First review all your previous questions, and mark them as answered if needed. How to know the sample total read in SRA ; How to download 10 sequence for specific disease in NCBI ; how to discover the dissimilar regions in alignment using pyhton? ; how to discover the dissimilar regions in alignment using pyhton? ; visualize CD-HIT output file ; how to split RNA-seq into codons by using python ; how to convert output of bash script to .csv ? ; how to apply DE-kupl in my data for differential expression ? ; HISAT2: Question regarding providing file path to indexed genome folder ; align using file.ht2 ; Bioinformatics ;

second,this question is too general. Give more details on your input and desired output. Also, what have you tried so far?

Maybe these public course slides from the Swedish National Bioinformatics Infrastructure course "Data Management Practices" will be helpful:

• Slides collection from https://doi.org/10.17044/scilifelab.c.6820587.v3
• Introduction to Data Management Practices for NGI

Please cite the respective authors of the modules, should you find information helpful, and reuse it in your company's materials.