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User: bioinformatics2020

gravatar for bioinformatics2020
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Posts by bioinformatics2020

<prev • 43 results • page 1 of 5 • next >
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Answer: A: New to NGS
... Support the website you're posting on AND learn about NGS/bioinformatics: https://www.biostarhandbook.com/ ...
written 1 day ago by bioinformatics2020 • 340
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Comment: C: How to extract identical characters in multiple text files?
... Could you give an example of how these BLASTp result files look like? ...
written 3 days ago by bioinformatics2020 • 340
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Comment: C: How to sum the genewise counts in edgeR ?
... Rpolicastro - I love seeing your tidyverse-esque responses on here. I always end up learning something new from ya. Quick question though. Whenever you create a sample data.frame, you always use this framework: structure(list(...... row.names = c(NA, -24L), class = "data.frame") Any reas ...
written 5 days ago by bioinformatics2020 • 340
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Comment: C: Loop in R script
... I made some minor adjustments! Please try now. :) ...
written 10 days ago by bioinformatics2020 • 340
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Comment: C: Loop in R script
... Can you send me what one of these files look like inside? ...
written 11 days ago by bioinformatics2020 • 340
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Comment: C: file handling in R
... Appreciate the tips! Edited my original post. ...
written 13 days ago by bioinformatics2020 • 340
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Answer: A: file handling in R
... if(!require("tidyverse")) install.packages("tidyverse") files <- purrr::map_dfr(list.files(pattern = "\\.txt$"), read_tsv) Then if you only want the Genes column: files <- files$Genes ...
written 13 days ago by bioinformatics2020 • 340
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Answer: A: How to extract a peptide sequence (interval) from a FASTA file?
... library(Biostrings) fa <- readBStringSet("file.fa") intervals <- read_tsv("intervals.txt") for(i in seq_along(fa)){ fa[[i]] <- subseq(fa[[i]], start = intervals$start[[i]], end = intervals$end[[i]]) } writeXStringSet(fa, "file.fa") ...
written 13 days ago by bioinformatics2020 • 340
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Comment: C: Loop in R script
... The main reason here was because I wanted to use `imap`, which allows you to iterate over the list of objects and their indices, and so I just wanted to be consistent throughout the calls. ...
written 13 days ago by bioinformatics2020 • 340
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Answer: A: Loop in R script
... Put this in the directory where you have the 200 files. Make sure you don't have any other text files because it uses the `list.files()` function to look for .txt files. if(!require("tidyverse")) install.packages("tidyverse") if(!require("magrittr")) install.packages("magrittr") libr ...
written 13 days ago by bioinformatics2020 • 340

Latest awards to bioinformatics2020

Popular Question 8 days ago, created a question with more than 1,000 views. For For CreateSeuratObject, Where Do the Values for min.cells and min.features come from?
Scholar 12 days ago, created an answer that has been accepted. For A: software of single-cell RNA-seq from fastq or fasta
Teacher 12 days ago, created an answer with at least 3 up-votes. For A: software of single-cell RNA-seq from fastq or fasta
Scholar 15 days ago, created an answer that has been accepted. For A: software of single-cell RNA-seq from fastq or fasta
Popular Question 22 days ago, created a question with more than 1,000 views. For Finding All Genes (Differential or Not) in Seurat's FindAllMarkers
Commentator 3 months ago, created a comment with at least 3 up-votes. For C: scVelo on Seurat umap
Popular Question 4 months ago, created a question with more than 1,000 views. For In Seurat, How Do nCount_RNA Differ from nFeature_RNA?
Scholar 6 months ago, created an answer that has been accepted. For A: software of single-cell RNA-seq from fastq or fasta
Teacher 6 months ago, created an answer with at least 3 up-votes. For A: software of single-cell RNA-seq from fastq or fasta
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