Closed Jiangjiangzhang6 closed 2 months ago
Please send me the 100 - 200 sequence or the files in the "_temp" folder (kentnf@gmail.com) to reproduce the error. This error should be caused by incorrect processing of hmmscan output files.
the bug has been fixed, please using git clone command to get the latest version.
dear friend: I run the command with "python ~/iTAK-2.0.2/iTAK.py -p 3 -o hap1.itak -c hap1.pep1" , but its error with show "ValueError: could not convert string to float:"
its very weird, when I run the test fasta in your software, its ok ,and have the result, so I think maybe the software need the special format, so I use the seqkit seq to generate the new file, but its also error. so maybe the id was error , the original was like "Cannabis1G00001.t1", modified "Cannabis1G00001t1", its still error. other ways to try, I extract the 100 sequences to run, its down. but when extract the 200 sequences, still error .
so how handle with this question.
thank you