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 Editor
First edit.
Awarded 663 times.
How to filter a SAM file by a bed file?
Awarded 10 hours ago
Scientific names of taxids with kraken 2.0.8 beta, command kraken2 --use-names error
Awarded 2 days ago
How to calculate Centimorgan lengths from run lengths in one-to-one dna profile comparison
Awarded Feb 16 at 11:45
Finding common and unique data set by comparing two files based on their column and to split the columns multiple strings to print in output
Awarded Feb 12 at 11:40
Why does the FASTA sequence for coronavirus look like DNA, not RNA?
Awarded Feb 9 at 18:25
How do I get the compartment Id and volume from SBML using libSBML Python?
Awarded Feb 8 at 8:10
How do I get the compartment Id and volume from SBML using libSBML Python?
Awarded Feb 8 at 1:45
(post deleted or otherwise unavailable)
Awarded Feb 6 at 8:45
Is the quality score of fastq used somewhere besides trimming/fastqc?
Awarded Feb 6 at 7:50
Make a fasta out of mapped reads without taking into account the reference
Awarded Feb 5 at 21:10
Why does this naive Python paired Fastq reader work?
Awarded Feb 5 at 15:50
Bedtools wrongly indicates zero coverage
Awarded Feb 3 at 19:00
A new paper suggests the Corona Virus has “Uncanny similarity of unique inserts in the 2019-nCoV spike protein to HIV-1” - What does this mean?
Awarded Jan 31 at 21:05
samtools / bamUtil | Meaning of <*> as Reference Name
Awarded Jan 30 at 15:00
how to calculate coverage of each base of mapped reads?
Awarded Jan 27 at 15:05
Pulling out a certain gene in a volcano plot
Awarded Jan 25 at 19:50
stacked bargraph with error bars
Awarded Jan 23 at 16:50
Making a boxplot or violinplot for several dataframe with different number of samples
Awarded Jan 23 at 11:05
Is there a point in recalibration of scores for variant calling?
Awarded Jan 22 at 11:10
Boxplot of read length distributions from multiple samples
Awarded Jan 21 at 3:05
Stacked barplot for single cell analysis
Awarded Jan 20 at 23:50
Error in my RNAseq analysis
Awarded Jan 17 at 15:35
Wrong format .ped in PLINK
Awarded Jan 17 at 14:55
How I can push a function to act on my files
Awarded Jan 16 at 20:00
Seurat define manually a cluster and find markers
Awarded Jan 16 at 8:20
Ribosomal RNA QC quantification using SILVA
Awarded Jan 14 at 19:00
'Wildcards' object has no attribute 'sample'
Awarded Jan 14 at 15:55
Genetic Genealogy related to SNP variants and INDEL variants
Awarded Jan 13 at 15:55
Script to allow gene set enrichment analysis of 10x genomics data in R
Awarded Jan 10 at 15:55
Any user friendly way to find rare mutations in whole genome raw?
Awarded Jan 7 at 23:40
Infer the new (Ban et. al) ribosomal nomenlature (ex. uL53 ) from the ribosomal protein's sequence
Awarded Jan 4 at 22:45
Are there any “canonical” sources of C. Elegans connectome?
Awarded Jan 4 at 9:20
(post deleted or otherwise unavailable)
Awarded Dec 28 '19 at 13:40
Parallelizing WGCNA k-means clustering and merging smaller clusters
Awarded Dec 24 '19 at 13:10
What is a read count?
Awarded Dec 24 '19 at 5:35
What should I do when I have “#NAME?” in my Log Fold Change data to calculate Z-score? replace with zero or what?
Awarded Dec 21 '19 at 17:20
“IndexError: list index out of range” in snakemake
Awarded Dec 17 '19 at 23:05
protein secondary structure matching/comparison scoring
Awarded Dec 15 '19 at 16:45
Detect differentially expressing cells
Awarded Dec 9 '19 at 11:30
Which of these enzymes is a better target for virtual screening?
Awarded Dec 8 '19 at 7:00
how to solve “dim(X) must have a positive length” at running ComBat function in R
Awarded Dec 2 '19 at 15:05
How can I run a command for multiple files?
Awarded Dec 2 '19 at 2:35
Simulating phenotype with the 1000 Genomes Project
Awarded Dec 1 '19 at 16:25
Converting Gene Symbol to Ensembl ID in R
Awarded Nov 29 '19 at 16:20
GATK 4.1.4.0 Mutect stats output
Awarded Nov 28 '19 at 12:45
TBLASTN error: Too many positional arguments
Awarded Nov 28 '19 at 1:10
CRISPR screening and systems biology
Awarded Nov 27 '19 at 16:15
(post deleted or otherwise unavailable)
Awarded Nov 26 '19 at 13:30
(post deleted or otherwise unavailable)
Awarded Nov 25 '19 at 20:20
Binding columns with matched elements
Awarded Nov 17 '19 at 20:50
different gene expression in the monocle
Awarded Nov 13 '19 at 2:15
How I can change the name of multiple files at once in R or terminal?
Awarded Nov 9 '19 at 22:40
How do researchers account for heterozygosity in genome assembly?
Awarded Nov 6 '19 at 9:55
What are Orthogonal DNA Sequences?
Awarded Nov 3 '19 at 1:55
bed file with N regions of GRCh38 reference?
Awarded Nov 1 '19 at 7:50
CIBERSORT runtime error eval failed
Awarded Oct 31 '19 at 10:35
How to merge two files on the first 3 columns?
Awarded Oct 29 '19 at 18:45
Is re-normalization of RNAseq data recommended for analysis of gene subsets?
Awarded Oct 29 '19 at 16:35
How to do `bedtools intersection` using pandas alone?
Awarded Oct 24 '19 at 7:05
Is there a way to measure cell line similarity using python?
Awarded Oct 23 '19 at 17:15
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