Raw_ Reads uses fastp quality control, then megahit is used for assembly, and metabat2 and metaclip are used for packing. As a result, the number of boxes is very small. Why? How to slove?
How can I remove warnings for per base sequence content, per sequence GC content and sequence duplication levels using trimmomatic or fastp. Thanks ![enter image …
Hi, After trimming the reads as discussed in below [https://www.biostars.org/p/9584040/#9584110][1] I used bowtie1 for alignment, but 99% of the reads were not aligned, **what is …
Hi all I have two sets of nanopore DNA sequencing data (experimental group and control group). Using the mCaller tool, I extracted the 6mA methylation …
We recently got a set of targeted genes sequenced(probably they used novaseq 6000). The panel is an extended brca panel for hereditary breast cancer screening. …
