keenhl

Results 10 issues of keenhl

Can Jellyfish read gzipped fastq files and, if not, can uncompressed fastq be piped into Jellyfish. Thanks,

Hi all, I tried to do gene prediction with Quast, but the process failed due to error. Quast was ran with the following gene prediction options: --eukaryote --gene-finding The error...

We have fast5 files generating using the RNA002 chemistry. We are interested in determining the methylation status (5mc) of these reads. How do we proceed to do this Bonito? Alternatively,...

We are trying to detect a deletion using Nanopore long read data. We think that the size of the deletion is something around 10-15 kb in size, although we are...

If a significant change in methylation is detected, at which base pair is this change? Is it the position indicated by the pos column or perhaps the middle of the...

If a significant change in methylation is determined at a particular position, how can one determine the direction of change. In other words, is there any way to determine if...

> devtools::install_github('satijalab/seurat-data') Using GitHub PAT from the git credential store. Error: Failed to install 'unknown package' from GitHub: HTTP error 401. Bad credentials Rate limit remaining: 51/60 Rate limit reset...

If you have an RNA sequence with U's, the U's will have to be converted to T's to get an alignment. Just something users might want to be aware of.

I am interested in combining methylation data. For example, I would like to combine cgXXXXXX_BC21 and cgXXXXXX_TC21 into a single value. There is a function in the sesame package called...

I have Tensorflow installed. When I check the version, it is 2.12. tensorflow::tf_config() 2023-02-27 15:55:21.780906: I tensorflow/core/platform/cpu_feature_guard.cc:182] This TensorFlow binary is optimized to use available CPU instructions in performance-critical operations....