Error loading paramSweep_v3 in DoubletFinder in R...

How to count number of occurrence consecutive pattern spanning over lines in Bash?...

Error in breseq during running bowtie2...

Nextflow No such variable: id...

Phasing genomes with shapeit5...

p.adjust with n < than number of tests...

How to get genotype data of SNVs from several new bam files?...

AWK to handle bed files...

How to use AWK for printing a line only if that line is different from the previous one?...

AnnotationHub Resource | Failed to load Resource | Download Issue in R...

Extracting certain locus from multiple samples from text file...

Loading a huge fastq file in biopython with FastqGeneralIterator...

How do I rewrite this expected depth of (genome) coverage function in R?...

awk: cmd. line:1:fatal: division by zero attempted...

Tab file mix up column when loading into R...

Can anyone tell me how to replace strings with floats in an np.array(of several genotypes) by freque...

How to generate a custom bed file to use for bedtools intersect?...

Interactive Manhattan plot with string chromosome names...

Pivotting the SNP Table , Converting CSV file to JSON using Bash...

If position from File B is found in interval of file A, print to new dataframe...

select uniquely mapped genes to SNP...

Using the NEAT Algorithm, will a child of two genomes always have the same structure as the most fit...

Finding overlaps between 2 ranges and their overlapped region lengths?...

How do I run this Bismark Bisulfite Sequencing program?...

Errors compiling Platanus v1.2.4 Genome Assembler on Mac OSX Big Sur...

R hypergeometric test between a character vector and a list, calculating p values in a loop...

create list of organisms based on pattern matching of sequence to a genome...

Looping over an R function...

Extracting lines of text depending on the len() of a particular column...

How to save Variant Call Format (VCF) file to disk in R using VariantAnnotation Package...