Million year ago respectively. In fact, we assembled a version1 genome by Illumina paired-end reads(150bp) with PacBio reads and scaffolded with Hi-C data. The Version1 genome LAI score was ~15. By the way, the final hifi-assembly genome size was larger than our exceptation from k-mer analysis about 50Mb. How can I upgrade my genome and any options or methods recommend?