Top new questions this week:
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I am trying to get dot-bracket-notations of single stranded RNA via the ViennaRNA python package (pypi.org/project/ViennaRNA/) at different temperatures. I have read in the docs (www….
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I’m using the following script to detect strandedness of my paired end RNA-seq data. …
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So I have been trying to get into visualizing proteins in python, so after some research I ended up on a tutorial that was teaching you how to visualize a protein from the COVID-19 virus, so I went …
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This question was also asked on Biostars I am using CNVkit on my data using hg38 as reference. The command that I am using is the following: …
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I’m conducting a simulation and I need to obtain polygenic risk scores (PRS) using genome wide association studies (GWAS) summary statistics. It is known that the GWAS will give BETA and OR for …
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I’d like to run dotPlotly from RStudio but I can’t find any description/help for this. Is it at all possible? Another side to this question: does anyone know any tool for dot plots for genome …
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I would like to extract date of acquisiton from mzXML and mzML files, using Python. Is it possible e.g. with Pyteomics? pymzml is only for mzML files. Are there other libraries that can do that? I …
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Greatest hits from previous weeks:
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I have a tab separated text file as shown below …
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I am learning about NGS analysis and im currently learning about QCing and removing adaptors. I am working on SRR1972920_1.fastq file. When running fastqc tool on that file, adapter contamination …
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I have a fasta file like >sample 1 gene 1 atgc >sample 1 gene 2 atgc >sample 2 gene 1 atgc I want to get the following output, with one break between …
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I have following accession numbers of the 10 chromosomes of Theobroma cacao genome. …
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In Seurats‘ documentation for FindClusters() function it is written that for around 3000 …
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I have a DNA sequence for which I would like to quickly find the reverse complement. Is there a quick way of doing this on the bash command line using only GNU tools?
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I would like to merge more than two sample in the Seurat, and the mergeseurat can only merge two sample. So what should I do now. The screenshot is my script.
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Can you answer these questions?
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Hi there I’m new to WDL and I need to complete a two-step workflow, Basically, what I need to do is to extract and merge two reads dataset (forward and reverse) for a sample and pass the merged, …
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I have a sequence of pdb files which I want to load in pymol window so that it gives an impression of a video. I am using cmd.load function in a loop and deleting the loaded file in the next step. But …
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I am trying to extract data from fast5-file with python 3.9.13 in Ubuntu. I have found a library “fast5_research”(This package comprises an API to HDF containers used by the research groups …
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