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 Editor
First edit.
Awarded 626 times.
Detect differentially expressing cells
Awarded Dec 9 at 11:30
Which of these enzymes is a better target for virtual screening?
Awarded Dec 8 at 7:00
how to solve “dim(X) must have a positive length” at running ComBat function in R
Awarded Dec 2 at 15:05
How can I run a command for multiple files?
Awarded Dec 2 at 2:35
Simulating phenotype with the 1000 Genomes Project
Awarded Dec 1 at 16:25
Converting Gene Symbol to Ensembl ID in R
Awarded Nov 29 at 16:20
GATK 4.1.4.0 Mutect stats output
Awarded Nov 28 at 12:45
TBLASTN error: Too many positional arguments
Awarded Nov 28 at 1:10
Whole gene knockout screening and systems biology
Awarded Nov 27 at 16:15
Custom GTF file
Awarded Nov 26 at 13:30
(post deleted or otherwise unavailable)
Awarded Nov 25 at 20:20
Binding columns with matched elements
Awarded Nov 17 at 20:50
different gene expression in the monocle
Awarded Nov 13 at 2:15
How I can change the name of multiple files at once in R or terminal?
Awarded Nov 9 at 22:40
How do researchers account for heterozygosity in genome assembly?
Awarded Nov 6 at 9:55
What are Orthogonal DNA Sequences?
Awarded Nov 3 at 1:55
bed file with N regions of GRCh38 reference?
Awarded Nov 1 at 7:50
CIBERSORT runtime error eval failed
Awarded Oct 31 at 10:35
How to merge two files on the first 3 columns?
Awarded Oct 29 at 18:45
Is re-normalization of RNAseq data recommended for analysis of gene subsets?
Awarded Oct 29 at 16:35
How to do `bedtools intersection` using pandas alone?
Awarded Oct 24 at 7:05
Is there a way to measure cell line similarity using python?
Awarded Oct 23 at 17:15
RNAseq data analysis
Awarded Oct 22 at 9:00
What do the symbols mean in minimap2's gap cost equation?
Awarded Oct 19 at 21:15
read and matching pattern with python
Awarded Oct 15 at 19:20
Smith-Waterman Pairwise Local Alignment Algorithm
Awarded Oct 13 at 15:15
Which correlation method to compute the correlation score between different clusters of Sc-RNAseq data?
Awarded Oct 13 at 12:55
What's the most efficient file format for the storage of DNA sequences?
Awarded Oct 11 at 10:20
RPGC normalisation creates artefacts at centromere
Awarded Oct 10 at 11:00
Convert PAF format to SAM/BAM format
Awarded Oct 9 at 13:20
Coverage required
Awarded Oct 4 at 13:15
Merging two files together
Awarded Oct 3 at 17:20
Merging two files together
Awarded Oct 3 at 5:55
Putting labels of different sizes on one PyMOl Object
Awarded Sep 30 at 16:10
How to edit the headers of multiple fasta files from multiple folders?
Awarded Sep 26 at 15:45
bedtools intersect on very large .bam file - -sorted confusion
Awarded Sep 25 at 21:35
Converting Gene Symbol to Ensembl ID in R
Awarded Sep 25 at 10:40
Identifying Indels from Chromatograms
Awarded Sep 24 at 11:50
How to load and split my two individual datasets when integrating datasets in Seurat?
Awarded Sep 23 at 16:45
Parsing specific features from Genbank by label?
Awarded Sep 21 at 12:25
Biopython Genbank writer not splitting long lines
Awarded Sep 18 at 20:05
TPM or rlog(CPM) for comparing expression?
Awarded Sep 17 at 21:15
Determining the quality of a publicly available genome assembly
Awarded Sep 17 at 8:35
In-sample and across samples normalized expression
Awarded Sep 16 at 12:10
(post deleted or otherwise unavailable)
Awarded Sep 15 at 10:20
Read alignment using Bowtie2
Awarded Sep 12 at 0:05
Dmpfold error “No such file or directory: 'best_qdope.pdb'” when running “run_dmpfold.sh”?
Awarded Sep 11 at 12:30
MiXCR: only create a single export file for all clonotypes
Awarded Sep 11 at 11:25
How to perform DE analysis for each sample
Awarded Sep 11 at 9:45
blast nt vs Genbank
Awarded Sep 10 at 19:00
Understanding Single Cell RNAseq Plots
Awarded Sep 9 at 17:10
(post deleted or otherwise unavailable)
Awarded Sep 5 at 20:45
(post deleted or otherwise unavailable)
Awarded Sep 5 at 9:55
(post deleted or otherwise unavailable)
Awarded Sep 4 at 3:15
How to run function “convolve” in parallel in R?
Awarded Sep 3 at 16:00
Create heat map that groups genes by expression within cluster in Seurat
Awarded Aug 29 at 22:15
How do I create a filtered gene list using expression medians
Awarded Aug 26 at 14:50
Is it valid to apply HMM based CNV calling on targeted sequencing (panel of hundreds of genes)
Awarded Aug 24 at 1:55
How do I create a filtered gene list using expression medians
Awarded Aug 23 at 18:50
(post deleted or otherwise unavailable)
Awarded Aug 23 at 15:05
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