Open Yixiangzhang1996 opened 1 year ago
Hi,
it means no sequence passes the filter in step 2:
--e FLOAT E-value cutoff for target sequences. [1e-7]
--id FLOAT Identity cutoff (in percentage) for target sequences. [80]
--qcov FLOAT Query cover cutoff (in percentage) for target sequences. [75]
--length INT Aligned length cutoff (in amino acid) for target sequences. [25]
If your sequences are very short (below 25 aa or 75 bp), then using the default value of --length
will lead to a removal or all sequences.
Hi Chen, I have encountered a similar issue with my sequences. In my case, I have 150-base pair paired-end (PE) sequences, and even after quality trimming, I still have sequences longer than 100 base pairs. Any suggestions or solutions you can provide for this problem. thank you for your patient.
<img width="641" alt="Screenshot 2024-01-04 at 8 30 21 P
M" src="https://github.com/xinehc/args_oap/assets/89136993/03d3ce0a-b954-486d-94f3-336953822b97"> (extracted fa) More information for you
Hello The error message, "CRITICAL: No target sequence remained after merging structure files, no further normalization will be made," indicates that there is an issue related to merging structure files and normalization in your analysis. This error occurs both with self-built databases and default databases.
Is it the data itself, or are the environment variables not configured properly?