Hi all, I'm using this code as a toy example to see if I understand how ggseqlogo works ```{r} # Create a data frame with …

I am wanting to extract the sequences in a fasta file as specific positions. I have downloaded my fasta file (f) in r by using …

Hi all, I am using the following code to make a scatter plot for a few genes. I could be able to change the Y-axis …

Hi! I need help with solving the following question with Python3: Write a Python program that reads a fastq file and calculate how many bases …

I would like to increase the font size of only the y axis ticks: ```sc.pl.dotplot(data, ["gene"], 'CellType',figsize=(4,10), dendrogram=False)``` Using ```plt.rcParams.update({'ytick.labelsize': 50})``` doesn’t work. Updating rcParams …

As part of a project I am working on I would like to align a sequence using Bowtie and then in addition to that alignment …

I have 10000 entries as a fasta file that contains nucleotide sequences of length 5. Eg:- AGGTC, AGCTC, CGCTC, .... 10000 entries. Now I have …

I have `RNAseq` data and trying to get the coverage of the reads over coding sequence but only for one gene for example `GAPDH`. and …

I am trying to understand how the X axis and Y- axis labeled; X -axis as Rank and Y is as fraction of read coverage …

<p>HI all,</p> <p>I have generated the read count data for my genomic locations using <a href='https://code.google.com/p/bedtools/'>bedtools</a>. I need to plot the read count with all …